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        <title>Histochemistry and Cell Biology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Histochemistry and Cell Biology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Histochemistry+and+Cell+Biology&t=Histochemistry+and+Cell+Biology&s=Search&f=source]]></link>
        <lastBuildDate>Sat, 20 Mar 2010 16:02:49 +0100</lastBuildDate>
        <item>
            <title>A comparative analysis of oncofetal fibronectin and tenascin-C incorporation in tumour vessels using human recombinant SIP format antibodies</title>
            <link>http://www.medworm.com/index.php?rid=3377657&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw57427050q778765%2F</link>
            <description>In conclusion, tumours differ in the pattern of Fn or Tn-C isoform positivity in the vessel wall, potentially
 representing a tumour type specific endothelial cell–tumour cell–stromal cell interaction. Carcinoma cells themselves are
 involved in vascular Tn-C matrix organization. Up to antigen distribution, Fn and Tn-C domain antibodies may serve as vehicles
 for antiangiogenetic and antifibrotic agents; oncFn/oncTn-C based targeting should be adapted individually.
 
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-010-0685-yAuthors
		Alexander Berndt, University Hospital Jena Institute of Pathology Ziegelmühlenweg 1 07743 Jena GermanyRobert Köllner, University Hospital Jena Institute of Pathology Ziegelmühlenweg 1 07743 Jena GermanyPetra Richter, University ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3377657</comments>
            <pubDate>Tue, 16 Mar 2010 14:49:23 +0100</pubDate>
            <guid isPermaLink="false">3377657</guid>        </item>
        <item>
            <title>Effects of dissolucytotic gold ions on recovering brain lesions</title>
            <link>http://www.medworm.com/index.php?rid=3377658&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm436361300056j43%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recent experimental research has shown that metallic gold releases charged gold atoms when placed intracerebrally and that
 the liberated gold ions affect inflammation in the brain. The observations suggest that metallic gold can be used as a safe
 suppressor of inflammation in the central nervous system.
 
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00418-010-0681-2Authors
		Gorm Danscher, University of Aarhus Department of Anatomy and Neurobiology 8000 Aarhus C DenmarkAgnete Larsen, University of Aarhus Department of Anatomy and Neurobiology 8000 Aarhus C Denmark
	

	
		Journal Histochemistry and Cell BiologyOnline ISSN 1432-119XPrint ISSN 0948-6143 (Source: Histochemistry and Cell Biology)</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3377658</comments>
            <pubDate>Tue, 16 Mar 2010 14:49:22 +0100</pubDate>
            <guid isPermaLink="false">3377658</guid>        </item>
        <item>
            <title>Developmental regulation of TRPC3 ion channel expression in the mouse cochlea</title>
            <link>http://www.medworm.com/index.php?rid=3369633&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F02336580380v845q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Canonical transient receptor potential type 3 (TRPC3) ion channels assemble from TRPC3 subunits and exhibit multiple activation
 mechanisms. TRPC3 has been proposed to contribute to Ca2+ entry supporting Ca2+ homeostasis in cochlear hair cells and to be activated by G protein-coupled receptor (GPCR) signaling in spiral ganglion
 neurons. The present study was designed to determine the spatiotemporal profile of TRPC3 expression during mouse cochlear
 ontogeny. TRPC3 immunofluorescence of cryosectioned cochleae was performed using E16–adult tissue. We found that prior to
 birth, TRPC3 expression was strongest in epithelial cells that form the cochlear partition. In the early postnatal period,
 to the onset of hearing (~P12), immunofluorescence was strongest in the hair ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3369633</comments>
            <pubDate>Sun, 14 Mar 2010 11:27:48 +0100</pubDate>
            <guid isPermaLink="false">3369633</guid>        </item>
        <item>
            <title>Differential expression of stem cell markers in human follicular bulge and interfollicular epidermal compartments</title>
            <link>http://www.medworm.com/index.php?rid=3369634&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy5031l5407200765%2F</link>
            <description>In this study, we whole mounted single human scalp hair follicles and examined
 their profiles using in situ immunohistochemistry and multicolor immunofluorescence in search of markers to distinguish between
 stem cells residing in the interfollicular epidermis (IFE) and bulge. Our study revealed that expression of several biomarkers
 localized uniquely to the basal IFE (CD34 and CD117), bulge region (CD200), or both (CK15, CD49f, and CD29). In addition,
 we found that both basal IFE and bulge stem cells did not express CD71 or CD24 suggesting their potential utility as negative
 selection markers. Dermal papilla but not basal IFE or bulge stem cells expressed CD90, making it a potential positive selection
 marker for dermal hair follicle stem cells. The markers tested in this study may en...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3369634</comments>
            <pubDate>Sun, 14 Mar 2010 11:27:47 +0100</pubDate>
            <guid isPermaLink="false">3369634</guid>        </item>
        <item>
            <title>Developmentally regulated expression of ectonucleotidases NTPDase5 and NTPDase6 and UDP-responsive P2Y receptors in the rat cochlea</title>
            <link>http://www.medworm.com/index.php?rid=3358218&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg773j07615p28072%2F</link>
            <description>This study reports the changes in expression of NTPDase5 and NTPDase6
 in the developing rat cochlea. These two intracellular members of the E-NTPDase family can be released in a soluble form and
 show preference for nucleoside 5′-diphosphates, such as UDP and GDP. Here, we demonstrate differential spatial and temporal
 patterns for NTPDase5 and NTPDase6 expression during cochlear development, which are indicative of both cytosolic and extracellular
 action via pyrimidines. NTPDase5 is noted during the early postnatal period in developing sensory hair cells and supporting
 Deiters’ cells of the organ of Corti, and primary auditory neurons located in the spiral ganglion. In contrast, NTPDase6 is
 confined to the embryonic and early postnatal hair cell bundles. NTPDase6 immunolocalisatio...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3358218</comments>
            <pubDate>Wed, 10 Mar 2010 16:14:07 +0100</pubDate>
            <guid isPermaLink="false">3358218</guid>        </item>
        <item>
            <title>Cell uptake of Zn(II)-phthalocyanine-containing liposomes by clathrin-mediated endocytosis</title>
            <link>http://www.medworm.com/index.php?rid=3315901&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr37h72560476r221%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The study of uptake mechanisms of therapeutic drugs has a growing interest in biomedical research. In this work the cell uptake
 and phototoxicity of the photosensitizer Zn(II)-phthalocyanine (ZnPc) in dipalmitoyl-phosphatidyl-choline liposomes have been
 studied in the presence or absence of inhibitors of macropinocytosis (cytochalasin D), and clathrin-mediated endocytosis (dynasore).
 No differences in the uptake or photodynamic damage were observed in A-549 cells subjected to incubation with either ZnPc
 alone or in combination with cytochalasin D. On the contrary, co-incubation of A-549 cells with ZnPc and dynasore resulted
 in a significant decrease of photodamage as well as negligible uptake of the photosensitizer. These results indicate that
 ZnPc is internalized...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3315901</comments>
            <pubDate>Fri, 26 Feb 2010 09:49:40 +0100</pubDate>
            <guid isPermaLink="false">3315901</guid>        </item>
        <item>
            <title>A pitfall in using BODIPY dyes to label lipid droplets for fluorescence microscopy</title>
            <link>http://www.medworm.com/index.php?rid=3315900&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F284155481446gu13%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The lipid droplet (LD) has become a focus of intense research. Fluorescence labeling is indispensable for the cell biological
 analysis of the LD, and a lipophilic fluorescence dye, BODIPY 493/503, which emits bright green fluorescence has been used
 extensively for LD labeling. The dye is convenient for double fluorescence labeling, but we noticed that it emits red fluorescence
 under certain conditions, which could lead to erroneous interpretations. We propose a protocol to preclude such a possibility.
 
 
	Content Type Journal ArticleCategory Short communicationDOI 10.1007/s00418-010-0678-xAuthors
		Yuki Ohsaki, Nagoya University Graduate School of Medicine Department of Anatomy and Molecular Cell Biology 65 Tsurumai, Showa Nagoya 466-8550 JapanYuki Shinohara, Nagoya...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3315900</comments>
            <pubDate>Fri, 26 Feb 2010 09:49:40 +0100</pubDate>
            <guid isPermaLink="false">3315900</guid>        </item>
        <item>
            <title>Albumin-based nanoparticles as magnetic resonance contrast agents: I. Concept, first syntheses and characterisation</title>
            <link>http://www.medworm.com/index.php?rid=3297774&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F86047745278405pl%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To develop a platform for molecular magnetic resonance imaging, we prepared gadolinium-bearing albumin-polylactic acid nanoparticles
 in the size range 20–40&amp;nbsp;nm diameter. Iterative cycles of design and testing upscaled the synthesis procedures to gram amounts
 for physicochemical characterisation and for pharmacokinetic testing. Morphological analyses showed that the nanoparticles
 were spheroidal with rough surfaces. Particle sizes were measured by direct transmission electron microscopical measurements
 from negatively contrasted preparations, and by use of photon correlation spectroscopy; the two methods each documented nanoparticle
 sizes less than 100&amp;nbsp;nm and generally 10–40&amp;nbsp;nm diameter, though with significant intrabatch and interbatch variabilit...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3297774</comments>
            <pubDate>Sat, 20 Feb 2010 06:50:20 +0100</pubDate>
            <guid isPermaLink="false">3297774</guid>        </item>
        <item>
            <title>Similar developmental patterns in immunolocalisation of stem cell factor and KIT in bovine meso- and metanephros</title>
            <link>http://www.medworm.com/index.php?rid=3287169&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F22m529g25p073q50%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The mesonephros is often regarded as a simplified version of the terminal renal organ, the metanephros. Both renal organs
 result from an epithelio-mesenchymal interaction between the Wolffian duct and the nephrogenic ridge. It appears that the
 epithelio-mesenchymal interaction makes use of similar signal cascades for both renal organs and that key events required
 for the development of the metanephros occur at earlier stages. In murine metanephroi, the stem cell factor (SCF)/-KIT-signal transduction pathway has recently been shown to regulate ureteric
 bud branching and epithelial cell differentiation. We immunohistochemically defined the time-sequence of KIT and SCF presence
 in both renal organs using bovine embryos/foetuses with crown rump length (CRL) of 1.7–24...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3287169</comments>
            <pubDate>Wed, 17 Feb 2010 18:27:55 +0100</pubDate>
            <guid isPermaLink="false">3287169</guid>        </item>
        <item>
            <title>Spatio-temporal changes of SDF1 and its CXCR4 receptor in the dorsal root ganglia following unilateral sciatic nerve injury as a model of neuropathic pain</title>
            <link>http://www.medworm.com/index.php?rid=3243111&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frn4568715q2833n0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is a growing evidence that chemokines and their receptors play a role in inducing and maintaining neuropathic pain.
 In the present study, unilateral chronic constriction injury (CCI) of rat sciatic nerve under aseptic conditions was used
 to investigate changes for stromal derived factor-1 (SDF1) and its CXCR4 receptor in lumbal (L4–L5) and cervical (C7–C8) dorsal
 root ganglia (DRG) from both sides of naïve, CCI-operated and sham-operated rats. All CCI-operated rats displayed mechanical
 allodynia and thermal hyperalgesia in hind paws ipsilateral to CCI, but forepaws exhibited only temporal changes of sensitivity
 not correlated with alterations in SDF1 and CXCR4 proteins. Naïve DRG displayed immunofluorescence for SDF1 (SDF1-IF) in the
 satellite glial ce...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3243111</comments>
            <pubDate>Tue, 02 Feb 2010 17:48:11 +0100</pubDate>
            <guid isPermaLink="false">3243111</guid>        </item>
        <item>
            <title>Thymic stromal lymphopoietin induces tight junction protein claudin-7 via NF-κB in dendritic cells</title>
            <link>http://www.medworm.com/index.php?rid=3193080&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F65020220v671r417%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Epithelial-derived thymic stromal lymphopoietin (TSLP) is an IL-7-like cytokine that triggers dendritic cell (DC)-mediated
 Th2-type inflammatory responses. The activated DCs can penetrate the epithelium to directly take up antigen without compromising
 the barrier function. Although it is reported that DCs express tight junction molecules and can establish tight junction-like
 structures with adjacent epithelial cells to preserve the epithelial barrier, the regulation of expression of tight junction
 molecules in DCs remains unknown. In the present study, to investigate the mechanical regulation of expression of tight junction
 molecules in DCs, XS52 DCs that was a long-term DC line established from the epidermis of a newborn BALB/c mouse, were treated
 with TSLP or to...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3193080</comments>
            <pubDate>Fri, 15 Jan 2010 00:42:28 +0100</pubDate>
            <guid isPermaLink="false">3193080</guid>        </item>
        <item>
            <title>Extensive infiltration of neutrophils in the acute phase of experimental autoimmune encephalomyelitis in C57BL/6 mice</title>
            <link>http://www.medworm.com/index.php?rid=3163188&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff401h5u471213x53%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To determine the possible involvement of neutrophils in the pathogenesis of experimental autoimmune encephalomyelitis (EAE),
 we examined their infiltration pattern during the course of MOG35–55-induced EAE in the C57BL/6 mice. Using immunohistochemistry and flow cytometry, we found that the number of neutrophils was
 significantly increased during onset of disease, remained high at the peak stage and dramatically declined thereafter. Moreover,
 dual labeling provided anatomical evidence of a prominent accumulation of neutrophils in the center and vicinity of lesion
 areas of demyelination, axonal loss or axonal degeneration at early stages of EAE. These observations provide evidence that
 neutrophils are one of the major sources of inflammatory cells to initiate EAE,...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3163188</comments>
            <pubDate>Sat, 09 Jan 2010 08:32:27 +0100</pubDate>
            <guid isPermaLink="false">3163188</guid>        </item>
        <item>
            <title>Characterization of endocytic compartments after holo-high density lipoprotein particle uptake in HepG2 cells</title>
            <link>http://www.medworm.com/index.php?rid=3128720&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F01w0r7528517454g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Holo-high density lipoprotein (HDL) particle uptake, besides selective lipid uptake, constitutes an alternative pathway to
 regulate cellular cholesterol homeostasis. In the current study, the cellular path of holo-HDL particles was investigated
 in human liver carcinoma cells (HepG2) using combined light and electron microscopical methods. The apolipoprotein moiety
 of HDL was visualized with different markers: horseradish peroxidase, colloidal gold and the fluorochrome Alexa568, used in fluorescence microscopy and after photooxidation correlatively at the ultrastructural level. Time course experiments
 showed a rapid uptake of holo-HDL particles, an accumulation in endosomal compartments, with a plateau after 1–2&amp;nbsp;h of continuous
 uptake, and a clearance 1–2&amp;n...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3128720</comments>
            <pubDate>Mon, 28 Dec 2009 19:14:06 +0100</pubDate>
            <guid isPermaLink="false">3128720</guid>        </item>
        <item>
            <title>In vivo liberation of silver ions from metallic silver surfaces</title>
            <link>http://www.medworm.com/index.php?rid=3123290&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flt151g634958681h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In vivo liberation of electrically charged silver atoms/silver ions from metallic silver pellets, silver grids and silver
 threads placed in the brain, skin and abdominal cavity was proved by way of the histochemical technique autometallography
 (AMG). A bio-film or “dissolution membrane” inserted between the metallic surface and macrophages was recognized on the surface
 of the implanted silver after a short period of time. Bio-released silver ions bound in silver–sulphur nanocrystals were traced
 within the first 24&amp;nbsp;h in the “dissolution membrane” and the “dissolucytotic” macrophages. In animals that had survived 10&amp;nbsp;days
 or more, silver nanocrystals were detected both extra- and intracellularly in places far away from the implant including reg...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3123290</comments>
            <pubDate>Thu, 24 Dec 2009 19:56:46 +0100</pubDate>
            <guid isPermaLink="false">3123290</guid>        </item>
        <item>
            <title>Dynamic movements of Ro52 cytoplasmic bodies along microtubules</title>
            <link>http://www.medworm.com/index.php?rid=3106600&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fem6261p1835012w8%2F</link>
            <description>In this study, we investigated the Ro52 cytoplasmic bodies using fluorescence microscopy. This analysis
 revealed that the Ro52 cytoplasmic bodies are diffusely located in the cytoplasm and exist independently of TRIM5α cytoplasmic
 bodies. Our results further showed that the Ro52 cytoplasmic bodies are not stained with MitoTracker dye and are not colocalized
 with the proteasome subunit Rpt5, the caveolae component caveolin-1, the endosome markers (EEA1, Rab5, and Rab7), and the
 lysosome marker LAMP2. These results indicate that the Ro52 cytoplasmic bodies are not mitochondria, proteasome-enriched structures,
 caveolae, endosomes, or lysosomes. Importantly, the Ro52 cytoplasmic bodies are highly motile and are located along the microtubule
 network. These results suggest that the Ro52 c...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3106600</comments>
            <pubDate>Wed, 16 Dec 2009 07:01:23 +0100</pubDate>
            <guid isPermaLink="false">3106600</guid>        </item>
        <item>
            <title>Age-dependent axonal expression of potassium channel proteins during development in mouse hippocampus</title>
            <link>http://www.medworm.com/index.php?rid=3088657&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc05111n8j2703884%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The development of the hippocampal network requires neuronal activity, which is shaped by the differential expression and
 sorting of a variety of potassium channels. Parallel to their maturation, hippocampal neurons undergo a distinct development
 of their ion channel profile. The age-dependent dimension of ion channel occurrence is of utmost importance as it is interdependently
 linked to network formation. However, data regarding the exact temporal expression of potassium channels during postnatal
 hippocampal development are scarce. We therefore studied the expression of several voltage-gated potassium channel proteins
 during hippocampal development in vivo and in primary cultures, focusing on channels that were sorted to the axonal compartment.
 The Kv1.1, Kv1.2, ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3088657</comments>
            <pubDate>Sat, 12 Dec 2009 14:16:41 +0100</pubDate>
            <guid isPermaLink="false">3088657</guid>        </item>
        <item>
            <title>Murine mCLCA5 is expressed in granular layer keratinocytes of stratified epithelia</title>
            <link>http://www.medworm.com/index.php?rid=3088658&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwk395x084h50v445%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;CLCA proteins represent a large family of proteins widely expressed in mammalian tissues with a unique expression pattern
 for each family member analyzed so far. However, their functions in normal and diseased tissues are poorly understood. Here,
 we present the cellular expression pattern of mCLCA5 in murine tissues using immunohistochemistry, confocal laser scanning
 microscopy and immune electron microscopy with specific antibodies and RT-qPCR following laser-capture microdissection. The
 mCLCA5 protein was localized to granular layer keratinocytes of virtually all stratified squamous epithelia of the body. Biochemical
 protein characterizations revealed that the amino-terminal cleavage product is fully secreted by the cell, while the carboxy-terminal
 cleavage prod...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3088658</comments>
            <pubDate>Fri, 11 Dec 2009 06:52:24 +0100</pubDate>
            <guid isPermaLink="false">3088658</guid>        </item>
        <item>
            <title>Dilated cardiomyopathy alters the expression patterns of CAR and other adenoviral receptors in human heart</title>
            <link>http://www.medworm.com/index.php?rid=3066376&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy4u32254482l5450%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Gene therapy trials for heart failure have demonstrated the key role of efficient gene transfer in achieving therapeutic efficacy.
 An attractive approach to improve adenoviral gene transfer is to use alternative virus serotypes with modified tropism. We
 performed a detailed analysis of cardiac expression of receptors for several adenovirus serotypes with a focus on differential
 expression of CAR and CD46, as adenoviruses targeting these receptors have been used in various applications. Explanted hearts
 from patients with DCM and healthy donors were analyzed using Q-RT-PCR, western blot and immunohistochemistry. Q-RT-PCR and
 Western analyses revealed robust expression of all receptors except CD80 in normal hearts with lower expression levels in
 DCM. Immunohistochem...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3066376</comments>
            <pubDate>Tue, 01 Dec 2009 20:57:22 +0100</pubDate>
            <guid isPermaLink="false">3066376</guid>        </item>
        <item>
            <title>Histochemical approach of cryobiopsy for glycogen distribution in living mouse livers under fasting and local circulation loss conditions</title>
            <link>http://www.medworm.com/index.php?rid=3055941&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F738641658264594l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Soluble proteins and glycogen particles, which are easily lost upon conventional chemical fixation, have been reported to
 be better preserved in paraffin-embedded sections by ‘cryobiopsy’ combined with freeze-substitution fixation (FS). In this
 study, we examined the distribution of glycogen in living mouse livers under physiologic and pathologic conditions with periodic
 acid-Schiff (PAS) staining by cryobiopsy. The livers of the fully fed mice showed high PAS-staining intensity in the cytoplasm
 of all hepatocytes. The PAS-staining intensity gradually decreased away from hepatocytes around portal tracts, depending on
 treatments with different α-amylase concentrations. At 6 or 12&amp;nbsp;h after fasting, PAS-staining intensity markedly decreased
 in restricted are...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3055941</comments>
            <pubDate>Tue, 01 Dec 2009 08:30:02 +0100</pubDate>
            <guid isPermaLink="false">3055941</guid>        </item>
        <item>
            <title>Expression of P2X6 receptors in the enteric nervous system of the rat gastrointestinal tract</title>
            <link>http://www.medworm.com/index.php?rid=3043897&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq1n56783332422xj%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Expression of P2X4 and P2X6 receptor subunits in the gastrointestinal tract of the rat was studied with double-labeling fluorescence immunohistochemistry.
 The results showed that P2X6 receptors were expressed widely in the submucosal and myenteric plexuses. In the myenteric plexus, P2X6 receptors were expressed mainly in large size neurons which resembled Dogiel type II neurons. These P2X6 receptor-immunoreactive (ir) neurons also expressed calbindin 28K, calretinin and neuronal nuclei (NeuN), proteins that are
 markers of intrinsic sensory neurons. In the submucosal plexus, all the calbindin 28K, calretinin and NeuN-ir cells were immunoreactive
 for P2X6 receptors. P2X6 receptors do not form homomultimers, but rather heteromultimers with either P2X2 or P2X4 receptors....</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3043897</comments>
            <pubDate>Sat, 28 Nov 2009 07:03:23 +0100</pubDate>
            <guid isPermaLink="false">3043897</guid>        </item>
        <item>
            <title>Extending the knowledge in histochemistry and cell biology</title>
            <link>http://www.medworm.com/index.php?rid=3043896&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F93gv712395875n16%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central to modern Histochemistry and Cell Biology stands the need for visualization of cellular and molecular processes. In the past several years, a variety of techniques
 has been achieved bridging traditional light microscopy, fluorescence microscopy and electron microscopy with powerful software-based
 post-processing and computer modeling. Researchers now have various tools available to investigate problems of interest from
 bird’s- up to worm’s-eye of view, focusing on tissues, cells, proteins or finally single molecules. Applications of new approaches
 in combination with well-established traditional techniques of mRNA, DNA or protein analysis have led to enlightening and
 prudent studies which have paved the way toward a better understanding of not only phys...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3043896</comments>
            <pubDate>Sat, 28 Nov 2009 07:03:23 +0100</pubDate>
            <guid isPermaLink="false">3043896</guid>        </item>
        <item>
            <title>Erratum to: Distribution of vitamin D binding protein expressing neurons in the rat hypothalamus</title>
            <link>http://www.medworm.com/index.php?rid=3043898&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fym90p28t32x214rp%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s00418-009-0664-3Authors
		Gustav F. Jirikowski, Friedrich Schiller Universität Jena, PF Department of Anatomy II Jena GermanyUlrike W. Kaunzner, Rockefeller University Laboratory of Neuroendocrinology New York NY USAAbeer El Emmam Dief, University of Alexandria Department of Physiology Alexandria EgyptJack D. Caldwell, Lake Erie College of Osteopathic Medicine Erie PA USA
	

	
		Journal Histochemistry and Cell BiologyOnline ISSN 1432-119XPrint ISSN 0948-6143 (Source: Histochemistry and Cell Biology)</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3043898</comments>
            <pubDate>Sat, 28 Nov 2009 07:03:22 +0100</pubDate>
            <guid isPermaLink="false">3043898</guid>        </item>
        <item>
            <title>Cytokeratin expression during mouse embryonic and early postnatal mammary gland development</title>
            <link>http://www.medworm.com/index.php?rid=3043899&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu317727365h12v67%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cytokeratins are intermediate filament proteins found in most epithelial cells including the mammary epithelium. Specific
 cytokeratin expression has been found to mark different epithelial cell lineages and also to associate with putative mammary
 stem/progenitor cells. However, a comparative analysis of the expression of cytokaratins during embryonic and postnatal mammary
 development is currently lacking. Moreover, it is not clear whether the different classes of putative mammary stem/progenitor
 cells exist during embryonic development. Here, we use double/triple-label immunofluorescence and immunohistochemistry to
 systematically compare the expression of cytokeratin 5 (K5), cytokeratin 6 (K6), cytokeratin 8 (K8), cytokeratin 14 (K14)
 and cytokeratin 19 (K19) in e...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3043899</comments>
            <pubDate>Wed, 25 Nov 2009 16:50:01 +0100</pubDate>
            <guid isPermaLink="false">3043899</guid>        </item>
        <item>
            <title>Head and neck squamous cancer stromal fibroblasts produce growth factors influencing phenotype of normal human keratinocytes</title>
            <link>http://www.medworm.com/index.php?rid=3016889&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqk40q4l8875j58jh%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Epithelial–mesenchymal interaction between stromal fibroblasts and cancer cells influences the functional properties of tumor
 epithelium, including the tumor progression and spread. We compared fibroblasts prepared from stroma of squamous cell carcinoma
 and normal dermal fibroblasts concerning their biological activity toward normal keratinocytes assessed by immunocytochemistry
 and profiling of gene activation for growth factors/cytokines by microarray chip technology. IGF-2 and BMP-4 were determined
 as candidate factors responsible for tumor-associated fibroblast activity that influences normal epithelia. This effect was
 confirmed by addition of recombinant IGF-2 and BMP4, respectively, to the culture medium. This hypothesis was also verified
 by inhibition expe...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016889</comments>
            <pubDate>Wed, 18 Nov 2009 19:15:19 +0100</pubDate>
            <guid isPermaLink="false">3016889</guid>        </item>
        <item>
            <title>Expression and immunolocalization of ERG1 potassium channels in the rat kidney</title>
            <link>http://www.medworm.com/index.php?rid=3011642&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F48j35p1214582367%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Potassium (K+) channels participate in K+ secretion, K+ recycling, and cell volume regulation and help to maintain the resting potential in mammalian kidneys. Previously, we identified
 a set of voltage-gated K+ channels (Kv1) in the inner medullary collecting duct of the rat kidney. In the present work, we identified the voltage-gated
 K+ channel ether-à-go-go-related gene (ERG) in the rat kidney. mRNAs of ERG1a and its N-terminal splice-variant ERG1b were detected. Immunoblots of the cortex and medulla revealed two molecular mass proteins of 135 and 80&amp;nbsp;kDa, consistent in
 size with the nonglycosylated ERG1a and ERG1b isoforms, respectively. However, bands of 155 and 95&amp;nbsp;kDa, corresponding to mature
 glycosylated ERG1a and ERG1b, respectively, were also obser...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3011642</comments>
            <pubDate>Wed, 18 Nov 2009 00:08:19 +0100</pubDate>
            <guid isPermaLink="false">3011642</guid>        </item>
        <item>
            <title>Erratum to: Ultrastructural characterization of giant endosomes induced by GTPase-deficient Rab5</title>
            <link>http://www.medworm.com/index.php?rid=2998950&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F56883h5m42r4l881%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s00418-009-0660-7Authors
		Catherine Sem Wegner, The Norwegian Radium Hospital, Oslo University Hospital Department of Biochemistry, Institute for Cancer Research Montebello 0310 Oslo NorwayLene Malerød, The Norwegian Radium Hospital, Oslo University Hospital Department of Biochemistry, Institute for Cancer Research Montebello 0310 Oslo NorwayNina Marie Pedersen, The Norwegian Radium Hospital, Oslo University Hospital Department of Biochemistry, Institute for Cancer Research Montebello 0310 Oslo NorwayCinzia Progida, University of Oslo Department of Molecular Biosciences 1041, Blindernveien 31 0316 Oslo NorwayOddmund Bakke, University of Oslo Department of Molecular Biosciences 1041, Blindernveien 31 0316 Oslo NorwayHarald Stenmark...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2998950</comments>
            <pubDate>Fri, 13 Nov 2009 18:22:11 +0100</pubDate>
            <guid isPermaLink="false">2998950</guid>        </item>
        <item>
            <title>Two submucosal nerve plexus in human intestines</title>
            <link>http://www.medworm.com/index.php?rid=2992299&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj0mgv24tj91m152v%2F</link>
            <description>We examined the architecture of human submucosal nerve networks of gut segments derived from 12 individuals (each six from
 small and large intestines). Twelve undivided submucosal wholemounts were prepared and immunohistochemically stained for peripherin
 (nerve elements) and for α-smooth muscle actin (remnants of attached muscle bundles). We found two ganglionic nerve networks.
 The plexus submucosus externus was generally monolayered and located under the outermost surface of the submucosal wholemounts.
 Its nerve fibre strands frequently joined each other in acute or obtuse angles, the meshes of the network were relatively
 wide and frequently polyangular shaped. The plexus submucosus internus was generally multi-(mostly two- or three-)layered
 and occupied at least the inner half of ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2992299</comments>
            <pubDate>Thu, 12 Nov 2009 18:38:52 +0100</pubDate>
            <guid isPermaLink="false">2992299</guid>        </item>
        <item>
            <title>Tissue reaction to three different types of tissue glues in an experimental aorta dissection model: a quantitative approach</title>
            <link>http://www.medworm.com/index.php?rid=2984323&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg113h28407415q72%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tissue glues are used during surgical treatment of acute aorta dissection although some glues release toxic products and thus
 alter the histological structure of the vessel wall. The aim of our study was to use a porcine experimental model of infrarenal
 aorta dissection to compare histological changes of the vessel wall 1, 6 and 12&amp;nbsp;months after application of BioGlue, Gelatin-resorcin-formaldehyde
 (GRF) glue and Tissucol. For quantification, stereological methods were used. All types of glue caused stenosis, GRF most
 and Tissucol least severely. With increasing postoperative survival time, stenosis was again reduced. Elastine length density
 decreased with increasing survival time in Control as well as in all Experimental groups. The immunohistochemical phenoty...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2984323</comments>
            <pubDate>Mon, 09 Nov 2009 19:13:40 +0100</pubDate>
            <guid isPermaLink="false">2984323</guid>        </item>
        <item>
            <title>Distribution, development and proliferation of interstitial cells of Cajal in murine colon: an immunohistochemical study from neonatal to adult life</title>
            <link>http://www.medworm.com/index.php?rid=2971798&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd288k13gk4054261%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This paper aimed at investigating the alterations in interstitial cells of Cajal (ICC) in the proximal, middle and distal
 colon of mice from 0-day to 56-day post-partum (P0–P56) by immunohistochemistry. The Kit+ ICC, which situated around myenteric nerve plexus (ICC–MY) were prominent at birth, meanwhile those cells within the smooth
 muscle layers (ICC–IM) and in the connective tissue beneath serosa (ICC–SS) began to appear. ICC–SM, which located at the
 submucosal border of circular muscle layer emerged at P6 in the proximal colon and subsequently in the distal colon at P8,
 and ICC in the oral side of colon revealed an earlier development in morphology and a higher density than that in the anal
 side. The density of ICC altered obviously during postnatal p...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2971798</comments>
            <pubDate>Thu, 05 Nov 2009 18:57:31 +0100</pubDate>
            <guid isPermaLink="false">2971798</guid>        </item>
        <item>
            <title>TRPC3 ion channel subunit immunolocalization in the cochlea</title>
            <link>http://www.medworm.com/index.php?rid=2953934&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6774w15q35448608%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Canonical transient receptor potential (TRPC) subunits assemble as tetramers to form ion channels with high calcium (Ca2+) permeability. Here, we investigated the possibility that TRPC3 ion channels are broadly expressed in the adult guinea pig
 and mouse cochleae. Using immunofluorescence, pronounced labeling occurred in the spiral ganglion (SG) neurons, inner hair
 cells (IHC), outer hair cells (OHC) and epithelial cells lining scala media. TRPC3 expression was homogeneous in the SG throughout
 the cochlea. In contrast, there was marked spatial variation in the immunolabeling in the cochlear hair cells with respect
 to location. This likely relates to the tonotopy of these cells. TRPC3 immunolabeling was more pronounced in the IHC than
 OHC. Both basal region IHC and ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2953934</comments>
            <pubDate>Sat, 31 Oct 2009 12:53:08 +0100</pubDate>
            <guid isPermaLink="false">2953934</guid>        </item>
        <item>
            <title>The shape of caveolae is omega-like after glutaraldehyde fixation and cup-like after cryofixation</title>
            <link>http://www.medworm.com/index.php?rid=2924680&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxn1n32132n167086%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Caveolae were defined as flask- or omega-shaped plasma membrane invaginations, abundant in adipocytes, fibroblasts, endothelial
 and smooth muscle cells. The major protein component of caveolar membranes is an integral membrane protein named caveolin.
 We compared the freeze-fracture behavior of caveolae in glutaraldehyde-fixed and cryofixed mouse fibroblast cells and found
 distinct differences. In glutaraldehyde-fixed cells almost all caveolae were cross-fractured through their pore and only very
 few caveolar membranes were membrane-fractured. We found the reverse situation in rapid frozen cells without any chemical
 fixation where most of the caveolae were membrane-fractured, showing different degrees of invagination from nearly flat to
 deeply invaginated. In ultra...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2924680</comments>
            <pubDate>Thu, 22 Oct 2009 18:56:12 +0100</pubDate>
            <guid isPermaLink="false">2924680</guid>        </item>
        <item>
            <title>Prostasin inhibits cell invasion in human choriocarcinomal JEG-3 cells</title>
            <link>http://www.medworm.com/index.php?rid=2922965&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb6214212v7654771%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Controlled invasion of the uterine wall by the trophoblast cells is pivotal for the successful pregnancy, and various kinds
 of protease are involved in this process. Serine protease prostasin has been shown to participate in the proteolytic activation
 of epithelial sodium channel as well as cleavage of epidermal growth factor receptor extracellular domain in human epithelial
 cells. Its physiological significance in human placentation has been suggested but not validated. In the present study, we
 found that prostasin was expressed at a relatively high level in human placenta trophoblasts in early pregnant weeks. In the
 in vitro cultured human choriocarcinomal JEG-3 cells, treatment with functional antibody against prostasin led to promotion
 in cell invasion capabil...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2922965</comments>
            <pubDate>Wed, 21 Oct 2009 19:27:48 +0100</pubDate>
            <guid isPermaLink="false">2922965</guid>        </item>
        <item>
            <title>Melanoma progression exhibits a significant impact on connexin expression patterns in the epidermal tumor microenvironment</title>
            <link>http://www.medworm.com/index.php?rid=2919497&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fat40825777774271%2F</link>
            <description>This study compares
 the extent of Cx26, Cx30 and Cx43 expression in the epidermal microenvironment of melanocytic nevi and melanomas and its association
 with melanoma thickness, proliferative index of the tumor and its microenvironment, and with 5-year metastasis and survival.
 We found that induction of Cx26 and Cx30 cell–cell border expression in the epidermal tumor microenvironment correlates to
 malignancy. Importantly, there was a significant correlation of tumor thickness with the vertical epidermal Cx26 and Cx30
 expression pattern and the horizontal Cx26 dissemination. Furthermore, horizontal Cx26 expression correlated with metastasis.
 Vertical epidermal expression patterns of Cx26 and Cx30 significantly correlated with the proliferative index in the epidermal
 tumor microenvi...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2919497</comments>
            <pubDate>Wed, 21 Oct 2009 09:05:42 +0100</pubDate>
            <guid isPermaLink="false">2919497</guid>        </item>
        <item>
            <title>Expression of cAMP response element-binding protein in the duct system of the mouse submandibular gland</title>
            <link>http://www.medworm.com/index.php?rid=2908034&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk110870153308502%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The submandibular gland (SMG) of mice shows a marked sexual dimorphism in which a duct portion called the granular convoluted
 tubule (GCT) is developed preferentially in males during puberty. The administration of testosterone to female mice causes
 the conversion of striated duct (SD) cells into GCT cells, but the underlying molecular mechanisms are unclear. Cyclic AMP
 response element-binding protein (CREB) is a transcription factor functioning downstream of a variety of signal transduction
 pathways. In the present study, we examined the expression, activation and cellular localization of CREB in the mouse SMG
 using Western blotting and immunohistochemistry. Both total CREB (t-CREB) and phosphorylated CREB (p-CREB) were significantly
 more abundant in the female t...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2908034</comments>
            <pubDate>Fri, 16 Oct 2009 18:01:46 +0100</pubDate>
            <guid isPermaLink="false">2908034</guid>        </item>
        <item>
            <title>Ultrastructural characterization of giant endosomes induced by GTPase-deficient Rab5</title>
            <link>http://www.medworm.com/index.php?rid=2898125&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe0778xj273115106%2F</link>
            <description>In this report, we have addressed this issue
 by generating a HEp2 cell line with inducible expression of Rab5(Q79L) and performing ultrastructural analysis of Rab5(Q79L)-induced
 endosomes. We find that Rab5(Q79L) not only induces formation of enlarged early endosomes but also causes enlargement of later
 endocytic profiles. Most strikingly, Rab5(Q79L) causes formation of enlarged multivesicular endosomes with a large number
 of intraluminal vesicles, and endosomes that contain both early and late endocytic markers are frequently observed. In addition,
 we observe defects in the sorting of the EGF receptor and the transferrin receptor through this compartment.
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-009-0643-8Authors
		Catherine Sem Wegener, The Norwegian ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2898125</comments>
            <pubDate>Wed, 14 Oct 2009 17:00:03 +0100</pubDate>
            <guid isPermaLink="false">2898125</guid>        </item>
        <item>
            <title>Switching of actin isoforms in skeletal muscle differentiation using mouse ES cells</title>
            <link>http://www.medworm.com/index.php?rid=2898124&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn64t64n11qt5075m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Among six actin isoforms, α-skeletal and α-cardiac actins have similar amino acid components and are highly conserved. Although
 skeletal muscles essentially express α-skeletal actins in the adult tissue, α-cardiac isoform actin is prominent in the embryonic
 muscle tissue. Switching of actin isoforms from α-cardiac to α-skeletal actin occurs during skeletal muscle differentiation.
 The cardiac type α-actin is expressed in the regeneration and patho-physiological states of the skeletal muscles as well.
 In the present study, we demonstrate the morphological switching of α-type actin isoforms from α-cardiac to α-skeletal actin
 in vitro using mouse ES cells for the first time. Immunofluorescent double staining with two specific antibodies revealed
 that α-card...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2898124</comments>
            <pubDate>Wed, 14 Oct 2009 17:00:03 +0100</pubDate>
            <guid isPermaLink="false">2898124</guid>        </item>
        <item>
            <title>Characterization of newly established bovine intestinal epithelial cell line</title>
            <link>http://www.medworm.com/index.php?rid=2898126&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6656n7v4671u8231%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Membranous epithelial cells (M cells) of the follicle-associated epithelium in Peyer’s patches have a high capacity for transcytosis
 of several viruses and microorganisms. Here, we report that we have successfully established a bovine intestinal epithelial
 cell line (BIE cells) and developed an in vitro M cell model. BIE cells have a cobblestone morphology and microvilli-like
 structures, and strongly express cell-to-cell junctional proteins and cytokeratin, which is a specific intermediate filament
 protein of epithelial cells. After co-culture with murine intestinal lymphocytes or treatment with supernatant from bovine
 PBMC cultured with IL-2, BIE cells acquired the ability of transcytosis. Therefore, BIE cells have typical characteristics
 of bovine intestinal e...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2898126</comments>
            <pubDate>Wed, 14 Oct 2009 17:00:02 +0100</pubDate>
            <guid isPermaLink="false">2898126</guid>        </item>
        <item>
            <title>Protein p0071, an armadillo plaque protein of adherens junctions, is predominantly expressed in distal renal tubules</title>
            <link>http://www.medworm.com/index.php?rid=2908035&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw465681x715gu7ml%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Protein p0071 is a member of the p120-subfamily of armadillo proteins and is well known as a junctional plaque component involved in cell–cell adhesion, especially in adherens junctions.
 By systematic immunohistochemical analysis of mouse and human kidney tissues, p0071 was prominently detected in distinct kidney
 tubules. Upon double-labeling immunolocalization experiments with segment-specific markers, p0071 was predominantly localized
 in distal straight and convoluted tubules and to a lesser extent in proximal tubules, in the ascending thin limb of loop of
 Henle and in the collecting ducts. In capillaries of the kidney, p0071 co-localized with VE-cadherin an endothelium-specific
 cadherin. Protein p0071 was also detected in both, renal cell carcinomas derived fr...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2908035</comments>
            <pubDate>Wed, 14 Oct 2009 17:00:01 +0100</pubDate>
            <guid isPermaLink="false">2908035</guid>        </item>
        <item>
            <title>Lung surfactant proteins in the early human placenta</title>
            <link>http://www.medworm.com/index.php?rid=2898127&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F671373772234v4v8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pulmonary surfactant is a complex mixture of phospholipids and four surfactant-associated proteins (SP-A, SP-B, SP-C and SP-D).
 The biological functions of SP-A and SP-D are primarily twofold, namely surfactant homeostasis and host defense. The hydrophobic
 surfactant proteins, SP-B and SP-C, are required for achieving the optimal surface tension reducing properties of surfactant
 by promoting the rapid adsorption of surfactant phospholipids along the alveolar surface. Despite the promising findings,
 only little is known about the extrapulmonary distribution of these proteins. Therefore, in this study, the presence of SP-A,
 SP-B, SP-C and SP-D in early human placenta has been investigated. First-trimester placental tissues (22–56&amp;nbsp;days) were obtained
 from wome...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2898127</comments>
            <pubDate>Tue, 13 Oct 2009 21:05:18 +0100</pubDate>
            <guid isPermaLink="false">2898127</guid>        </item>
        <item>
            <title>Induction and cellular expression of tartrate resistant acid phosphatase during dextran sodium sulphate induced colitis in rats</title>
            <link>http://www.medworm.com/index.php?rid=2889852&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp6126p33u6762786%2F</link>
            <description>In conclusion, induction
 of TRAP provides an early sign of macrophage responsiveness in DSS induced colitis.
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-009-0647-4Authors
		Pernilla Lång, Karolinska Institutet, Karolinska University Hospital Huddinge Division of Pathology F46, Department of Laboratory Medicine 141 86 Stockholm SwedenStefan Lange, Sahlgrenska University Hospital Department of Clinical Bacteriology Göteborg SwedenDick Delbro, University of Karlstad Department of Chemistry and Biomedical Sciences Karlstad SwedenGöran Andersson, Karolinska Institutet, Karolinska University Hospital Huddinge Division of Pathology F46, Department of Laboratory Medicine 141 86 Stockholm Sweden
	

	
		Journal Histochemistry and Cell BiologyOnline ISSN 1432-119XPrin...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2889852</comments>
            <pubDate>Sun, 11 Oct 2009 07:12:19 +0100</pubDate>
            <guid isPermaLink="false">2889852</guid>        </item>
        <item>
            <title>Isolation and in vitro characterisation of dental pulp stem cells from natal teeth</title>
            <link>http://www.medworm.com/index.php?rid=2881073&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc4162168q046506n%2F</link>
            <description>This report described the first successful
 isolation and characterisation of hNDP-SCs.
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-009-0646-5Authors
		Erdal Karaöz, Kocaeli University Stem Cell and Gene Therapy Research and Applied Center 41380 Kocaeli TurkeyBurcu Nur Doğan, University of Marmara Department of Pedodontics, Faculty of Dentistry 34100 Istanbul TurkeyAyça Aksoy, Kocaeli University Stem Cell and Gene Therapy Research and Applied Center 41380 Kocaeli TurkeyGülçin Gacar, Kocaeli University Stem Cell and Gene Therapy Research and Applied Center 41380 Kocaeli TurkeySerap Akyüz, University of Marmara Department of Pedodontics, Faculty of Dentistry 34100 Istanbul TurkeySelda Ayhan, Kocaeli University Stem Cell and Gene Therapy Research and Applied...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2881073</comments>
            <pubDate>Fri, 09 Oct 2009 06:06:52 +0100</pubDate>
            <guid isPermaLink="false">2881073</guid>        </item>
        <item>
            <title>Dynamics of leading lamellae of living fibroblasts visualized by high-speed scanning probe microscopy</title>
            <link>http://www.medworm.com/index.php?rid=2881074&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft863208021207u83%2F</link>
            <description>In this study, we aimed at improving the temporal resolution of scanning probe microscopy (SPM) for observing living cells
 by introducing soft cantilevers, low feedback-gain operations, and cantilever deflection imaging. We achieved visualization
 of the mechanical architecture in leading lamellae of living fibroblasts at a temporal resolution of around 10&amp;nbsp;s, which is
 higher than that of conventional contact-mode SPM. Time-lapse SPM could be used to monitor not only cytoskeletal dynamics
 but also the dynamics of numerous microgranules. Statistical analysis of microgranular motion revealed that the microgranules
 have superdiffusive behaviors and significant directional order of motion. We also found that the direction of their motion
 is correlated with the direction of growing act...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2881074</comments>
            <pubDate>Fri, 09 Oct 2009 06:06:50 +0100</pubDate>
            <guid isPermaLink="false">2881074</guid>        </item>
        <item>
            <title>Localization of fatty acid binding protein of epidermal type common to dendritic cells and presumptive macrophages in Peyer’s patches and epithelial M cells of mouse intestine</title>
            <link>http://www.medworm.com/index.php?rid=2850783&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe771n22887104044%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Fatty acid binding protein of epidermal type (E-FABP) was expressed/localized in most, if not all, populations of the dendritic
 cells in the subepithelial domes, follicles and interfollicular regions of Peyer’s patches and presumptive macrophages in
 their germinal centers, and all M cells in the follicle-associated epithelium of mouse intestine. The immunoreactivity in
 both of the cell populations makes it easy to recognize the accumulation of DCs in the subepithelial domes in close proximity
 to the base of M cells, which is essential for luminal antigens to be transported to Peyer’s patches. E-FABP may play some
 important roles in the mucosal immune reaction through Peyer’s patches and associated structures.
 
	Content Type Journal ArticleCategory Original P...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2850783</comments>
            <pubDate>Tue, 29 Sep 2009 04:05:08 +0100</pubDate>
            <guid isPermaLink="false">2850783</guid>        </item>
        <item>
            <title>Altered expression of P2X3 in vagal and spinal afferents following esophagitis in rats</title>
            <link>http://www.medworm.com/index.php?rid=2850784&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnlu7117023103lp0%2F</link>
            <description>The objective of this study was to investigate
 the expression of P2X3 receptors in spinal and vagal sensory neurons and esophageal tissues following esophagitis in rats. Two groups of rats were
 used including 7&amp;nbsp;days fundus-ligated (7D-ligated) esophagitis and sham-operated controls. Esophagitis was produced by ligating
 the fundus and partial obstruction of pylorus that initiated reflux of gastric contents. The sham-operated rats underwent
 midline incision without surgical manipulation of the stomach. Expressions of P2X3 receptors in thoracic dorsal root ganglia (DRGs), nodose ganglia (NGs), and esophageal tissues were evaluated by RT–PCR,
 western blot and immunohistochemistry. Esophageal neurons were identified by retrograde transport of Fast Blue from the esophagus.
 There wer...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2850784</comments>
            <pubDate>Mon, 28 Sep 2009 14:40:37 +0100</pubDate>
            <guid isPermaLink="false">2850784</guid>        </item>
        <item>
            <title>Ovarian hormones regulate expression of the focal adhesion proteins, talin and paxillin, in rat uterine luminal but not glandular epithelial cells</title>
            <link>http://www.medworm.com/index.php?rid=2836031&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbg31582860047142%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;During early pregnancy in the rat, focal adhesions disassemble in uterine luminal epithelial cells at the time of implantation
 to facilitate their removal so that the implanting blastocyst can invade into the underlying endometrial decidual cells. This
 study investigated the effect of ovarian hormones on the distribution and protein expression of two focal adhesion proteins,
 talin and paxillin, in rat uterine luminal and glandular epithelial cells under various hormone regimes. Talin and paxillin
 showed a major distributional change between different hormone regimes. Talin and paxillin were highly concentrated along
 the basal cell surface of uterine luminal epithelial cells in response to oestrogen treatment. However, this prominent staining
 of talin and paxillin ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2836031</comments>
            <pubDate>Thu, 24 Sep 2009 16:42:00 +0100</pubDate>
            <guid isPermaLink="false">2836031</guid>        </item>
        <item>
            <title>Characterization of bovine fetal Leydig cells by KIT expression</title>
            <link>http://www.medworm.com/index.php?rid=2812123&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg382142540x58w55%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The origin of fetal Leydig cells (FLC) and whether they share a common lineage with adult Leydig cells (ALC) is still under
 debate, and a marker to reliably track and isolate fetal Leydig precursor cells remains to be identified. We analyzed KIT
 positive (KIT+) cells in gonads from bovine fetuses with crown-rump-length (CRL) 2.5–85&amp;nbsp;cm by immunohistochemistry, and found
 that KIT expression was gender-specific. In female gonads, expression was mainly associated with epithelial cell cords, which
 extended from the surface epithelium towards the KIT-negative inner stroma. In male gonads of fetuses, after CRL 2.9&amp;nbsp;cm, KIT
 expression was strikingly strong in interstitial cells (IC). Only a few KIT+ cells were detected in the epithelial cell cords
 and in the st...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2812123</comments>
            <pubDate>Fri, 18 Sep 2009 16:11:29 +0100</pubDate>
            <guid isPermaLink="false">2812123</guid>        </item>
        <item>
            <title>Selection of buffer pH by the isoelectric point of the antigen for the efficient heat-induced epitope retrieval: re-appraisal for nuclear protein pathobiology</title>
            <link>http://www.medworm.com/index.php?rid=2812122&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg3pn8711rrn838l1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Epitope retrieval (ER) using heating causes a dramatic improvement in the sensitivity of immunohistochemistry for formalin-fixed
 paraffin-embedded (FFPE) tissue sections. Here, the relationship between the pH of the retrieval buffer used for heat-induced
 epitope retrieval (HIER) and the isoelectric points (pI) of the antigen recognized by antibodies against nuclear proteins
 (mainly human pituitary transcription factors in this study) was investigated using FFPE tissue sections. A universal buffer,
 with a buffering capacity over a wide pH range from 2.0 to 12.0, was used for HIER. We found that the intensity of staining
 for most nuclear proteins after HIER depended simply on the pH of the buffer. Importantly, for efficient HIER, antigens with
 acidic pI required bas...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2812122</comments>
            <pubDate>Fri, 18 Sep 2009 16:11:29 +0100</pubDate>
            <guid isPermaLink="false">2812122</guid>        </item>
        <item>
            <title>High expression of antizyme inhibitor 2, an activator of ornithine decarboxylase in steroidogenic cells of human gonads</title>
            <link>http://www.medworm.com/index.php?rid=2812124&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F56767p646v95223n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;High activity of ornithine decarboxylase (ODC), the rate-limiting enzyme of polyamine synthesis, is typically present in rapidly
 proliferating normal and malignant cells. The mitotically inactive steroidogenic cells in rodent testis and ovaries, however,
 also display high ODC activity. The activity of ODC in these cells responds to luteinizing hormone, and inhibition of ODC
 reduces the production of steroid hormones. Polyamines and ODC also control proliferation of germ cells and spermiogenesis.
 The activity of ODC, especially in proliferating cells, is regulated by antizyme inhibitor (AZIN). This protein displaces
 ODC from a complex with its inhibitor, antizyme. We have previously identified and cloned a second AZIN, i.e. antizyme inhibitor
 2 (AZIN2), which has t...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2812124</comments>
            <pubDate>Wed, 16 Sep 2009 18:49:51 +0100</pubDate>
            <guid isPermaLink="false">2812124</guid>        </item>
        <item>
            <title>Distribution of the epilepsy-related Lgi1 protein in rat cortical neurons</title>
            <link>http://www.medworm.com/index.php?rid=2812125&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl1u271km31268838%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Lgi1 protein is involved in the pathogenesis of autosomal dominant lateral temporal epilepsy because mutations in the
 leucine-rich, glioma-inactivated 1 (LGI1) gene have been found in affected subjects and families; however, the function of
 Lgi1 is still unclear. Definition of the fine intracellular distribution of Lgi1 in normal cortical tissue would add in understanding
 its role and envisage pathogenetic mechanisms. Therefore, we analyzed normal rat cortex for Lgi1 by combining biochemistry,
 immunohistochemistry and immunoelectron microscopy. Our results demonstrate that Lgi1 is a cytoplasmic protein distributed
 both in the soma and in the processes of neurons: it occurs on the rough endoplasmic reticulum, the site of synthesis, in
 the Golgi complex, where i...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2812125</comments>
            <pubDate>Wed, 16 Sep 2009 18:49:50 +0100</pubDate>
            <guid isPermaLink="false">2812125</guid>        </item>
        <item>
            <title>Global gene expression profiling reveals a key role of CD44 in hepatic oval-cell reaction after 2-AAF/CCl4 injury in rodents</title>
            <link>http://www.medworm.com/index.php?rid=2812126&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcu7136r2utv62685%2F</link>
            <description>In this study, we treated rats with 2-acetylaminofluorene/carbon tetrachloride to
 induce hepatic oval cells. By expression microarray analysis, we investigated global gene expression profiles in liver tissue,
 with an emphasis on adhesion molecules, extracellular matrix proteins, matrix metalloproteinases (MMPs), growth factors/cytokines,
 and receptors that might contribute to the distinct behaviors of oval cells. Genes upregulated at least twofold were selected.
 We then performed immunostaining to verify the microarray results and identified expression of MMP-7 and CD44 in oval cells.
 Staining of cytokeratin (CK)-19, an oval-cell marker, was similar between oval cells located next to periportal areas and
 those located far within the parenchyma. In contrast, CD44 staining was more int...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2812126</comments>
            <pubDate>Wed, 16 Sep 2009 18:49:49 +0100</pubDate>
            <guid isPermaLink="false">2812126</guid>        </item>
        <item>
            <title>Osteogenic properties of late adherent subpopulations of human bone marrow stromal cells</title>
            <link>http://www.medworm.com/index.php?rid=2743592&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy5805ww2l5337712%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The nonadherent (NA) population of bone-marrow-derived mononuclear cells (MNC) has been demonstrated to be a source of osteogenic
 precursors in addition to the plastic-adherent mesenchymal stromal cells (MSC). In the current study, two subpopulations of
 late adherent (LA) osteoprogenitors were obtained by subsequent replating of NA cells, and their phenotypic, functional, and
 molecular properties were compared with those of early adherent (EA) MSC. Approximately 35% of MNC were LA cells, and they
 acquired a homogeneous expression of MSC antigens later than EA cells. In EA-MSC, the alkaline phosphatase (ALP) activity
 increased significantly from time of seeding to the first confluence, whereas in LA cells it raised later, after the addition
 of mineralization medium...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2743592</comments>
            <pubDate>Thu, 27 Aug 2009 16:33:52 +0100</pubDate>
            <guid isPermaLink="false">2743592</guid>        </item>
        <item>
            <title>DEHP effects on retinal vessels in newborn rats: a qualitative and quantitative analysis</title>
            <link>http://www.medworm.com/index.php?rid=2729516&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp67238482528m066%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Di-(2-ethylhexyl)-phthalate (DEHP), employed in polyvinyl chloride fabrication and released by endotracheal tubes, is known
 to cause alterations to several mammalian tissues, markedly in immature animals. The high incidence and severity of bronchopulmonary
 dysplasia and retinopathy in preterm babies submitted to endotracheal intubation prompted us to investigate the effects of
 DEHP in lung and retina perinatal development. We previously demonstrated that in rats delivered and breast-fed by DEHP-treated
 mothers lung alveolarisation is severely impaired. In the present research, the maturation of retinal vessels was studied
 in (a) flat-mounted retinas obtained after intracardiac injection of FITC-conjugated dextran, (b) flat-mounted retinas incubated
 with FITC-conju...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2729516</comments>
            <pubDate>Sat, 22 Aug 2009 18:53:12 +0100</pubDate>
            <guid isPermaLink="false">2729516</guid>        </item>
        <item>
            <title>Fibulin-1 and fibrinogen in human atherosclerotic lesions</title>
            <link>http://www.medworm.com/index.php?rid=2719214&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fagx773468t418773%2F</link>
            <description>In this study, the deposition patterns of fibulin-1 and fibrinogen were examined in human coronary artery atherosclerotic
 lesions excised by atherectomy from 20 patients. Fibulin-1 deposition was found to be closely overlapping with fibrinogen
 located within the atherosclerotic lesions and in regions containing fresh thrombi. Pronounced intracellular fibulin-1 immunostaining
 was apparent in lesion areas rich in macrophages and foam cells, although THP-1 macrophages and foam cells were found not
 to express fibulin-1. Strong ECM deposition of fibulin-1 was observed in acellular atheromatous and myxomatous regions. By
 contrast, fibulin-1 was present at relatively low levels in the ECM associated with smooth muscle cells within and outside
 of lesions and was not detected in sclerotic reg...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2719214</comments>
            <pubDate>Wed, 19 Aug 2009 17:50:06 +0100</pubDate>
            <guid isPermaLink="false">2719214</guid>        </item>
        <item>
            <title>Relocalization of a microtubule-anchoring protein, ninein, from the centrosome to dendrites during differentiation of mouse neurons</title>
            <link>http://www.medworm.com/index.php?rid=2719215&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn572161ug810g268%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Microtubules in typical cells form radial arrays with their plus-ends pointing toward the cell periphery. In contrast, microtubules
 in dendrites of neurons are free from centrosomes and have a unique arrangement in which about half have a polarity with a
 minus-end distal orientation. Mechanisms for generation and maintenance of the microtubule arrangement in dendrites are not
 well understood. Here, we examined dendritic localization of a centrosomal protein, ninein, which has microtubule-anchoring
 and stabilizing functions. Immunohistochemical analysis of developing mouse cerebral and cerebellar cortices showed that ninein
 is localized at the centrosome in undifferentiated neural precursors. In contrast, ninein was barely detected in migrating
 neurons, such as tho...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2719215</comments>
            <pubDate>Wed, 19 Aug 2009 08:29:31 +0100</pubDate>
            <guid isPermaLink="false">2719215</guid>        </item>
        <item>
            <title>Characterization of mesenchymal stem cells from rat bone marrow: ultrastructural properties, differentiation potential and immunophenotypic markers</title>
            <link>http://www.medworm.com/index.php?rid=2719216&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu0515x7q76471641%2F</link>
            <description>In this study, morphological and immunophenotypic properties of BM-MSCs were examined in detail. Differentiation
 potential and growth kinetics of adult rat BM-MSCs were also determined. Immunohistochemistry and RT-PCR results indicated
 that BM-MSCs expressed myogenic (desmin, myogenin, myosin IIa, and α-SMA), neurogenic (γ-enolase, MAP2a,b, c-fos, nestin,
 GFAP and beta III tubulin), and osteogenic (osteonectin, osteocalcin, osteopontin, Runx-2, BMP-2, BMP-4 and type I collagen)
 markers without stimulation towards differentiation. These expression patterns indicated why these cells can easily differentiate
 into multiple lineages both in vitro and in vivo. Ultrastructural characteristics of rBM-MSCs showed more developed and metabolically
 active cells.
 
	Content Type Journal Article...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2719216</comments>
            <pubDate>Tue, 18 Aug 2009 09:37:12 +0100</pubDate>
            <guid isPermaLink="false">2719216</guid>        </item>
        <item>
            <title>Effects of folic acid and homocysteine on spinal cord morphology of the chicken embryo</title>
            <link>http://www.medworm.com/index.php?rid=2701865&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F54763822j4476050%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Maternal ingestion of folic acid (FA) reduces neural tube defects, which are associated with high homocysteine levels. Present
 study evaluated the effects of FA and homocysteine on cell proliferation and cell adhesion, as well as on apoptosis, throughout
 the development of the spinal cord and mesenchyme of chicken embryos. Normal closure of the neural tube and a regular distribution
 of the mesenchymal cells were observed in control and FA-treated embryos. All homocysteine-treated embryos and also 6 of 10
 embryos treated with FA&amp;nbsp;+&amp;nbsp;homocysteine showed failure of closure of the neural tube. Homocysteine decreased the thickness
 of the mantle and marginal layers of the spinal cord, and FA did not prevent this effect. FA treatment reversed the decrease
 of prol...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2701865</comments>
            <pubDate>Wed, 12 Aug 2009 15:36:16 +0100</pubDate>
            <guid isPermaLink="false">2701865</guid>        </item>
        <item>
            <title>Topographical variation in the distributions of versican, aggrecan and perlecan in the foetal human spine reflects their diverse functional roles in spinal development</title>
            <link>http://www.medworm.com/index.php?rid=2698950&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffmg7871g10652356%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We evaluated the immunohistochemical distribution of three major proteoglycans of cartilage, i.e., aggrecan, versican and
 perlecan vis-a-vis collagens I and II in the developing human spine of first-trimester foetuses. Aggrecan and perlecan were
 prominently immunolocalised in the cartilaginous vertebral body rudiments and to a lesser extent within the foetal intervertebral
 disc. In contrast, versican was only expressed in the developing intervertebral disc interspace. Using domain-specific monoclonal
 antibodies against the various modules of versican, we discovered the V0 isoform as the predominant form present. Versican
 immunolocalisations conducted with antibodies directed to epitopes in its N and C termini and GAG-α and GAG-β core protein
 domains provided evi...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2698950</comments>
            <pubDate>Tue, 11 Aug 2009 00:03:13 +0100</pubDate>
            <guid isPermaLink="false">2698950</guid>        </item>
        <item>
            <title>Roundness variation in JPEG images affects the automated process of nuclear immunohistochemical quantification: correction with a linear regression model</title>
            <link>http://www.medworm.com/index.php?rid=2681391&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fau040l558g4q4441%2F</link>
            <description>This study attempts to show, with respect to immunohistochemically stained nuclei, which morphometric
 parameters may be altered by the different levels of JPEG compression, and the implications of these alterations for automated
 nuclear counts, and further, develops a method for correcting this discrepancy in the nuclear count. For this purpose, 47
 DIs from different tissues were captured in uncompressed TIFF format and converted to 1:3, 1:23 and 1:46 compression JPEG
 images. Sixty-five positive objects were selected from these images, and six morphological parameters were measured and compared
 for each object in TIFF images and those of the different compression levels using a set of previously developed and tested
 macros. Roundness proved to be the only morphological parameter that...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2681391</comments>
            <pubDate>Mon, 03 Aug 2009 20:43:54 +0100</pubDate>
            <guid isPermaLink="false">2681391</guid>        </item>
        <item>
            <title>The inability of fully grown germinal vesicle stage oocyte cytoplasm to transcriptionally silence transferred transcribing nuclei</title>
            <link>http://www.medworm.com/index.php?rid=2666826&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm651526826624218%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;For somatic cell nuclear transfer cytoplasts from metaphase II, oocytes are exclusively used. However, it is evident that
 certain reprogramming activities are present in oocytes even at earlier stages of maturation. These activities are, however,
 only poorly characterised. The main reason for this is that even the intrinsic oocyte processes are insufficiently understood.
 The mammalian oocyte is a highly specialised cell that harbours many specific characteristics. One of these is its particularly
 large size when compared to somatic cells. As the oocyte enters the growth phase its volume, as well as the amount of material,
 increases considerably. Thus, it is clear that the oocyte must possess the machinery to accomplish this incredible material
 accumulation. When t...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2666826</comments>
            <pubDate>Fri, 31 Jul 2009 19:48:02 +0100</pubDate>
            <guid isPermaLink="false">2666826</guid>        </item>
        <item>
            <title>Toward visualization of nanomachines in their native cellular environment</title>
            <link>http://www.medworm.com/index.php?rid=2666825&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdm521h5127706644%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The cellular nanocosm is made up of numerous types of macromolecular complexes or biological nanomachines. These form functional modules that are
 organized into complex subcellular networks. Information on the ultra-structure of these nanomachines has mainly been obtained
 by analyzing isolated structures, using imaging techniques such as X-ray crystallography, NMR, or single particle electron
 microscopy (EM). Yet there is a strong need to image biological complexes in a native state and within a cellular environment,
 in order to gain a better understanding of their functions. Emerging methods in EM are now making this goal reachable. Cryo-electron
 tomography bypasses the need for conventional fixatives, dehydration and stains, so that a close-to-native environment ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2666825</comments>
            <pubDate>Fri, 31 Jul 2009 19:48:02 +0100</pubDate>
            <guid isPermaLink="false">2666825</guid>        </item>
        <item>
            <title>Atypical fast SERCA1a protein expression in slow myofibers and differential S-nitrosylation prevented by exercise during long term bed rest</title>
            <link>http://www.medworm.com/index.php?rid=2662314&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F375272621340673h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We monitored changes in SERCA isoform specific expression and S-nitrosylation in myofibers of lower limb soleus (SOL) and
 vastus lateralis (VL) muscle biopsies before and after 60&amp;nbsp;days of voluntary long term bed rest (BR) without (BR-CTRL group,
 n&amp;nbsp;=&amp;nbsp;8) and with exercise countermeasure (BR-EX group, n&amp;nbsp;=&amp;nbsp;8). Before BR, a typical myofiber type-specific distribution of fast and slow SERCA1/2a isoforms was seen. After BR, a
 subpopulation (approx. 15%) of slow myofibers in BR-CTRL additionally expressed the fast SERCA1a isoform which was not seen
 in BR-EX. After BR, SERCA1a S-nitrosylation patterns analyzed by the biotin-switch assay decreased in disused SOL only but
 increased in both muscles following exercise. Differential SERCA1a S-nitrosylati...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2662314</comments>
            <pubDate>Thu, 30 Jul 2009 19:54:24 +0100</pubDate>
            <guid isPermaLink="false">2662314</guid>        </item>
        <item>
            <title>Monocarboxylate transporter genes in the mammary gland of lactating cows</title>
            <link>http://www.medworm.com/index.php?rid=2653189&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm23196208nx11223%2F</link>
            <description>This study is the first to examine the expression of the 14 monocarboxylate transporter genes (MCT1–MCT14) in the mammary
 gland of mammals. RT-PCR, Western blot, immunohistochemistry, and immunofluorescence confocal laser microscopy were applied
 in a comprehensive approach to assess the expression and cellular localization of MCTs in the mammary gland of lactating cattle.
 RT-PCR revealed the existence of nine MCT isoforms, namely MCT1, MCT2, MCT3, MCT4, MCT5, MCT8, MCT10, MCT13, and MCT14 in
 cow mammary gland. The amplified cDNA segments were confirmed by sequence analysis and deposited in the GenBank. Using the
 commercially available antibodies against MCT1–MCT8, Western blotting verified the protein expression of MCT1, MCT2, MCT3,
 MCT4, MCT5, and MCT8 in the cow mammary gland. ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2653189</comments>
            <pubDate>Mon, 27 Jul 2009 21:50:22 +0100</pubDate>
            <guid isPermaLink="false">2653189</guid>        </item>
        <item>
            <title>Probing cell-surface dynamics and mechanics at different scales</title>
            <link>http://www.medworm.com/index.php?rid=2648528&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F864957l60182t024%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recent advances in our understanding of the cell surfaces strongly rely on new physical methods and concepts. During last
 decades, microscopy techniques combined with statistical analysis and modelling have significantly improved the toolkit of
 life scientists. They provide quantitative ways to analyse diverse biological functions such as cell signalling and cell adhesion
 at different scales. Here, I review quantitative approaches to cell-surface dynamics and mechanics. I focus on two specific
 topics: how membrane molecules dynamically organize in membranes and how cell-surface mechanics can contribute to tissue morphogenesis.
 
	Content Type Journal ArticleCategory ReviewsDOI 10.1007/s00418-009-0620-2Authors
		Pierre-François Lenne, Université Aix-Marseille II, C...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2648528</comments>
            <pubDate>Sun, 26 Jul 2009 22:19:41 +0100</pubDate>
            <guid isPermaLink="false">2648528</guid>        </item>
        <item>
            <title>Limiting transport steps and novel interactions of Connexin-43 along the secretory pathway</title>
            <link>http://www.medworm.com/index.php?rid=2644566&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj20223065400256u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Connexins are four-transmembrane-domain proteins expressed in all vertebrates which form permeable gap junction channels that
 connect cells. Here, we analysed Connexin-43 (Cx43) transport to the plasma membrane and studied the effects of small GTPases
 acting along the secretory pathway. We show that both GTP- and GDP-restricted Sar1 prevents exit of Cx43 from the endoplasmic
 reticulum (ER), but only GTP-restricted Sar1 arrests Cx43 in COP II-coated ER exit sites and accumulates 14-3-3 proteins in
 the ER fraction. FRET-FLIM data confirm that already in ER exit sites Cx43 exists in oligomeric form, suggesting an in vivo
 role for 14-3-3 in Cx43 oligomerization. Exit of Cx43 from the ER can be blocked by other factors—such as expression of the
 β subunit of the COP ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2644566</comments>
            <pubDate>Sat, 25 Jul 2009 00:28:52 +0100</pubDate>
            <guid isPermaLink="false">2644566</guid>        </item>
        <item>
            <title>Complementary developmental expression of the two tyrosine hydroxylase transcripts in zebrafish</title>
            <link>http://www.medworm.com/index.php?rid=2639474&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn1g682466u381264%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tyrosine hydroxylase (TH) is a rate-limiting enzyme in the biosynthesis of catecholamines. In zebrafish, two genes encoding
 TH have been identified. We cloned them and studied their expression in zebrafish. In adult tissues, th1 mRNA was more abundant than th2 mRNA in the brain and eyes, whereas th2 mRNA was more abundant in the liver, kidney, heart and gills. In developing brain, th1 mRNA was readily detected at 1&amp;nbsp;day post-fertilization using qPCR and in situ hybridization, whereas th2 mRNA appeared later. th1 was found in 17 catecholaminergic groups in larval brain, whereas th2 was found in four additional groups. A monoclonal antibody commonly used against TH detected preferentially TH1 protein.
 The two th genes, probably originated as a result of genome dupli...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2639474</comments>
            <pubDate>Thu, 23 Jul 2009 09:00:46 +0100</pubDate>
            <guid isPermaLink="false">2639474</guid>        </item>
        <item>
            <title>Microtubule-dependent formation of the stigmoid body as a cytoplasmic inclusion distinct from pathological aggresomes</title>
            <link>http://www.medworm.com/index.php?rid=2590911&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx031p12v65757343%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The stigmoid body (STB) is a neurocytoplasmic inclusion containing huntingtin-associated protein 1 (HAP1), an interactor of
 huntingtin, and its formation is induced by transfection of HAP1-cDNA into cultured cells. Although STB is believed to play
 a protective role in polyglutamine diseases, including Huntington’s disease and spinal and bulbar muscular atrophy, by sequestering
 the causative proteins, huntingtin and androgen receptor, respectively, its physiological function and formation remain poorly
 understood. Therefore, STB is occasionally confused with another cytoplasmic inclusion observed in polyglutamine diseases,
 the aggresome. Here we examined the subcellular dynamics of STB and compared it immunohistochemically and cytochemically with
 the aggresome in...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2590911</comments>
            <pubDate>Mon, 06 Jul 2009 20:15:14 +0100</pubDate>
            <guid isPermaLink="false">2590911</guid>        </item>
        <item>
            <title>TRPV2 expression in rat oral mucosa</title>
            <link>http://www.medworm.com/index.php?rid=2590912&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk216p835k3l68744%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The oral mucosa is a highly specialised, stratified epithelium that confers protection from infection and physical, chemical
 and thermal stimuli. The non-keratinised junctional epithelium surrounds each tooth like a collar and is easily attacked by
 foreign substances from the oral sulcus. We found that TRPV2, a temperature-gated channel, is highly expressed in junctional
 epithelial cells, but not in oral sulcular epithelial cells or oral epithelial cells. Dual or triple immunolabelling with
 immunocompetent cell markers also revealed TRPV2 expression in Langerhans cells and in dendritic cells and macrophages. Electron
 microscopy disclosed TRPV2 immunoreactivity in the unmyelinated and thinly myelinated axons within the connective tissue underlying
 the epithelium. T...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2590912</comments>
            <pubDate>Mon, 06 Jul 2009 20:00:27 +0100</pubDate>
            <guid isPermaLink="false">2590912</guid>        </item>
        <item>
            <title>Quantitative electron microscopy shows uniform incorporation of triglycerides into existing lipid droplets</title>
            <link>http://www.medworm.com/index.php?rid=2550118&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe151256701788uj4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The lipid droplet (LD) is an organelle with a lipid ester core and a surface phospholipid monolayer. The mechanism of LD biogenesis
 is not well understood. The present study aimed to elucidate the LD growth process, for which we developed a new electron
 microscopic method that quantifies the proportion of existing and newly synthesized triglycerides in individual LDs. Our method
 takes advantage of the reactivity of unsaturated fatty acids and osmium tetroxide, which imparts LDs an electron density that
 reflects fatty acid composition. With this method, existing triglyceride-rich LDs in 3Y1 fibroblasts were observed to incorporate
 newly synthesized triglycerides at a highly uniform rate. This uniformity and its persistence even after microtubules were
 depolymerized...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2550118</comments>
            <pubDate>Fri, 26 Jun 2009 07:12:55 +0100</pubDate>
            <guid isPermaLink="false">2550118</guid>        </item>
        <item>
            <title>The murine AE4 promoter predominantly drives type B intercalated cell specific transcription</title>
            <link>http://www.medworm.com/index.php?rid=2503757&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe18w1j22k6w5738t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;AE4 is an anion exchanger almost exclusively expressed in the collecting ducts of the kidney. This very restricted expression
 prompted us to analyze its transcription in more detail. 5′ RACE yielded alternative transcriptional start sites that are
 predicted to code for N-terminal protein variants. Comparison of the 5′ genomic sequence between species identified a transcriptionally
 active region with three conserved spans. In transgenic mice β-galactosidase expression driven by this fragment resembled
 endogenous AE4 expression and was predominantly restricted to type B intercalated cells. Hence this promoter could prove useful
 to target type B intercalated cells by genetic approaches.
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-009-...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503757</comments>
            <pubDate>Mon, 22 Jun 2009 06:43:26 +0100</pubDate>
            <guid isPermaLink="false">2503757</guid>        </item>
        <item>
            <title>Pleiotrophin is expressed in avian somites and tendon anlagen</title>
            <link>http://www.medworm.com/index.php?rid=2503759&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwg36265v032151m7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pleiotrophin (Ptn) is a secreted, developmentally regulated growth factor associated with the extracellular matrix. During
 mammalian embryogenesis, Ptn has been suggested to play a role in the development of various embryonic structures including
 nervous system and skeleton. In the avian embryo, Ptn has been proposed to be involved in limb cartilage development, but
 embryonic Ptn expression has not been comprehensively studied. We isolated a cDNA fragment containing the full-length coding sequence of
 chick Ptn and studied the expression of Ptn in detail until embryonic day 10. We, furthermore, isolated a 6,385-bp phage clone containing the Ptn cDNA of 2,551&amp;nbsp;bp and additional 3,787&amp;nbsp;bp downstream of the published Ptn cDNA sequence classifying a yet Ptn-unrel...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503759</comments>
            <pubDate>Mon, 15 Jun 2009 07:22:23 +0100</pubDate>
            <guid isPermaLink="false">2503759</guid>        </item>
        <item>
            <title>Expression of glutamate receptor subunits in human cancers</title>
            <link>http://www.medworm.com/index.php?rid=2503758&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6630077557772p64%2F</link>
            <description>This study was designed to systematically
 analyze the expression of ionotropic and metabotropic glutamate receptor subunits in various human cancer cell lines, compare
 expression levels to those in human brain tissue and, using electrophysiological techniques, explore whether cancer cells
 respond to glutamate receptor agonists and antagonists. Expression analysis of glutamate receptor subunits NR1-NR3B, GluR1-GluR7, KA1, KA2 and mGluR1-mGluR8 was performed by means of RT-PCR in human rhabdomyosarcoma/medulloblastoma (TE671), neuroblastoma (SK-NA-S), thyroid carcinoma
 (FTC 238), lung carcinoma (SK-LU-1), astrocytoma (MOGGCCM), multiple myeloma (RPMI 8226), glioma (U87-MG and U343), lung carcinoma
 (A549), colon adenocarcinoma (HT 29), T cell leukemia cells (Jurkat E6.1), breast carcinom...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503758</comments>
            <pubDate>Mon, 15 Jun 2009 07:22:23 +0100</pubDate>
            <guid isPermaLink="false">2503758</guid>        </item>
        <item>
            <title>Autometallographic enhancement of the Golgi-Cox staining enables high resolution visualization of dendrites and spines</title>
            <link>http://www.medworm.com/index.php?rid=2467950&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw5gk16820366621n%2F</link>
            <description>We present a method for autometallographic (AMG) enhancement of the Golgi-Cox staining enabling high resolution visualization
 of dendrites and spines. The method is cheaper and more flexible than conventional enhancement procedures performed with commercial
 photographic developers. The staining procedure is thoroughly described and we demonstrate with qualitative and quantitative
 data, how histological tissue sectioning, Golgi-Cox immersion time and different AMG enhancement length may influence the
 staining of dendrites and spines in the rat hippocampus. The described method will be of value for future behavioural-anatomical
 studies, examining changes in dendrite branching and spine density caused by brain diseases and their subsequent treatment.
 
	Content Type Journal ArticleCatego...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2467950</comments>
            <pubDate>Sun, 07 Jun 2009 10:35:26 +0100</pubDate>
            <guid isPermaLink="false">2467950</guid>        </item>
        <item>
            <title>Localization, function and regulation of the two intestinal fatty acid-binding protein types</title>
            <link>http://www.medworm.com/index.php?rid=2462727&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F89866784n3852144%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although intestinal (I) and liver (L) fatty acid binding proteins (FABP) have been widely studied, the physiological significance
 of the presence of the two FABP forms (I- and L-FABP) in absorptive cells remains unknown as do the differences related to
 their distribution along the crypt-villus axis, regional expression, ontogeny and regulation in the human intestine. Our morphological
 experiments supported the expression of I- and L-FABP as early as 13 weeks of gestation. Whereas cytoplasmic immunofluorescence
 staining of L-FABP was barely detectable in the lower half of the villus and in the crypt epithelial cells, I-FABP was visualized
 in epithelial cells of the crypt-villus axis in all intestinal segments until the adult period in which the staining was maximize...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2462727</comments>
            <pubDate>Fri, 05 Jun 2009 09:47:20 +0100</pubDate>
            <guid isPermaLink="false">2462727</guid>        </item>
        <item>
            <title>The neurotoxicological effects of mastoparan Polybia-MPII at the murine neuromuscular junction: an ultrastructural and immunocytochemical study</title>
            <link>http://www.medworm.com/index.php?rid=2462728&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F01g12645l8w015l6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Polybia-MPII (INWLKLGKMVIDAL-NH2), a mastoparan isolated from the crude venom of the swarming wasp Polybia paulista, was injected into the left hind limb of Swiss white mice. Between 3&amp;nbsp;h and 21&amp;nbsp;days later the mice were killed and the soleus
 muscles from both hind limbs were removed. Sections of the muscles were made for transmission electron microscopy and immunocytochemistry.
 Transmission electron microscopy showed that both the volume fraction occupied by synaptic vesicles and synaptic vesicle density
 was greatly reduced after exposure to Polybia-MPII, although there was no significant structural damage to the plasma membrane
 of the terminal boutons and mitochondria were indistinguishable from those in normal, control boutons. Immunocytochemistry
 reveal...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2462728</comments>
            <pubDate>Fri, 05 Jun 2009 09:47:19 +0100</pubDate>
            <guid isPermaLink="false">2462728</guid>        </item>
        <item>
            <title>Characterisation and expression of SPLUNC2, the human orthologue of rodent parotid secretory protein</title>
            <link>http://www.medworm.com/index.php?rid=2462729&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7u12481402135768%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We recently described the Palate Lung Nasal Clone (PLUNC) family of proteins as an extended group of proteins expressed in
 the upper airways, nose and mouth. Little is known about these proteins, but they are secreted into the airway and nasal lining
 fluids and saliva where, due to their structural similarity with lipopolysaccharide-binding protein and bactericidal/permeability-increasing
 protein, they may play a role in the innate immune defence. We now describe the generation and characterisation of novel affinity-purified
 antibodies to SPLUNC2, and use them to determine the expression of this, the major salivary gland PLUNC. Western blotting
 showed that the antibodies identified a number of distinct protein bands in saliva, whilst immunohistochemical analysis de...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2462729</comments>
            <pubDate>Fri, 05 Jun 2009 09:47:17 +0100</pubDate>
            <guid isPermaLink="false">2462729</guid>        </item>
        <item>
            <title>New multiple labelling method for improved satellite cell identification in human muscle: application to a cohort of power-lifters and sedentary men</title>
            <link>http://www.medworm.com/index.php?rid=2455937&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr648p5l1w1331q00%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Presently applied methods to identify and quantify human satellite cells (SCs) give discrepant results. We introduce a new
 immunofluorescence method that simultaneously monitors two SC markers (NCAM and Pax7), the basal lamina and nuclei. Biopsies
 from power-lifters, power-lifters using anabolic substances and untrained subjects were re-examined. Significantly different
 results from those with staining for NCAM and nuclei were observed. There were three subtypes of SCs; NCAM+/Pax7+ (94%), NCAM+/Pax7− (4%) and NCAM−/Pax7+ (1%) but large individual variability existed. The proportion of SCs per nuclei within the basal lamina of myofibres (SC/N)
 was similar for all groups reflecting a balance between the number of SCs and myonuclei to maintain homeostasis. We empha...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2455937</comments>
            <pubDate>Sun, 31 May 2009 08:12:01 +0100</pubDate>
            <guid isPermaLink="false">2455937</guid>        </item>
        <item>
            <title>Human parotid and submandibular glands express and secrete surfactant proteins A, B, C and D</title>
            <link>http://www.medworm.com/index.php?rid=2455938&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F67961332m0763665%2F</link>
            <description>This study aimed to evaluate the expression and presence of surfactant proteins (SP) A, B, C, and D in human salivary glands
 and saliva. The expression of mRNA for SP-A, -B, -C and -D was analyzed by RT-PCR in healthy parotid and submandibular glands.
 Deposition of all surfactant proteins was determined with monoclonal antibodies by means of Western blot analysis and immunohistochemistry
 in healthy tissues and saliva of volunteers. Our results show that all four surfactant proteins SP-A, SP-B, SP-C and SP-D
 are peptides of saliva and salivary glands. Based on the known direct and indirect antimicrobial effects of collectins, the
 surfactant-associated proteins A and D appear to be involved in immune defense inside the oral cavity. Furthermore, by lowering
 surface tension between saliv...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2455938</comments>
            <pubDate>Sat, 30 May 2009 08:20:33 +0100</pubDate>
            <guid isPermaLink="false">2455938</guid>        </item>
        <item>
            <title>The expression pattern of the 70-kDa heat shock protein Hspa2 in mouse tissues</title>
            <link>http://www.medworm.com/index.php?rid=2432115&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F146150160564xnu2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The highest expression level of a 70-kDa heat shock protein family member Hspa2 is detected specifically in meiotic and post-meiotic
 male germ cells, which is reflected by original name of this protein, i.e., testis-specific Hsp70. However, this chaperon
 protein could be also detected in certain somatic tissues. Here, the extra-testicular expression pattern of mouse Hspa2 was
 analyzed. We found expression of Hspa2 in various epithelial cells including lining of bronchioles and oviduct, columnar epithelium
 of endometrium, epithelial reticular cells of thymus, transitional epithelium of the urinary bladder, or ependymal cells covering
 walls of the ventricular system of the brain. Surprisingly, Hspa2 was a putative secretory protein in intestine, endometrial
 glands a...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2432115</comments>
            <pubDate>Fri, 22 May 2009 06:47:09 +0100</pubDate>
            <guid isPermaLink="false">2432115</guid>        </item>
        <item>
            <title>Expression of CPI-17 in smooth muscle during embryonic development and in neointimal lesion formation</title>
            <link>http://www.medworm.com/index.php?rid=2422725&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8212414565240805%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ca2+ sensitivity of smooth muscle (SM) contraction is determined by CPI-17, an inhibitor protein for myosin light chain phosphatase
 (MLCP). CPI-17 is highly expressed in mature SM cells, but the expression level varies under pathological conditions. Here,
 we determined the expression of CPI-17 in embryonic SM tissues and arterial neointimal lesions using immunohistochemistry.
 As seen in adult animals, the predominant expression of CPI-17 was detected at SM tissues on mouse embryonic sections, whereas
 MLCP was ubiquitously expressed. Compared with SM α-actin, CPI-17 expression doubled in arterial SM from embryonic day E10
 to E14. Like SM α-actin and other SM marker proteins, CPI-17 was expressed in embryonic heart, and the expression was down-regulated
 at E17. In...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2422725</comments>
            <pubDate>Wed, 13 May 2009 06:07:29 +0100</pubDate>
            <guid isPermaLink="false">2422725</guid>        </item>
        <item>
            <title>Oligomerized Tie2 localizes to clathrin-coated pits in response to angiopoietin-1</title>
            <link>http://www.medworm.com/index.php?rid=2402520&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk84gt1k7777t122t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The tyrosine kinase receptor Tie2 is expressed on endothelial cells, and together with its ligand angiopoietin-1 (Ang1), is
 important for angiogenesis and vascular stability. Upon activation by Ang1, Tie2 is rapidly internalized and degraded, a mechanism
 most likely necessary to attenuate receptor activity. Using immunogold electron microscopy, we show that on the surface of
 endothelial cells, Tie2 is arranged in variably sized clusters containing dimers and higher order oligomers. Clusters of Tie2
 were expressed on the apical and basolateral plasma membranes, and on the tips of microvilli. Upon activation by Ang1, Tie2
 co-localized with the clathrin heavy chain at the apical and basolateral plasma membranes and within endothelial cells indicating
 that Tie2 intern...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2402520</comments>
            <pubDate>Fri, 08 May 2009 05:58:45 +0100</pubDate>
            <guid isPermaLink="false">2402520</guid>        </item>
        <item>
            <title>Protein phosphatase 1A (PPM1A) is involved in human cytotrophoblast cell invasion and migration</title>
            <link>http://www.medworm.com/index.php?rid=2386506&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb435261153h66013%2F</link>
            <description>The objective of this study was to
 investigate the expression of PPM1A in normal and malignant human placenta and its role in trophoblast invasion, which shares
 many similarities with invasion of tumor cells. By Western blotting and immunocytochemistry, significantly higher expression
 of PPM1A in human placental villi at term was found as compared with that during the first trimester. Furthermore, the expression
 level of PPM1A protein in hydatidiform moles was lower compared with that during normal pregnancy. We further investigated
 the function of PPM1A in extravillous trophoblast cell line HTR8/SVneo. Transwell migration and Matrigel invasion assays demonstrated
 that PPM1A siRNA significantly promoted the motility and invasiveness of the cells. Gelatin zymography showed that knockd...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2386506</comments>
            <pubDate>Thu, 30 Apr 2009 06:03:25 +0100</pubDate>
            <guid isPermaLink="false">2386506</guid>        </item>
        <item>
            <title>The elevated expression of calcitonin receptor by cells recruited into the endothelial layer and neo-intima of atherosclerotic plaque</title>
            <link>http://www.medworm.com/index.php?rid=2386507&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr1048016vp687118%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Calcitonin receptor-immunoreactive (CTR-ir) endothelial and foam cells were identified in atherosclerotic plaque within the
 abdominal and thoracic aortas of rabbits fed a cholesterol-supplemented diet. Initially, cells within the endothelial layers
 of nascent atherosclerotic plaque of arteries were also CD34-positive, a marker of precursor cells of the haematopoietic lineage.
 In a further rabbit model with more advanced cardiovascular disease, CTR-ir cells were located deeper within the plaque as
 well as within the endothelial layer overlying the neo-intima. Finally, in the third model, in which the 4-week period on
 the atherogenic diet was followed by a 12-week period of regression on a normal chow diet, during which serum cholesterol
 levels returned to the norma...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2386507</comments>
            <pubDate>Thu, 30 Apr 2009 06:03:23 +0100</pubDate>
            <guid isPermaLink="false">2386507</guid>        </item>
        <item>
            <title>Human signal peptide had advantage over mouse in secretory expression</title>
            <link>http://www.medworm.com/index.php?rid=2386508&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1t56rt92n7381g64%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The signal peptide is a critical component in the secretory expression of protein in eukaryotic cells. It has been verified
 that the signal peptide of mouse nerve growth factor could mediate the secretory expression of beta-endorphin in cultured
 non-neuronal cells. Although there is a counterpart of nerve growth factor in human genome, no research about the signal sequence
 from human genome has been reported. The function of mediating secretory expression is affected by many factors. We assumed
 that the counterpart from human genome could function as the signal peptide from mouse nerve growth factor does and these
 two signal sequences had different efficiency in mediating secretory expression of beta-endorphin, but we could not figure
 out which one had a better fu...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2386508</comments>
            <pubDate>Thu, 30 Apr 2009 06:03:22 +0100</pubDate>
            <guid isPermaLink="false">2386508</guid>        </item>
        <item>
            <title>The expression of receptivity markers in the fallopian tube epithelium</title>
            <link>http://www.medworm.com/index.php?rid=2366939&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk2627w5882v63404%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pinopodes represent the morphological and integrins, the biomollecular markers of endometrial receptivity. We studied using
 scanning electron microscopy, the expression of pinopodes on tubal samples and their corresponding endometria, from 21 women
 of reproductive age (7 from proliferative phase, 7 from day LH +5 and 7 from day LH +7). In addition, we examined the immunohistochemical
 staining of integrins αvβ3, αvβ5 and their ligands, fibronectin (FN) and osteopontin (OPN) in the same tubal epithelium samples.
 Pinopodes were detected on the tubal epithelium exclusively during day LH +7, coincident with their formation in the endometrium
 and synchronous to αvβ3 sharp increase in the oviduct epithelium, suggesting a regulation similar to the endometrium. In con...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2366939</comments>
            <pubDate>Thu, 23 Apr 2009 08:26:42 +0100</pubDate>
            <guid isPermaLink="false">2366939</guid>        </item>
        <item>
            <title>Galectin-1 induced activation of the mitochondrial apoptotic pathway: evidence for a connection between death-receptor and mitochondrial pathways in human Jurkat T lymphocytes</title>
            <link>http://www.medworm.com/index.php?rid=2358435&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp41342213g13mqm8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Galectin-1 (gal-1) triggers T cell death by several distinct intracellular pathways including the activation of the death-receptor
 pathway. The aim of this study was to investigate whether gal-1 induced activation of the death-receptor pathway in Jurkat
 T lymphocytes mediates apoptosis via the mitochondrial pathway linked by truncated Bid (tBid). We demonstrate that gal-1 induced
 proteolytic cleavage of the death agonist Bid, a member of the Bcl-2/Bcl-xL family and a substrate of activated caspase-8,
 was inhibited by caspase-8 inhibitor II (Z-IETD-FMK). Downstream of Bid, gal-1 stimulated mitochondrial cytochrome c release as well as the activation and proteolytic processing of initiator procaspase-9 were effectively decreased by caspase-8
 inhibitor II. Blocking of...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2358435</comments>
            <pubDate>Tue, 21 Apr 2009 10:04:22 +0100</pubDate>
            <guid isPermaLink="false">2358435</guid>        </item>
        <item>
            <title>Hepatoblast and mesenchymal cell-specific gene-expression in fetal rat liver and in cultured fetal rat liver cells</title>
            <link>http://www.medworm.com/index.php?rid=2358484&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw66153612x07473l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to determine whether passaged rat fetal liver cells are functional hepatoblasts. Hepatocyte/hepatoblast-
 and liver myofibroblast-gene-expressions were studied in adult and fetal rat liver tissues as well as in primary and passaged
 cultures of isolated rat fetal liver cells at both the mRNA and protein level. Desmin- and Alpha-Smooth Muscle Actin (SMA)-positive
 cells were located in the walls of liver vessels, whereas Desmin-positive/SMA-negative cells were distributed within the liver
 parenchyma. Primary cultures contained Prox1-positive hepatoblasts, Desmin/SMA-positive myofibroblasts and only a few Desmin-positive/SMA-negative
 cells. Albumin and alpha-fetoprotein (AFP) could be detected in the primary cultures and to a lesser extent afte...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2358484</comments>
            <pubDate>Tue, 21 Apr 2009 10:04:20 +0100</pubDate>
            <guid isPermaLink="false">2358484</guid>        </item>
        <item>
            <title>A cell culture system for the induction of Mallory bodies: Mallory bodies and aggresomes represent different types of inclusion bodies</title>
            <link>http://www.medworm.com/index.php?rid=2358468&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe37758r781705qg1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mallory bodies (MBs) represent keratin-rich inclusion bodies observed in human alcoholic liver disease and in several chronic
 non-alcoholic liver diseases. The mechanism of their formation and their relationship to other inclusion bodies such as aggresomes
 is incompletely understood. We could induce keratin aggregates typical of MBs in cultured clone 9 rat hepatocytes by transgenic
 expression of wild-type and mutant aquaporin2 or α1-antitrypsin and under various forms of other cellular stress. By immunocytochemical
 analysis, p62 and poly-ubiquitin, components of classical MBs, could be demonstrated in the keratin aggregates of clone 9
 hepatocytes. In addition, histone deacetylase 6, a microtubule-associated deacetylase, was identified as a novel component
 of the ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2358468</comments>
            <pubDate>Tue, 21 Apr 2009 10:04:20 +0100</pubDate>
            <guid isPermaLink="false">2358468</guid>        </item>
        <item>
            <title>Localization of Nopp140 within mammalian cells during interphase and mitosis</title>
            <link>http://www.medworm.com/index.php?rid=2358451&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn36956x78j686185%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We investigated distribution of the nucleolar phosphoprotein Nopp140 within mammalian cells, using immunofluorescence confocal
 microscopy and immunoelectron microscopy. During interphase, three-dimensional image reconstructions of confocal sections
 revealed that nucleolar labelling appeared as several tiny spheres organized in necklaces. Moreover, after an immunogold labelling
 procedure, gold particles were detected not only over the dense fibrillar component but also over the fibrillar centres of
 nucleoli in untreated and actinomycin D-treated cells. Labelling was also consistently present in Cajal bodies. After pulse-chase
 experiments with BrUTP, colocalization was more prominent after a 10- to 15-min chase than after a 5-min chase. During mitosis,
 confocal anal...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2358451</comments>
            <pubDate>Tue, 21 Apr 2009 10:04:20 +0100</pubDate>
            <guid isPermaLink="false">2358451</guid>        </item>
        <item>
            <title>Doxycycline accelerates renal cyst growth and fibrosis in the pcy/pcy mouse model of type 3 nephronophthisis, a form of recessive polycystic kidney disease</title>
            <link>http://www.medworm.com/index.php?rid=2358499&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm8264v32r8j12762%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Nephronophthisis belongs to a family of recessive cystic kidney diseases and may arise from mutations in multiple genes. In
 this report we have used a spontaneous mouse mutant of type 3 nephronophthisis to examine whether the doxycycline-inducible
 synthesis of Timp-2, a natural inhibitor of matrix metalloproteinases, can influence renal cyst growth in transgenic mice.
 Metalloproteinases may exert either a negative or a positive effect on the progression of cystic kidney disease, and we reasoned
 that this may be most effectively examined by using a natural inhibitor. Surprisingly, already the application of doxycycline,
 which also inhibits matrix metalloproteinases, accelerated renal cyst growth and led to increased renal fibrosis, an additional
 effect of Timp-2 wa...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2358499</comments>
            <pubDate>Tue, 21 Apr 2009 10:04:19 +0100</pubDate>
            <guid isPermaLink="false">2358499</guid>        </item>
        <item>
            <title>LPA-induced mutually exclusive subcellular localization of active RhoA and Arp2 mRNA revealed by sequential FRET and FISH</title>
            <link>http://www.medworm.com/index.php?rid=2339996&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F42l2k512431ug630%2F</link>
            <description>In this study we have identified
 lysophosphatidic acid (LPA) as a potent inducer of Arp2 mRNA localization to protrusions in fibroblasts via the RhoA-ROCK
 pathway. As RhoA is known to be activated locally in the cells, we sought to understand how spatial activation of Rho affects
 Arp2 mRNA localization. By sequentially performing fluorescence resonance energy transfer (FRET) and fluorescence in situ
 hybridization (FISH), we have visualized active RhoA and Arp2 mRNA in the same cells. Upon LPA stimulation, approximately
 two times more cells than those in the serum-free medium showed mutually exclusive localization of active RhoA and Arp2 mRNA.
 These results demonstrate the importance of localized activation of Rho in Arp2 mRNA localization and provide new insights
 as to how Rho regul...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2339996</comments>
            <pubDate>Tue, 14 Apr 2009 06:01:46 +0100</pubDate>
            <guid isPermaLink="false">2339996</guid>        </item>
        <item>
            <title>Intracellular dynamics of topoisomerase I inhibitor, CPT-11, by slit-scanning confocal Raman microscopy</title>
            <link>http://www.medworm.com/index.php?rid=2339997&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuq762244119w8857%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Most molecular imaging technologies require exogenous probes and may have some influence on the intracellular dynamics of
 target molecules. In contrast, Raman scattering light measurement can identify biomolecules in their innate state without
 application of staining methods. Our aim was to analyze intracellular dynamics of topoisomerase I inhibitor, CPT-11, by using
 slit-scanning confocal Raman microscopy, which can take Raman images with high temporal and spatial resolution. We could acquire
 images of the intracellular distribution of CPT-11 and its metabolite SN-38 within several minutes without use of any exogenous
 tags. Change of subcellular drug localization after treatment could be assessed by Raman imaging. We also showed intracellular
 conversion from CPT-...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2339997</comments>
            <pubDate>Tue, 14 Apr 2009 06:01:45 +0100</pubDate>
            <guid isPermaLink="false">2339997</guid>        </item>
        <item>
            <title>The metastasis-associated genes MTA1 and MTA3 are abundantly expressed in human placenta and chorionic carcinoma cells</title>
            <link>http://www.medworm.com/index.php?rid=2339998&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3515467g522v9542%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Normal placenta development relies on the ability of trophoblast cells to invade into the uterus and to build up an extensively
 vascularized feto-maternal tissue, necessary for the nutrition of the embryo. The ability of cell migration, invasion, and
 the ability to induce neovascularization are likewise hallmarks of cancer cells. The metastasis-associated genes MTA1 and
 MTA3 are known to be involved in cancer cell migration by regulation of cell adhesion proteins and to induce the expression
 of neoangiogenic cytokines, as recently shown by us for ovarian cancer cells. Therefore, we analyzed the expression of MTA1
 and MTA3 in normal human placenta tissues and the chorionic cancer cell lines BeWo, JEG, and JAR. Immunohistochemical analysis
 revealed a rather strong e...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2339998</comments>
            <pubDate>Sun, 12 Apr 2009 05:48:49 +0100</pubDate>
            <guid isPermaLink="false">2339998</guid>        </item>
        <item>
            <title>Dermatan sulfate domains defined by the novel antibody GD3A12, in normal tissues and ovarian adenocarcinomas</title>
            <link>http://www.medworm.com/index.php?rid=2339999&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg573t79u150h8420%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Dermatan sulfate (DS) expression in normal tissue and ovarian cancer was investigated using the novel, phage display-derived
 antibody GD3A12 that was selected against embryonic glycosaminoglycans (GAGs). Antibody GD3A12 was especially reactive with
 DS rich in IdoA-GalNAc4S disaccharide units. IdoA residues are important for antibody recognition as DS polymers with low
 numbers of IdoA residues were less reactive, and expression of the DS epimerase in ovarian carcinoma cells was associated
 with expression of the GD3A12 epitope. Moreover, staining of antibody GD3A12 was abolished by chondroitinase-B lyase digestion.
 Expression of DS domains defined by antibody GD3A12 was confined to connective tissue of most organs examined and presented
 as a typical fibrillar-type o...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2339999</comments>
            <pubDate>Fri, 10 Apr 2009 05:58:04 +0100</pubDate>
            <guid isPermaLink="false">2339999</guid>        </item>
        <item>
            <title>C-type natriuretic peptide receptor expression in pancreatic alpha cells</title>
            <link>http://www.medworm.com/index.php?rid=2340000&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0vx208h7566t438g%2F</link>
            <description>In conclusion, the NPR-C receptor is expressed
 in normal and neoplastic human alpha cells. These findings suggest a role for natriuretic peptides in the regulation of glucagon
 secretion from human alpha cells.
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-009-0591-3Authors
		Matthew D. Burgess, James A. Haley VA Hospital Surgery and Research &amp; Development Services Research Service (151), 13000 Bruce B. Downs Boulevard Tampa FL 33612-4745 USAKim D. Moore, James A. Haley VA Hospital Surgery and Research &amp; Development Services Research Service (151), 13000 Bruce B. Downs Boulevard Tampa FL 33612-4745 USAGay M. Carter, James A. Haley VA Hospital Surgery and Research &amp; Development Services Research Service (151), 13000 Bruce B. Downs Boulevard Tampa FL 33612-4745 US...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2340000</comments>
            <pubDate>Wed, 08 Apr 2009 08:06:31 +0100</pubDate>
            <guid isPermaLink="false">2340000</guid>        </item>
        <item>
            <title>Distinct temporospatial expression patterns of glycolysis-related proteins in human hepatocellular carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=2340001&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcg862145x5j60u0w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hepatocellular carcinoma (HCC) represents the sixth most frequent human cancer worldwide and is characterized by rapid progression
 as well as resistance to systemic chemotherapy. Recently, glycolysis has emerged as a potent driving force of tumor growth
 and therapy failure. The precise role of glycolysis for the pathogenesis of human HCC has not been elucidated thus far. Therefore,
 we have conducted a comprehensive analysis of the expression patterns of central glycolysis-related factors [glucose transporter-1
 and -2 (Glut-1 and Glut-2), phosphoglycerate kinase-1 (PGK-1) and hypoxia-inducible factor-1α (HIF-1α)] in a large cohort
 of benign and malignant human liver samples. PGK-1 protein and gene expression was scant in normal liver, elevated in cirrhotic
 livers...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2340001</comments>
            <pubDate>Tue, 07 Apr 2009 05:48:02 +0100</pubDate>
            <guid isPermaLink="false">2340001</guid>        </item>
        <item>
            <title>Basement membranes in skin: unique matrix structures with diverse functions?</title>
            <link>http://www.medworm.com/index.php?rid=2323751&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg41v8337hh53j256%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The view of extracellular matrix (ECM) has evolved from a merely scaffolding and space filling tissue element to an interface
 actively controlling cellular activities and tissue functions. A highly specialized form of ECM is the basement membrane (BM),
 an ubiquitous sheet-like polymeric structure composed of a set of distinct glycoproteins and proteoglycans. In this review
 we are largely focusing on function and assembly of BM in skin (1) at the dermo-epidermal interface and (2) in the resident
 micro-vasculature. The role of the non-polymeric components perlecan and particularly nidogen is exemplified by reviewing
 experiments based on genetic approaches and adequate experimental skin models in vivo and in vitro. While in mice total deficiency
 of one of these compo...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2323751</comments>
            <pubDate>Tue, 31 Mar 2009 05:46:24 +0100</pubDate>
            <guid isPermaLink="false">2323751</guid>        </item>
        <item>
            <title>Multiple stimulations for muscle–nerve–blood vessel unit in compensatory hypertrophied skeletal muscle of rat surgical ablation model</title>
            <link>http://www.medworm.com/index.php?rid=2323754&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm774300kg9300152%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tissue inflammation and multiple cellular responses in the compensatory enlarged plantaris (OP Plt) muscle induced by surgical
 ablation of synergistic muscles (soleus and gastrocnemius) were followed over 10 weeks after surgery. Contralateral surgery
 was performed in adult Wistar male rats. Cellular responses in muscle fibers, blood vessels and nerve fibers were analyzed
 by immunohistochemistry and electron microscopy. Severe muscle fiber damage and disappearance of capillaries associated with
 apparent tissue edema were observed in the peripheral portion of OP Plt muscles during the first week, whereas central portions
 were relatively preserved. Marked cell activation/proliferation was also mainly observed in peripheral portions. Similarly,
 activated myogenic cell...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2323754</comments>
            <pubDate>Thu, 26 Mar 2009 08:04:54 +0100</pubDate>
            <guid isPermaLink="false">2323754</guid>        </item>
        <item>
            <title>Chemical analysis of osmium tetroxide staining in adipose tissue using imaging ToF-SIMS</title>
            <link>http://www.medworm.com/index.php?rid=2294710&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx0078760v1630871%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osmium tetroxide (OsO4) is a commonly used stain for unsaturated lipids in electron and optical microscopy of cells and tissues. In this work, the
 localization of osmium oxide and specific lipids was independently monitored in mouse adipose tissue by using time-of-flight
 secondary ion mass spectrometry with Bi cluster primary ions. Substance-specific ion images recorded after OsO4 staining showed that unsaturated C18 fatty acids were colocalized with osmium oxide, corroborating the view that osmium tetroxide
 binds to unsaturated lipids. In contrast, saturated fatty acids (C14, C16 and C18) and also unsaturated C16 fatty acids show
 largely complementary localizations to osmium oxide. Furthermore, the distributions of saturated and unsaturated diglycerides
 are consis...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2294710</comments>
            <pubDate>Wed, 25 Mar 2009 06:55:19 +0100</pubDate>
            <guid isPermaLink="false">2294710</guid>        </item>
        <item>
            <title>Anabolic-androgenic steroid does not enhance compensatory muscle hypertrophy but significantly diminish muscle damages in the rat surgical ablation model</title>
            <link>http://www.medworm.com/index.php?rid=2294706&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx139k86846464384%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cellular responses in the compensatory hypertrophied (plantaris) muscle induced by surgical ablation of synergistic muscles
 (soleus and gastrocnemius) were determined during 10-week anabolic androgenic steroid (AAS) treatment. Adult Wistar male rats
 were divided randomly into the Control and Steroid groups, and contralateral surgery was performed. Nandrolone decanoate was
 administered to the Steroid group. [3H]thymidine and [14C]leucine labeling were used to determine the serial changes in cellular mitotic activity and amino acid uptake. Myogenic
 cells and cellular responses in blood vessels and nerve fibers were analyzed by immunohistochemistry. Significantly lower
 cellular mitotic activity associated with lower volume of muscle fiber necrosis was observed in the ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2294706</comments>
            <pubDate>Wed, 25 Mar 2009 06:55:19 +0100</pubDate>
            <guid isPermaLink="false">2294706</guid>        </item>
        <item>
            <title>Evidence for distinct populations of human Merkel cells</title>
            <link>http://www.medworm.com/index.php?rid=2294714&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F67534w2726x73227%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Merkel cells (MCs) are neuroendocrine cells of unknown origin located in the skin. They are identified at electron microscopic
 level by electron dense granules, at light microscopic level by the presence of cytokeratins 8, 18, 19 and 20. Contradictory
 reports concerning the presence of other molecules of epithelial as well as neural origin prompted us to investigate whether
 there are distinct populations of human MCs. Here, we show the heterogeneous expression of villin, N-CAM, NGF-R, and neurofilaments
 in MCs. Synaptophysin is found in all MCs but with different intensity, nestin is absent. Expression patterns vary between
 interfollicular epidermis, hair follicles and glabrous epidermis. We conclude that there are distinct populations of MCs,
 but all populations ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2294714</comments>
            <pubDate>Wed, 25 Mar 2009 06:55:18 +0100</pubDate>
            <guid isPermaLink="false">2294714</guid>        </item>
        <item>
            <title>Expression and localization of growth hormone receptor in the oviduct of cyclic and pregnant pigs and mid-implantation conceptuses</title>
            <link>http://www.medworm.com/index.php?rid=2283080&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv630874827137600%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Previously it was shown that growth hormone (GH) and its receptor (GH-R) are involved in growth-promoting events during early
 embryonic development. However, it is still unknown if GH-induced GH-R signalling may support other functions within the oviduct.
 The purpose of our study was to analyse GH-R expression and localization in the porcine oviduct during different stages of
 the oestrus cycle and pregnancy (days 2–3 post inseminationem to days 65–71). As shown by reverse transcription polymerase chain reaction (RT-PCR), GH-R is expressed in the porcine oviduct
 during all stages of the oestrus cycle and pregnancy, respectively. Additionally, GH-R mRNA was detected in porcine conceptuses
 collected at day 18 of pregnancy. Using immunohistochemistry, GH-R was excl...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2283080</comments>
            <pubDate>Wed, 18 Mar 2009 07:04:27 +0100</pubDate>
            <guid isPermaLink="false">2283080</guid>        </item>
        <item>
            <title>An active mechanism flanks and modulates the export of the small ribosomal subunits</title>
            <link>http://www.medworm.com/index.php?rid=2283081&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3404786424w67748%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The modalities of export of the ribosomal subunits from the nucleolus to the nuclear pores have been only partially clarified
 since it is not yet clear whether the movements depend purely on diffusion or also from an active process. Recently, we suggested
 the existence of an active transport mechanism of a subset (10–12%) of the small ribosomal subunits (SSU) (Cisterna et al.
 in 2006, Faseb J). Here, we give further evidence that an active, motor protein-mediated process exists for the SSU transport
 from the nucleolus to the nuclear pore. We demonstrate that the blockade of ATP synthesis and antibody-mediated inhibition
 of nuclear myosin or actin induce structural and functional modifications of the nucleolus, suggestive of transcriptional
 activity decrease. Mor...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2283081</comments>
            <pubDate>Wed, 18 Mar 2009 07:04:25 +0100</pubDate>
            <guid isPermaLink="false">2283081</guid>        </item>
        <item>
            <title>Differential membrane redistribution of P2X receptor isoforms in response to osmotic and hyperglycemic stress in the rat lens</title>
            <link>http://www.medworm.com/index.php?rid=2273019&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F973r60426x928255%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;P2X1, 2, 3, 4, 6 and 7 are all expressed in a differentiation-dependent manner in the rat lens. However, in the lens outer cortex the subcellular
 distribution of all P2X isoforms is predominantly associated with a pool of receptors located in cytoplasmic vesicles. Here
 we investigate whether osmotic and hyperglycemic stress can alter the subcellular distribution of this cytoplasmic pool of
 P2X receptors. We show that in a discrete zone of the deeper outer cortex an isoform and stimulus-specific shift in the subcellular
 distribution of P2X receptors occurs from the cytoplasm to defined membrane domains. In response to hypertonic stress P2X1 and P2X4 isoforms became more closely associated with the broad sides of fiber cells, while under hypotonic conditions P2X4 and ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2273019</comments>
            <pubDate>Sat, 14 Mar 2009 13:17:01 +0100</pubDate>
            <guid isPermaLink="false">2273019</guid>        </item>
        <item>
            <title>c-Kit-negative fibroblast-like cells express platelet-derived growth factor receptor α in the murine gastrointestinal musculature</title>
            <link>http://www.medworm.com/index.php?rid=2268239&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7r15477642311335%2F</link>
            <description>In this study, we examined
 PDGFRα immunoreactivity in the murine gastrointestinal tract. PDGFRα-immunopositive (PDGFRα-ip) cells were observed in the
 musculature in all parts of the gastrointestinal tract. Although PDGFRα-ip cells were distinct from ICC and neurons, these
 cells were closely associated with intramuscular ICC and enteric nerve fibers. In the myenteric layer, PDGFRα-ip cells formed
 a cellular network with their ramified processes and encompassed myenteric ganglia. Numerous PDGFRα-ip cells were observed
 in the subserosal plane and showed a multipolar shape. The distribution pattern of the PDGFRα-ip cells in the ICC-deficient
 W
 
 v
 
 /W
 
 v
 mutant mice was the same as that in normal mice. PDGFRα-ip cells that showed intense immunoreactivity of SK3 potassium ch...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2268239</comments>
            <pubDate>Thu, 12 Mar 2009 09:58:22 +0100</pubDate>
            <guid isPermaLink="false">2268239</guid>        </item>
        <item>
            <title>Perivascular cells of the supraspinatus tendon express both tendon- and stem cell-related markers</title>
            <link>http://www.medworm.com/index.php?rid=2268227&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff462p84278p14142%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tendons and ligaments are often affected by mechanical injuries or chronic impairment but other than muscle or bone they possess
 a low healing capacity. So far, little is known about regeneration of tendons and the role of tendon precursor cells in that
 process. We hypothesize that perivascular cells of tendon capillaries are progenitors for functional tendon cells and are
 characterized by expression of marker genes and proteins typical for mesenchymal stem cells and functional tendon cells. Immunohistochemical
 characterization of biopsies derived from intact human supraspinatus tendons was performed. From these biopsies perivascular
 cells were isolated, cultured, and characterized using RT-PCR and Western blotting. We have shown for the first time that
 perivascul...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2268227</comments>
            <pubDate>Thu, 12 Mar 2009 09:58:22 +0100</pubDate>
            <guid isPermaLink="false">2268227</guid>        </item>
        <item>
            <title>Juvenile polyps have gastric differentiation with MUC5AC expression and downregulation of CDX2 and SMAD4</title>
            <link>http://www.medworm.com/index.php?rid=2249448&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa416763545563k86%2F</link>
            <description>In conclusion, juvenile polyps have gastric transdifferentiation
 associated with downregulation of CDX2 and SMAD4, lending support to the role of the BMP/SMAD pathway in CDX2 regulation.
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-009-0579-zAuthors
		Rita Barros, IPATIMUP, Instituto de Patologia e Imunologia Molecular da Universidade do Porto Rua Dr. Roberto Frias si/na 4200 Porto PortugalNuno Mendes, IPATIMUP, Instituto de Patologia e Imunologia Molecular da Universidade do Porto Rua Dr. Roberto Frias si/na 4200 Porto PortugalJames R. Howe, University of Iowa College of Medicine Department of Surgery Iowa City USACelso A. Reis, IPATIMUP, Instituto de Patologia e Imunologia Molecular da Universidade do Porto Rua Dr. Roberto Frias si/na 4200 Porto PortugalCarme...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2249448</comments>
            <pubDate>Fri, 06 Mar 2009 09:46:08 +0100</pubDate>
            <guid isPermaLink="false">2249448</guid>        </item>
        <item>
            <title>Cellular organization of normal mouse liver: a histological, quantitative immunocytochemical, and fine structural analysis</title>
            <link>http://www.medworm.com/index.php?rid=2233953&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe3t2q7h561m08251%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The cellular organization of normal mouse liver was studied using light and electron microscopy and quantitative immunocytochemical
 techniques. The general histological organization of the mouse liver is similar to livers of other mammalian species, with
 a lobular organization based on the distributions of portal areas and central venules. The parenchymal hepatocytes were detected
 with immunocytochemical techniques to recognize albumin or biotin containing cells. The macrophage Kupffer cells were identified
 with F4-80 immunocytochemistry, Ito stellate cells were identified with GFAP immunocytochemistry, and endothelial cells were
 labeled with the CD-34 antibody. Kupffer cells were labeled with intravascularly administered fluorescently labeled latex
 microspheres o...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2233953</comments>
            <pubDate>Tue, 03 Mar 2009 10:52:28 +0100</pubDate>
            <guid isPermaLink="false">2233953</guid>        </item>
        <item>
            <title>Anniversaries, peroxisomes and reactive oxygen species</title>
            <link>http://www.medworm.com/index.php?rid=2223093&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F72565t1g26788786%2F</link>
            <description>Content Type Journal ArticleCategory EditorialDOI 10.1007/s00418-009-0574-4Authors
		Michael Schrader, University of Aveiro Centre for Cell Biology and Department of Biology 3810-193 Aveiro Portugal
	

	
		Journal Histochemistry and Cell BiologyOnline ISSN 1432-119XPrint ISSN 0948-6143 (Source: Histochemistry and Cell Biology)</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2223093</comments>
            <pubDate>Thu, 26 Feb 2009 10:34:29 +0100</pubDate>
            <guid isPermaLink="false">2223093</guid>        </item>
        <item>
            <title>Freeze-fracture electron microscopic study of tight junction strands in HEK293 cells and MDCK II cells expressing claudin-1 mutants in the second extracellular loop</title>
            <link>http://www.medworm.com/index.php?rid=2223094&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx215073728276700%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Claudins constitute tight junction (TJ) strands. In order to examine the function of the second extracellular loop (ECL2),
 we constructed 1CLΔFY and 1CLΔPL in which highly conserved amino acids, FY or PL, in the ECL2 of mouse claudin-1 were deleted.
 They were then tagged with either EGFP at the NH2-terminus (EGFP1CLΔFY and EGFP1CLΔPL) or the myc-epitope at the COOH-terminus (1CLΔFYmyc and 1CLΔPLmyc). The expression of
 EGFP1CLΔFY and EGFP1CLΔPL in TJ-free HEK293 cells formed TJ strands resembling those formed by wild-type claudin-1. The expression
 of 1CLΔPLmyc in TJ-bearing MDCK II cells induced aberrant TJ strands in the lateral plasma membranes whose intramembranous
 particles were almost equally distributed in the P- and E-face. In contrast, 1CLΔFYmyc fo...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2223094</comments>
            <pubDate>Thu, 26 Feb 2009 10:34:28 +0100</pubDate>
            <guid isPermaLink="false">2223094</guid>        </item>
        <item>
            <title>Lipopolysaccharide-binding protein: localization in secretory granules of Paneth cells in the mouse small intestine</title>
            <link>http://www.medworm.com/index.php?rid=2223095&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm326197650r66126%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lipopolysaccharide (LPS)-binding protein (LBP) is an acute-phase protein involved in the host’s response to endotoxin and
 mainly synthesized and secreted to the blood by the liver. But in addition, LBP is also made by extrahepatic cells, including
 the enterocyte-like cell line Caco-2. To study in closer detail the synthesis and storage of LBP in the intestinal mucosal
 epithelium, we performed an immunolocalization of LBP in mouse small intestine. By immunofluorescence microscopy, an antibody
 recognizing the 58–60&amp;nbsp;kDa protein of LBP distinctly labeled a small population of cells located deep into the crypts. This
 cell population was also positive for lysozyme and α-defensin 4, identifying Paneth cells as the main intestinal LBP-producing
 cells. By immunog...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2223095</comments>
            <pubDate>Thu, 26 Feb 2009 10:34:24 +0100</pubDate>
            <guid isPermaLink="false">2223095</guid>        </item>
        <item>
            <title>Molecular mapping deep within a living human organ: analysis of microvessel function on the timescale of seconds and with sub-micrometre spatial resolution</title>
            <link>http://www.medworm.com/index.php?rid=2223096&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F555236x6773385qj%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Visualising vascular endothelial cell function in individual blood microvessels allows elucidation of molecular interactions
 at the vascular wall, the first barrier between blood-borne therapeutic agent and its target. Functional analysis in situ
 requires sub-micrometer spatial resolution and tagged molecules generating contrast in living blood vessels. Light microscopy
 fulfills these requirements, particularly if fluorescent tags deliver the contrast. However, vascular arborisations in living
 organs defy morpho-functional analysis, filling tissues with closely meshed three-dimensional networks which are inaccessible
 to optical imaging. We protocol here successful morpho-functional analysis of microvascular processing in a living organ,
 the human placental cotyled...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2223096</comments>
            <pubDate>Thu, 26 Feb 2009 10:34:23 +0100</pubDate>
            <guid isPermaLink="false">2223096</guid>        </item>
        <item>
            <title>Human mast cells express leptin and leptin receptors</title>
            <link>http://www.medworm.com/index.php?rid=2223097&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe871q4k667j193x7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mast cells are immune cells that produce and secrete a variety of mediators and cytokines that influence various inflammatory
 and immune processes. Leptin is a cytokine regulating metabolic, endocrine as well as immune functions via the leptin receptor
 which is expressed by many immune cells. However, there are no data about leptin receptor expression in mast cells. Immunohistochemical
 and immunofluorescent double stainings showed the expression of leptin and leptin receptors in mast cells in human skin and
 several parts of the respiratory, gastrointestinal and urogenital tract. Leptin was expressed in mast cells expressing the
 classification marker chymase, whereas a variable expression was observed in tryptase positive mast cells. For leptin receptors,
 the expre...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2223097</comments>
            <pubDate>Wed, 25 Feb 2009 10:34:44 +0100</pubDate>
            <guid isPermaLink="false">2223097</guid>        </item>
        <item>
            <title>Claudin-11 is over-expressed and dislocated from the blood–testis barrier in Sertoli cells associated with testicular intraepithelial neoplasia in men</title>
            <link>http://www.medworm.com/index.php?rid=2223098&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F621750v6789568tj%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In mouse testis, claudin-11 is responsible for the formation of specific parallel TJ strands of the blood–testis barrier (BTB).
 Concerning the human BTB, there is no information about the transmembrane TJ proteins. We recently demonstrated the loss of
 functional integrity of the BTB in testicular intraepithelial neoplasia (TIN), associated with a dislocation of the peripheral
 TJ proteins ZO-1 and ZO-2. Here, we determined the expression and distribution of claudin-11 at the human BTB in seminiferous
 tubules with normal spermatogenesis (NSP) and TIN. Immunostaining of claudin-11 revealed intense signals at the basal BTB
 region in seminiferous epithelium with NSP. Within TIN tubules, claudin-11 immunostaining became diffuse and cytoplasmic.
 Double immunogold label...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2223098</comments>
            <pubDate>Wed, 25 Feb 2009 10:34:40 +0100</pubDate>
            <guid isPermaLink="false">2223098</guid>        </item>
        <item>
            <title>Peroxisomes in airway epithelia and future prospects of these organelles for pulmonary cell biology</title>
            <link>http://www.medworm.com/index.php?rid=2205403&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu64753642454555w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Peroxisomes are intimately involved in the metabolism of reactive oxygen species, in the synthesis of ether lipids and of
 polyunsaturated fatty acids as well as in the β-oxidation of bioactive and toxic lipid derivatives. Therefore, the metabolic
 pathways of this organelle might play an important role in pulmonary biology by protection of inner pulmonary surface epithelia
 against oxidative stress, induced by the high oxygen levels in the air and/or by regulation of the lipid homeostasis in pulmonary
 epithelia and the pulmonary surfactant film. In this article, original results on the distribution of peroxisomal marker proteins,
 involved in the biogenesis, ROS- and lipid-metabolism of this organelle in the bronchiolar epithelium and the alveolar region
 of the adul...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2205403</comments>
            <pubDate>Fri, 20 Feb 2009 06:51:45 +0100</pubDate>
            <guid isPermaLink="false">2205403</guid>        </item>
        <item>
            <title>The fate of chondrocytes during ageing of human thyroid cartilage</title>
            <link>http://www.medworm.com/index.php?rid=2205402&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4p7780746468gn12%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Human laryngeal cartilages, especially thyroid cartilage, exhibit gender-specific ageing. In contrast to male thyroid cartilages,
 the ventral half of the female thyroid cartilage plate remains unmineralized until advanced age. In cartilage specimens from
 laryngectomies and autopsies, apoptosis was studied immunohistochemically and the oxidative mitochondrial enzyme nicotinamide
 adenine dinucleotide hydride tetrazolium reductase (NADH-TR) was localized histochemically. In addition, very fresh specimens
 from laryngectomies were fixed under addition of ruthenium hexamine trichloride or tannin to fixation solution to study cell
 organelles of chondrocytes by electron microscopic methods. In general, apoptotic chondrocytes decreased in thyroid cartilages
 of both genders...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2205402</comments>
            <pubDate>Fri, 20 Feb 2009 06:51:45 +0100</pubDate>
            <guid isPermaLink="false">2205402</guid>        </item>
        <item>
            <title>Degradation of excess peroxisomes in mammalian liver cells by autophagy and other mechanisms</title>
            <link>http://www.medworm.com/index.php?rid=2205401&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc221v43611273275%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Here we discuss the mechanisms for the degradation of excess peroxisomes in mammalian hepatocytes which include (a) autophagy,
 (b) the action of peroxisomal Lon protease and (c) the membrane disrupting effect of 15-lipoxygenase. A recent study using
 Atg7 conditional-knock-out mice revealed that 70–80% of excess peroxisomes are degraded by the autophagic process. The remaining
 20–30% of excess peroxisomes is most probably degraded by the action of peroxisomal Lon protease. Finally, a selective disruption
 of the peroxisomal membrane has been shown to be mediated by 15-lipoxygenase activity which is followed by diffusion of matrix
 proteins into the cytoplasm and cytoplasmic proteolysis.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00418-009-0564-6Aut...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2205401</comments>
            <pubDate>Fri, 20 Feb 2009 06:51:45 +0100</pubDate>
            <guid isPermaLink="false">2205401</guid>        </item>
        <item>
            <title>MAPK mediates Hsp25 signaling in incisor development</title>
            <link>http://www.medworm.com/index.php?rid=2205404&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F183431n665185211%2F</link>
            <description>In this study, we investigated incisor development and
 growth in the mouse based on MAPK signaling. Moreover, heat-shock protein (Hsp)-25 is well known to be a useful marker of
 odontoblast differentiation. We used anisomycin (a protein-synthesis inhibitor that activates MAPKs) and U0126 (a MAPK inhibitor
 that blocks ERK1/2 phosphorylation) to examine the role of MAPKs in Hsp25 signaling in the development of the mouse incisor.
 We performed immunohistochemistry and in vitro culture using incisor tooth germ, and found that phospho-ERK (pERK), pMEK,
 and Hsp25 localized in developing incisor ameloblasts and anisomycin failed to produce incisor development. In addition, Western
 blotting results showed that anisomycin stimulated the phosphorylation of ERK, MEK, and Hsp25, and that some of ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2205404</comments>
            <pubDate>Thu, 19 Feb 2009 09:48:23 +0100</pubDate>
            <guid isPermaLink="false">2205404</guid>        </item>
        <item>
            <title>Three-dimensional colocalization analysis of plasma-derived apolipoprotein B with amyloid plaques in APP/PS1 transgenic mice</title>
            <link>http://www.medworm.com/index.php?rid=2205405&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0752k8h748425r28%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Parenchymal accumulation of amyloid-beta (Aβ) is a hallmark pathological feature of Alzheimer’s disease. An emerging hypothesis
 is that blood-to-brain delivery of Aβ may increase with compromised blood–brain barrier integrity. In plasma, substantial
 Aβ is associated with triglyceride-rich lipoproteins (TRLs) secreted by the liver and intestine. Utilizing apolipoprotein B as an exclusive marker of hepatic and intestinal TRLs, here we show utilizing an highly sensitive
 3-dimensional immuno-microscopy imaging technique, that in APP/PS1 amyloid transgenic mice, concomitant with substantially
 increased plasma Aβ, there is a significant colocalization of apolipoprotein B with cerebral amyloid plaque. The findings
 are consistent with the possibility that circulati...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2205405</comments>
            <pubDate>Thu, 19 Feb 2009 09:48:21 +0100</pubDate>
            <guid isPermaLink="false">2205405</guid>        </item>
        <item>
            <title>Oct4 is expressed in Nestin-positive cells as a marker for pancreatic endocrine progenitor</title>
            <link>http://www.medworm.com/index.php?rid=2201075&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj0v75rn316p66312%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There are abundant progenitor cells in the developing pancreas, but molecular markers for these cells are lacking. Octamer-binding
 transcription factor-4 (Oct4) is an important transcription factor for keeping the features of self-renewal and pluripotency
 of embryonic stem cells. It’s well known that Oct4, as a totipotent stem cells marker, just is expressed in totipotent stem
 cells. In the present study, we collected ten human fetal pancreases, and found that Oct4 mRNA and protein were expressed
 in human fetal pancreas samples by RT-PCR, western blot and immunohistochemistry assays. Using double-staining, we demonstrated
 that Oct4 was not co-expressed with Chromogranin A (a peptide expressed in endocrine cells), but partially co-expressed with
 Ngn3 (a transcrip...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2201075</comments>
            <pubDate>Wed, 18 Feb 2009 08:50:42 +0100</pubDate>
            <guid isPermaLink="false">2201075</guid>        </item>
        <item>
            <title>Phagocytic leukocytes and reactive oxygen species</title>
            <link>http://www.medworm.com/index.php?rid=2201077&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh0gj119123060r33%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Phagocytic leukocytes, when appropriately stimulated, display a respiratory burst in which they consume oxygen and produce
 superoxide anions. Superoxide is produced by the phagocyte NADPH-oxidase system which is a multiprotein complex that is dissociated
 in quiescent cells and is assembled into the functional oxidase following stimulation of these cells. Also associated with
 the respiratory burst is the generation of other reactive oxygen species. The identity of components of the NADPH-oxidase
 system and their interactions are known in considerable molecular detail. Understanding of the regulation of superoxide production
 is less well known. This review also points out the important role of microscopy in complementing biochemical studies to understand
 better the ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2201077</comments>
            <pubDate>Wed, 18 Feb 2009 08:50:41 +0100</pubDate>
            <guid isPermaLink="false">2201077</guid>        </item>
        <item>
            <title>Peroxisomes and reactive oxygen species, a lasting challenge</title>
            <link>http://www.medworm.com/index.php?rid=2201076&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26m273611376l504%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Oxidases generating and enzymes scavenging H2O2 predestine peroxisomes (PO) to a pivotal organelle in oxygen metabolism. Catalase, the classical marker enzyme of PO, exhibits
 both catalatic and peroxidatic activity. The latter is responsible for the staining with 3,3′-diamino-benzidine, which greatly
 facilitated the visualization of the organelle and promoted further studies on PO. d-Amino acid oxidase catalyzes with strict stereospecificity the oxidative deamination of d-amino acids. The oxidase is significantly more active in the kidney than in liver and more in periportal than pericentral
 rat hepatocytes. Peroxisomes in these tissues differ in their enzyme activity and protein concentration not only in adjacent
 cells but even within the same one. Moreover, the ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2201076</comments>
            <pubDate>Wed, 18 Feb 2009 08:50:41 +0100</pubDate>
            <guid isPermaLink="false">2201076</guid>        </item>
        <item>
            <title>Peroxisomes: 40 years of histochemical staining, personal reminiscences</title>
            <link>http://www.medworm.com/index.php?rid=2191059&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyl25t4h27833551x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The historical circumstances that led to the discovery of the 3,3′-diamino-benzidine (DAB) method for staining of peroxisomes
 40&amp;nbsp;years ago are reviewed. In the course of studies on the uptake and absorption of horse radish peroxidase in mammalian liver,
 in sections incubated for detection of peroxidase activity in DAB, it was noted that peroxisomes also stained positively for
 peroxidase activity. Subsequently, it was revealed that the peroxidatic activity of catalase, which is abundantly present
 in peroxisomes, is responsible for that staining. This notion was confirmed in quantitative biochemical studies with crystalline
 beef liver catalase and in tracer studies using catalase as an ultrastructural tracer. The application of the DAB method led
 to the disco...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2191059</comments>
            <pubDate>Sat, 14 Feb 2009 10:19:21 +0100</pubDate>
            <guid isPermaLink="false">2191059</guid>        </item>
        <item>
            <title>Biogenesis of peroxisomes and mitochondria: linked by division</title>
            <link>http://www.medworm.com/index.php?rid=2191060&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp826w6211l47u275%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Peroxisomes and mitochondria are metabolically linked organelles, which are crucial to human health and development. The search
 for components involved in their dynamics and maintenance led to the interesting finding that mitochondria and peroxisomes
 share components of their division machinery. Recently, it became clear that this is a common strategy used by mammals, fungi
 and plants. Furthermore, a closer interrelationship between peroxisomes and mitochondria has been proposed, which might have
 an impact on functionality and disease conditions. Here, we briefly highlight the major findings, views and open questions
 concerning peroxisomal formation, division, and interrelationship with mitochondria.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00418-...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2191060</comments>
            <pubDate>Sat, 14 Feb 2009 10:19:20 +0100</pubDate>
            <guid isPermaLink="false">2191060</guid>        </item>
        <item>
            <title>Molecular characterization and analysis of a truncated serotonin receptor gene expressed in neural and reproductive tissues of abalone</title>
            <link>http://www.medworm.com/index.php?rid=2188266&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2865737jl28l1412%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In molluscs, the neurotransmitter serotonin (5-HT) has been linked to a variety of biological roles including gamete maturation
 and spawning. The possible involvement of 5-HT in abalone gamete release was demonstrated by a dose-dependent increase in
 Haliotis rubra gonad contractile bioactivity following 5-HT stimulation. Physiological functions associated with 5-HT, are mediated through
 binding to 5-HT receptors. A cDNA encoding a putative 5-HT receptor consisting of 359 amino acids was isolated from the tropical
 abalone H. asinina, termed 5-HT1&amp;nbsp;ha. The 5-HT1&amp;nbsp;ha shares G-protein-coupled receptor motifs with metazoan 5-HT receptors, including predicted transmembrane domains, active
 sites for protein kinase action, and N-linked glycosylation sites. However,...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2188266</comments>
            <pubDate>Fri, 13 Feb 2009 08:14:04 +0100</pubDate>
            <guid isPermaLink="false">2188266</guid>        </item>
        <item>
            <title>Expression of Snail is associated with myofibroblast phenotype development in oral squamous cell carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=2173455&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj0p26542g3775162%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Snail is a regulator of epithelial–mesenchymal transition (EMT) and considered crucial to carcinoma metastasis, myofibroblast
 transdifferentiation, and fibroblast activation. To investigate the role of Snail in oral squamous cell carcinoma (OSCC),
 its immunohistochemical expression was analysed in 129 OSCC samples and correlated to nodal metastasis, histological grade,
 E-cadherin, and alpha smooth-muscle-actin (αSMA). The results were compared to findings in 23 basal cell carcinomas (BCC).
 Additionally, the influence of TGFβ1 and EGF on Snail, E-cadherin, vimentin, and αSMA expression was analysed in two OSCC
 cell lines. As a result, Snail-positive cells were mainly found in the stroma of the OSCC invasive front without statistically
 significant correlation t...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2173455</comments>
            <pubDate>Sat, 07 Feb 2009 10:10:04 +0100</pubDate>
            <guid isPermaLink="false">2173455</guid>        </item>
        <item>
            <title>Adipophilin distribution and colocalisation with lipid droplets in skeletal muscle</title>
            <link>http://www.medworm.com/index.php?rid=2134902&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe0n1404281608nj2%2F</link>
            <description>In conclusion, this study indicates that the IMCL pool is heterogenous, as the
 majority but not all IMCL contain adipophilin.
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-009-0558-4Authors
		Christopher S. Shaw, University of Birmingham Exercise Metabolism Research Group, School of Sport and Exercise Sciences Edgbaston Birmingham B15 2TT UKMark Sherlock, University of Birmingham School of Clinical and Experimental Medicine, College of Medicine and Dental Sciences Edgbaston Birmingham B15 2TT UKPaul M. Stewart, University of Birmingham School of Clinical and Experimental Medicine, College of Medicine and Dental Sciences Edgbaston Birmingham B15 2TT UKAnton J. M. Wagenmakers, University of Birmingham Exercise Metabolism Research Group, School of Sport and Exercis...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2134902</comments>
            <pubDate>Sat, 24 Jan 2009 12:39:27 +0100</pubDate>
            <guid isPermaLink="false">2134902</guid>        </item>
        <item>
            <title>Progressive renal dysfunction and macrophage infiltration in interstitial fibrosis in an adenine-induced tubulointerstitial nephritis mouse model</title>
            <link>http://www.medworm.com/index.php?rid=2129319&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh643j87t6k63q0x2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Adenine phosphoribosyltransferase deficiency in mice or an excessive oral intake of adenine leads to the accumulation of 2,8-dihydroxyadenine
 (DHA) in renal tubules and that causes progressive renal dysfunction accompanied by interstitial fibrosis. However, the precise
 mechanism responsible for DHA-induced progressive fibrosis is not fully understood. The present study investigates the possible
 involvement of monocytes/macrophages in the progressive fibrosis induced by feeding adenine to mice. Urinary calculi were
 deposited in tubules on day 7 after the initiation of adenine feeding. Elevation of the serum creatinine level and loss of
 body weight were observed in a time-dependent manner, suggesting the development of typical renal dysfunction induced by the
 adenin...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2129319</comments>
            <pubDate>Thu, 22 Jan 2009 09:05:37 +0100</pubDate>
            <guid isPermaLink="false">2129319</guid>        </item>
        <item>
            <title>Synthesis and intracellular transportation of type I procollagen during functional differentiation of odontoblasts</title>
            <link>http://www.medworm.com/index.php?rid=2129320&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk576j31030294315%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The expression of type I collagen, the most component of dentin extracellular matrix proteins (ECMs) in odontoblast is correlated
 with the activity of dentin formation. Since odontoblast possesses a distinct cellular process for protein transport into
 the dentinal tubule, it is important to examine the intracellular protein localization. However, a study focusing on odontoblast
 processes has not been performed. Type I collagen is synthesized as procollagen, which is immediately converted to collagen
 upon secretion. After characterization of antiserum to rat type I procollagen, we investigated the intracellular localization
 of type I procollagen in odontoblasts during and after dentinogenesis, using immunohistochemistry and in situ hybridization.
 The level of mRNA ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2129320</comments>
            <pubDate>Wed, 21 Jan 2009 23:22:54 +0100</pubDate>
            <guid isPermaLink="false">2129320</guid>        </item>
        <item>
            <title>Immunohistochemical analysis of cAMP response element-binding protein in mouse testis during postnatal development and spermatogenesis</title>
            <link>http://www.medworm.com/index.php?rid=2112449&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5xwj5n40262r6440%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Basal activity and cellular localization of cAMP response element-binding protein (CREB) was examined in mouse testis during
 postnatal development and spermatogenesis. Testes of ICR mice sampled on postnatal day (PND) 3, 7, 14, 21, 28, 35, 42, and
 49 were analyzed using Western blotting. Basal CREB activity was significantly higher in early phase (PND 3–7) developing
 testes than in intermediate- and late-phase developing (PND 14–42) and adult testes (PND 49). Furthermore, immunohistochemical
 analysis demonstrated the change of CREB phosphorylation in various testicular cell types during postnatal development. In
 particular, CREB phosphorylation in seminiferous tubules of the adult testis varied according to the spermatogenic cycle,
 while phosphorylation was ev...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2112449</comments>
            <pubDate>Fri, 16 Jan 2009 12:47:02 +0100</pubDate>
            <guid isPermaLink="false">2112449</guid>        </item>
        <item>
            <title>Metallophilic macrophages are fully developed in the thymus of autoimmune regulator (Aire)-deficient mice</title>
            <link>http://www.medworm.com/index.php?rid=2112450&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl5t03012752g75q4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Thymic metallophilic macrophages represent a significant component in the thymus physiology. Recently, we showed their presence
 to be dependent on functional lymphotoxin-β receptor (LTβR) signaling pathway. However, it is unknown whether the development
 of metallophilic macrophages also requires the Autoimmune regulator (Aire) transcription factor, as suggested by some studies
 for medullary thymic epithelial cells, or perhaps the presence of Aire-expressing thymic epithelial cells themselves. Therefore,
 we investigated the presence of metallophilic macrophages in Aire-deficient thymus. Our study shows that the metallophilic
 macrophages are fully developed in the Aire-deficient thymus; their development is not regulated via Aire transcription factor
 and does not ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2112450</comments>
            <pubDate>Fri, 16 Jan 2009 12:47:01 +0100</pubDate>
            <guid isPermaLink="false">2112450</guid>        </item>
        <item>
            <title>Localization of plasma membrane bound NTPDases in the murine reproductive tract</title>
            <link>http://www.medworm.com/index.php?rid=2087246&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff14503k244411n31%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Extracellular nucleotides might influence aspects of the biology of reproduction in that ATP affects smooth muscle contraction,
 participates in steroidogenesis and spermatogenesis, and also regulates transepithelial transport, as in oviducts. Activation
 of cellular nucleotide purinergic receptors is influenced by four plasma membrane-bound members of the ectonucleoside triphosphate
 diphosphohydrolase (E-NTPDase) family, namely NTPDase1, NTPDase2, NTPDase3, and NTPDase8 that differ in their ecto-enzymatic
 properties. The purpose of this study was to characterize the expression profile of the membrane-bound NTPDases in the murine
 female and male reproductive tracts by immunological techniques (immunolabelling, Western blotting) and by enzymatic assays,
 in situ and o...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2087246</comments>
            <pubDate>Tue, 06 Jan 2009 16:16:23 +0100</pubDate>
            <guid isPermaLink="false">2087246</guid>        </item>
        <item>
            <title>The ascorbic acid transporter SVCT2 is expressed in slow-twitch skeletal muscle fibres</title>
            <link>http://www.medworm.com/index.php?rid=2087245&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp551txu511416727%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ascorbic acid, the reduced form of vitamin C, functions as a potent antioxidant as well as in cell differentiation. Ascorbate
 is taken up by mammalian cells through the specific sodium/ascorbate co-transporters SVCT1 and SVCT2. Although skeletal muscle
 contains about 50% of the whole-body vitamin C, the expression of SVCT transporters has not been clearly addressed in this
 tissue. In this work, we analysed the expression pattern of SVCT2 during embryonic myogenesis using the chick as model system.
 We cloned the chick orthologue of SVCT2 (cSVCT2) that shares 93% identity with the mouse transporter. cSVCT2 mRNA and protein
 are expressed during chick embryonic muscle development. Immunohistochemical analyses showed that SVCT2 is preferentially
 expressed by type I slo...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2087245</comments>
            <pubDate>Tue, 06 Jan 2009 16:16:23 +0100</pubDate>
            <guid isPermaLink="false">2087245</guid>        </item>
        <item>
            <title>Differential expression of the integrins α6Aβ4 and α6Bβ4 along the crypt–villus axis in the human small intestine</title>
            <link>http://www.medworm.com/index.php?rid=2065577&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj4288860p6245132%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The integrin α6 subunit exists as two different variants, termed α6A and α6B. These two variants have been shown to harbor
 potentially distinct biochemical properties but little is known about their cellular function. The aim of this work was to
 characterize the expression of the integrin α6A and B variants in relation to cell proliferation and differentiation in the
 human small intestinal epithelium. The results showed distinct expression patterns for the two variants along the crypt–villus
 axis. Indeed, proliferative cells of the crypt were found to predominantly express α6A, while differentiated enterocytes and
 Paneth cells expressed the α6B variant. A similar relationship was observed in intestinal cell models by competitive RT-PCR.
 Further studies in ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2065577</comments>
            <pubDate>Wed, 24 Dec 2008 08:51:29 +0100</pubDate>
            <guid isPermaLink="false">2065577</guid>        </item>
        <item>
            <title>Tracing and ablation of single cells in the mammalian blastocyst using fluorescent DNA staining and multi-photon laser microscopy</title>
            <link>http://www.medworm.com/index.php?rid=2061606&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv7n71grg64n70786%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Comparing the vital DNA dyes Hoechst33342 and DAPI in their ability to visualise cell nuclei of the late rabbit blastocyst,
 both dyes were found to be equally suited despite differences in staining intensity in embryonic versus extraembryonic tissues
 and in nuclear versus cytoplasmic domains at the subcellular level: Both dyes stain all nuclei of a given cell layer (e.g.
 epiblast or hypoblast) evenly and provide satisfactory fluorescence contrast throughout the blastocyst, while not interfering
 with normal development up to 10&amp;nbsp;h in vitro. Using short period (60–300&amp;nbsp;min) irradiation experiments with either dye, single-photon
 (405&amp;nbsp;nm) and multi-photon (800&amp;nbsp;nm) laser excitation was compared in different areas of the same embryo and parameters of ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2061606</comments>
            <pubDate>Sun, 21 Dec 2008 08:18:08 +0100</pubDate>
            <guid isPermaLink="false">2061606</guid>        </item>
        <item>
            <title>DEHP effects on histology and cell proliferation in lung of newborn rats</title>
            <link>http://www.medworm.com/index.php?rid=2056375&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk4h0535180327068%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Di-(2-ethylhexyl)-phthalate (DEHP), the plasticizer employed in the fabrication of polyvinyl chloride, is known to be released
 by many medical devices, namely endotracheal tubes currently utilised for pulmonary ventilation of pre-term newborns. When
 experimentally administered, especially to rodents, the phthalate reportedly causes alterations to several tissues, immature
 animals being even more responsive targets than adult ones. In the present research, female rats were fed with DEHP in the
 last week of pregnancy and after delivery, and lung of their pups was morphologically and immunohistochemically analysed.
 We detected significant alveolar simplification (larger but fewer alveoli with decreased septation), with consequent sensible
 reduction of gas-exchange su...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2056375</comments>
            <pubDate>Fri, 19 Dec 2008 08:15:23 +0100</pubDate>
            <guid isPermaLink="false">2056375</guid>        </item>
        <item>
            <title>Preserved expression of fibroblast growth factor (FGF)-2 and FGF receptor 1 in brain and spinal cord of amyotrophic lateral sclerosis patients</title>
            <link>http://www.medworm.com/index.php?rid=2056374&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4hp646053j96010x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Impaired trophic support of motor neurons appears to be an important pathogenic factor in amyotrophic lateral sclerosis (ALS).
 We investigated the mRNA expression of the pluripotent fibroblast growth factor 2 (FGF-2) and its receptors in post mortem
 spinal cord of ALS and control patients. FGF-2 and FGF receptor (FGFR) 1 and 2 transcripts were first studied in the spinal
 cord using RT-PCR. The cellular distribution of FGF-2 and FGFR mRNA in the spinal cord, motor cortex and brain stem was then
 assessed by in situ hybridization histochemistry. RT-PCR revealed the presence of FGF-2 and FGF receptor 1 and 2 transcripts
 with no obvious differences between ALS and control spinal cord. Comparing mRNA expression in the motoneuron-containing ventral
 horn with the clinical...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2056374</comments>
            <pubDate>Fri, 19 Dec 2008 08:15:23 +0100</pubDate>
            <guid isPermaLink="false">2056374</guid>        </item>
        <item>
            <title>Knockdown of tight junction protein claudin-2 prevents bile canalicular formation in WIF-B9 cells</title>
            <link>http://www.medworm.com/index.php?rid=2047691&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F82598150wq202109%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The polarization of hepatocytes involves formation of functionally distinct sinusoidal (basolateral) and bile canalicular
 (apical) plasma membrane domains that are separated by tight junctions. Although various molecular mechanisms and signaling
 cascades including polarity complex proteins may contribute to bile canalicular formation in hepatocytes, the role of tight
 junction proteins in bile canalicular formation remains unclear. To investigate the role of the integral tight junction protein
 claudin-2 in bile canalicular formation, we depleted claudin-2 expression by siRNA in the polarized hepatic cell line WIF-B9
 after treatment with or without phenobarbital. When WIF-B9 cells were treated with phenobarbital, claudin-2 expression and
 tight junction strands were ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2047691</comments>
            <pubDate>Tue, 16 Dec 2008 07:56:39 +0100</pubDate>
            <guid isPermaLink="false">2047691</guid>        </item>
        <item>
            <title>In situ detection of methylated DNA by histo endonuclease-linked detection of methylated DNA sites: a new principle of analysis of DNA methylation</title>
            <link>http://www.medworm.com/index.php?rid=2018156&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn749l8u222h11420%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s00418-008-0545-1Authors
		Takehiko Koji, Nagasaki University Graduate School of Biomedical Sciences Department of Histology and Cell Biology 1-12-4 Sakamoto Nagasaki 852-8523 JapanShiho Kondo, Nagasaki University Graduate School of Biomedical Sciences Department of Histology and Cell Biology 1-12-4 Sakamoto Nagasaki 852-8523 JapanYoshitaka Hishikawa, Nagasaki University Graduate School of Biomedical Sciences Department of Histology and Cell Biology 1-12-4 Sakamoto Nagasaki 852-8523 JapanShucai An, Nagasaki University Graduate School of Biomedical Sciences Department of Histology and Cell Biology 1-12-4 Sakamoto Nagasaki 852-8523 JapanYoko Sato, Nagasaki University Graduate School of Biomedical Sciences Department of Histology and C...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2018156</comments>
            <pubDate>Fri, 05 Dec 2008 09:17:57 +0100</pubDate>
            <guid isPermaLink="false">2018156</guid>        </item>
        <item>
            <title>Vinculin and cellular retinol-binding protein-1 are markers for quiescent and activated hepatic stellate cells in formalin-fixed paraffin embedded human liver</title>
            <link>http://www.medworm.com/index.php?rid=2018157&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff22178651v75494p%2F</link>
            <description>In conclusion, we therefore propose to use CRBP-1 and/or vinculin to stain HSCs in human liver tissues.
 
	Content Type Journal ArticleCategory Original PaperDOI 10.1007/s00418-008-0544-2Authors
		Elke Van Rossen, Vrije Universiteit Brussel Department of Cell Biology, Faculty of Medicine and Pharmacy Jette BelgiumSara Vander Borght, University of Leuven Laboratory of Morphology and Molecular Pathology Leuven BelgiumLeo Adrianus van Grunsven, Vrije Universiteit Brussel Department of Cell Biology, Faculty of Medicine and Pharmacy Jette BelgiumHendrik Reynaert, Vrije Universiteit Brussel Department of Cell Biology, Faculty of Medicine and Pharmacy Jette BelgiumVeerle Bruggeman, Katholieke Universiteit Leuven Division Livestock-Nutrition-Quality, Department of Biosystems Leuven BelgiumRune Blo...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2018157</comments>
            <pubDate>Thu, 04 Dec 2008 07:10:03 +0100</pubDate>
            <guid isPermaLink="false">2018157</guid>        </item>
        <item>
            <title>In vivo and in vitro effects of SREBP-1 on diabetic renal tubular lipid accumulation and RNAi-mediated gene silencing study</title>
            <link>http://www.medworm.com/index.php?rid=2011579&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj53432ll32787264%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Lipid deposits can injury the kidney of diabetic patients and models. Sterol regulatory element binding protein-1 (SREBP-1)
 is transcription factor regulating the synthesis of fatty acid and triglyceride. At present whether the expression of SREBP-1
 makes some effects on the lipid accumulation in diabetic kidney is not still clear completely. The purpose of our in vivo
 and in vitro study is to investigate the relationship between the expression of SREBP-1 and lipid abnormal metabolism in the
 type 1 diabetic rats and explore to inhibit SREBP-1 gene expression by RNA interfere in human renal proximal tubular epithelial
 cells line (HKC cells). The animal experiment showed that triglyceride and SREBP-1 were up-regulated in proximal tubule of
 diabetic rats’ kidney, w...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2011579</comments>
            <pubDate>Tue, 02 Dec 2008 07:32:18 +0100</pubDate>
            <guid isPermaLink="false">2011579</guid>        </item>
        <item>
            <title>Cellular expression of a monocarboxylate transporter (MCT1) in the mammary gland and sebaceous gland of mice</title>
            <link>http://www.medworm.com/index.php?rid=2011580&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F20156t21p016vv61%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Proton-coupled monocarboxylate transporters (MCTs) are essential for the transport of lactate, ketone bodies, and other monocarboxylates
 through the plasma membrane, but the direction and substrates of transporting in loco remain unclear. The present study examined
 the expression and subcellular localization of MCTs in lipogenic organs. An in situ hybridization survey of major MCT subtypes
 detected an intense expression of MCT1 mRNA in the mammary gland, Harderian gland, and sebaceous gland. The MCT1 immunoreactivity
 was found baso-laterally in acinar cells of the mammary and Harderian glands. Alveolar cells of sebaceous glands in the skin,
 eyelids, and penis contained the membrane-associated MCT1 immunoreactivity along the entire length of the cell surface at
 the...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2011580</comments>
            <pubDate>Tue, 02 Dec 2008 07:32:17 +0100</pubDate>
            <guid isPermaLink="false">2011580</guid>        </item>
        <item>
            <title>Ultrastructural localization of actin and actin-binding proteins in the nucleus</title>
            <link>http://www.medworm.com/index.php?rid=1999355&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj02800235wr76145%2F</link>
            <description>We report for the first time the presence of tropomyosin and p190RhoGAP in the cell nucleus, and the spatial
 colocalization of actin with spectrin, paxillin, and α-actinin in the nucleolus.
 
	Content Type Journal ArticleCategory Short CommunicationDOI 10.1007/s00418-008-0539-zAuthors
		Hana Dingová, Academy of Sciences of the Czech Republic Institute of Molecular Genetics, v.v.i Vídeňská 1083 142 20 Prague 4 Czech RepublicJana Fukalová, Academy of Sciences of the Czech Republic Institute of Molecular Genetics, v.v.i Vídeňská 1083 142 20 Prague 4 Czech RepublicMiloslava Maninová, Academy of Sciences of the Czech Republic Institute of Molecular Genetics, v.v.i Vídeňská 1083 142 20 Prague 4 Czech RepublicVlada V. Philimonenko, Academy of Sciences of the Czech Republic Institute...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1999355</comments>
            <pubDate>Fri, 28 Nov 2008 14:03:17 +0100</pubDate>
            <guid isPermaLink="false">1999355</guid>        </item>
        <item>
            <title>New morphological aspects of blood islands formation in the embryonic mouse hearts</title>
            <link>http://www.medworm.com/index.php?rid=1996833&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg539721481850405%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Vasculogenesis in embryonic hearts proceeds by formation of aggregates consisting of erythroblasts and endothelial cells.
 These aggregates are called blood-islands or blood-island-like structures. We aimed to characterize blood islands in mouse
 embryonic hearts at stages spanning from 11&amp;nbsp;dpc through 13&amp;nbsp;dpc, i.e. prior to the establishment of the coronary circulation.
 Our observations suggested that there are two types of blood islands. One formed by migrating nucleated erythroblasts, which
 associated with migrating endothelial cell and the second by in situ emergence of two kinds of cells belonging to separate
 populations: one resembling an erythroblast progenitor and the second resembling an endothelial-cell progenitor. The subepicardial
 blood islands c...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996833</comments>
            <pubDate>Thu, 27 Nov 2008 09:20:59 +0100</pubDate>
            <guid isPermaLink="false">1996833</guid>        </item>
        <item>
            <title>Distribution of vitamin D binding protein expressing neurons in the rat hypothalamus</title>
            <link>http://www.medworm.com/index.php?rid=1996834&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxr78g73617181033%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We observed immunostaining for vitamin D binding protein (DBP) in rat hypothalamus. Part of the supraoptic and of the paraventricular
 neurons showed DBP immunoreactivity, in part colocalized with Arg-vasopressin. DBP was also observed in widespread axonal
 projections throughout the lateral hypothalamus, the median eminence and the posterior pituitary lobe. A portion of ependymal
 cells, the choroids plexus epithelium and some of the endocrine cells in the anterior pituitary lobe contained DBP immunoreactivity.
 In situ hybridization of semithin sections with a synthetic oligonucleotide probe to DBP mRNA resulted in staining of magnocellular
 hypothalamic neurons, but not of ependymal cells or anterior lobe cells. Our observations indicate an intrinsic expression
 of D...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996834</comments>
            <pubDate>Wed, 26 Nov 2008 19:59:48 +0100</pubDate>
            <guid isPermaLink="false">1996834</guid>        </item>
        <item>
            <title>Characterization of the inflammatory and fibrotic response in a mouse model of cardiac pressure overload</title>
            <link>http://www.medworm.com/index.php?rid=1985264&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F15g624kn84778k82%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Myocardial fibrosis is an integral component of most cardiac pathologic conditions and contributes to the development of both
 systolic and diastolic dysfunction. Because of the availability of genetically manipulated animals, mouse models are essential
 for understanding the mechanisms involved in the pathogenesis of cardiac fibrosis. Accordingly, we characterized the inflammatory
 and fibrotic response in a mouse model of cardiac pressure overload due to transverse aortic constriction (TAC). Following
 TAC, mouse hearts exhibited induction of chemokines and proinflammatory cytokines, associated with macrophage, but not neutrophil,
 infiltration. Induction of inflammatory cytokines was followed by a late upregulation of transforming growth factor (TGF)-β
 isoforms, ac...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1985264</comments>
            <pubDate>Sun, 23 Nov 2008 06:47:00 +0100</pubDate>
            <guid isPermaLink="false">1985264</guid>        </item>
        <item>
            <title>Extracellular matrix control of mammary gland morphogenesis and tumorigenesis: insights from imaging</title>
            <link>http://www.medworm.com/index.php?rid=1964353&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc412459656107n4u%2F</link>
            <description>We describe how the ECM directs mammary gland formation and function, and discuss how a cell’s inability to
 interpret these signals—whether as a result of genetic insults or physicochemical alterations in the ECM—disorganizes the
 gland and promotes malignancy. By restoring context and forcing cells to properly interpret these native signals, aberrant
 behavior can be quelled and organization re-established. Traditional imaging approaches have been a key complement to the
 standard biochemical, molecular, and cell biology approaches used in these studies. Utilizing imaging modalities with enhanced
 spatial resolution in live tissues may uncover additional means by which the ECM regulates tissue structure, on different
 length scales, through its pericellular organization (short-scal...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1964353</comments>
            <pubDate>Fri, 14 Nov 2008 08:00:19 +0100</pubDate>
            <guid isPermaLink="false">1964353</guid>        </item>
        <item>
            <title>Enzyme-assisted photosensitization activates different apoptotic pathways in Rose Bengal acetate treated HeLa cells</title>
            <link>http://www.medworm.com/index.php?rid=1964354&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu6135q76k120x500%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Photosensitization of tumor cells after incubation with Rose Bengal acetate (RB-Ac) induces multiple organelle photodamage
 followed by apoptotic cell death. We used immunocytochemical techniques in multicolor fluorescence microscopy to elucidate
 whether this occurs through the simultaneous activation of different apoptotic pathways, in HeLa cells. We detected in situ
 the activated forms of caspases 9 and 3, and the translocation from the mitochondria to the nucleus of the apoptosis inducing
 factor; DNA electrophoretic techniques were also used to assess the occurrence of nuclear DNA cleavage into either high- or
 low-molecular-weight fragments. Both the caspase-dependent and caspase-independent apoptotic pathways are activated. The genomic
 DNA is degraded into high...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1964354</comments>
            <pubDate>Fri, 14 Nov 2008 08:00:14 +0100</pubDate>
            <guid isPermaLink="false">1964354</guid>        </item>
        <item>
            <title>Chick embryo chorioallantoic membrane model systems to study and visualize human tumor cell metastasis</title>
            <link>http://www.medworm.com/index.php?rid=1961287&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk600u2200623h461%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Since their introduction almost a century ago, chick embryo model systems involving the technique of chorioallantoic grafting
 have proved invaluable in the in vivo studies of tumor development and angiogenesis and tumor cell dissemination. The ability
 of the chick embryo’s chorioallantoic membrane (CAM) to efficiently support the growth of inoculated xenogenic tumor cells
 greatly facilitates analysis of human tumor cell metastasis. During spontaneous metastasis, the highly vascularized CAM sustains
 rapid tumor formation within several days following cell grafting. The dense capillary network of the CAM also serves as a
 repository of aggressive tumor cells that escaped from the primary tumor and intravasated into the host vasculature. This
 spontaneous metastasis ...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1961287</comments>
            <pubDate>Thu, 13 Nov 2008 15:45:16 +0100</pubDate>
            <guid isPermaLink="false">1961287</guid>        </item>
        <item>
            <title>Increased expression of glycodelin mRNA and protein in rat lungs during ovalbumin-induced allergic airway inflammation</title>
            <link>http://www.medworm.com/index.php?rid=1961288&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F84x2n3n04q406q22%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Asthma is a chronic inflammatory disease accompanied by airway obstruction and hyper-responsiveness. Asthmatic inflammation
 is characterized by the expression of multiple genes for inflammatory mediators. Glycodelin is a glycoprotein with several
 functions in cell recognition and differentiation. There is substantial evidence that glycodelin may be a mediator for immunomodulatory
 and immunosuppressive effects on several human tissues. To determine the potential role of glycodelin in the pulmonary immune
 response, we examined the distribution of the glycodelin mRNA and protein in an experimental rat model of allergen-induced
 airway inflammation. The experimental model developed an airway response to inhaled nebulized ovalbumin in adult rats. Two
 groups of rats (ova...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1961288</comments>
            <pubDate>Wed, 12 Nov 2008 22:21:42 +0100</pubDate>
            <guid isPermaLink="false">1961288</guid>        </item>
        <item>
            <title>Localization of ank1.5 in the sarcoplasmic reticulum precedes that of SERCA and RyR: relationship with the organization of obscurin in developing sarcomeres</title>
            <link>http://www.medworm.com/index.php?rid=1955525&amp;cid=s_35968_61_f&amp;fid=35968&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj877u676x1885u6h%2F</link>
            <description>We report here studies on the localization of obscurin and ank1.5 in embryonic
 and postnatal rodent skeletal muscles. Using two antibodies against epitopes in the N- and C-terminus of obscurin, two distinct
 patterns of localization were observed. Before birth, the antibodies against the N- and the C-terminus of obscurin stained
 the Z-disk and M-band, respectively. At the same time, ank1.5 was detected at the Z-disk, rising the possibility that obscurin
 molecules at M-band may not be able to interact with ank1.5. Localization of ank1.5 at Z-disks in E14 muscle fibers revealed
 that ank1.5 is among the earliest SR proteins to assemble, since its organization preceded that of other SR proteins, like
 SERCA and RyR. After birth, the antibody against the N-terminus of obscurin stained the M...</description>
            <author>Histochemistry and Cell Biology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1955525</comments>
            <pubDate>Tue, 11 Nov 2008 07:58:41 +0100</pubDate>
            <guid isPermaLink="false">1955525</guid>        </item>
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