Further similarities between astrocytes and perisinusoidal stellate cells of liver (Ito cells): Colocalization of desmin and glial fibrillary acidic protein in astroglial primary cultures
The colocalization of desmin and glial fibrillary acidic protein (GFAP) in astrocytes was inferred from previous studies demonstrating a unique antigenic composition comprising GFAP, desmin and vimentin in perisinusoidal stellate cells (PSC) of liver which share several features with astrocytes. In...
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Veröffentlicht in: | Biology of the cell 1997-06, Vol.89 (3), p.169-177 |
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description | The colocalization of desmin and glial fibrillary acidic protein (GFAP) in astrocytes was inferred from previous studies demonstrating a unique antigenic composition comprising GFAP, desmin and vimentin in perisinusoidal stellate cells (PSC) of liver which share several features with astrocytes. In the present study the colocalization of GFAP and desmin was investigated by double-immunolabeling experiments in 12-day-old rat astroglial primary cultures with antiserum against GFAP and two commercial monoclonal antibodies against desmin, antibodies of clone DEU-10 and clone DEB-5. These antibodies selectively decorated the perisinusoidal stellate cells (PSC) of liver for which desmin is known to be a marker. The results obtained with astroglial cells demonstrate that both GFAP and desmin are coexpressed in morphologically different types, process-bearing and process-lacking astrocytes. The expression of desmin was apparently more pronounced in process-lacking astrocytes and was considerably lower in process-bearing ones. In process-lacking astrocytes, in contrast to filamentous cytoplasmic staining for GFAP, the immunoreactivity for desmin was non-filamentous and was irregularly spread in the perinuclear cytoplasm of the cells, while in process-bearing astrocytes the pattern of staining for desmin was similar to that of GFAP. The variability in the intensity and pattern of staining for desmin in astrocytes might be due to transitional stages of differentiation for part of the cells. This interpretation was supported by the presence of GFAP in the cells weakly expressing smooth muscle alpha-actin and the absence of GFAP in the cells enriched with microfilaments. |
doi_str_mv | 10.1016/S0248-4900(97)80034-2 |
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In the present study the colocalization of GFAP and desmin was investigated by double-immunolabeling experiments in 12-day-old rat astroglial primary cultures with antiserum against GFAP and two commercial monoclonal antibodies against desmin, antibodies of clone DEU-10 and clone DEB-5. These antibodies selectively decorated the perisinusoidal stellate cells (PSC) of liver for which desmin is known to be a marker. The results obtained with astroglial cells demonstrate that both GFAP and desmin are coexpressed in morphologically different types, process-bearing and process-lacking astrocytes. The expression of desmin was apparently more pronounced in process-lacking astrocytes and was considerably lower in process-bearing ones. In process-lacking astrocytes, in contrast to filamentous cytoplasmic staining for GFAP, the immunoreactivity for desmin was non-filamentous and was irregularly spread in the perinuclear cytoplasm of the cells, while in process-bearing astrocytes the pattern of staining for desmin was similar to that of GFAP. The variability in the intensity and pattern of staining for desmin in astrocytes might be due to transitional stages of differentiation for part of the cells. This interpretation was supported by the presence of GFAP in the cells weakly expressing smooth muscle alpha-actin and the absence of GFAP in the cells enriched with microfilaments.</description><identifier>ISSN: 0248-4900</identifier><identifier>EISSN: 1768-322X</identifier><identifier>DOI: 10.1016/S0248-4900(97)80034-2</identifier><identifier>PMID: 9429301</identifier><language>eng</language><publisher>England: Elsevier SAS</publisher><subject>Actins - analysis ; Animals ; antigenic composition ; Astrocytes - chemistry ; Astrocytes - cytology ; Cells, Cultured ; Desmin - analysis ; differentiation smooth muscle alpha-actin ; double-immunolabeling ; Fluorescent Antibody Technique, Indirect ; Glial Fibrillary Acidic Protein - analysis ; intermediate filaments ; Liver - chemistry ; Liver - cytology ; Muscle, Smooth - chemistry ; Rats ; Rats, Sprague-Dawley ; Rats, Wistar ; Staining and Labeling</subject><ispartof>Biology of the cell, 1997-06, Vol.89 (3), p.169-177</ispartof><rights>1997</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-fde7ce9ae975f86664cceb93ad6bf51cc51f2eb7be2c3a4d3cf45bffea10830e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9429301$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Buniatian, Gayane Hrachia</creatorcontrib><title>Further similarities between astrocytes and perisinusoidal stellate cells of liver (Ito cells): Colocalization of desmin and glial fibrillary acidic protein in astroglial primary cultures</title><title>Biology of the cell</title><addtitle>Biol Cell</addtitle><description>The colocalization of desmin and glial fibrillary acidic protein (GFAP) in astrocytes was inferred from previous studies demonstrating a unique antigenic composition comprising GFAP, desmin and vimentin in perisinusoidal stellate cells (PSC) of liver which share several features with astrocytes. In the present study the colocalization of GFAP and desmin was investigated by double-immunolabeling experiments in 12-day-old rat astroglial primary cultures with antiserum against GFAP and two commercial monoclonal antibodies against desmin, antibodies of clone DEU-10 and clone DEB-5. These antibodies selectively decorated the perisinusoidal stellate cells (PSC) of liver for which desmin is known to be a marker. The results obtained with astroglial cells demonstrate that both GFAP and desmin are coexpressed in morphologically different types, process-bearing and process-lacking astrocytes. The expression of desmin was apparently more pronounced in process-lacking astrocytes and was considerably lower in process-bearing ones. In process-lacking astrocytes, in contrast to filamentous cytoplasmic staining for GFAP, the immunoreactivity for desmin was non-filamentous and was irregularly spread in the perinuclear cytoplasm of the cells, while in process-bearing astrocytes the pattern of staining for desmin was similar to that of GFAP. The variability in the intensity and pattern of staining for desmin in astrocytes might be due to transitional stages of differentiation for part of the cells. This interpretation was supported by the presence of GFAP in the cells weakly expressing smooth muscle alpha-actin and the absence of GFAP in the cells enriched with microfilaments.</description><subject>Actins - analysis</subject><subject>Animals</subject><subject>antigenic composition</subject><subject>Astrocytes - chemistry</subject><subject>Astrocytes - cytology</subject><subject>Cells, Cultured</subject><subject>Desmin - analysis</subject><subject>differentiation smooth muscle alpha-actin</subject><subject>double-immunolabeling</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Glial Fibrillary Acidic Protein - analysis</subject><subject>intermediate filaments</subject><subject>Liver - chemistry</subject><subject>Liver - cytology</subject><subject>Muscle, Smooth - chemistry</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rats, Wistar</subject><subject>Staining and Labeling</subject><issn>0248-4900</issn><issn>1768-322X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks2KFTEQhYMo43X0EQaykplFa9Lpv7iR4eLowIALFdyFdFLRknTnmqRHxlfz5Uzf27h1VVD1cahTdQi54OwVZ7x7_YnVzVA1krFL2V8NjImmqh-RHe-7oRJ1_fUx2f1DnpJnKf1gjDVyaM_ImWxqKRjfkT83S8zfIdKEE3odMSMkOkL-BTBTnXIM5iGXlp4tPUDEhPOSAlrtacrgvc5ATamJBkc93hepy9scTr2rN3QffDDa42-dMcwrZCFNOB8Fv3ksOg7HiEUpPlBt0KKhhxgyFAa3FU7cIeK0QmbxeYmQnpMnTvsEL7Z6Tr7cvPu8_1DdfXx_u7--q4xo2lw5C70BqUH2rRu6rmuMgVEKbbvRtdyYlrsaxn6E2gjdWGFc047OgeZsEAzEOXl50i1r_VwgZTVhWv3pGcKSVC9b3nbloP8DeSf6ruVDAS82cBknsGpzpra3lPnb0xyKrXuEqJJBmA1YjGCysgEVZ2rNgTrmQK1PVrJXxxyoWvwF_XOrag</recordid><startdate>19970601</startdate><enddate>19970601</enddate><creator>Buniatian, Gayane Hrachia</creator><general>Elsevier SAS</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>19970601</creationdate><title>Further similarities between astrocytes and perisinusoidal stellate cells of liver (Ito cells): Colocalization of desmin and glial fibrillary acidic protein in astroglial primary cultures</title><author>Buniatian, Gayane Hrachia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-fde7ce9ae975f86664cceb93ad6bf51cc51f2eb7be2c3a4d3cf45bffea10830e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Actins - analysis</topic><topic>Animals</topic><topic>antigenic composition</topic><topic>Astrocytes - chemistry</topic><topic>Astrocytes - cytology</topic><topic>Cells, Cultured</topic><topic>Desmin - analysis</topic><topic>differentiation smooth muscle alpha-actin</topic><topic>double-immunolabeling</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Glial Fibrillary Acidic Protein - analysis</topic><topic>intermediate filaments</topic><topic>Liver - chemistry</topic><topic>Liver - cytology</topic><topic>Muscle, Smooth - chemistry</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rats, Wistar</topic><topic>Staining and Labeling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Buniatian, Gayane Hrachia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Buniatian, Gayane Hrachia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Further similarities between astrocytes and perisinusoidal stellate cells of liver (Ito cells): Colocalization of desmin and glial fibrillary acidic protein in astroglial primary cultures</atitle><jtitle>Biology of the cell</jtitle><addtitle>Biol Cell</addtitle><date>1997-06-01</date><risdate>1997</risdate><volume>89</volume><issue>3</issue><spage>169</spage><epage>177</epage><pages>169-177</pages><issn>0248-4900</issn><eissn>1768-322X</eissn><abstract>The colocalization of desmin and glial fibrillary acidic protein (GFAP) in astrocytes was inferred from previous studies demonstrating a unique antigenic composition comprising GFAP, desmin and vimentin in perisinusoidal stellate cells (PSC) of liver which share several features with astrocytes. In the present study the colocalization of GFAP and desmin was investigated by double-immunolabeling experiments in 12-day-old rat astroglial primary cultures with antiserum against GFAP and two commercial monoclonal antibodies against desmin, antibodies of clone DEU-10 and clone DEB-5. These antibodies selectively decorated the perisinusoidal stellate cells (PSC) of liver for which desmin is known to be a marker. The results obtained with astroglial cells demonstrate that both GFAP and desmin are coexpressed in morphologically different types, process-bearing and process-lacking astrocytes. The expression of desmin was apparently more pronounced in process-lacking astrocytes and was considerably lower in process-bearing ones. In process-lacking astrocytes, in contrast to filamentous cytoplasmic staining for GFAP, the immunoreactivity for desmin was non-filamentous and was irregularly spread in the perinuclear cytoplasm of the cells, while in process-bearing astrocytes the pattern of staining for desmin was similar to that of GFAP. The variability in the intensity and pattern of staining for desmin in astrocytes might be due to transitional stages of differentiation for part of the cells. This interpretation was supported by the presence of GFAP in the cells weakly expressing smooth muscle alpha-actin and the absence of GFAP in the cells enriched with microfilaments.</abstract><cop>England</cop><pub>Elsevier SAS</pub><pmid>9429301</pmid><doi>10.1016/S0248-4900(97)80034-2</doi><tpages>9</tpages></addata></record> |
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subjects | Actins - analysis Animals antigenic composition Astrocytes - chemistry Astrocytes - cytology Cells, Cultured Desmin - analysis differentiation smooth muscle alpha-actin double-immunolabeling Fluorescent Antibody Technique, Indirect Glial Fibrillary Acidic Protein - analysis intermediate filaments Liver - chemistry Liver - cytology Muscle, Smooth - chemistry Rats Rats, Sprague-Dawley Rats, Wistar Staining and Labeling |
title | Further similarities between astrocytes and perisinusoidal stellate cells of liver (Ito cells): Colocalization of desmin and glial fibrillary acidic protein in astroglial primary cultures |
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