Transcription and translation of gp600 and receptor-associated protein (RAP) in active Heymann nephritis
Active Heymann nephritis (HN) of rat, an autoimmune glomerular disease, is a model for human membranous glomerulonephropathy. The autoantigen of HN is a glycoprotein of approximately 600 kd that is present in both rat and human kidneys. Another kidney protein of 39-45 kd called receptor-associated p...
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Veröffentlicht in: | The American journal of pathology 1995-06, Vol.146 (6), p.1481-1487 |
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description | Active Heymann nephritis (HN) of rat, an autoimmune glomerular disease, is a model for human membranous glomerulonephropathy. The autoantigen of HN is a glycoprotein of approximately 600 kd that is present in both rat and human kidneys. Another kidney protein of 39-45 kd called receptor-associated protein (RAP) is associated with gp600. In normal kidney very little gp600 and RAP can be detected in glomeruli. This study was undertaken to determine whether the synthesis of gp600 and RAP would increase after development of active HN. Kidneys from normal (n = 5) and active (n = 11) HN rats were studied for expression of gp600 and RAP and their mRNAs by immunofluorescence and in situ hybridization. In all HN kidneys in contrast to normal kidneys both the transcription and translation of gp600 were markedly increased in glomeruli and proximal tubules. Transcription and translation of RAP were also increased but less so than gp600. The site of increased transcription of gp600 and RAP in glomeruli was clearly localized to the visceral glomerular epithelial cells.
This is the first study to show increased transcription of gp600 and RAP in active HN and the first study to identify the visceral glomerular epithelial cell as the cell for the increased transcription. |
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This is the first study to show increased transcription of gp600 and RAP in active HN and the first study to identify the visceral glomerular epithelial cell as the cell for the increased transcription.</description><identifier>ISSN: 0002-9440</identifier><identifier>EISSN: 1525-2191</identifier><identifier>PMID: 7778686</identifier><language>eng</language><publisher>United States: ASIP</publisher><subject>Animals ; Autoantigens - analysis ; Carrier Proteins - biosynthesis ; Carrier Proteins - immunology ; Female ; Fluorescent Antibody Technique ; Glomerulonephritis - genetics ; Glomerulonephritis - metabolism ; Glycoproteins - biosynthesis ; Glycoproteins - immunology ; Heymann Nephritis Antigenic Complex ; In Situ Hybridization ; Kidney Glomerulus - immunology ; LDL-Receptor Related Protein-Associated Protein ; Membrane Glycoproteins - biosynthesis ; Membrane Glycoproteins - immunology ; Protein Biosynthesis - genetics ; Rats ; Rats, Inbred Lew ; Transcription, Genetic - genetics ; Up-Regulation</subject><ispartof>The American journal of pathology, 1995-06, Vol.146 (6), p.1481-1487</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1870916/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1870916/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7778686$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Makker, SP</creatorcontrib><creatorcontrib>Widstrom, R</creatorcontrib><creatorcontrib>Huang, J</creatorcontrib><title>Transcription and translation of gp600 and receptor-associated protein (RAP) in active Heymann nephritis</title><title>The American journal of pathology</title><addtitle>Am J Pathol</addtitle><description>Active Heymann nephritis (HN) of rat, an autoimmune glomerular disease, is a model for human membranous glomerulonephropathy. The autoantigen of HN is a glycoprotein of approximately 600 kd that is present in both rat and human kidneys. Another kidney protein of 39-45 kd called receptor-associated protein (RAP) is associated with gp600. In normal kidney very little gp600 and RAP can be detected in glomeruli. This study was undertaken to determine whether the synthesis of gp600 and RAP would increase after development of active HN. Kidneys from normal (n = 5) and active (n = 11) HN rats were studied for expression of gp600 and RAP and their mRNAs by immunofluorescence and in situ hybridization. In all HN kidneys in contrast to normal kidneys both the transcription and translation of gp600 were markedly increased in glomeruli and proximal tubules. Transcription and translation of RAP were also increased but less so than gp600. The site of increased transcription of gp600 and RAP in glomeruli was clearly localized to the visceral glomerular epithelial cells.
This is the first study to show increased transcription of gp600 and RAP in active HN and the first study to identify the visceral glomerular epithelial cell as the cell for the increased transcription.</description><subject>Animals</subject><subject>Autoantigens - analysis</subject><subject>Carrier Proteins - biosynthesis</subject><subject>Carrier Proteins - immunology</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>Glomerulonephritis - genetics</subject><subject>Glomerulonephritis - metabolism</subject><subject>Glycoproteins - biosynthesis</subject><subject>Glycoproteins - immunology</subject><subject>Heymann Nephritis Antigenic Complex</subject><subject>In Situ Hybridization</subject><subject>Kidney Glomerulus - immunology</subject><subject>LDL-Receptor Related Protein-Associated Protein</subject><subject>Membrane Glycoproteins - biosynthesis</subject><subject>Membrane Glycoproteins - immunology</subject><subject>Protein Biosynthesis - genetics</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>Transcription, Genetic - genetics</subject><subject>Up-Regulation</subject><issn>0002-9440</issn><issn>1525-2191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUNtKxDAQLaLoevkEoU9eHgpJmk3SF0HEGwiK6HOYJrPbSJvUJKv491ZdRB-GmTPncA4zG8WMztm8YrShm8WMEMKqhnOyU-ym9DJBUSuyXWxLKZVQYlZ0TxF8MtGN2QVfgrdl_tr08I3DolyOgpBvIqLBMYdYQUrBOMhoyzGGjM6XJ4_nD6flNIDJ7g3LG_wYwPvS49hFl13aL7YW0Cc8WPe94vnq8uniprq7v769OL-rOtbUuQKLtLU11GYBsuUtV2oqAq3lAILLtqZNq4QhwFTLUDZ0wYQxdo7GKmVFvVec_fiOq3ZAa9BP9_R6jG6A-KEDOP2f8a7Ty_CmqZKkoV8GR2uDGF5XmLIeXDLY9-AxrJKWsmZ8TtkkPPyb9Bux_u3EH__wnVt27y6iTgP0_aSmGl5GyoUWmnJF60-XgocS</recordid><startdate>19950601</startdate><enddate>19950601</enddate><creator>Makker, SP</creator><creator>Widstrom, R</creator><creator>Huang, J</creator><general>ASIP</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19950601</creationdate><title>Transcription and translation of gp600 and receptor-associated protein (RAP) in active Heymann nephritis</title><author>Makker, SP ; Widstrom, R ; Huang, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h293t-ade1bd3a3cfa7b4b488b480abd4aa647b319b86c0a28b2e791f26ccd5ecd88d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Autoantigens - analysis</topic><topic>Carrier Proteins - biosynthesis</topic><topic>Carrier Proteins - immunology</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>Glomerulonephritis - genetics</topic><topic>Glomerulonephritis - metabolism</topic><topic>Glycoproteins - biosynthesis</topic><topic>Glycoproteins - immunology</topic><topic>Heymann Nephritis Antigenic Complex</topic><topic>In Situ Hybridization</topic><topic>Kidney Glomerulus - immunology</topic><topic>LDL-Receptor Related Protein-Associated Protein</topic><topic>Membrane Glycoproteins - biosynthesis</topic><topic>Membrane Glycoproteins - immunology</topic><topic>Protein Biosynthesis - genetics</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>Transcription, Genetic - genetics</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Makker, SP</creatorcontrib><creatorcontrib>Widstrom, R</creatorcontrib><creatorcontrib>Huang, J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Makker, SP</au><au>Widstrom, R</au><au>Huang, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcription and translation of gp600 and receptor-associated protein (RAP) in active Heymann nephritis</atitle><jtitle>The American journal of pathology</jtitle><addtitle>Am J Pathol</addtitle><date>1995-06-01</date><risdate>1995</risdate><volume>146</volume><issue>6</issue><spage>1481</spage><epage>1487</epage><pages>1481-1487</pages><issn>0002-9440</issn><eissn>1525-2191</eissn><abstract>Active Heymann nephritis (HN) of rat, an autoimmune glomerular disease, is a model for human membranous glomerulonephropathy. The autoantigen of HN is a glycoprotein of approximately 600 kd that is present in both rat and human kidneys. Another kidney protein of 39-45 kd called receptor-associated protein (RAP) is associated with gp600. In normal kidney very little gp600 and RAP can be detected in glomeruli. This study was undertaken to determine whether the synthesis of gp600 and RAP would increase after development of active HN. Kidneys from normal (n = 5) and active (n = 11) HN rats were studied for expression of gp600 and RAP and their mRNAs by immunofluorescence and in situ hybridization. In all HN kidneys in contrast to normal kidneys both the transcription and translation of gp600 were markedly increased in glomeruli and proximal tubules. Transcription and translation of RAP were also increased but less so than gp600. The site of increased transcription of gp600 and RAP in glomeruli was clearly localized to the visceral glomerular epithelial cells.
This is the first study to show increased transcription of gp600 and RAP in active HN and the first study to identify the visceral glomerular epithelial cell as the cell for the increased transcription.</abstract><cop>United States</cop><pub>ASIP</pub><pmid>7778686</pmid><tpages>7</tpages></addata></record> |
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subjects | Animals Autoantigens - analysis Carrier Proteins - biosynthesis Carrier Proteins - immunology Female Fluorescent Antibody Technique Glomerulonephritis - genetics Glomerulonephritis - metabolism Glycoproteins - biosynthesis Glycoproteins - immunology Heymann Nephritis Antigenic Complex In Situ Hybridization Kidney Glomerulus - immunology LDL-Receptor Related Protein-Associated Protein Membrane Glycoproteins - biosynthesis Membrane Glycoproteins - immunology Protein Biosynthesis - genetics Rats Rats, Inbred Lew Transcription, Genetic - genetics Up-Regulation |
title | Transcription and translation of gp600 and receptor-associated protein (RAP) in active Heymann nephritis |
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