Plasminogen activator inhibitor-1 is an immediate early response gene in regenerating rat liver
Plasminogen activator inhibitor-1 (PAI-1), a M(r) 50,000 serine protease inhibitor, is the major physiological inhibitor of plasminogen activation. Quiescent rat hepatocytes do not express the PAI-1 gene in vivo; however, PAI-1 is synthesized both by primary cultures of rat hepatocytes and by hepato...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1994-03, Vol.54 (5), p.1337-1343 |
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description | Plasminogen activator inhibitor-1 (PAI-1), a M(r) 50,000 serine protease inhibitor, is the major physiological inhibitor of plasminogen activation. Quiescent rat hepatocytes do not express the PAI-1 gene in vivo; however, PAI-1 is synthesized both by primary cultures of rat hepatocytes and by hepatoma cells in vitro. Furthermore, PAI-1 is expressed by fibroblastic cells in vitro, in response to mitogen stimulation, suggesting a possible connection between hepatocyte PAI-1 expression and cell proliferation. To determine whether PAI-1 is an early growth response gene in hepatocytes in vivo, we analyzed its expression in regenerating rat liver. Male rats underwent partial (70%) hepatectomy (PH) or sham operation (SO), and liver samples were analyzed by Northern blot analysis and in situ hybridization. PAI-1 mRNA was not present at time 0 h, nor at any other time in SO rats but was induced rapidly in regenerating livers, peaking at 2 h and declining to negligible levels by 8 h posthepatectomy. This induction was not inhibited by cycloheximide. In situ hybridization analysis localized PAI-1 transcripts to hepatocytes. Immunohistochemical analysis demonstrated PAI-1-specific staining in hepatocytes in the livers of both PH and SO rats, but the temporal and spatial distribution profiles differed between PH and SO rats. Our studies demonstrate that PAI-1 is an immediate early response gene, transiently expressed in regenerating liver, expression of which may be important in hepatocyte growth and proliferation in vivo. |
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J ; BRUZDZINSKI, C. J ; RAPER, S. E ; GELEHRTER, T. D</creator><creatorcontrib>THORNTON, A. J ; BRUZDZINSKI, C. J ; RAPER, S. E ; GELEHRTER, T. D</creatorcontrib><description>Plasminogen activator inhibitor-1 (PAI-1), a M(r) 50,000 serine protease inhibitor, is the major physiological inhibitor of plasminogen activation. Quiescent rat hepatocytes do not express the PAI-1 gene in vivo; however, PAI-1 is synthesized both by primary cultures of rat hepatocytes and by hepatoma cells in vitro. Furthermore, PAI-1 is expressed by fibroblastic cells in vitro, in response to mitogen stimulation, suggesting a possible connection between hepatocyte PAI-1 expression and cell proliferation. To determine whether PAI-1 is an early growth response gene in hepatocytes in vivo, we analyzed its expression in regenerating rat liver. Male rats underwent partial (70%) hepatectomy (PH) or sham operation (SO), and liver samples were analyzed by Northern blot analysis and in situ hybridization. PAI-1 mRNA was not present at time 0 h, nor at any other time in SO rats but was induced rapidly in regenerating livers, peaking at 2 h and declining to negligible levels by 8 h posthepatectomy. This induction was not inhibited by cycloheximide. In situ hybridization analysis localized PAI-1 transcripts to hepatocytes. Immunohistochemical analysis demonstrated PAI-1-specific staining in hepatocytes in the livers of both PH and SO rats, but the temporal and spatial distribution profiles differed between PH and SO rats. Our studies demonstrate that PAI-1 is an immediate early response gene, transiently expressed in regenerating liver, expression of which may be important in hepatocyte growth and proliferation in vivo.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 8118825</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Animals ; Biological and medical sciences ; Blotting, Northern ; Cell cycle, cell proliferation ; Cell Division - physiology ; Cell physiology ; Fundamental and applied biological sciences. Psychology ; Gene Expression - genetics ; Genes, Immediate-Early - physiology ; Hepatectomy ; Immunohistochemistry ; In Situ Hybridization ; Liver - cytology ; Liver - physiology ; Liver - surgery ; Liver Regeneration - genetics ; Male ; Molecular and cellular biology ; Plasminogen Activator Inhibitor 1 - analysis ; Plasminogen Activator Inhibitor 1 - genetics ; Rats ; Rats, Inbred F344 ; Receptors, Cell Surface - genetics ; Receptors, Urokinase Plasminogen Activator ; RNA, Messenger - analysis ; RNA, Messenger - genetics ; Time Factors ; Tissue Plasminogen Activator - genetics ; Transcription, Genetic - genetics ; Urokinase-Type Plasminogen Activator - genetics</subject><ispartof>Cancer research (Chicago, Ill.), 1994-03, Vol.54 (5), p.1337-1343</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3960799$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8118825$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>THORNTON, A. J</creatorcontrib><creatorcontrib>BRUZDZINSKI, C. J</creatorcontrib><creatorcontrib>RAPER, S. E</creatorcontrib><creatorcontrib>GELEHRTER, T. D</creatorcontrib><title>Plasminogen activator inhibitor-1 is an immediate early response gene in regenerating rat liver</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Plasminogen activator inhibitor-1 (PAI-1), a M(r) 50,000 serine protease inhibitor, is the major physiological inhibitor of plasminogen activation. Quiescent rat hepatocytes do not express the PAI-1 gene in vivo; however, PAI-1 is synthesized both by primary cultures of rat hepatocytes and by hepatoma cells in vitro. Furthermore, PAI-1 is expressed by fibroblastic cells in vitro, in response to mitogen stimulation, suggesting a possible connection between hepatocyte PAI-1 expression and cell proliferation. To determine whether PAI-1 is an early growth response gene in hepatocytes in vivo, we analyzed its expression in regenerating rat liver. Male rats underwent partial (70%) hepatectomy (PH) or sham operation (SO), and liver samples were analyzed by Northern blot analysis and in situ hybridization. PAI-1 mRNA was not present at time 0 h, nor at any other time in SO rats but was induced rapidly in regenerating livers, peaking at 2 h and declining to negligible levels by 8 h posthepatectomy. This induction was not inhibited by cycloheximide. In situ hybridization analysis localized PAI-1 transcripts to hepatocytes. Immunohistochemical analysis demonstrated PAI-1-specific staining in hepatocytes in the livers of both PH and SO rats, but the temporal and spatial distribution profiles differed between PH and SO rats. Our studies demonstrate that PAI-1 is an immediate early response gene, transiently expressed in regenerating liver, expression of which may be important in hepatocyte growth and proliferation in vivo.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Cell cycle, cell proliferation</subject><subject>Cell Division - physiology</subject><subject>Cell physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression - genetics</subject><subject>Genes, Immediate-Early - physiology</subject><subject>Hepatectomy</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Liver - cytology</subject><subject>Liver - physiology</subject><subject>Liver - surgery</subject><subject>Liver Regeneration - genetics</subject><subject>Male</subject><subject>Molecular and cellular biology</subject><subject>Plasminogen Activator Inhibitor 1 - analysis</subject><subject>Plasminogen Activator Inhibitor 1 - genetics</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Urokinase Plasminogen Activator</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - genetics</subject><subject>Time Factors</subject><subject>Tissue Plasminogen Activator - genetics</subject><subject>Transcription, Genetic - genetics</subject><subject>Urokinase-Type Plasminogen Activator - genetics</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9LxDAQxYMo67r6EYQcxFshaZImOcriPxD0oOcySdPdSJquSXdhv70Ri1dP78283wzMnKAlFUxVknNxipaEEFUJLutzdJHzZykFJWKBFopSpWqxRO1bgDz4OG5cxGAnf4BpTNjHrTe-uIpinzFE7IfBdR4mhx2kcMTJ5d0Ys8Nl0BW-NH5cgsnHDS6Cgz-4dInOegjZXc26Qh8P9-_rp-rl9fF5ffdSbWutp4r2VoPioKWVxlhrFOtAKsuZJprbrieuN0oaQQSzwBynneWqNrWgtTAG2Ard_u7dpfFr7_LUDj5bFwJEN-5zKxumBCPsX5A2WjVCkQJez-DelNPbXfIDpGM7v67kN3MO2ULoE0Tr8x_GdEOk1uwbZyN5iA</recordid><startdate>19940301</startdate><enddate>19940301</enddate><creator>THORNTON, A. J</creator><creator>BRUZDZINSKI, C. J</creator><creator>RAPER, S. E</creator><creator>GELEHRTER, T. D</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19940301</creationdate><title>Plasminogen activator inhibitor-1 is an immediate early response gene in regenerating rat liver</title><author>THORNTON, A. J ; BRUZDZINSKI, C. J ; RAPER, S. E ; GELEHRTER, T. D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h299t-1fc9a84a97c7bbccb83da78c439094cdf0efb87b5053ca3e41dc482b25125bba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Cell cycle, cell proliferation</topic><topic>Cell Division - physiology</topic><topic>Cell physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression - genetics</topic><topic>Genes, Immediate-Early - physiology</topic><topic>Hepatectomy</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization</topic><topic>Liver - cytology</topic><topic>Liver - physiology</topic><topic>Liver - surgery</topic><topic>Liver Regeneration - genetics</topic><topic>Male</topic><topic>Molecular and cellular biology</topic><topic>Plasminogen Activator Inhibitor 1 - analysis</topic><topic>Plasminogen Activator Inhibitor 1 - genetics</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Receptors, Urokinase Plasminogen Activator</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - genetics</topic><topic>Time Factors</topic><topic>Tissue Plasminogen Activator - genetics</topic><topic>Transcription, Genetic - genetics</topic><topic>Urokinase-Type Plasminogen Activator - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>THORNTON, A. J</creatorcontrib><creatorcontrib>BRUZDZINSKI, C. J</creatorcontrib><creatorcontrib>RAPER, S. E</creatorcontrib><creatorcontrib>GELEHRTER, T. D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>THORNTON, A. J</au><au>BRUZDZINSKI, C. J</au><au>RAPER, S. E</au><au>GELEHRTER, T. D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasminogen activator inhibitor-1 is an immediate early response gene in regenerating rat liver</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1994-03-01</date><risdate>1994</risdate><volume>54</volume><issue>5</issue><spage>1337</spage><epage>1343</epage><pages>1337-1343</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Plasminogen activator inhibitor-1 (PAI-1), a M(r) 50,000 serine protease inhibitor, is the major physiological inhibitor of plasminogen activation. Quiescent rat hepatocytes do not express the PAI-1 gene in vivo; however, PAI-1 is synthesized both by primary cultures of rat hepatocytes and by hepatoma cells in vitro. Furthermore, PAI-1 is expressed by fibroblastic cells in vitro, in response to mitogen stimulation, suggesting a possible connection between hepatocyte PAI-1 expression and cell proliferation. To determine whether PAI-1 is an early growth response gene in hepatocytes in vivo, we analyzed its expression in regenerating rat liver. Male rats underwent partial (70%) hepatectomy (PH) or sham operation (SO), and liver samples were analyzed by Northern blot analysis and in situ hybridization. PAI-1 mRNA was not present at time 0 h, nor at any other time in SO rats but was induced rapidly in regenerating livers, peaking at 2 h and declining to negligible levels by 8 h posthepatectomy. This induction was not inhibited by cycloheximide. In situ hybridization analysis localized PAI-1 transcripts to hepatocytes. Immunohistochemical analysis demonstrated PAI-1-specific staining in hepatocytes in the livers of both PH and SO rats, but the temporal and spatial distribution profiles differed between PH and SO rats. Our studies demonstrate that PAI-1 is an immediate early response gene, transiently expressed in regenerating liver, expression of which may be important in hepatocyte growth and proliferation in vivo.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>8118825</pmid><tpages>7</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Blotting, Northern Cell cycle, cell proliferation Cell Division - physiology Cell physiology Fundamental and applied biological sciences. Psychology Gene Expression - genetics Genes, Immediate-Early - physiology Hepatectomy Immunohistochemistry In Situ Hybridization Liver - cytology Liver - physiology Liver - surgery Liver Regeneration - genetics Male Molecular and cellular biology Plasminogen Activator Inhibitor 1 - analysis Plasminogen Activator Inhibitor 1 - genetics Rats Rats, Inbred F344 Receptors, Cell Surface - genetics Receptors, Urokinase Plasminogen Activator RNA, Messenger - analysis RNA, Messenger - genetics Time Factors Tissue Plasminogen Activator - genetics Transcription, Genetic - genetics Urokinase-Type Plasminogen Activator - genetics |
title | Plasminogen activator inhibitor-1 is an immediate early response gene in regenerating rat liver |
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