Activated Protein C Stimulates the Fibrinolytic Activity of Cultured Endothelial Cells and Decreases Antiactivator Activity

The effects of bovine activated protein C (APC) on the fibrinolytic activity of cultured bovine aortic endothelial cells were investigated. Confluent monolayers were incubated with purified APC under various conditions and changes in total fibrinolytic activity and in the level of plasminogen activa...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1985-02, Vol.82 (4), p.1121-1125
Hauptverfasser: Sakata, Yoichi, Curriden, Scott, Lawrence, Dan, Griffin, John H., Loskutoff, David J.
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container_issue 4
container_start_page 1121
container_title Proceedings of the National Academy of Sciences - PNAS
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creator Sakata, Yoichi
Curriden, Scott
Lawrence, Dan
Griffin, John H.
Loskutoff, David J.
description The effects of bovine activated protein C (APC) on the fibrinolytic activity of cultured bovine aortic endothelial cells were investigated. Confluent monolayers were incubated with purified APC under various conditions and changes in total fibrinolytic activity and in the level of plasminogen activator and plasminogen activator inhibitor (antiactivator) were monitored. The addition of APC to the cells in the absence of other blood or plasma components led to a rapid, dose-dependent increase of fibrinolytic activity both in the media and in cellular extracts. For example, 3.4 μ g of APC per ml resulted in a 15-fold increase of fibrinolytic activity in the medium within 1 hour. The enhanced fibrinolytic activity reflected increases in both the urokinase-related and tissue-type plasminogen activators produced by these cells. Interestingly, treatment of cells with APC also caused a rapid, dose-dependent decrease in antiactivator activity. Diisopropyl fluorophosphate-inactivated APC did not decrease antiactivator or increase plasminogen activator. Although a small but significant direct (i.e., cell-independent) effect of APC on both fibrinolytic activity and antiactivator activity could be demonstrated, the major portion of these changes appeared to be cell-mediated. These observations indicate that the fibrinolytic potential of cultured endothelial cells is increased by APC and that the enzyme active site is essential for this change. Moreover, the results suggest that one of the primary mechanisms for this stimulation of endothelial cell fibrinolytic activity involves an APC-mediated decrease in antiactivator.
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Confluent monolayers were incubated with purified APC under various conditions and changes in total fibrinolytic activity and in the level of plasminogen activator and plasminogen activator inhibitor (antiactivator) were monitored. The addition of APC to the cells in the absence of other blood or plasma components led to a rapid, dose-dependent increase of fibrinolytic activity both in the media and in cellular extracts. For example, 3.4 μ g of APC per ml resulted in a 15-fold increase of fibrinolytic activity in the medium within 1 hour. The enhanced fibrinolytic activity reflected increases in both the urokinase-related and tissue-type plasminogen activators produced by these cells. Interestingly, treatment of cells with APC also caused a rapid, dose-dependent decrease in antiactivator activity. Diisopropyl fluorophosphate-inactivated APC did not decrease antiactivator or increase plasminogen activator. Although a small but significant direct (i.e., cell-independent) effect of APC on both fibrinolytic activity and antiactivator activity could be demonstrated, the major portion of these changes appeared to be cell-mediated. These observations indicate that the fibrinolytic potential of cultured endothelial cells is increased by APC and that the enzyme active site is essential for this change. 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Confluent monolayers were incubated with purified APC under various conditions and changes in total fibrinolytic activity and in the level of plasminogen activator and plasminogen activator inhibitor (antiactivator) were monitored. The addition of APC to the cells in the absence of other blood or plasma components led to a rapid, dose-dependent increase of fibrinolytic activity both in the media and in cellular extracts. For example, 3.4 μ g of APC per ml resulted in a 15-fold increase of fibrinolytic activity in the medium within 1 hour. The enhanced fibrinolytic activity reflected increases in both the urokinase-related and tissue-type plasminogen activators produced by these cells. Interestingly, treatment of cells with APC also caused a rapid, dose-dependent decrease in antiactivator activity. Diisopropyl fluorophosphate-inactivated APC did not decrease antiactivator or increase plasminogen activator. 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Blood cells</subject><subject>Blood plasma</subject><subject>Cattle</subject><subject>Cells</subject><subject>Cells, Cultured</subject><subject>Cultured cells</subject><subject>Electrophoresis</subject><subject>Endothelial cells</subject><subject>Endothelium - metabolism</subject><subject>Fibrinolysis - drug effects</subject><subject>Fibrinolytics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gels</subject><subject>General aspects, investigation methods, hemostasis, fibrinolysis</subject><subject>Glycoproteins - metabolism</subject><subject>Glycoproteins - pharmacology</subject><subject>Molecular and cellular biology</subject><subject>Plasminogen Activators - biosynthesis</subject><subject>Plasminogen Inactivators</subject><subject>Protein C</subject><subject>Ungulates</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkUuLFDEUhQtRxnZ060IQshB31eZRlcfCRVPOqDCgoK7DrVTiZEhXtUlqsPHPm7bbogVXgZzvnHuTU1XPCV4TLNib3QhpLem6WRNCyYNqRbAiNW8UflitMKailg1tHldPUrrDGKtW4ovqgklBVMNX1a-Nyf4esh3Q5zhl60fUoS_Zb-dQLhPKtxZd-z76cQr77A36w_u8R5ND3RzyHIv1ahymQgYPAXU2hIRgHNA7a6KFVFI2Y_ZwHDTFJeJp9chBSPbZ6bysvl1ffe0-1Def3n_sNje1aTgndVlfEm4UOBBMcoGZoMCVgbYVDSuaUtZBz3rnBHN86MkgBwW0xVZBO1B2Wb095u7mfmsHY8ccIehd9FuIez2B1_8qo7_V36d7zZSgmBf_65M_Tj9mm7Le-mTKM2G005y0aBVvyocXcH0ETZxSitYtMwjWh7b0oS0tqW70oa1ieHm-2YKf6in6q5MOyUBwEUbj04Ipwrgk8mzBQ_xfdRmj3RxCtj_z2bz_gkV_cdTvUilqAWhLBGe_AQ7CwNY</recordid><startdate>19850201</startdate><enddate>19850201</enddate><creator>Sakata, Yoichi</creator><creator>Curriden, Scott</creator><creator>Lawrence, Dan</creator><creator>Griffin, John H.</creator><creator>Loskutoff, David J.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19850201</creationdate><title>Activated Protein C Stimulates the Fibrinolytic Activity of Cultured Endothelial Cells and Decreases Antiactivator Activity</title><author>Sakata, Yoichi ; Curriden, Scott ; Lawrence, Dan ; Griffin, John H. ; Loskutoff, David J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4661-424816c9afa738670372a69ca5574348199efab3bff73f6db1d8d9a250e9a5d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Aorta - metabolism</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Blood cells</topic><topic>Blood coagulation. Blood cells</topic><topic>Blood plasma</topic><topic>Cattle</topic><topic>Cells</topic><topic>Cells, Cultured</topic><topic>Cultured cells</topic><topic>Electrophoresis</topic><topic>Endothelial cells</topic><topic>Endothelium - metabolism</topic><topic>Fibrinolysis - drug effects</topic><topic>Fibrinolytics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gels</topic><topic>General aspects, investigation methods, hemostasis, fibrinolysis</topic><topic>Glycoproteins - metabolism</topic><topic>Glycoproteins - pharmacology</topic><topic>Molecular and cellular biology</topic><topic>Plasminogen Activators - biosynthesis</topic><topic>Plasminogen Inactivators</topic><topic>Protein C</topic><topic>Ungulates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sakata, Yoichi</creatorcontrib><creatorcontrib>Curriden, Scott</creatorcontrib><creatorcontrib>Lawrence, Dan</creatorcontrib><creatorcontrib>Griffin, John H.</creatorcontrib><creatorcontrib>Loskutoff, David J.</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>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sakata, Yoichi</au><au>Curriden, Scott</au><au>Lawrence, Dan</au><au>Griffin, John H.</au><au>Loskutoff, David J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activated Protein C Stimulates the Fibrinolytic Activity of Cultured Endothelial Cells and Decreases Antiactivator Activity</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1985-02-01</date><risdate>1985</risdate><volume>82</volume><issue>4</issue><spage>1121</spage><epage>1125</epage><pages>1121-1125</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>The effects of bovine activated protein C (APC) on the fibrinolytic activity of cultured bovine aortic endothelial cells were investigated. Confluent monolayers were incubated with purified APC under various conditions and changes in total fibrinolytic activity and in the level of plasminogen activator and plasminogen activator inhibitor (antiactivator) were monitored. The addition of APC to the cells in the absence of other blood or plasma components led to a rapid, dose-dependent increase of fibrinolytic activity both in the media and in cellular extracts. For example, 3.4 μ g of APC per ml resulted in a 15-fold increase of fibrinolytic activity in the medium within 1 hour. The enhanced fibrinolytic activity reflected increases in both the urokinase-related and tissue-type plasminogen activators produced by these cells. Interestingly, treatment of cells with APC also caused a rapid, dose-dependent decrease in antiactivator activity. Diisopropyl fluorophosphate-inactivated APC did not decrease antiactivator or increase plasminogen activator. 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1091-6490
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subjects Animals
Aorta - metabolism
Biological and medical sciences
Blood
Blood cells
Blood coagulation. Blood cells
Blood plasma
Cattle
Cells
Cells, Cultured
Cultured cells
Electrophoresis
Endothelial cells
Endothelium - metabolism
Fibrinolysis - drug effects
Fibrinolytics
Fundamental and applied biological sciences. Psychology
Gels
General aspects, investigation methods, hemostasis, fibrinolysis
Glycoproteins - metabolism
Glycoproteins - pharmacology
Molecular and cellular biology
Plasminogen Activators - biosynthesis
Plasminogen Inactivators
Protein C
Ungulates
title Activated Protein C Stimulates the Fibrinolytic Activity of Cultured Endothelial Cells and Decreases Antiactivator Activity
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