Generation of coagulation factor V activity by cultured rabbit alveolar macrophages

Alveolar macrophages are cell's important in immune defense and inflammation in the lung, and the coagulation system participates in these reactions. In earlier experiments, it was found that alveolar macrophages contain and produce tissue factor, the extrinsic clotting pathway activator. The p...

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Veröffentlicht in:The Journal of experimental medicine 1984-12, Vol.160 (6), p.1880-1890
Hauptverfasser: ROTHBERGER, H, MCGEE, M. P
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container_end_page 1890
container_issue 6
container_start_page 1880
container_title The Journal of experimental medicine
container_volume 160
creator ROTHBERGER, H
MCGEE, M. P
description Alveolar macrophages are cell's important in immune defense and inflammation in the lung, and the coagulation system participates in these reactions. In earlier experiments, it was found that alveolar macrophages contain and produce tissue factor, the extrinsic clotting pathway activator. The present experiments explore possible production by alveolar macrophages of the sequence of the clotting proteins that interact to form thrombin following initiation of coagulation by tissue factor. In studies using alveolar macrophages purified from rabbits, factor V activity was not detected in cell preparations assayed directly after isolation. However, after short-term culture, we found generation and release of factor V activity by these cells, which was predominantly from subpopulations with densities of 1.060-1.068 g/ml, corresponding to intermediate stages of alveolar macrophage maturation. Cell viability and protein synthesis were required for generation of the activity as shown by inhibitory effects of cell lysis before culture and by effects observed after including puromycin in cultures with viable cells. The activity generated was characterized as factor V by demonstrating specific functional requirements in one- and two-stage coagulation tests. There was no detectable generation in these cultures of factors II, VII, X, or the more recently described factor X-independent monocyte/macrophage prothrombinases. Factor V activity generated by alveolar macrophages may contribute to prothrominase assembly, activation of clotting, and fibrin formation within the alveolus.
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Cell viability and protein synthesis were required for generation of the activity as shown by inhibitory effects of cell lysis before culture and by effects observed after including puromycin in cultures with viable cells. The activity generated was characterized as factor V by demonstrating specific functional requirements in one- and two-stage coagulation tests. There was no detectable generation in these cultures of factors II, VII, X, or the more recently described factor X-independent monocyte/macrophage prothrombinases. Factor V activity generated by alveolar macrophages may contribute to prothrominase assembly, activation of clotting, and fibrin formation within the alveolus.</description><identifier>ISSN: 0022-1007</identifier><identifier>EISSN: 1540-9538</identifier><identifier>DOI: 10.1084/jem.160.6.1880</identifier><identifier>PMID: 6512491</identifier><identifier>CODEN: JEMEAV</identifier><language>eng</language><publisher>New York, NY: Rockefeller University Press</publisher><subject>Animals ; Biological and medical sciences ; Blood coagulation. Blood cells ; Cells, Cultured ; Coagulation factors ; Endotoxins - pharmacology ; Factor V - immunology ; Factor V - metabolism ; Factor Va ; Female ; Fundamental and applied biological sciences. Psychology ; Lung - cytology ; Macrophages - metabolism ; Molecular and cellular biology ; Puromycin - pharmacology ; Rabbits ; Thrombin - pharmacology ; Time Factors</subject><ispartof>The Journal of experimental medicine, 1984-12, Vol.160 (6), p.1880-1890</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-bb5039f3144714a27589c5e4a4741bf3dd4f1e6b6e009bf2e1e43163ebf968fe3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=9199772$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6512491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ROTHBERGER, H</creatorcontrib><creatorcontrib>MCGEE, M. P</creatorcontrib><title>Generation of coagulation factor V activity by cultured rabbit alveolar macrophages</title><title>The Journal of experimental medicine</title><addtitle>J Exp Med</addtitle><description>Alveolar macrophages are cell's important in immune defense and inflammation in the lung, and the coagulation system participates in these reactions. In earlier experiments, it was found that alveolar macrophages contain and produce tissue factor, the extrinsic clotting pathway activator. The present experiments explore possible production by alveolar macrophages of the sequence of the clotting proteins that interact to form thrombin following initiation of coagulation by tissue factor. In studies using alveolar macrophages purified from rabbits, factor V activity was not detected in cell preparations assayed directly after isolation. However, after short-term culture, we found generation and release of factor V activity by these cells, which was predominantly from subpopulations with densities of 1.060-1.068 g/ml, corresponding to intermediate stages of alveolar macrophage maturation. Cell viability and protein synthesis were required for generation of the activity as shown by inhibitory effects of cell lysis before culture and by effects observed after including puromycin in cultures with viable cells. The activity generated was characterized as factor V by demonstrating specific functional requirements in one- and two-stage coagulation tests. There was no detectable generation in these cultures of factors II, VII, X, or the more recently described factor X-independent monocyte/macrophage prothrombinases. Factor V activity generated by alveolar macrophages may contribute to prothrominase assembly, activation of clotting, and fibrin formation within the alveolus.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood coagulation. Blood cells</subject><subject>Cells, Cultured</subject><subject>Coagulation factors</subject><subject>Endotoxins - pharmacology</subject><subject>Factor V - immunology</subject><subject>Factor V - metabolism</subject><subject>Factor Va</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Lung - cytology</subject><subject>Macrophages - metabolism</subject><subject>Molecular and cellular biology</subject><subject>Puromycin - pharmacology</subject><subject>Rabbits</subject><subject>Thrombin - pharmacology</subject><subject>Time Factors</subject><issn>0022-1007</issn><issn>1540-9538</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU2LFDEQDaKs4-rVm9AH8dZtKkmnOxdBlnUVFjz4cQ1JpjKbJd0Zk-6B-fdmmWHQU1G8V69e1SPkLdAO6Cg-PuLUgaSd7GAc6TOygV7QVvV8fE42lDLWAqXDS_KqlEdKQYheXpEr2QMTCjbkxx3OmM0S0twk37hkdms8td64JeXmd1NrOITl2Nhj49a4rBm3TTbWhqUx8YApmtxMxuW0fzA7LK_JC29iwTfnek1-fbn9efO1vf9-9-3m833rBIiltbanXHlePQ0gDBv6UbkehRGDAOv5dis8oLQSKVXWMwQUHCRH65UcPfJr8umku1_thFuH85JN1PscJpOPOpmg_0fm8KB36aAZjEPPRBX4cBbI6c-KZdFTKA5jNDOmtejqCBSnrBK7E7HeWEpGf1kCVD_FoGsMusagpX6KoQ68-9fahX7-e8Xfn3FTnIk-m9mFcqEpUGoYGP8L3zeSYg</recordid><startdate>19841201</startdate><enddate>19841201</enddate><creator>ROTHBERGER, H</creator><creator>MCGEE, M. 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Blood cells</topic><topic>Cells, Cultured</topic><topic>Coagulation factors</topic><topic>Endotoxins - pharmacology</topic><topic>Factor V - immunology</topic><topic>Factor V - metabolism</topic><topic>Factor Va</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Lung - cytology</topic><topic>Macrophages - metabolism</topic><topic>Molecular and cellular biology</topic><topic>Puromycin - pharmacology</topic><topic>Rabbits</topic><topic>Thrombin - pharmacology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ROTHBERGER, H</creatorcontrib><creatorcontrib>MCGEE, M. 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P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation of coagulation factor V activity by cultured rabbit alveolar macrophages</atitle><jtitle>The Journal of experimental medicine</jtitle><addtitle>J Exp Med</addtitle><date>1984-12-01</date><risdate>1984</risdate><volume>160</volume><issue>6</issue><spage>1880</spage><epage>1890</epage><pages>1880-1890</pages><issn>0022-1007</issn><eissn>1540-9538</eissn><coden>JEMEAV</coden><abstract>Alveolar macrophages are cell's important in immune defense and inflammation in the lung, and the coagulation system participates in these reactions. In earlier experiments, it was found that alveolar macrophages contain and produce tissue factor, the extrinsic clotting pathway activator. The present experiments explore possible production by alveolar macrophages of the sequence of the clotting proteins that interact to form thrombin following initiation of coagulation by tissue factor. In studies using alveolar macrophages purified from rabbits, factor V activity was not detected in cell preparations assayed directly after isolation. However, after short-term culture, we found generation and release of factor V activity by these cells, which was predominantly from subpopulations with densities of 1.060-1.068 g/ml, corresponding to intermediate stages of alveolar macrophage maturation. Cell viability and protein synthesis were required for generation of the activity as shown by inhibitory effects of cell lysis before culture and by effects observed after including puromycin in cultures with viable cells. The activity generated was characterized as factor V by demonstrating specific functional requirements in one- and two-stage coagulation tests. There was no detectable generation in these cultures of factors II, VII, X, or the more recently described factor X-independent monocyte/macrophage prothrombinases. 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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Animals
Biological and medical sciences
Blood coagulation. Blood cells
Cells, Cultured
Coagulation factors
Endotoxins - pharmacology
Factor V - immunology
Factor V - metabolism
Factor Va
Female
Fundamental and applied biological sciences. Psychology
Lung - cytology
Macrophages - metabolism
Molecular and cellular biology
Puromycin - pharmacology
Rabbits
Thrombin - pharmacology
Time Factors
title Generation of coagulation factor V activity by cultured rabbit alveolar macrophages
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