Endothelial cells in culture produce a vasoconstrictor substance

We report that cultured vascular endothelial cells release into the culture medium a vasoconstrictor peptide, a substance we call an endotheliumderived constricting factor (EDCF). Conditioned medium from cultured bovine aortic and pulmonary artery endothelial cells caused sustained, dose‐dependent i...

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Veröffentlicht in:Journal of cellular physiology 1987-08, Vol.132 (2), p.263-270
Hauptverfasser: O'Brien, Richard F., Robbins, Richard J., McMurtry, Ivan F.
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container_title Journal of cellular physiology
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creator O'Brien, Richard F.
Robbins, Richard J.
McMurtry, Ivan F.
description We report that cultured vascular endothelial cells release into the culture medium a vasoconstrictor peptide, a substance we call an endotheliumderived constricting factor (EDCF). Conditioned medium from cultured bovine aortic and pulmonary artery endothelial cells caused sustained, dose‐dependent isometric constriction of vascular rings isolated from bovine coronary and pulmonary arteries and rat and guinea pig pulmonary arteries and aortas. The medium also caused vasoconstriction when infused into isolated, perfused rabbit hearts and rat kidneys. Conditioned medium from bovine aortic intimal explants also contained constrictor activity, whereas medium from denuded intimal explants, cultured microvascular endothelial cells, vascular smooth muscle cells, or lung fibroblasts did not. Constrictor activity increased progressively in the culture medium over 2–12 h of incubation. Thrombin stimulated the release of constrictor activity; hypoxia, anoxia and meclofenamate had no effect and the calcium ionophore A23187 inhibited EDCF release. The EDCF caused a characteristic slow‐onset and sustained constriction of the vascular rings that relaxed slowly over 60–90 min following removal. The constriction was not affected by inhibitors of arachidonic acid metabolism or by antagonists of serotonergic, histaminergic, aloha‐adrenergic, opioid, leukotriene, angiotensin II, or substance P receptors; constriction was reversed partly by verapamil and acetylcholine and completely by nitroprusside and isoproterenol. EDCF was heat stable, not extractable into organic solvents, and completely destroyed by trypsin and neutral protease. Cycloheximide blocked the production of EDCF. These properties and the results of polyacrylamide gel filtration experiments suggested that EDCF was a peptide with a molecular weight of 3,000 daltons. These findings show that endothelial cells in culture produce a vasoconstrictor substance and support the idea that endothelial cell products play a role in mediating vascular tone.
doi_str_mv 10.1002/jcp.1041320210
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Conditioned medium from cultured bovine aortic and pulmonary artery endothelial cells caused sustained, dose‐dependent isometric constriction of vascular rings isolated from bovine coronary and pulmonary arteries and rat and guinea pig pulmonary arteries and aortas. The medium also caused vasoconstriction when infused into isolated, perfused rabbit hearts and rat kidneys. Conditioned medium from bovine aortic intimal explants also contained constrictor activity, whereas medium from denuded intimal explants, cultured microvascular endothelial cells, vascular smooth muscle cells, or lung fibroblasts did not. Constrictor activity increased progressively in the culture medium over 2–12 h of incubation. Thrombin stimulated the release of constrictor activity; hypoxia, anoxia and meclofenamate had no effect and the calcium ionophore A23187 inhibited EDCF release. The EDCF caused a characteristic slow‐onset and sustained constriction of the vascular rings that relaxed slowly over 60–90 min following removal. The constriction was not affected by inhibitors of arachidonic acid metabolism or by antagonists of serotonergic, histaminergic, aloha‐adrenergic, opioid, leukotriene, angiotensin II, or substance P receptors; constriction was reversed partly by verapamil and acetylcholine and completely by nitroprusside and isoproterenol. EDCF was heat stable, not extractable into organic solvents, and completely destroyed by trypsin and neutral protease. Cycloheximide blocked the production of EDCF. These properties and the results of polyacrylamide gel filtration experiments suggested that EDCF was a peptide with a molecular weight of 3,000 daltons. 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Psychology ; Molecular and cellular biology ; Muscle Contraction - drug effects ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - physiology ; Peptide Biosynthesis ; Pulmonary Artery - metabolism ; Rabbits ; Rats ; Secretion. 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Cell. Physiol</addtitle><description>We report that cultured vascular endothelial cells release into the culture medium a vasoconstrictor peptide, a substance we call an endotheliumderived constricting factor (EDCF). Conditioned medium from cultured bovine aortic and pulmonary artery endothelial cells caused sustained, dose‐dependent isometric constriction of vascular rings isolated from bovine coronary and pulmonary arteries and rat and guinea pig pulmonary arteries and aortas. The medium also caused vasoconstriction when infused into isolated, perfused rabbit hearts and rat kidneys. Conditioned medium from bovine aortic intimal explants also contained constrictor activity, whereas medium from denuded intimal explants, cultured microvascular endothelial cells, vascular smooth muscle cells, or lung fibroblasts did not. Constrictor activity increased progressively in the culture medium over 2–12 h of incubation. Thrombin stimulated the release of constrictor activity; hypoxia, anoxia and meclofenamate had no effect and the calcium ionophore A23187 inhibited EDCF release. The EDCF caused a characteristic slow‐onset and sustained constriction of the vascular rings that relaxed slowly over 60–90 min following removal. The constriction was not affected by inhibitors of arachidonic acid metabolism or by antagonists of serotonergic, histaminergic, aloha‐adrenergic, opioid, leukotriene, angiotensin II, or substance P receptors; constriction was reversed partly by verapamil and acetylcholine and completely by nitroprusside and isoproterenol. EDCF was heat stable, not extractable into organic solvents, and completely destroyed by trypsin and neutral protease. Cycloheximide blocked the production of EDCF. These properties and the results of polyacrylamide gel filtration experiments suggested that EDCF was a peptide with a molecular weight of 3,000 daltons. These findings show that endothelial cells in culture produce a vasoconstrictor substance and support the idea that endothelial cell products play a role in mediating vascular tone.</description><subject>Animals</subject><subject>aorta</subject><subject>Aorta, Thoracic - metabolism</subject><subject>Biological and medical sciences</subject><subject>Calcimycin - pharmacology</subject><subject>Cattle</subject><subject>Cell physiology</subject><subject>Cells, Cultured</subject><subject>Culture Media</subject><subject>endothelial-derived constricting factor</subject><subject>Endothelins</subject><subject>Endothelium - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Molecular and cellular biology</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - physiology</subject><subject>Peptide Biosynthesis</subject><subject>Pulmonary Artery - metabolism</subject><subject>Rabbits</subject><subject>Rats</subject><subject>Secretion. Exocytosis</subject><subject>Thrombin - pharmacology</subject><subject>Vasoconstriction - drug effects</subject><subject>Vasoconstrictor Agents - metabolism</subject><subject>Vasoconstrictor Agents - pharmacology</subject><subject>vasoconstrictors</subject><subject>Vasodilator Agents - pharmacology</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkDtPwzAURi0EKuWxsiFlQGwpfj82UFWeFTCAGC3HsUVKmhQ7AfrvMWpVxMTkK93zXX86ABwhOEIQ4rOZXaSBIoIhRnALDBFUIqec4W0wTADKFaNoF-zFOIMQKkXIAAwIQhQLOATnk6Zsu1dXV6bOrKvrmFVNZvu664PLFqEte-syk32Y2Nq2iV2obNeGLPZF7Exj3QHY8aaO7nD97oPny8nT-DqfPlzdjC-muWWQwtwXnFGDpHKUciixVIRJRGSJGfUFoYrJ0nOBvSk8g7KkRihEBOEl9RgzTvbB6epu6vTeu9jpeRV_CpvGtX3UQnBOFFP_gogqLLiQCRytQBvaGIPzehGquQlLjaD-cauTW_3rNgWO15f7Yu7KDb6WmfYn672J1tQ-JD9V3GCCUsk4TZhaYZ9V7Zb_fKpvx49_KuSrbBU797XJmvCmuSCC6Zf7Kz0dP4nb6Z3U9-QboH-fSA</recordid><startdate>198708</startdate><enddate>198708</enddate><creator>O'Brien, Richard F.</creator><creator>Robbins, Richard J.</creator><creator>McMurtry, Ivan F.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>198708</creationdate><title>Endothelial cells in culture produce a vasoconstrictor substance</title><author>O'Brien, Richard F. ; Robbins, Richard J. ; McMurtry, Ivan F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5040-fb654a189e44608289358138d254fb34958df672fabf508d4a7913736d4f22563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Animals</topic><topic>aorta</topic><topic>Aorta, Thoracic - metabolism</topic><topic>Biological and medical sciences</topic><topic>Calcimycin - pharmacology</topic><topic>Cattle</topic><topic>Cell physiology</topic><topic>Cells, Cultured</topic><topic>Culture Media</topic><topic>endothelial-derived constricting factor</topic><topic>Endothelins</topic><topic>Endothelium - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Molecular and cellular biology</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - physiology</topic><topic>Peptide Biosynthesis</topic><topic>Pulmonary Artery - metabolism</topic><topic>Rabbits</topic><topic>Rats</topic><topic>Secretion. Exocytosis</topic><topic>Thrombin - pharmacology</topic><topic>Vasoconstriction - drug effects</topic><topic>Vasoconstrictor Agents - metabolism</topic><topic>Vasoconstrictor Agents - pharmacology</topic><topic>vasoconstrictors</topic><topic>Vasodilator Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Brien, Richard F.</creatorcontrib><creatorcontrib>Robbins, Richard J.</creatorcontrib><creatorcontrib>McMurtry, Ivan F.</creatorcontrib><collection>Istex</collection><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Brien, Richard F.</au><au>Robbins, Richard J.</au><au>McMurtry, Ivan F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endothelial cells in culture produce a vasoconstrictor substance</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J. Cell. Physiol</addtitle><date>1987-08</date><risdate>1987</risdate><volume>132</volume><issue>2</issue><spage>263</spage><epage>270</epage><pages>263-270</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><coden>JCLLAX</coden><abstract>We report that cultured vascular endothelial cells release into the culture medium a vasoconstrictor peptide, a substance we call an endotheliumderived constricting factor (EDCF). Conditioned medium from cultured bovine aortic and pulmonary artery endothelial cells caused sustained, dose‐dependent isometric constriction of vascular rings isolated from bovine coronary and pulmonary arteries and rat and guinea pig pulmonary arteries and aortas. The medium also caused vasoconstriction when infused into isolated, perfused rabbit hearts and rat kidneys. Conditioned medium from bovine aortic intimal explants also contained constrictor activity, whereas medium from denuded intimal explants, cultured microvascular endothelial cells, vascular smooth muscle cells, or lung fibroblasts did not. Constrictor activity increased progressively in the culture medium over 2–12 h of incubation. Thrombin stimulated the release of constrictor activity; hypoxia, anoxia and meclofenamate had no effect and the calcium ionophore A23187 inhibited EDCF release. The EDCF caused a characteristic slow‐onset and sustained constriction of the vascular rings that relaxed slowly over 60–90 min following removal. The constriction was not affected by inhibitors of arachidonic acid metabolism or by antagonists of serotonergic, histaminergic, aloha‐adrenergic, opioid, leukotriene, angiotensin II, or substance P receptors; constriction was reversed partly by verapamil and acetylcholine and completely by nitroprusside and isoproterenol. EDCF was heat stable, not extractable into organic solvents, and completely destroyed by trypsin and neutral protease. Cycloheximide blocked the production of EDCF. These properties and the results of polyacrylamide gel filtration experiments suggested that EDCF was a peptide with a molecular weight of 3,000 daltons. These findings show that endothelial cells in culture produce a vasoconstrictor substance and support the idea that endothelial cell products play a role in mediating vascular tone.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>3114270</pmid><doi>10.1002/jcp.1041320210</doi><tpages>8</tpages></addata></record>
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subjects Animals
aorta
Aorta, Thoracic - metabolism
Biological and medical sciences
Calcimycin - pharmacology
Cattle
Cell physiology
Cells, Cultured
Culture Media
endothelial-derived constricting factor
Endothelins
Endothelium - metabolism
Fundamental and applied biological sciences. Psychology
Molecular and cellular biology
Muscle Contraction - drug effects
Muscle, Smooth, Vascular - drug effects
Muscle, Smooth, Vascular - physiology
Peptide Biosynthesis
Pulmonary Artery - metabolism
Rabbits
Rats
Secretion. Exocytosis
Thrombin - pharmacology
Vasoconstriction - drug effects
Vasoconstrictor Agents - metabolism
Vasoconstrictor Agents - pharmacology
vasoconstrictors
Vasodilator Agents - pharmacology
title Endothelial cells in culture produce a vasoconstrictor substance
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