Immunohistochemical localization of defensin in human coronary vessels
Neutrophil defensins comprise a family of cationic peptides that possess potent antimicrobial activity. Defensins are normally sequestered in cytoplasmic granules with their primary site of action in phagolysosomes, although some peptide is released into the circulation during the course of infectio...
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Veröffentlicht in: | The American journal of pathology 1997-03, Vol.150 (3), p.1009-1020 |
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description | Neutrophil defensins comprise a family of cationic peptides that possess potent antimicrobial activity. Defensins are normally sequestered in cytoplasmic granules with their primary site of action in phagolysosomes, although some peptide is released into the circulation during the course of infection or inflammation. In view of the fact that neutrophils adhere to the endothelium and that defensins have been reported to bind to human endothelial cells in vitro, we used immunohistochemistry to study the distribution of these peptides in normal and in atherosclerotic human coronary arteries. Defensin was found primarily in the intima of normal and atherosclerotic vessels, most prominently in association with intimal smooth muscle cells. Both large- and small-vessel endothelium stained focally for defensin. Defensin was also found in the media near the external elastic lamina and in some periadventitial vessels. The same distribution was seen in vessels that had been perfusion fixed immediately upon procurement, excluding diffusion of defensin from PMNs ex vivo. These data indicate that neutrophil defensin is present in the walls of human coronary arteries. The deposition of defensin in vessels may contribute to the pathophysiological consequences of inflammation in addition to their role in host defense. |
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Defensins are normally sequestered in cytoplasmic granules with their primary site of action in phagolysosomes, although some peptide is released into the circulation during the course of infection or inflammation. In view of the fact that neutrophils adhere to the endothelium and that defensins have been reported to bind to human endothelial cells in vitro, we used immunohistochemistry to study the distribution of these peptides in normal and in atherosclerotic human coronary arteries. Defensin was found primarily in the intima of normal and atherosclerotic vessels, most prominently in association with intimal smooth muscle cells. Both large- and small-vessel endothelium stained focally for defensin. Defensin was also found in the media near the external elastic lamina and in some periadventitial vessels. The same distribution was seen in vessels that had been perfusion fixed immediately upon procurement, excluding diffusion of defensin from PMNs ex vivo. These data indicate that neutrophil defensin is present in the walls of human coronary arteries. The deposition of defensin in vessels may contribute to the pathophysiological consequences of inflammation in addition to their role in host defense.</description><identifier>ISSN: 0002-9440</identifier><identifier>EISSN: 1525-2191</identifier><identifier>PMID: 9060838</identifier><identifier>CODEN: AJPAA4</identifier><language>eng</language><publisher>Bethesda, MD: ASIP</publisher><subject>Anti-Infective Agents - analysis ; Anti-Infective Agents - metabolism ; Antibodies - analysis ; Arteriosclerosis - pathology ; Arteriosclerosis - physiopathology ; Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood Proteins - analysis ; Blood Proteins - immunology ; Blood Proteins - metabolism ; Cardiology. Vascular system ; Coronary Vessels - chemistry ; Coronary Vessels - metabolism ; Defensins ; Endothelium, Vascular - chemistry ; Female ; Fibrinolysis - physiology ; Humans ; Immunohistochemistry ; Male ; Medical sciences ; Reference Values ; Tunica Intima - chemistry ; Tunica Intima - cytology ; Tunica Media - chemistry ; Tunica Media - cytology</subject><ispartof>The American journal of pathology, 1997-03, Vol.150 (3), p.1009-1020</ispartof><rights>1997 INIST-CNRS</rights><rights>Copyright American Society for Investigative Pathology Mar 1997</rights><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/PMC1857878/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1857878/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2601313$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9060838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barnathan, ES</creatorcontrib><creatorcontrib>Raghunath, PN</creatorcontrib><creatorcontrib>Tomaszewski, JE</creatorcontrib><creatorcontrib>Ganz, T</creatorcontrib><creatorcontrib>Cines, DB</creatorcontrib><creatorcontrib>Higazi A, al-R</creatorcontrib><title>Immunohistochemical localization of defensin in human coronary vessels</title><title>The American journal of pathology</title><addtitle>Am J Pathol</addtitle><description>Neutrophil defensins comprise a family of cationic peptides that possess potent antimicrobial activity. Defensins are normally sequestered in cytoplasmic granules with their primary site of action in phagolysosomes, although some peptide is released into the circulation during the course of infection or inflammation. In view of the fact that neutrophils adhere to the endothelium and that defensins have been reported to bind to human endothelial cells in vitro, we used immunohistochemistry to study the distribution of these peptides in normal and in atherosclerotic human coronary arteries. Defensin was found primarily in the intima of normal and atherosclerotic vessels, most prominently in association with intimal smooth muscle cells. Both large- and small-vessel endothelium stained focally for defensin. Defensin was also found in the media near the external elastic lamina and in some periadventitial vessels. The same distribution was seen in vessels that had been perfusion fixed immediately upon procurement, excluding diffusion of defensin from PMNs ex vivo. These data indicate that neutrophil defensin is present in the walls of human coronary arteries. The deposition of defensin in vessels may contribute to the pathophysiological consequences of inflammation in addition to their role in host defense.</description><subject>Anti-Infective Agents - analysis</subject><subject>Anti-Infective Agents - metabolism</subject><subject>Antibodies - analysis</subject><subject>Arteriosclerosis - pathology</subject><subject>Arteriosclerosis - physiopathology</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Proteins - analysis</subject><subject>Blood Proteins - immunology</subject><subject>Blood Proteins - metabolism</subject><subject>Cardiology. Vascular system</subject><subject>Coronary Vessels - chemistry</subject><subject>Coronary Vessels - metabolism</subject><subject>Defensins</subject><subject>Endothelium, Vascular - chemistry</subject><subject>Female</subject><subject>Fibrinolysis - physiology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Reference Values</subject><subject>Tunica Intima - chemistry</subject><subject>Tunica Intima - cytology</subject><subject>Tunica Media - chemistry</subject><subject>Tunica Media - cytology</subject><issn>0002-9440</issn><issn>1525-2191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkFtLxDAQhYso63r5CUIR0adCJukleRFEvMGCL_ocZpPUZkmTtWkV_fVGdhEVwoThfJw5MzvZHCpaFRQE7GZzQggtRFmS_ewgxlVqa8bJLJsJUhPO-Dy7fej7yYfOxjGozvRWoctdSNV-4miDz0Oba9MaH63P0-umHn2uwhA8Dh_5m4nRuHiU7bXoojne_ofZ8-3N0_V9sXi8e7i-WhQdK8VYICNLzZRutK4ZEUukjJaoTZk6xbSuUC-VUkTQEngJQGtFoQFdiraFmiI7zC43vutp2RutjB8HdHI92D6lkQGt_Kt428mX8CaBVw1veDI43xoM4XUycZS9jco4h96EKcqG84rRhiXw9B-4CtPg03KSAhdVCgcJOvkd5yfH9rxJP9vqGNNJ2wG9svEHozUBBt-zLjZYZ1-6dzsYGXt0LpmCxNUaKiKZBEIE-wJKe5LO</recordid><startdate>19970301</startdate><enddate>19970301</enddate><creator>Barnathan, ES</creator><creator>Raghunath, PN</creator><creator>Tomaszewski, JE</creator><creator>Ganz, T</creator><creator>Cines, DB</creator><creator>Higazi A, al-R</creator><general>ASIP</general><general>American Society for Investigative Pathology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19970301</creationdate><title>Immunohistochemical localization of defensin in human coronary vessels</title><author>Barnathan, ES ; Raghunath, PN ; Tomaszewski, JE ; Ganz, T ; Cines, DB ; Higazi A, al-R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h349t-a30bd3cd7dd6309ba2324ade4630c3dd5adbccc09241841126c2171d49ff162a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Anti-Infective Agents - analysis</topic><topic>Anti-Infective Agents - metabolism</topic><topic>Antibodies - analysis</topic><topic>Arteriosclerosis - pathology</topic><topic>Arteriosclerosis - physiopathology</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Proteins - analysis</topic><topic>Blood Proteins - immunology</topic><topic>Blood Proteins - metabolism</topic><topic>Cardiology. Vascular system</topic><topic>Coronary Vessels - chemistry</topic><topic>Coronary Vessels - metabolism</topic><topic>Defensins</topic><topic>Endothelium, Vascular - chemistry</topic><topic>Female</topic><topic>Fibrinolysis - physiology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Reference Values</topic><topic>Tunica Intima - chemistry</topic><topic>Tunica Intima - cytology</topic><topic>Tunica Media - chemistry</topic><topic>Tunica Media - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barnathan, ES</creatorcontrib><creatorcontrib>Raghunath, PN</creatorcontrib><creatorcontrib>Tomaszewski, JE</creatorcontrib><creatorcontrib>Ganz, T</creatorcontrib><creatorcontrib>Cines, DB</creatorcontrib><creatorcontrib>Higazi A, al-R</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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</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>Barnathan, ES</au><au>Raghunath, PN</au><au>Tomaszewski, JE</au><au>Ganz, T</au><au>Cines, DB</au><au>Higazi A, al-R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunohistochemical localization of defensin in human coronary vessels</atitle><jtitle>The American journal of pathology</jtitle><addtitle>Am J Pathol</addtitle><date>1997-03-01</date><risdate>1997</risdate><volume>150</volume><issue>3</issue><spage>1009</spage><epage>1020</epage><pages>1009-1020</pages><issn>0002-9440</issn><eissn>1525-2191</eissn><coden>AJPAA4</coden><abstract>Neutrophil defensins comprise a family of cationic peptides that possess potent antimicrobial activity. Defensins are normally sequestered in cytoplasmic granules with their primary site of action in phagolysosomes, although some peptide is released into the circulation during the course of infection or inflammation. In view of the fact that neutrophils adhere to the endothelium and that defensins have been reported to bind to human endothelial cells in vitro, we used immunohistochemistry to study the distribution of these peptides in normal and in atherosclerotic human coronary arteries. Defensin was found primarily in the intima of normal and atherosclerotic vessels, most prominently in association with intimal smooth muscle cells. Both large- and small-vessel endothelium stained focally for defensin. Defensin was also found in the media near the external elastic lamina and in some periadventitial vessels. The same distribution was seen in vessels that had been perfusion fixed immediately upon procurement, excluding diffusion of defensin from PMNs ex vivo. These data indicate that neutrophil defensin is present in the walls of human coronary arteries. The deposition of defensin in vessels may contribute to the pathophysiological consequences of inflammation in addition to their role in host defense.</abstract><cop>Bethesda, MD</cop><pub>ASIP</pub><pmid>9060838</pmid><tpages>12</tpages></addata></record> |
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subjects | Anti-Infective Agents - analysis Anti-Infective Agents - metabolism Antibodies - analysis Arteriosclerosis - pathology Arteriosclerosis - physiopathology Atherosclerosis (general aspects, experimental research) Biological and medical sciences Blood and lymphatic vessels Blood Proteins - analysis Blood Proteins - immunology Blood Proteins - metabolism Cardiology. Vascular system Coronary Vessels - chemistry Coronary Vessels - metabolism Defensins Endothelium, Vascular - chemistry Female Fibrinolysis - physiology Humans Immunohistochemistry Male Medical sciences Reference Values Tunica Intima - chemistry Tunica Intima - cytology Tunica Media - chemistry Tunica Media - cytology |
title | Immunohistochemical localization of defensin in human coronary vessels |
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