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Mechanisms of platelet and leukocyte recruitment in experimental colitis
Both leukocytes and platelets accumulate in the colonic microvasculature during experimental colitis, leading to microvascular dysfunction and tissue injury. The objective of this study was to determine whether the recruitment of leukocytes and platelets in inflamed colonic venules are codependent p...
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Published in: | American journal of physiology: Gastrointestinal and liver physiology 2007-11, Vol.293 (5), p.G1054-G1060 |
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container_end_page | G1060 |
container_issue | 5 |
container_start_page | G1054 |
container_title | American journal of physiology: Gastrointestinal and liver physiology |
container_volume | 293 |
creator | Vowinkel, Thorsten Wood, Katherine C Stokes, Karen Y Russell, Janice Tailor, Anitaben Anthoni, Christoph Senninger, Norbert Krieglstein, Christian F Granger, D Neil |
description | Both leukocytes and platelets accumulate in the colonic microvasculature during experimental colitis, leading to microvascular dysfunction and tissue injury. The objective of this study was to determine whether the recruitment of leukocytes and platelets in inflamed colonic venules are codependent processes. The rolling and adherence of leukocytes and platelets in colonic venules of mice with dextran sodium sulfate (DSS)-induced colitis were monitored by intravital videomicroscopy. DSS elicited an increased recruitment of both rolling and adherent leukocytes and platelets. DSS-colitic mice rendered thrombocytopenic with anti-platelet serum exhibited profound reductions in leukocyte adhesion. Neutropenia, induced with anti-neutrophil serum, significantly reduced the adhesion of leukocytes and the accumulation of platelet-leukocyte aggregates while greatly enhancing the number of platelets that roll and adhere directly to venular endothelial cells. The enhanced platelet adhesion associated with neutropenia was mediated by platelet P-selectin interactions with endothelial cell P-selectin glycoprotein ligand (PSGL-1). DSS colitis was also associated with an increased expression of PSGL-1 in the colonic vasculature. These findings indicate that the recruitment of leukocytes and platelets in inflamed colonic venules are co-dependent processes. |
doi_str_mv | 10.1152/ajpgi.00350.2007 |
format | article |
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The objective of this study was to determine whether the recruitment of leukocytes and platelets in inflamed colonic venules are codependent processes. The rolling and adherence of leukocytes and platelets in colonic venules of mice with dextran sodium sulfate (DSS)-induced colitis were monitored by intravital videomicroscopy. DSS elicited an increased recruitment of both rolling and adherent leukocytes and platelets. DSS-colitic mice rendered thrombocytopenic with anti-platelet serum exhibited profound reductions in leukocyte adhesion. Neutropenia, induced with anti-neutrophil serum, significantly reduced the adhesion of leukocytes and the accumulation of platelet-leukocyte aggregates while greatly enhancing the number of platelets that roll and adhere directly to venular endothelial cells. The enhanced platelet adhesion associated with neutropenia was mediated by platelet P-selectin interactions with endothelial cell P-selectin glycoprotein ligand (PSGL-1). DSS colitis was also associated with an increased expression of PSGL-1 in the colonic vasculature. These findings indicate that the recruitment of leukocytes and platelets in inflamed colonic venules are co-dependent processes.</description><identifier>ISSN: 0193-1857</identifier><identifier>EISSN: 1522-1547</identifier><identifier>DOI: 10.1152/ajpgi.00350.2007</identifier><identifier>PMID: 17884975</identifier><identifier>CODEN: APGPDF</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Blood clots ; Blood Platelets - physiology ; Colitis - blood ; Colitis - physiopathology ; Disease Models, Animal ; Endothelium, Vascular - physiology ; Gastroenterology ; Inflammatory bowel disease ; Leukocytes ; Leukocytes - physiology ; Male ; Mice ; Mice, Inbred C57BL ; Proteins</subject><ispartof>American journal of physiology: Gastrointestinal and liver physiology, 2007-11, Vol.293 (5), p.G1054-G1060</ispartof><rights>Copyright American Physiological Society Nov 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-d75b2bd1cda6e0b6990295754fe476281ccc3fc515069d81eeeb4fb223a41e0c3</citedby><cites>FETCH-LOGICAL-c432t-d75b2bd1cda6e0b6990295754fe476281ccc3fc515069d81eeeb4fb223a41e0c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17884975$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vowinkel, Thorsten</creatorcontrib><creatorcontrib>Wood, Katherine C</creatorcontrib><creatorcontrib>Stokes, Karen Y</creatorcontrib><creatorcontrib>Russell, Janice</creatorcontrib><creatorcontrib>Tailor, Anitaben</creatorcontrib><creatorcontrib>Anthoni, Christoph</creatorcontrib><creatorcontrib>Senninger, Norbert</creatorcontrib><creatorcontrib>Krieglstein, Christian F</creatorcontrib><creatorcontrib>Granger, D Neil</creatorcontrib><title>Mechanisms of platelet and leukocyte recruitment in experimental colitis</title><title>American journal of physiology: Gastrointestinal and liver physiology</title><addtitle>Am J Physiol Gastrointest Liver Physiol</addtitle><description>Both leukocytes and platelets accumulate in the colonic microvasculature during experimental colitis, leading to microvascular dysfunction and tissue injury. The objective of this study was to determine whether the recruitment of leukocytes and platelets in inflamed colonic venules are codependent processes. The rolling and adherence of leukocytes and platelets in colonic venules of mice with dextran sodium sulfate (DSS)-induced colitis were monitored by intravital videomicroscopy. DSS elicited an increased recruitment of both rolling and adherent leukocytes and platelets. DSS-colitic mice rendered thrombocytopenic with anti-platelet serum exhibited profound reductions in leukocyte adhesion. Neutropenia, induced with anti-neutrophil serum, significantly reduced the adhesion of leukocytes and the accumulation of platelet-leukocyte aggregates while greatly enhancing the number of platelets that roll and adhere directly to venular endothelial cells. The enhanced platelet adhesion associated with neutropenia was mediated by platelet P-selectin interactions with endothelial cell P-selectin glycoprotein ligand (PSGL-1). DSS colitis was also associated with an increased expression of PSGL-1 in the colonic vasculature. These findings indicate that the recruitment of leukocytes and platelets in inflamed colonic venules are co-dependent processes.</description><subject>Animals</subject><subject>Blood clots</subject><subject>Blood Platelets - physiology</subject><subject>Colitis - blood</subject><subject>Colitis - physiopathology</subject><subject>Disease Models, Animal</subject><subject>Endothelium, Vascular - physiology</subject><subject>Gastroenterology</subject><subject>Inflammatory bowel disease</subject><subject>Leukocytes</subject><subject>Leukocytes - physiology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Proteins</subject><issn>0193-1857</issn><issn>1522-1547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpdkM1LxDAQxYMo7rp69yTBg7eu-Wzao4i6wooXPYc0nWrWbFuTFNz_3u4HCJ6GGd57zPshdEnJnFLJbs2q_3BzQrgkc0aIOkLT8cwyKoU6RlNCS57RQqoJOotxRQiRjNJTNKGqKESp5BQtXsB-mtbFdcRdg3tvEnhI2LQ19jB8dXaTAAewYXBpDW3CrsXw00Nw2814bDvvkovn6KQxPsLFYc7Q--PD2_0iW74-Pd_fLTMrOEtZrWTFqpra2uRAqrwsCSulkqIBoXJWUGstb6ykkuRlXVAAqERTMcaNoEAsn6GbfW4fuu8BYtJrFy14b1rohqjzQiguJR-F1_-Eq24I7fibZpzJQoqR2wyRvciGLsYAje7HYiZsNCV6i1jvEOsdYr1FPFquDrlDtYb6z3Bgyn8Bj_d4ZQ</recordid><startdate>200711</startdate><enddate>200711</enddate><creator>Vowinkel, Thorsten</creator><creator>Wood, Katherine C</creator><creator>Stokes, Karen Y</creator><creator>Russell, Janice</creator><creator>Tailor, Anitaben</creator><creator>Anthoni, Christoph</creator><creator>Senninger, Norbert</creator><creator>Krieglstein, Christian F</creator><creator>Granger, D Neil</creator><general>American Physiological Society</general><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></search><sort><creationdate>200711</creationdate><title>Mechanisms of platelet and leukocyte recruitment in experimental colitis</title><author>Vowinkel, Thorsten ; Wood, Katherine C ; Stokes, Karen Y ; Russell, Janice ; Tailor, Anitaben ; Anthoni, Christoph ; Senninger, Norbert ; Krieglstein, Christian F ; Granger, D Neil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-d75b2bd1cda6e0b6990295754fe476281ccc3fc515069d81eeeb4fb223a41e0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Blood clots</topic><topic>Blood Platelets - physiology</topic><topic>Colitis - blood</topic><topic>Colitis - physiopathology</topic><topic>Disease Models, Animal</topic><topic>Endothelium, Vascular - physiology</topic><topic>Gastroenterology</topic><topic>Inflammatory bowel disease</topic><topic>Leukocytes</topic><topic>Leukocytes - physiology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vowinkel, Thorsten</creatorcontrib><creatorcontrib>Wood, Katherine C</creatorcontrib><creatorcontrib>Stokes, Karen Y</creatorcontrib><creatorcontrib>Russell, Janice</creatorcontrib><creatorcontrib>Tailor, Anitaben</creatorcontrib><creatorcontrib>Anthoni, Christoph</creatorcontrib><creatorcontrib>Senninger, Norbert</creatorcontrib><creatorcontrib>Krieglstein, Christian F</creatorcontrib><creatorcontrib>Granger, D Neil</creatorcontrib><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><jtitle>American journal of physiology: Gastrointestinal and liver physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vowinkel, Thorsten</au><au>Wood, Katherine C</au><au>Stokes, Karen Y</au><au>Russell, Janice</au><au>Tailor, Anitaben</au><au>Anthoni, Christoph</au><au>Senninger, Norbert</au><au>Krieglstein, Christian F</au><au>Granger, D Neil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanisms of platelet and leukocyte recruitment in experimental colitis</atitle><jtitle>American journal of physiology: Gastrointestinal and liver physiology</jtitle><addtitle>Am J Physiol Gastrointest Liver Physiol</addtitle><date>2007-11</date><risdate>2007</risdate><volume>293</volume><issue>5</issue><spage>G1054</spage><epage>G1060</epage><pages>G1054-G1060</pages><issn>0193-1857</issn><eissn>1522-1547</eissn><coden>APGPDF</coden><abstract>Both leukocytes and platelets accumulate in the colonic microvasculature during experimental colitis, leading to microvascular dysfunction and tissue injury. The objective of this study was to determine whether the recruitment of leukocytes and platelets in inflamed colonic venules are codependent processes. The rolling and adherence of leukocytes and platelets in colonic venules of mice with dextran sodium sulfate (DSS)-induced colitis were monitored by intravital videomicroscopy. DSS elicited an increased recruitment of both rolling and adherent leukocytes and platelets. DSS-colitic mice rendered thrombocytopenic with anti-platelet serum exhibited profound reductions in leukocyte adhesion. Neutropenia, induced with anti-neutrophil serum, significantly reduced the adhesion of leukocytes and the accumulation of platelet-leukocyte aggregates while greatly enhancing the number of platelets that roll and adhere directly to venular endothelial cells. The enhanced platelet adhesion associated with neutropenia was mediated by platelet P-selectin interactions with endothelial cell P-selectin glycoprotein ligand (PSGL-1). DSS colitis was also associated with an increased expression of PSGL-1 in the colonic vasculature. These findings indicate that the recruitment of leukocytes and platelets in inflamed colonic venules are co-dependent processes.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>17884975</pmid><doi>10.1152/ajpgi.00350.2007</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blood clots Blood Platelets - physiology Colitis - blood Colitis - physiopathology Disease Models, Animal Endothelium, Vascular - physiology Gastroenterology Inflammatory bowel disease Leukocytes Leukocytes - physiology Male Mice Mice, Inbred C57BL Proteins |
title | Mechanisms of platelet and leukocyte recruitment in experimental colitis |
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