CD18-independent neutrophil and mononuclear leukocyte emigration into the peritoneum of rabbits
The CD18 mAb 60.3 and the CD49d mAb HP1/2 were given at the time of intraperitoneal instillation of either protease peptone or live Escherichia coli bacteria and at 12 h. Leukocyte emigration was evaluated at 4 and 24 h. PMN emigration 4 h after protease peptone instillation and injection of both mA...
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Veröffentlicht in: | The Journal of clinical investigation 1993-09, Vol.92 (3), p.1168-1173 |
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description | The CD18 mAb 60.3 and the CD49d mAb HP1/2 were given at the time of intraperitoneal instillation of either protease peptone or live Escherichia coli bacteria and at 12 h. Leukocyte emigration was evaluated at 4 and 24 h. PMN emigration 4 h after protease peptone instillation and injection of both mAbs was 10% of that in saline treatment. It was 15% of that in saline treatment after mAb 60.3 alone and unchanged by mAb HP1/2. At 24 h PMN emigration in response to protease peptone was not prevented by either CD18 or CD49d mAbs, however, when given together emigration was 10% of saline-treated animals. Mononuclear cell emigration to protease peptone was enhanced at 4 h by both CD18 and CD49d mAbs. The CD18 mAb did not augment mononuclear emigration in response to live bacteria. At 24 h, neither the CD18 nor the CD49d mAb alone blocked emigration of mononuclear cells, but the combination of the two did. These studies demonstrate that: (a) early (4 h) PMN emigration is CD11/CD18 dependent; (b) late (24 h) PMN emigration is CD11/CD18 independent; and (c) mononuclear cells utilize the integrins CD18 and CD49d. |
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K ; HARLAN, J. M</creator><creatorcontrib>WINN, R. K ; HARLAN, J. M</creatorcontrib><description>The CD18 mAb 60.3 and the CD49d mAb HP1/2 were given at the time of intraperitoneal instillation of either protease peptone or live Escherichia coli bacteria and at 12 h. Leukocyte emigration was evaluated at 4 and 24 h. PMN emigration 4 h after protease peptone instillation and injection of both mAbs was 10% of that in saline treatment. It was 15% of that in saline treatment after mAb 60.3 alone and unchanged by mAb HP1/2. At 24 h PMN emigration in response to protease peptone was not prevented by either CD18 or CD49d mAbs, however, when given together emigration was 10% of saline-treated animals. Mononuclear cell emigration to protease peptone was enhanced at 4 h by both CD18 and CD49d mAbs. The CD18 mAb did not augment mononuclear emigration in response to live bacteria. At 24 h, neither the CD18 nor the CD49d mAb alone blocked emigration of mononuclear cells, but the combination of the two did. These studies demonstrate that: (a) early (4 h) PMN emigration is CD11/CD18 dependent; (b) late (24 h) PMN emigration is CD11/CD18 independent; and (c) mononuclear cells utilize the integrins CD18 and CD49d.</description><identifier>ISSN: 0021-9738</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI116686</identifier><identifier>PMID: 8104195</identifier><identifier>CODEN: JCINAO</identifier><language>eng</language><publisher>Ann Arbor, MI: American Society for Clinical Investigation</publisher><subject>Animals ; Antigens, CD - physiology ; Biological and medical sciences ; CD18 Antigens ; Chemotaxis, Leukocyte ; Escherichia coli Infections - immunology ; Fundamental and applied biological sciences. Psychology ; Integrin alpha Chains ; Leukocytes, Mononuclear - physiology ; Neutrophils - physiology ; Peritoneal Cavity - cytology ; Rabbits ; Receptors, Very Late Antigen - physiology ; Vertebrates: blood, hematopoietic organs, reticuloendothelial system</subject><ispartof>The Journal of clinical investigation, 1993-09, Vol.92 (3), p.1168-1173</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-8be6d09b299b7aa051064e0fd8e8e5dec209b0a5e740f7ba8e657e23085053c93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC288254/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC288254/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4918373$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8104195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WINN, R. K</creatorcontrib><creatorcontrib>HARLAN, J. M</creatorcontrib><title>CD18-independent neutrophil and mononuclear leukocyte emigration into the peritoneum of rabbits</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>The CD18 mAb 60.3 and the CD49d mAb HP1/2 were given at the time of intraperitoneal instillation of either protease peptone or live Escherichia coli bacteria and at 12 h. Leukocyte emigration was evaluated at 4 and 24 h. PMN emigration 4 h after protease peptone instillation and injection of both mAbs was 10% of that in saline treatment. It was 15% of that in saline treatment after mAb 60.3 alone and unchanged by mAb HP1/2. At 24 h PMN emigration in response to protease peptone was not prevented by either CD18 or CD49d mAbs, however, when given together emigration was 10% of saline-treated animals. Mononuclear cell emigration to protease peptone was enhanced at 4 h by both CD18 and CD49d mAbs. The CD18 mAb did not augment mononuclear emigration in response to live bacteria. At 24 h, neither the CD18 nor the CD49d mAb alone blocked emigration of mononuclear cells, but the combination of the two did. These studies demonstrate that: (a) early (4 h) PMN emigration is CD11/CD18 dependent; (b) late (24 h) PMN emigration is CD11/CD18 independent; and (c) mononuclear cells utilize the integrins CD18 and CD49d.</description><subject>Animals</subject><subject>Antigens, CD - physiology</subject><subject>Biological and medical sciences</subject><subject>CD18 Antigens</subject><subject>Chemotaxis, Leukocyte</subject><subject>Escherichia coli Infections - immunology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Integrin alpha Chains</subject><subject>Leukocytes, Mononuclear - physiology</subject><subject>Neutrophils - physiology</subject><subject>Peritoneal Cavity - cytology</subject><subject>Rabbits</subject><subject>Receptors, Very Late Antigen - physiology</subject><subject>Vertebrates: blood, hematopoietic organs, reticuloendothelial system</subject><issn>0021-9738</issn><issn>1558-8238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkb1u2zAUhYkigeOmHfoAATgEBTooJUVRJIcMgZM0Dgx0aWeCoq5sJhKpkFQBv31V2DDS5d7hfOf-IvSFkhtKRfn9ebWmtK5l_QEtKeeykCWTZ2hJSEkLJZi8QB9TeiGEVhWvFmghKamo4kukV_dUFs63MMIcfMYephzDuHM9Nr7FQ_DBT7YHE3EP02uw-wwYBreNJrvgsfM54LwDPEJ0Ocz2AYcOR9M0LqdP6LwzfYLPx3yJfj8-_Fo9FZufP9aru01hmZK5kA3ULVFNqVQjjCGckroC0rUSJPAWbDmLxHAQFelEYyTUXEDJiOSEM6vYJbo91B2nZoDWzptE0-sxusHEvQ7G6f8V73Z6G_7oUsqSV7P_69Efw9sEKevBJQt9bzyEKWnBVU0FoTP47QDaGFKK0J16UKL_PUOfnjGzV--HOpHH68_69VE3yZq-i8Zbl05YpahkgrG_Eq6Tjw</recordid><startdate>19930901</startdate><enddate>19930901</enddate><creator>WINN, R. K</creator><creator>HARLAN, J. M</creator><general>American Society for Clinical Investigation</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>19930901</creationdate><title>CD18-independent neutrophil and mononuclear leukocyte emigration into the peritoneum of rabbits</title><author>WINN, R. K ; HARLAN, J. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-8be6d09b299b7aa051064e0fd8e8e5dec209b0a5e740f7ba8e657e23085053c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Antigens, CD - physiology</topic><topic>Biological and medical sciences</topic><topic>CD18 Antigens</topic><topic>Chemotaxis, Leukocyte</topic><topic>Escherichia coli Infections - immunology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Integrin alpha Chains</topic><topic>Leukocytes, Mononuclear - physiology</topic><topic>Neutrophils - physiology</topic><topic>Peritoneal Cavity - cytology</topic><topic>Rabbits</topic><topic>Receptors, Very Late Antigen - physiology</topic><topic>Vertebrates: blood, hematopoietic organs, reticuloendothelial system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WINN, R. K</creatorcontrib><creatorcontrib>HARLAN, J. M</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>The Journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WINN, R. K</au><au>HARLAN, J. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD18-independent neutrophil and mononuclear leukocyte emigration into the peritoneum of rabbits</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>1993-09-01</date><risdate>1993</risdate><volume>92</volume><issue>3</issue><spage>1168</spage><epage>1173</epage><pages>1168-1173</pages><issn>0021-9738</issn><eissn>1558-8238</eissn><coden>JCINAO</coden><abstract>The CD18 mAb 60.3 and the CD49d mAb HP1/2 were given at the time of intraperitoneal instillation of either protease peptone or live Escherichia coli bacteria and at 12 h. Leukocyte emigration was evaluated at 4 and 24 h. PMN emigration 4 h after protease peptone instillation and injection of both mAbs was 10% of that in saline treatment. It was 15% of that in saline treatment after mAb 60.3 alone and unchanged by mAb HP1/2. At 24 h PMN emigration in response to protease peptone was not prevented by either CD18 or CD49d mAbs, however, when given together emigration was 10% of saline-treated animals. Mononuclear cell emigration to protease peptone was enhanced at 4 h by both CD18 and CD49d mAbs. The CD18 mAb did not augment mononuclear emigration in response to live bacteria. At 24 h, neither the CD18 nor the CD49d mAb alone blocked emigration of mononuclear cells, but the combination of the two did. These studies demonstrate that: (a) early (4 h) PMN emigration is CD11/CD18 dependent; (b) late (24 h) PMN emigration is CD11/CD18 independent; and (c) mononuclear cells utilize the integrins CD18 and CD49d.</abstract><cop>Ann Arbor, MI</cop><pub>American Society for Clinical Investigation</pub><pmid>8104195</pmid><doi>10.1172/JCI116686</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens, CD - physiology Biological and medical sciences CD18 Antigens Chemotaxis, Leukocyte Escherichia coli Infections - immunology Fundamental and applied biological sciences. Psychology Integrin alpha Chains Leukocytes, Mononuclear - physiology Neutrophils - physiology Peritoneal Cavity - cytology Rabbits Receptors, Very Late Antigen - physiology Vertebrates: blood, hematopoietic organs, reticuloendothelial system |
title | CD18-independent neutrophil and mononuclear leukocyte emigration into the peritoneum of rabbits |
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