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pubmed-article:11343213pubmed:dateCreated2001-5-8lld:pubmed
pubmed-article:11343213pubmed:abstractTextMigration of polymorphonuclear neutrophils (PMNL) from the vascular compartment into the pleural space occurs rapidly during the development of parapneumonic effusions. This study investigated the polarized secretion of interleukin (IL)-8 in activated pleural mesothelial cells (PMC) and the migration of PMNL across resting, activated PMC monolayers. Results show that PMC produce IL-8 in a polar manner. When PMC were stimulated with Staphylococcus aureus or IL-1beta at the basal or at the apical surface, significantly (P< .05) more IL-8 was released toward the apical surface. This polarized production of IL-8 was confirmed by in situ hybridization. PMNL migration was higher from the basilar to apical than from the apical to basilar surface of PMC. Neutralizing antibodies against IL-8 and intercellular adhesion molecule (ICAM)-1 significantly (P< .001) blocked PMNL migration across activated monolayers. Thus, during pleural inflammation, PMC regulate the influx of PMNL into the pleural space by polar production of IL-8 and expression of ICAM-1.lld:pubmed
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pubmed-article:11343213pubmed:authorpubmed-author:MohammedK AKAlld:pubmed
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pubmed-article:11343213pubmed:pagination1638-45lld:pubmed
pubmed-article:11343213pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:11343213pubmed:year2001lld:pubmed
pubmed-article:11343213pubmed:articleTitlePolar production of interleukin-8 by mesothelial cells promotes the transmesothelial migration of neutrophils: role of intercellular adhesion molecule-1.lld:pubmed
pubmed-article:11343213pubmed:affiliationDivision of Pulmonary and Critical Care Medicine, Department of Veterans Affairs Medical Center, and Indiana University School of Medicine, Indianapolis, IN, USA.lld:pubmed
pubmed-article:11343213pubmed:publicationTypeJournal Articlelld:pubmed
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pubmed-article:11343213pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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