Neutrophil Adhesion to Human Endothelial Cells is Induced by the Membrane Attack Complex: The Roles of P-Selectin and Platelet Activating Factor
dc.contributor.author | Ward, Peter A. | en_US |
dc.contributor.author | Warren, Jeffrey S. | en_US |
dc.contributor.author | Kilgore, Kenneth S. | en_US |
dc.date.accessioned | 2006-09-11T14:55:35Z | |
dc.date.available | 2006-09-11T14:55:35Z | |
dc.date.issued | 1998-12 | en_US |
dc.identifier.citation | Kilgore, Kenneth S.; Ward, Peter A.; Warren, Jeffrey S.; (1998). "Neutrophil Adhesion to Human Endothelial Cells is Induced by the Membrane Attack Complex: The Roles of P-Selectin and Platelet Activating Factor." Inflammation 22(6): 583-598. <http://hdl.handle.net/2027.42/44521> | en_US |
dc.identifier.issn | 0360-3997 | en_US |
dc.identifier.issn | 1573-2576 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/44521 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9824773&dopt=citation | en_US |
dc.description.abstract | A variety of inflammatory diseases are accompanied by activation of the complement system. We examined the role of the membrane attack complex (MAC) in mediating neutrophil adhesion to endothelial cells. To assemble the MAC in endothelial cell monolayers, a C5b-like molecule was created through the treatment of purified C5 with the oxidizing agent chloramine-T, followed by addition of the remaining components (C6-C9) that constitute the MAC. Use of this method abrogated potentially confounding effects mediated by other complement components (e.g., C5a). MAC assembly resulted in a rapid (30 min), concentration-dependent increase in neutrophil adherence. A monoclonal antibody directed against P-selectin inhibited MAC-mediated neutrophil adhesion. A whole cell EIA confirmed P-selectin expression after formation of the MAC. Incubation of neutrophils with the platelet-activating factor receptor antagonist, CF 3988, also significantly decreased adhesion, indicating that PAF plays a role in MAC-mediated adhesion. These results suggest that the MAC can promote neutrophil adhesion through P-selectin and PAF-mediated mechanisms. | en_US |
dc.format.extent | 1785463 bytes | |
dc.format.extent | 3115 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Kluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Media | en_US |
dc.subject.other | Pathology | en_US |
dc.subject.other | Pharmacology/Toxicology | en_US |
dc.subject.other | Medicine & Public Health | en_US |
dc.subject.other | Internal Medicine | en_US |
dc.subject.other | Rheumatology | en_US |
dc.title | Neutrophil Adhesion to Human Endothelial Cells is Induced by the Membrane Attack Complex: The Roles of P-Selectin and Platelet Activating Factor | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Pathology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Pathology, University of Michigan Medical School, 1301 Catherine Road, Ann Arbor, Michigan, 48109–0602 | en_US |
dc.contributor.affiliationum | Department of Pathology, University of Michigan Medical School, 1301 Catherine Road, Ann Arbor, Michigan, 48109–0602 | en_US |
dc.contributor.affiliationum | Department of Pathology, University of Michigan Medical School, 1301 Catherine Road, Ann Arbor, Michigan, 48109–0602 | en_US |
dc.contributor.affiliationumcampus | Ann Arbor | en_US |
dc.identifier.pmid | 9824773 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/44521/1/10753_2004_Article_415305.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1023/A:1022362413939 | en_US |
dc.identifier.source | Inflammation | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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