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Human neutrophils exhibit disparate chemotactic factor gene expression

dc.contributor.authorStrieter, Robert M.en_US
dc.contributor.authorKasahara, K.en_US
dc.contributor.authorAllen, R.en_US
dc.contributor.authorShowell, H. J.en_US
dc.contributor.authorStandiford, Theodore J.en_US
dc.contributor.authorKunkel, Steven L.en_US
dc.date.accessioned2006-04-10T13:32:07Z
dc.date.available2006-04-10T13:32:07Z
dc.date.issued1990-12-14en_US
dc.identifier.citationStrieter, R.M., Kasahara, K., Allen, R., Showell, H.J., Standiford, T.J., Kunkel, S.L. (1990/12/14)."Human neutrophils exhibit disparate chemotactic factor gene expression." Biochemical and Biophysical Research Communications 173(2): 725-730. <http://hdl.handle.net/2027.42/28272>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WBK-4HM8G72-19/2/b0dcb376a3b130b4675eb8cb7b849fc0en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28272
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1701991&dopt=citationen_US
dc.description.abstractThe evolution of acute inflammation from initiation through resolution is associated with the changing character of the infiltrating leukocytes. Recruitment of these leukocytes is dependent upon the generation of chemotactic factors that have either global or specific activity for a particular leukocyte. In this manuscript we present data demonstrating that human neutrophils can express mRNA for neutrophil chemotactic factor/interleukin 8 (IL-8), but fail to express mRNA for monocyte chemotactic protein (MCP-1). The expression of IL-8 was observed upon adherence or in response to stimulation with lipopolysaccharide. Maximal IL-8 antigenic production was noted at 24 hrs. These studies demonstrate a disparate expression of chemotactic cytokines by neutrophils.en_US
dc.format.extent490248 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleHuman neutrophils exhibit disparate chemotactic factor gene expressionen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Medicine, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Medicine, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Immunology, Pfizer Central Research, Groton, Connecticut, USAen_US
dc.identifier.pmid1701991en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28272/1/0000021.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0006-291X(05)80095-6en_US
dc.identifier.sourceBiochemical and Biophysical Research Communicationsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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