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Aging and eliciting agents: Effect on murine peritoneal macrophage monokine bioactivity

dc.contributor.authorChen, Yifangen_US
dc.contributor.authorBradley, Suzanne F.en_US
dc.date.accessioned2006-04-10T15:51:47Z
dc.date.available2006-04-10T15:51:47Z
dc.date.issued1993en_US
dc.identifier.citationChen, Yifang, Bradley, Suzanne F. (1993)."Aging and eliciting agents: Effect on murine peritoneal macrophage monokine bioactivity." Experimental Gerontology 28(2): 145-159. <http://hdl.handle.net/2027.42/30935>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T6J-47RJ08P-31/2/6e64133e19d16d1e63071b7685580894en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30935
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8325351&dopt=citationen_US
dc.description.abstractDecreased responsiveness of the aged to infection may be associated with a decline in monokine production. Prior studies in macrophages have used different eliciting agents, and results have varied. We assessed the effect of age on interleukin-1 (IL-1), tumor necrosis factor (TNF), and interleukin-6 (IL-6) in unelicited, thioglycollate (TG)-elicited, and complete Freund's adjuvant (CFA)-elicited peritoneal macrophages. Resident macrophages or CFA-elicited macrophages from middle aged or aged mice produced significantly less monokine bioactivity than resident or CFA-elicited macrophages from young mice. Monokine bioactivity from TG-elicited macrophages from aged and middle aged mice was significantly increased when compared with macrophages of young mice. Eliciting agents may alter macrophage populations and interactions with other cells leading to changes in monokine bioactivity with aging.en_US
dc.format.extent953192 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleAging and eliciting agents: Effect on murine peritoneal macrophage monokine bioactivityen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelGeriatricsen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Veterans Affairs Medical Center, 2215 Fuller Road, Ann Arbor, Michigan 48105, USA; Divisions of Geriatric Medicine and Infectious Diseases, Department of Internal Medicine, University of Michigan Medical School, 2215 Fuller Road, Ann Arbor, Michigan 48105, USA.en_US
dc.contributor.affiliationumDivisions of Geriatric Medicine and Infectious Diseases, Department of Internal Medicine, University of Michigan Medical School, 2215 Fuller Road, Ann Arbor, Michigan 48105, USA; Department of Veterans Affairs Medical Center, 2215 Fuller Road, Ann Arbor, Michigan 48105, USA.en_US
dc.identifier.pmid8325351en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30935/1/0000605.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0531-5565(93)90004-Wen_US
dc.identifier.sourceExperimental Gerontologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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