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The beta form is the dominant interleukin released by murine peritoneal macrophages

dc.contributor.authorChensue, Stephen W.en_US
dc.contributor.authorShmyr-Forsch, C.en_US
dc.contributor.authorOtterness, Ivan G.en_US
dc.contributor.authorKunkel, Steven L.en_US
dc.date.accessioned2006-04-07T20:50:18Z
dc.date.available2006-04-07T20:50:18Z
dc.date.issued1989-04-14en_US
dc.identifier.citationChensue, S. W., Shmyr-Forsch, C., Otterness, I. G., Kunkel, S. L. (1989/04/14)."The beta form is the dominant interleukin released by murine peritoneal macrophages." Biochemical and Biophysical Research Communications 160(1): 404-408. <http://hdl.handle.net/2027.42/27968>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WBK-4DN93SM-HD/2/2f1f00409ded73cccd0e274c89b989c2en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27968
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2653321&dopt=citationen_US
dc.description.abstractUsing highly specific polyclonal antisera raised against recombinant murine IL-1 [alpha] and [beta], we performed solid-phase immunoabsorption studies on supernates of resident and adjuvant-elicited CBA/J mouse peritoneal macrophages. Antibody specificity was established by reciprocal absorption studies and Western blot analysis. Supernates obtained from macrophages cultured for 18 hr in the presence of 1[mu]g/ml lipopolysaccharide (LPS) were subjected to immunoabsorption. Approximately 78-90% of the released bioactive material was IL-1 and about 80% of this could be attributed to IL-1 [beta]. Analogous to that reported for human monocytes, these data suggest that IL-1 [beta] is the predominant released form of IL-1.en_US
dc.format.extent333017 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleThe beta form is the dominant interleukin released by murine peritoneal macrophagesen_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.affiliationumPfizer Central Research, Groton, Connecticut 06340, USA; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.en_US
dc.contributor.affiliationumPfizer Central Research, Groton, Connecticut 06340, USA; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.en_US
dc.contributor.affiliationumPfizer Central Research, Groton, Connecticut 06340, USA; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.en_US
dc.contributor.affiliationumPfizer Central Research, Groton, Connecticut 06340, USA; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.en_US
dc.identifier.pmid2653321en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27968/1/0000399.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0006-291X(89)91670-7en_US
dc.identifier.sourceBiochemical and Biophysical Research Communicationsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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