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Differing calcium requirements for regulatory effects of ATP, ATP[gamma]S and adenosine on O2 responses of human neutrophils

dc.contributor.authorWard, Peter A.en_US
dc.contributor.authorCunningham, Thomas W.en_US
dc.contributor.authorWalker, Blair A. M.en_US
dc.contributor.authorJohnson, Kent J.en_US
dc.date.accessioned2006-04-07T20:15:13Z
dc.date.available2006-04-07T20:15:13Z
dc.date.issued1988-07-29en_US
dc.identifier.citationWard, Peter A., Cunningham, Thomas W., Walker, Blair A. M., Johnson, Kent J. (1988/07/29)."Differing calcium requirements for regulatory effects of ATP, ATP[gamma]S and adenosine on O2 responses of human neutrophils." Biochemical and Biophysical Research Communications 154(2): 746-751. <http://hdl.handle.net/2027.42/27213>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WBK-4DNHXJT-N3/2/6100b82da5ff6ba3a5eef25114d97f58en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27213
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2840905&dopt=citationen_US
dc.description.abstractIn formyl peptide stimulated human neutrophils the enhancement of O2 responses by ATP and ATP[gamma]S requires extracellular calcium. In contrast, the inhibitory effects of adenosine are independent of a calcium requirement. Rates of O2 generation are not affected by these adenine compounds. Rather, ATP and ATP[gamma]S cause a sustained period of generation whereas adenosine causes an abrupt early termination of the O2 response. The differing calcium requirements for regulatory effects of adenine compounds on O2 responses of stimulated neutrophils suggests that ATP (or ATP[gamma]S) and adenosine may exert their effects at different points in the pathway of signal transduction events.en_US
dc.format.extent332608 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleDiffering calcium requirements for regulatory effects of ATP, ATP[gamma]S and adenosine on O2 responses of human neutrophilsen_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.affiliationumThe University of Michigan Medical School Department of Pathology 1301 Catherine St., Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumThe University of Michigan Medical School Department of Pathology 1301 Catherine St., Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumThe University of Michigan Medical School Department of Pathology 1301 Catherine St., Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumThe University of Michigan Medical School Department of Pathology 1301 Catherine St., Ann Arbor, MI 48109, USAen_US
dc.identifier.pmid2840905en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27213/1/0000217.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0006-291X(88)90203-3en_US
dc.identifier.sourceBiochemical and Biophysical Research Communicationsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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