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Understanding the dynamics of cellular responsiveness to modifications of metabolic substrates in perifusion

dc.contributor.authorBrand, Rhonda M.en_US
dc.contributor.authorLyons, Richard H.en_US
dc.contributor.authorMidgley, A. Reesen_US
dc.date.accessioned2007-04-06T18:05:07Z
dc.date.available2007-04-06T18:05:07Z
dc.date.issued1994-07en_US
dc.identifier.citationBrand, Rhonda M.; Lyons, R. H.; Midgley, A. Rees (1994)."Understanding the dynamics of cellular responsiveness to modifications of metabolic substrates in perifusion." Journal of Cellular Physiology 160(1): 10-16. <http://hdl.handle.net/2027.42/49889>en_US
dc.identifier.issn0021-9541en_US
dc.identifier.issn1097-4652en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/49889
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8021289&dopt=citationen_US
dc.description.abstractA novel microperifusion system with capabilities for continuous, real-time, potentiometric monitoring of extracellular hydrogen ion concentration has been used to define the response of HeLa cells to abrupt changes in extracellular energy sources or introduction of an inhibitor of glycolysis. Glycolytic inhibition, induced by removal of glucose or introduction of iodoacetate, each led to a rapid, continuous decrease in acid release. The response to iodoacetate took longer than removal of glucose, perhaps due to the time required for binding and activation. Once inhibition began, however, the rate of change was greater than following glucose removal. Conversely, recovery time following iodoacetate inhibition was much slower than with glucose removal. Unlike the response to short-term glucose depletion, a second pulse of iodoacetate resulted in a faster response followed by an even longer recovery time. The response to switching between glucose and glutamine began almost without evident delay. The response patterns revealed that HeLa cells prefer glutamine to glucose, but, in the presence of both energy sources, some glucose continues to be used. In summary, these results indicate that continuous, real-time monitoring of the kinetics of hydrogen-ion release can be used to gain new insights into the dynamics of cellular response to perturbations of extracellular energy sources. © 1994 Wiley-Liss, Inc.en_US
dc.format.extent827865 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCell & Developmental Biologyen_US
dc.titleUnderstanding the dynamics of cellular responsiveness to modifications of metabolic substrates in perifusionen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelKinesiology and Sportsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumReproductive Sciences Program, the University of Michigan, Ann Arbor, Michigan 48109-0404 ; Bioengineering Program, the University of Michigan, Ann Arbor, Michigan 48109-0404en_US
dc.contributor.affiliationumReproductive Sciences Program, the University of Michigan, Ann Arbor, Michigan 48109-0404 ; Department of Biochemistry, the University of Michigan, Ann Arbor, Michigan 48109-0404en_US
dc.contributor.affiliationumReproductive Sciences Program, the University of Michigan, Ann Arbor, Michigan 48109-0404 ; Bioengineering Program, the University of Michigan, Ann Arbor, Michigan 48109-0404 ; National Center for Infertility Research at Michigan, the University of Michigan, Ann Arbor, Michigan 48109-0404 ; Reproductive Sciences Program, the University of Michigan, Ann Arbor, Michigan 48109-0404en_US
dc.identifier.pmid8021289en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/49889/1/1041600103_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/jcp.1041600103en_US
dc.identifier.sourceJournal of Cellular Physiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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