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PMID: 8021289 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

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

Journal of cellular physiology ·Vol. 160 ·No. 1 ·1994-07-00 ·Pages 10-6

Brand RM, Lyons RH, Midgley AR

Abstract

A 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.

MeSH Terms
Energy Metabolism Glucose/metabolism Glutamine/metabolism Glycolysis/physiology HeLa Cells Humans Hydrogen-Ion Concentration Iodoacetates/pharmacology Iodoacetic Acid Substrate Specificity Time Factors
Chemicals
Iodoacetates Glutamine Glucose Iodoacetic Acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Brand R M
Reproductive Sciences Program, University of Michigan, Ann Arbor 48109-0404.
Lyons R H
Midgley A R
Article Info
Journal
Journal of cellular physiology
Abbr.
J Cell Physiol
ISSN
0021-9541
Published
1994-07-00
Pages
10-6
Language
English
Region
United States
NLM ID
0050222
Subset
IM
Grants
NICHD NIH HHS · R01 HD18018 · United States
NICHD NIH HHS · U54 HD29184 · United States
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