End products of glucose and glutamine metabolism by cultured cell lines
- 1 April 1988
- journal article
- research article
- Published by Wiley in Journal of Cellular Physiology
- Vol. 135 (1) , 151-155
- https://doi.org/10.1002/jcp.1041350122
Abstract
Rates of CO2 production from glucose and glutamine, intracellular metabolite levels, and release of metabolic end products into the culture medium were determined for 13 cultured cell lines, including a glycolysis-defective mutant. All the non-mutant lines synthesized pyruvate, lactate, alanine, proline, aspartate, and citrate, so that the metabolism of glucose and glutamine resulted mainly in the production of these compounds and only to a lesser extent in complete oxidation to CO2. These data and the pattern of metabolites produced by the mutant line were consistent with a model characterized by incomplete glutamine oxidation leading to end product accumulation. Multiple linear regression analysis identified the metabolite levels most highly correlated with the intracellular citrate level and with the amount of citrate released into the medium. The analysis also showed that the rates of CO2 production from glucose and glutamine were themselves positively correlated, suggesting that the oxidation of the two substrates is coordinately controlled under normal culture conditions.This publication has 13 references indexed in Scilit:
- End products of glucose and glutamine metabolism by L929 cells.Journal of Biological Chemistry, 1987
- Substrate utilization for lactate and energy production by heat‐shocked L929 cellsJournal of Cellular Physiology, 1986
- Glutamine is responsible for stimulating glycolysis by L929 cellsJournal of Cellular Physiology, 1986
- The pathways of glutamate and glutamine oxidation by tumor cell mitochondria. Role of mitochondrial NAD(P)+-dependent malic enzyme.Journal of Biological Chemistry, 1984
- Glycolysis, glutaminolysis and cell proliferationCell Biology International Reports, 1982
- Effect of glucose on aspartate and glutamate synthesis by human diploid fibroblastsJournal of Cellular Physiology, 1981
- Mitochondrial malic enzymes. Mitochondrial NAD(P)+-dependent malic enzyme activity and malate-dependent pyruvate formation are progression-linked in Morris hepatomas.Journal of Biological Chemistry, 1980
- Isolation of a Chinese hamster fibroblast mutant defective in hexose transport and aerobic glycolysis: its use to dissect the malignant phenotype.Proceedings of the National Academy of Sciences, 1980
- Reciprocal regulation of glucose and glutamine utilization by cultured human diploid fibroblastsJournal of Cellular Physiology, 1978
- Amino Acid Metabolism in Mammalian Cell CulturesScience, 1959