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Research Article Free access | 10.1172/JCI113707

Oxypurine cycle in human erythrocytes regulated by pH, inorganic phosphate, and oxygen.

P A Berman, D A Black, L Human, and E H Harley

Department of Chemical Pathology, University of Cape Town Medical School, South Africa.

Find articles by Berman, P. in: PubMed | Google Scholar

Department of Chemical Pathology, University of Cape Town Medical School, South Africa.

Find articles by Black, D. in: PubMed | Google Scholar

Department of Chemical Pathology, University of Cape Town Medical School, South Africa.

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Department of Chemical Pathology, University of Cape Town Medical School, South Africa.

Find articles by Harley, E. in: PubMed | Google Scholar

Published September 1, 1988 - More info

Published in Volume 82, Issue 3 on September 1, 1988
J Clin Invest. 1988;82(3):980–986. https://doi.org/10.1172/JCI113707.
© 1988 The American Society for Clinical Investigation
Published September 1, 1988 - Version history
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Abstract

The effect of pH, PO2, and inorganic phosphate on the uptake and metabolism of hypoxanthine by erythrocytes has been studied. Uptake of hypoxanthine and accumulation of inosine 5'-monophosphate (IMP) were markedly increased at acid pH, high external phosphate concentrations, and low PO2. Release of accumulated IMP as hypoxanthine occurred at alkaline pH values and low external phosphate concentrations. Conditions favoring IMP accumulation gave rise, in the absence of hypoxanthine, to a corresponding increase in 5'-phosphoribosyl-1-pyrophosphate. Intracellular phosphate concentrations were markedly pH dependent and a model is presented whereby hypoxanthine uptake and release are controlled by intracellular concentrations of inorganic phosphate and 2,3-bisphosphoglycerate. These allosteric effectors influence, in opposing ways, two enzymes governing IMP accumulation, namely 5'-phosphoribosyl-1-pyrophosphate synthetase and 5'-nucleotidase. These metabolic properties suggest that the erythrocyte could play a role in the removal of hypoxanthine from anoxic tissue.

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