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Am J Physiol Cell Physiol 296: C151-C161, 2009. First published November 5, 2008; doi:10.1152/ajpcell.00359.2008
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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

{alpha}- and β-Monosaccharide transport in human erythrocytes

Jeffry M. Leitch and Anthony Carruthers

Department of Biochemistry & Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts

Submitted 9 July 2008 ; accepted in final form 4 November 2008

Equilibrative sugar uptake in human erythrocytes is characterized by a rapid phase, which equilibrates 66% of the cell water, and by a slow phase, which equilibrates 33% of the cell water. This behavior has been attributed to the preferential transport of β-sugars by erythrocytes (Leitch JM, Carruthers A. Am J Physiol Cell Physiol 292: C974–C986, 2007). The present study tests this hypothesis. The anomer theory requires that the relative compartment sizes of rapid and slow transport phases are determined by the proportions of β- and {alpha}-sugar in aqueous solution. This is observed with D-glucose and 3-O-methylglucose but not with 2-deoxy-D-glucose and D-mannose. The anomer hypothesis predicts that the slow transport phase, which represents {alpha}-sugar transport, is eliminated when anomerization is accelerated to generate the more rapidly transported β-sugar. Exogenous, intracellular mutarotase accelerates anomerization but has no effect on transport. The anomer hypothesis requires that transport inhibitors inhibit rapid and slow transport phases equally. This is observed with the endofacial site inhibitor cytochalasin B but not with the exofacial site inhibitors maltose or phloretin, which inhibit only the rapid phase. Direct measurement of {alpha}- and β-sugar uptake demonstrates that erythrocytes transport {alpha}- and β-sugars with equal avidity. These findings refute the hypothesis that erythrocytes preferentially transport β-sugars. We demonstrate that biphasic 3-O-methylglucose equilibrium exchange kinetics refute the simple carrier hypothesis for protein-mediated sugar transport but are compatible with a fixed-site transport mechanism regulated by intracellular ATP and cell shape.

carrier-mediated transport; transport kinetics; transport regulation



Address for reprint requests and other correspondence: A. Carruthers, Dept. of Biochemistry & Molecular Pharmacology, Univ. of Massachusetts Medical School, 364 Plantation St., Worcester, MA 01605 (e-mail: anthony.carruthers{at}umassmed.edu)




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