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Glucose transporters in the 21st Century

American Journal of Physiology-Endocrinology and Metabolism · 2009 · Vol. 298(2) · pp. E141–E145
Bernard ThorensMike Mueckler

Abstract

The ability to take up and metabolize glucose at the cellular level is a property shared by the vast majority of existing organisms. Most mammalian cells import glucose by a process of facilitative diffusion mediated by members of the Glut (SLC2A) family of membrane transport proteins. Fourteen Glut proteins are expressed in the human and they include transporters for substrates other than glucose, including fructose, myoinositol, and urate. The primary physiological substrates for at least half of the 14 Glut proteins are either uncertain or unknown. The well-established glucose transporter isoforms, Gluts 1-4, are known to have distinct regulatory and/or kinetic properties that reflect their specific roles in cellular and whole body glucose homeostasis. Separate review articles on many of the Glut proteins have recently appeared in this journal. Here, we provide a very brief summary of the known properties of the 14 Glut proteins and suggest some avenues of future investigation in this area.

Gout, Hyperuricemia, Uric AcidMetabolism, Diabetes, and CancerDiet, Metabolism, and DiseaseGlucose transporterTransporterGene isoformGlucose homeostasisBiochemistryBiologyFructoseCell biologyChemistryInsulin

MeSH terms

GlucoseHumansMembrane Transport ProteinsGlucose Transport Proteins, Facilitative
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References
The SLC2 family of facilitated hexose and polyol transporters
Pflügers Archiv - European Journal of Physiology · 2004 · 492 citations
The facilitative glucose transporter GLUT3: 20 years of distinction
American Journal of Physiology-Endocrinology and Metabolism · 2008 · 471 citations
Regulation of the fructose transporter GLUT5 in health and disease
American Journal of Physiology-Endocrinology and Metabolism · 2008 · 472 citations
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