Scinovex
review Open AccessTop 1% cited

Facilitative glucose transporters

European Journal of Biochemistry · 1994 · Vol. 219(3) · pp. 713–725
Mike Mueckler

Abstract

Facilitative glucose transport is mediated by members of the Glut protein family that belong to a much larger superfamily of 12 transmembrane segment transporters. Six members of the Glut family have been described thus far. These proteins are expressed in a tissue- and cell-specific manner and exhibit distinct kinetic and regulatory properties that reflect their specific functional roles. Glut1 is a widely expressed isoform that provides many cells with their basal glucose requirement. It also plays a special role in transporting glucose across epithelial and endothelial barrier tissues. Glut2 is a high-Km isoform expressed in hepatocytes, pancreatic beta cells, and the basolateral membranes of intestinal and renal epithelial cells. It acts as a high-capacity transport system to allow the uninhibited (non-rate-limiting) flux of glucose into or out of these cell types. Glut3 is a low-Km isoform responsible for glucose uptake into neurons. Glut4 is expressed exclusively in the insulin-sensitive tissues, fat and muscle. It is responsible for increased glucose disposal in these tissues in the postprandial state and is important in whole-body glucose homeostasis. Glut5 is a fructose transporter that is abundant in spermatozoa and the apical membrane of intestinal cells. Glut7 is the transporter present in the endoplasmic reticulum membrane that allows the flux of free glucose out of the lumen of this organelle after the action of glucose-6-phosphatase on glucose 6-phosphate. This review summarizes recent advances concerning the structure, function, and regulation of the Glut proteins.

Metabolism, Diabetes, and CancerAmino Acid Enzymes and MetabolismMetabolism and Genetic DisordersGlucose transporterGLUT2GLUT1BiologyGLUT4GLUT3Cell biologyGlucose uptakeEndoplasmic reticulumBiochemistry

MeSH terms

Amino Acid SequenceAnimalsDiabetes Mellitus, Type 1Gene Expression RegulationGlucoseHumansInsulinMolecular Sequence DataMonosaccharide Transport ProteinsSequence AlignmentProtein Structure, Tertiary
Citations
1,091
FWCI
21.40
field-weighted impact
References
182
Percentile
100%
vs. same field & year
Citations per year
Cited by
References
Rates and tissue sites of non-insulin- and insulin-mediated glucose uptake in humans
American Journal of Physiology-Endocrinology and Metabolism · 1988 · 650 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.