Facilitative glucose transport is mediated by members of the Glut prot
ein family that belong to a much larger superfamily of 12 transmembran
e segment transporters. Six members of the Glut family have been descr
ibed thus far. These proteins are expressed in a tissue- and cell-spec
ific manner and exhibit distinct kinetic and regulatory properties tha
t 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 epitheli
al and endothelial barrier tissues. Glut2 is a high-K-m isoform expres
sed in hepatocytes, pancreatic beta cells, and the basolateral membran
es of intestinal and renal epithelial cells. It acts as a high-capacit
y transport system to allow the uninhibited (non-rate-limiting) flux o
f glucose into or out of these cell types. Glut3 is a low-K-m isoform
responsible for glucose uptake into neurons. Glut4 is expressed exclus
ively in the insulin-sensitive tissues, fat and muscle. It is responsi
ble for increased glucose disposal in these tissues in the postprandia
l state and is important in whole-body glucose homeostasis. Glut3 is a
fructose transporter that is abundant in spermatozoa and the apical m
embrane of intestinal cells. Glut7 is the transporter present in the e
ndoplasmic reticulum membrane that allows the flux of free glucose out
of the lumen of this organelle after the action of glucose-6-phosphat
ase on glucose 6-phosphate. This review summarizes recent advances con
cerning the structure, function, and regulation of the Glut proteins.