Mammalian glucose transporters: structure and molecular regulation.
Mammalian glucose transporters: structure and molecular regulation.
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DOI:
10.1016/b978-0-12-571147-0.50015-9
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发表时间:
1991
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影响因子:
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通讯作者:
Charles F. Burant;W. Sivitz;Hirofumi Fukumoto;Toshiaki Kayano;Shinya Nagamatsu;Susumo Seino;J. E. Pessin;Graeme I. Bell
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文献类型:
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作者:
Charles F. Burant;W. Sivitz;Hirofumi Fukumoto;Toshiaki Kayano;Shinya Nagamatsu;Susumo Seino;J. E. Pessin;Graeme I. Bell
Publisher Summary This chapter focuses on recent advances in the molecular biology of glucose transport and on the different mechanisms by which it may be regulated. The regulation of glucose transport in vivo is complex and involves two classes of membrane proteins. One class, that is, the Na+-dependent glucose transporters—the SLGT family—is involved in the active transport of dietary glucose from the lumen of the small intestine and reabsorption of filtered glucose in the proximal tubule of the kidney. The second class of glucose transporters found in mammalian cells, the facilitative glucose transporters, represents ubiquitous proteins that appear to be present on all cells. They have distinct but overlapping patterns of tissue distribution and are responsible for mediating the passive transport of glucose across the cell membrane down its concentration gradient. The facilitative glucose carriers are a family of structurally related membrane proteins and currently cDNA clones encoding five members of this family—the GLUT family—have been isolated and characterized and the search for additional members of this family is continuing. The facilitative glucose transporters have acquired distinct physiological and biochemical properties that allow them to serve specific functions in the tissues in which they are expressed. The distribution of GLUT family provides the basis for a novel but very specific mechanism by which insulin can rapidly and reversibly stimulate glucose uptake by increasing the concentration of GLUT4 at the cell surface.