Mechanism and regulation of GLUT-4 vesicle fusion in muscle and fat cells

被引:91
作者
Foster, LJ
Klip, A
机构
[1] Hosp Sick Children, Cell Biol Programme, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2000年 / 279卷 / 04期
关键词
vesicle traffic; soluble N-ethylmaleimide-sensitive factor attachment protein receptor; syntaxin; 4; 23-kDa synaptosome-associated protein-like; protein; vesicle-associated membrane protein 2;
D O I
10.1152/ajpcell.2000.279.4.C877
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Twenty years ago it was shown that recruitment of glucose transporters from an internal membrane compartment to the plasma membrane led to increased glucose uptake into fat and muscle cells stimulated by insulin. The final step of this process is the fusion of glucose transporter 4 (GLUT-4)-containing vesicles with the plasma membrane. The identification of a neuronal soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) complex as a requirement for synaptic vesicle-plasma membrane fusion led to the search for homologous complexes outside the nervous system. Indeed, isoforms of the neuronal SNAREs were identified in muscle and fat cells and were shown to be required for GLUT-4 incorporation into the cell membrane. In addition, proteins that bind to nonneuronal SNAREs were cloned and proposed to regulate vesicle fusion. We have summarized the molecular mechanisms leading to membrane fusion in nonneuronal systems, focusing on the role of SNAREs and accessory proteins (Munc18c, synip, Rab4, and VAP-33) in incorporation of GLUT-4 into the plasma membrane. Potential modes of regulation of this process are discussed, including SNARE phosphorylation and interaction with the cytoskeleton.
引用
收藏
页码:C877 / C890
页数:14
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