Rab GTPases implicated in inherited and acquired disorders

被引:74
作者
Mitra, Shreya [1 ]
Cheng, Kwai W. [1 ]
Mills, Gordon B. [1 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77054 USA
关键词
Rab GTPases; Vesicular trafficking; Endocytosis; GLUT4; Cancer; Rab25; GRISCELLI-SYNDROME TYPE-2; INDUCED GLUT4 TRANSLOCATION; GDP-DISSOCIATION INHIBITOR; NUCLEOTIDE EXCHANGE FACTOR; ACTIVATING PROTEIN AS160; BREAST-CANCER; FUNCTIONAL-CHARACTERIZATION; ALPHA-5-BETA-1; INTEGRIN; VESICULAR TRANSPORT; REGULATED TRANSPORT;
D O I
10.1016/j.semcdb.2010.12.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The endocytotic machinery imports, transports and exports receptors and associated molecules between the plasma membrane and various cytoplasmic chambers resulting in selective recycling, degradation, or secretion of molecules and signaling complexes. Trafficking of receptors, growth factors, nutrients, cytokines, integrins as well as pathogens dictates the kinetics and magnitude of signal transduction cascades. Understandably, alterations in the 'fate' of such cargo complexes have profound physiologic and pathophysiologic implications. Rab GTPases regulate endocytosis by decorating intracellular vesicles and targeting these vesicles along with their cargoes to appropriate subcellular compartments. In the last decade, the number of genetic diseases driven by germline mutations in Rab GTPases or their interacting proteins [1-3], has increased and there is growing evidence of aberrant Rab GTPase function in acquired pathophysiologies such as immune deficiency, infection, obesity, diabetes and cancer. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:57 / 68
页数:12
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