Chaperone-mediated autophagy: Molecular mechanisms and physiological relevance

被引:203
|
作者
Orenstein, Samantha J. [1 ]
Cuervo, Ana Maria [1 ]
机构
[1] Albert Einstein Coll Med, Dept Dev & Mol Biol, Marion Bessin Liver Res Ctr, Inst Aging Res, Bronx, NY 10461 USA
关键词
Chaperones; Lysosomes; Membrane proteins; Protein translocation; Proteases; Proteolysis; RAT-LIVER LYSOSOMES; ALPHA-SYNUCLEIN; PEPTIDE SEQUENCES; PROTEIN-DEGRADATION; CYTOSOLIC PROTEINS; SELECTIVE PATHWAY; HUMAN-FIBROBLASTS; SERUM WITHDRAWAL; MEMBRANE; RECEPTOR;
D O I
10.1016/j.semcdb.2010.02.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chaperone-mediated autophagy (CMA) is a selective lysosomal pathway for the degradation of cytosolic proteins. We review in this work some of the recent findings on this pathway regarding the molecular mechanisms that contribute to substrate targeting, binding and translocation across the lysosomal membrane. We have placed particular emphasis on the critical role that changes in the lipid composition of the lysosomal membrane play in the regulation of CMA, as well as the modulatory effect of other novel CMA components. In the second part of this review, we describe the physiological relevance of CMA and its role as one of the cellular mechanisms involved in the response to stress. Changes with age in CMA activity and the contribution of failure of CMA to the phenotype of aging and to the pathogenesis of several age-related pathologies are also described. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:719 / 726
页数:8
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