Autophagy, a guardian against neurodegeneration

被引:171
作者
Garcia-Arencibia, Moises [1 ]
Hochfeld, Warren E. [1 ]
Toh, Pearl P. C. [1 ]
Rubinsztein, David C. [1 ]
机构
[1] Univ Cambridge, Cambridge Inst Med Res, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 0XY, England
基金
英国惠康基金;
关键词
Autophagy; Alzheimer disease; Neurodegeneration; Huntington disease; MULTIPLE SULFATASE DEFICIENCY; HUNTINGTONS-DISEASE; CONJUGATION SYSTEM; AXONAL-TRANSPORT; ALPHA-SYNUCLEIN; MOUSE MODELS; CELL-DEATH; TOXICITY; PROTEIN; POLYGLUTAMINE;
D O I
10.1016/j.semcdb.2010.02.008
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Autophagy is an intracellular degradation process responsible for the clearance of most long-lived proteins and organelles. Cytoplasmic components are enclosed by double-membrane autophagosomes, which subsequently fuse with lysosomes for degradation. Autophagy dysfunction may contribute to the pathology of various neurodegenerative disorders, which manifest abnormal protein accumulation. As autophagy induction enhances the clearance of aggregate-prone intracytoplasmic proteins that cause neurodegeneration (like mutant huntingtin, tau and ataxin 3) and confers cytoprotective roles in cell and animal models, upregulating autophagy may be a tractable therapeutic strategy for diseases caused by such proteins. Here, we will review the molecular machinery of autophagy and its role in neurodegenerative diseases. Drugs and associated signalling pathways that may be targeted for pharmacological induction of autophagy will also be discussed. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:691 / 698
页数:8
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