Autophagy for tissue homeostasis and neuroprotection

被引:161
作者
Marino, Guillermo [1 ,2 ]
Madeo, Frank [3 ]
Kroemer, Guido [1 ,4 ,5 ,6 ]
机构
[1] Inst Gustave Roussy, INSERM, U848, F-94805 Villejuif, France
[2] Univ Paris 11, F-94805 Villejuif, France
[3] Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria
[4] Ctr Rech Cordeliers, F-75005 Paris, France
[5] Hop Europeen Georges Pompidou, AP HP, F-75908 Paris, France
[6] Univ Paris 05, F-75270 Paris, France
关键词
AGGREGATE-PRONE PROTEINS; BETA-CELL MASS; PHYSIOLOGICAL FUNCTIONS; HUNTINGTONS-DISEASE; MEDIATED AUTOPHAGY; SKELETAL-MUSCLE; ALPHA-SYNUCLEIN; MOUSE MODEL; GENE ATG5; CLEARANCE;
D O I
10.1016/j.ceb.2010.10.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although autophagy has frequently been viewed as a cell death mechanism in the mammalian system, it is now considered as indispensable for the homeostasis of cells, tissues, and organisms. Basal or stress-induced autophagy plays essential and diverse roles in a variety of tissues, due to its cytoprotective properties. In this review, we briefly discuss the different homeostatic functions of autophagy that have been finely dissected in mammals through the generation and characterization of animal models with tissue-specific autophagic alterations. In addition, and given the importance of constitutive autophagy in neuronal tissues, we describe in more detail the specific roles of autophagy in the central nervous system (CNS). Finally, we discuss the contribution of autophagy malfunctions to the development of several common neurological disorders and the potential benefits of pharmacologically induced autophagy for the avoidance of neurodegeneration.
引用
收藏
页码:198 / 206
页数:9
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