Does autophagy have a license to kill mammalian cells?

被引:208
作者
Scarlatti, F. [2 ]
Granata, R. [2 ]
Meijer, A. J. [3 ]
Codogno, P. [1 ]
机构
[1] Univ Paris 11, INSERM, U756, F-92296 Chatenay Malabry, France
[2] Univ Turin, Dept Internal Med, Lab Cellular & Mol Endocrinol, Turin, Italy
[3] Univ Amsterdam, Acad Med Ctr, Dept Med Biochem, NL-1105 AZ Amsterdam, Netherlands
关键词
apoptosis; macroautophagy; necrosis; signalling; NF-KAPPA-B; CANCER DEVELOPMENT; INDUCED APOPTOSIS; KINASE-B; DEATH; SURVIVAL; PROTEIN; MACROAUTOPHAGY; INHIBITION; RAPAMYCIN;
D O I
10.1038/cdd.2008.101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macroautophagy is an evolutionarily conserved vacuolar, self-digesting mechanism for cellular components, which end up in the lysosomal compartment. In mammalian cells, macroautophagy is cytoprotective, and protects the cells against the accumulation of damaged organelles or protein aggregates, the loss of interaction with the extracellular matrix, and the toxicity of cancer therapies. During periods of nutrient starvation, stimulating macroautophagy provides the fuel required to maintain an active metabolism and the production of ATP. Macroautophagy can inhibit the induction of several forms of cell death, such as apoptosis and necrosis. However, it can also be part of the cascades of events that lead to cell death, either by collaborating with other cell death mechanisms or by causing cell death on its own. Loss of the regulation of bulk macroautophagy can prime self-destruction by cells, and some forms of selective autophagy and non-canonical forms of macroautophagy have been shown to be associated with cell demise. There is now mounting evidence that autophagy and apoptosis share several common regulatory elements that are crucial in any attempt to understand the dual role of autophagy in cell survival and cell death.
引用
收藏
页码:12 / 20
页数:9
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