The role of autophagy in mammalian development: Cell makeover rather than cell death

被引:433
作者
Cecconi, Francesco [1 ,2 ]
Levine, Beth [3 ,4 ,5 ]
机构
[1] Univ Roma Tor Vergata, Dept Biol, Dulbecco Telethon Inst, I-00133 Rome, Italy
[2] IRCCS Fondaz Santa Lucia, Lab Mol Neuroembryol, I-00143 Rome, Italy
[3] Univ Texas SW Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[5] Univ Texas SW Med Ctr Dallas, Dept Microbiol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.devcel.2008.08.012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy is important for the degradation of bulk cytoplasm, long-lived proteins, and entire organelles. In lower eukaryotes, autophagy functions as a cell death mechanism or as a stress response during development. However, autophagy's significance in vertebrate development, and the role (if any) of vertebrate-specific factors in its regulation, remains unexplained. Through careful analysis of the current autophagy gene mutant mouse models, we propose that in mammals, autophagy may be involved in specific cytosolic rearrangements needed for proliferation, death, and differentiation during embryogenesis and postnatal development. Thus, autophagy is a process of cytosolic "renovation," crucial in cell fate decisions.
引用
收藏
页码:344 / 357
页数:14
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