Caspase-dependent non-apoptotic processes in development

被引:122
作者
Nakajima, Yu-ichiro [1 ,2 ]
Kuranaga, Erina [2 ,3 ]
机构
[1] Tohoku Univ, Frontier Res Inst Interdisciplinary Sci FRIS, Sendai, Miyagi 9808578, Japan
[2] Tohoku Univ, Grad Sch Life Sci, Lab Histogenet Dynam, Sendai, Miyagi 9808578, Japan
[3] RIKEN, Ctr Dev Biol, Lab Histogenet Dynam, Kobe, Hyogo 6500047, Japan
关键词
PROGRAMMED CELL-DEATH; CYTOCHROME-C; CAENORHABDITIS-ELEGANS; DROSOPHILA; DIFFERENTIATION; ACTIVATION; PATHWAY; MIGRATION; CYCLE; INDIVIDUALIZATION;
D O I
10.1038/cdd.2017.36
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
Caspases are at the core of executing apoptosis by orchestrating cellular destruction with proteolytic cascades. Caspase-mediated proteolysis also controls diverse nonlethal cellular activities such as proliferation, differentiation, cell fate decision, and cytoskeletal reorganization. During the last decade or so, genetic studies of Drosophila have contributed to our understanding of the in vivo mechanism of the non-apoptotic cellular responses in developmental contexts. Furthermore, recent studies using C. elegans suggest that apoptotic signaling may play unexpected roles, which influence ageing and normal development at the organism level. In this review, we describe how the caspase activity is elaborately controlled during vital cellular processes at the level of subcellular localization, the duration and timing to avoid full apoptotic consequences, and also discuss the novel roles of non-apoptotic caspase signaling in adult homeostasis and physiology.
引用
收藏
页码:1422 / 1430
页数:9
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