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凋亡小体:半胱天冬酶激活的引擎

Apoptosomes: engines for caspase activation.

作者信息

Adams Jerry M, Cory Suzanne

机构信息

The Walter and Eliza Hall Institute of Medical Research, Melbourne, 3050, Victoria, Australia.

出版信息

Curr Opin Cell Biol. 2002 Dec;14(6):715-20. doi: 10.1016/s0955-0674(02)00381-2.

Abstract

Activation of the caspases that initiate apoptosis typically requires cognate scaffold proteins, including CED-4 in Caenorhabditis elegans, Apaf-1 in mammals and Dark in Drosophila. Each scaffold protein oligomerizes procaspases into a complex called the apoptosome, but the regulation and biological roles of the scaffolds differ. Whereas CED-4 is restrained by the Bcl-2 homologue CED-9, Apaf-1 is inhibited by its WD40 repeat region, until it is activated by cytochrome c, derived from damaged mitochondria. Although Dark also has a WD40 region, its activation does not seem to involve cytochrome c. CED-4 is essential for apoptosis in the worm and Dark for many apoptotic responses in the fly, but the Apaf-1/caspase-9 system probably amplifies rather than initiates the mammalian caspase cascade.

摘要

引发细胞凋亡的半胱天冬酶的激活通常需要同源支架蛋白,包括秀丽隐杆线虫中的CED-4、哺乳动物中的Apaf-1和果蝇中的Dark。每种支架蛋白都会将半胱天冬酶原寡聚成一种称为凋亡小体的复合物,但这些支架蛋白的调节方式和生物学作用有所不同。CED-4受Bcl-2同源物CED-9的抑制,而Apaf-1则受其WD40重复区域的抑制,直到它被受损线粒体释放的细胞色素c激活。尽管Dark也有一个WD40区域,但其激活似乎不涉及细胞色素c。CED-4对蠕虫的细胞凋亡至关重要,Dark对果蝇的许多凋亡反应至关重要,但Apaf-1/半胱天冬酶-9系统可能是放大而不是启动哺乳动物的半胱天冬酶级联反应。

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