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应激诱导凋亡后细胞核内凋亡蛋白酶激活因子-1和细胞色素c的重新分布。

Nuclear Apaf-1 and cytochrome c redistribution following stress-induced apoptosis.

作者信息

Ruiz-Vela Antonio, González de Buitrago Gonzalo, Martínez-A Carlos

机构信息

Department of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, Universidad Autónoma de Madrid, Campus de Cantoblanco, Madrid, Spain.

出版信息

FEBS Lett. 2002 Apr 24;517(1-3):133-8. doi: 10.1016/s0014-5793(02)02607-8.

Abstract

Apoptotic protease activating factor-1 (Apaf-1) and cytochrome c are cofactors critical for inducing caspase-9 activation following stress-induced apoptosis. One consequence of caspase-9 activation is nuclear-cytoplasmic barrier disassembly, which is required for nuclear caspase-3 translocation. In the nucleus, caspase-3 triggers proteolysis of the caspase-activated DNA nuclease (CAD) inhibitor, causing CAD induction and subsequent DNA degradation. Here we demonstrate that apoptotic cells show perinuclear cytochrome c aggregation, which may be critical for nuclear redistribution of cytochrome c and Apaf-1. We thus indicate that the nuclear redistribution of these cofactors concurs with the previously reported caspase-9-induced nuclear disassembly, and may represent an early apoptotic hallmark.

摘要

凋亡蛋白酶激活因子-1(Apaf-1)和细胞色素c是应激诱导凋亡后诱导半胱天冬酶-9激活的关键辅助因子。半胱天冬酶-9激活的一个后果是核质屏障解体,这是核内半胱天冬酶-3易位所必需的。在细胞核中,半胱天冬酶-3触发半胱天冬酶激活的DNA核酸酶(CAD)抑制剂的蛋白水解,导致CAD诱导及随后的DNA降解。在此我们证明,凋亡细胞显示核周细胞色素c聚集,这可能对细胞色素c和Apaf-1的核重新分布至关重要。因此我们指出,这些辅助因子的核重新分布与先前报道的半胱天冬酶-9诱导的核解体同时发生,并且可能代表早期凋亡标志。

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