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

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...

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Veröffentlicht in:FEBS letters 2002-04, Vol.517 (1), p.133-138
Hauptverfasser: Ruiz-Vela, Antonio, González de Buitrago, Gonzalo, Martı́nez-A, Carlos
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Sprache:eng
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Zusammenfassung: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.
ISSN:0014-5793
1873-3468
DOI:10.1016/S0014-5793(02)02607-8