Caspase 8-mediated cleavage of the pro-apoptotic BCL-2 family member BID in p53-dependent apoptosis

被引:36
作者
Fischer, B
Coelho, D
Dufour, P
Bergerat, JP
Denis, JM
Gueulette, J
Bischoff, P [1 ]
机构
[1] Univ Strasbourg, Lab Cancerol Expt & Radiobiol, EA 3430, Inst Rech Contre Canc Appareil Digestif, Strasbourg, France
[2] Catholic Univ Louvain, Fac Med, Lab Radiobiol & Radioprotect, Brussels, Belgium
关键词
bid; p53; apoptosis; caspases; mitochondria; transduction pathways; fast neutrons;
D O I
10.1016/S0006-291X(03)01004-0
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
The objective of this study was to characterize the apoptotic pathways activated by fast neutrons in the human lymphoblastoid cell line TK6 and in its p53 -/- derivative. Our results demonstrate that while p53 is not required for neutron-induced apoptosis, as previously shown, it does affect the kinetics of apoptosis and the molecular pathways leading to the activation of effector caspases. Indeed, rapid p53-dependent apoptosis was associated with the activation of caspase 9, 8, 3, and 7 and the cleavage of BID by caspase 8. In contrast, the slow-occurring p53-independent apoptotic process, mediated by caspase 7, took place without BID cleavage and loss of transmembrane mitochondrial potential. Altogether, our findings highlight an essential role for caspase 8-mediated BID cleavage, in the course of p53-dependent apoptosis triggered by fast neutrons in lymphoid cells. They also demonstrate that this mechanism is not involved in p53-independent apoptosis. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:516 / 522
页数:7
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