Control of apoptosis by IP3 and ryanodine receptor driven calcium signals

被引:129
作者
Hajnóczky, G [1 ]
Csordás, G [1 ]
Madesh, M [1 ]
Pacher, P [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1054/ceca.2000.0169
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intracellular calcium signals mediated by IP3 and ryanodine receptors (IP3R/RyR) play a central role in cell survival, but emerging evidence suggests that IP3R/RyR are also important in apoptotic cell death. Switch from the life program to the death program may involve coincident detection of proapoptotic stimuli and calcium signals or changes in the spatiotemporal pattern of the calcium signal or changes at the lever of effecters activated by the calcium signal (e.g. calpain, calcineurin). The fate of the cell is often determined in the mitochondria, where calcium spikes may support cell survival through stimulation of ATP production or initiate apoptosis via opening of the permeability transition pore and release of apoptotic factors such as cytochrome c. The functional importance of these mitochondrial calcium signalling pathways has been underscored by the elucidation of a highly effective, local Ca2+ coupling between IP3R/RyR and mitochondrial Ca2+ uptake sites. This article will focus on the IP3R/RyR-dependent pathways to apoptosis, particularly on the mitochondrial phase of the death cascade. (C) 2000 Harcourt Publishers Ltd.
引用
收藏
页码:349 / 363
页数:15
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