Induction of mitochondrial dysfunction by poly(ADP-ribose) polymer: Implication for neuronal cell death

被引:29
作者
Baek, Seung-Hoon [2 ]
Bae, Ok-Nam [3 ]
Kim, Eun-Kyoung [1 ]
Yu, Seong-Woon [1 ]
机构
[1] DGIST, Dept Brain Sci, Taegu 711873, South Korea
[2] Ajou Univ, Coll Pharm, Suwon 443749, South Korea
[3] Hanyang Univ, Coll Pharm, Ansan 426791, South Korea
关键词
apoptosis-inducing factor; mitochondria; neuronal cell death; poly(ADP-ribose) polymer; APOPTOSIS-INDUCING FACTOR; PERMEABILITY TRANSITION PORE; PAR POLYMER; CLEAVAGE;
D O I
10.1007/s10059-013-0172-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Poly(ADP-ribose) polymerase-1 (PARP-1) mediates neuronal cell death in a variety of pathological conditions involving severe DNA damage. Poly(ADP-ribose) (PAR) polymer is a product synthesized by PARP-1. Previous studies suggest that PAR polymer heralds mitochondrial apoptosis-inducing factor (AIF) release and thereby, signals neuronal cell death. However, the details of the effects of PAR polymer on mitochondria remain to be elucidated. Here we report the effects of PAR polymer on mitochondria in cells in situ and isolated brain mitochondria in vitro. We found that PAR polymer causes depolarization of mitochondrial membrane potential and opening of the mitochondrial permeability transition pore early after injury. Furthermore, PAR polymer specifically induces AIF release, but not cytochrome c from isolated brain mitochondria. These data suggest PAR polymer as an endogenous mitochondrial toxin and will further our understanding of the PARP-1-dependent neuronal cell death paradigm.
引用
收藏
页码:258 / 266
页数:9
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