National Institute of Biological Sciences, 7 Science Park Road, Zhongguancun Life Science Park, Beijing 102206, China.
School of Life Sciences, Peking University, Beijing 100871, China.
Mol Cell. 2016 Jul 21;63(2):229-239. doi: 10.1016/j.molcel.2016.06.016.
In response to apoptotic stimuli, mitochondria in mammalian cells release cytochrome c and other apoptogenic proteins, leading to the subsequent activation of caspases and apoptotic cell death. This process is promoted by the pro-apoptotic members of the Bcl-2 family of proteins, such as Bim and Bax, which, respectively, initiate and execute cytochrome c release from the mitochondria. Here we report the discovery of a small molecule that efficiently blocks Bim-induced apoptosis after Bax is activated on the mitochondria. The cellular target of this small molecule was identified to be the succinate dehydrogenase subunit B (SDHB) protein of complex II of the mitochondrial electron transfer chain (ETC). The molecule protects the integrity of the ETC and allows treated cells to continue to proliferate after apoptosis induction. Moreover, this molecule blocked dopaminergic neuron death and reversed Parkinson-like behavior in a rat model of Parkinson's disease.
在响应凋亡刺激时,哺乳动物细胞中的线粒体释放细胞色素 c 和其他促凋亡蛋白,导致随后 caspase 的激活和凋亡细胞死亡。这个过程是由 Bcl-2 家族蛋白的促凋亡成员促进的,如 Bim 和 Bax,它们分别启动和执行线粒体中细胞色素 c 的释放。在这里,我们报告了一种小分子的发现,该小分子在 Bax 在线粒体上被激活后,有效地阻止了 Bim 诱导的凋亡。这种小分子的细胞靶标被鉴定为线粒体电子传递链(ETC)复合物 II 的琥珀酸脱氢酶亚基 B(SDHB)蛋白。该分子保护 ETC 的完整性,并允许处理后的细胞在凋亡诱导后继续增殖。此外,该分子阻断多巴胺能神经元死亡,并在帕金森病大鼠模型中逆转帕金森样行为。