Cancer Research UK Beatson Institute, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
Nat Rev Mol Cell Biol. 2020 Feb;21(2):85-100. doi: 10.1038/s41580-019-0173-8. Epub 2019 Oct 21.
Through their many and varied metabolic functions, mitochondria power life. Paradoxically, mitochondria also have a central role in apoptotic cell death. Upon induction of mitochondrial apoptosis, mitochondrial outer membrane permeabilization (MOMP) usually commits a cell to die. Apoptotic signalling downstream of MOMP involves cytochrome c release from mitochondria and subsequent caspase activation. As such, targeting MOMP in order to manipulate cell death holds tremendous therapeutic potential across different diseases, including neurodegenerative diseases, autoimmune disorders and cancer. In this Review, we discuss new insights into how mitochondria regulate apoptotic cell death. Surprisingly, recent data demonstrate that besides eliciting caspase activation, MOMP engages various pro-inflammatory signalling functions. As we highlight, together with new findings demonstrating cell survival following MOMP, this pro-inflammatory role suggests that mitochondria-derived signalling downstream of pro-apoptotic cues may also have non-lethal functions. Finally, we discuss the importance and roles of mitochondria in other forms of regulated cell death, including necroptosis, ferroptosis and pyroptosis. Collectively, these new findings offer exciting, unexplored opportunities to target mitochondrial regulation of cell death for clinical benefit.
通过其多种多样的代谢功能,线粒体为生命提供能量。矛盾的是,线粒体在细胞凋亡中也起着核心作用。在线粒体凋亡诱导后,线粒体外膜通透性(MOMP)通常会使细胞死亡。MOMP 下游的凋亡信号涉及细胞色素 c 从线粒体释放和随后的半胱天冬酶激活。因此,靶向 MOMP 以操纵细胞死亡在包括神经退行性疾病、自身免疫性疾病和癌症在内的多种疾病中具有巨大的治疗潜力。在这篇综述中,我们讨论了线粒体如何调节细胞凋亡的新见解。令人惊讶的是,最近的数据表明,除了引发半胱天冬酶激活外,MOMP 还参与了各种促炎信号功能。正如我们所强调的,结合新发现的 MOMP 后细胞存活的证据,这种促炎作用表明,促凋亡信号下游的线粒体衍生信号也可能具有非致死功能。最后,我们讨论了线粒体在其他形式的受调控细胞死亡(包括坏死性凋亡、铁死亡和细胞焦亡)中的重要性和作用。总的来说,这些新发现为靶向线粒体对细胞死亡的调控以获得临床益处提供了令人兴奋的、尚未开发的机会。