Dawson Ted M, Dawson Valina L
Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205; email:
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Annu Rev Pharmacol Toxicol. 2017 Jan 6;57:437-454. doi: 10.1146/annurev-pharmtox-010716-105001.
Mitochondria lie at the crossroads of neuronal survival and cell death. They play important roles in cellular bioenergetics, control intracellular Ca homeostasis, and participate in key metabolic pathways. Mutations in genes involved in mitochondrial quality control cause a myriad of neurodegenerative diseases. Mitochondria have evolved strategies to kill cells when they are not able to continue their vital functions. This review provides an overview of the role of mitochondria in neurologic disease and the cell death pathways that are mediated through mitochondria, including their role in accidental cell death, the regulated cell death pathways of apoptosis and parthanatos, and programmed cell death. It details the current state of parthanatic cell death and discusses potential therapeutic strategies targeting initiators and effectors of mitochondrial-mediated cell death in neurologic disorders.
线粒体处于神经元存活与细胞死亡的交叉点。它们在细胞生物能量学中发挥重要作用,控制细胞内钙稳态,并参与关键的代谢途径。参与线粒体质量控制的基因突变会导致多种神经退行性疾病。当线粒体无法继续其重要功能时,它们会进化出杀死细胞的策略。本文综述了线粒体在神经疾病中的作用以及通过线粒体介导的细胞死亡途径,包括它们在意外细胞死亡、凋亡和PARP-1依赖性坏死性凋亡等程序性细胞死亡途径中的作用。详细阐述了PARP-1依赖性坏死性凋亡的现状,并讨论了针对神经疾病中线粒体介导的细胞死亡起始因子和效应因子的潜在治疗策略。