University of the Pacific, Thomas J. Long School of Pharmacy, Department of Physiology and Pharmacology, Stockton, CA 95211, USA.
Cold Spring Harb Perspect Med. 2012 Aug 1;2(8):a009365. doi: 10.1101/cshperspect.a009365.
Parkinson's disease is a debilitating disorder characterized by a progressive loss of dopaminergic neurons caused by programmed cell death. The aim of this review is to provide an up-to-date summary of the major programmed cell death pathways as they relate to PD. For a long time, programmed cell death has been synonymous with apoptosis but there now is evidence that other types of programmed cell death exist, such as autophagic cell death or programmed necrosis, and that these types of cell death are relevant to PD. The pathways and signals covered here include namely the death receptors, BCL-2 family, caspases, calpains, cdk5, p53, PARP-1, autophagy, mitophagy, mitochondrial fragmentation, and parthanatos. The review will present evidence from postmortem PD studies, toxin-induced models (especially MPTP/MPP+, 6-hydroxydopamine and rotenone), and from α-synuclein, LRRK2, Parkin, DJ-1, and PINK1 genetic models of PD, both in vitro and in vivo.
帕金森病是一种进行性致残性疾病,其特征是多巴胺能神经元进行性丧失,由程序性细胞死亡引起。本综述的目的是提供与 PD 相关的主要程序性细胞死亡途径的最新总结。长期以来,程序性细胞死亡一直是细胞凋亡的代名词,但现在有证据表明,还存在其他类型的程序性细胞死亡,如自噬性细胞死亡或程序性坏死,这些类型的细胞死亡与 PD 有关。本文涵盖的途径和信号包括死亡受体、BCL-2 家族、半胱天冬酶、钙蛋白酶、cdk5、p53、PARP-1、自噬、线粒体自噬、线粒体碎片化和 parthanatos。本综述将从帕金森病死后研究、毒素诱导模型(特别是 MPTP/MPP+、6-羟多巴胺和鱼藤酮)以及α-突触核蛋白、LRRK2、Parkin、DJ-1 和 PINK1 的遗传 PD 模型中提供证据,包括体外和体内。