Cheng Si-Ying, Wang Shu-Chao, Lei Ming, Wang Zhen, Xiong Kun
Xiangya Medical School, Central South University, Changsha, Hunan Province, China.
Department of Anatomy and Neurobiology, School of Basic Medical Sciences, Central South University, Changsha, Hunan Province, China.
Neural Regen Res. 2018 Mar;13(3):556-562. doi: 10.4103/1673-5374.228762.
Calpains are a group of calcium-dependent proteases that are over activated by increased intracellular calcium levels under pathological conditions. A wide range of substrates that regulate necrotic, apoptotic and autophagic pathways are affected by calpain. Calpain plays a very important role in neuronal death and various neurological disorders. This review introduces recent research progress related to the regulatory mechanisms of calpain in neuronal death. Various neuronal programmed death pathways including apoptosis, autophagy and regulated necrosis can be divided into receptor interacting protein-dependent necroptosis, mitochondrial permeability transition-dependent necrosis, pyroptosis and poly (ADP-ribose) polymerase 1-mediated parthanatos. Calpains cleave series of key substrates that may lead to cell death or participate in cell death. Regarding the investigation of calpain-mediated programed cell death, it is necessary to identify specific inhibitors that inhibit calpain mediated neuronal death and nervous system diseases.
钙蛋白酶是一组钙依赖性蛋白酶,在病理条件下,细胞内钙水平升高会使其过度激活。钙蛋白酶会影响一系列调节坏死、凋亡和自噬途径的底物。钙蛋白酶在神经元死亡和各种神经疾病中起着非常重要的作用。本综述介绍了与钙蛋白酶在神经元死亡中的调节机制相关的最新研究进展。包括凋亡、自噬和程序性坏死在内的各种神经元程序性死亡途径可分为受体相互作用蛋白依赖性坏死性凋亡、线粒体通透性转换依赖性坏死、焦亡和聚(ADP-核糖)聚合酶1介导的Parthanatos。钙蛋白酶可切割一系列可能导致细胞死亡或参与细胞死亡的关键底物。关于钙蛋白酶介导的程序性细胞死亡的研究,有必要鉴定出抑制钙蛋白酶介导的神经元死亡和神经系统疾病的特异性抑制剂。