Graduate School and Faculty of Pharmaceutical Sciences, Suzuka University of Medical Science, 3500-3 Minamitamagaki, Suzuka, 513-8670, Japan.
Neurochem Res. 2018 Jan;43(1):50-58. doi: 10.1007/s11064-017-2303-z. Epub 2017 May 18.
Nitric oxide (NO), which is produced from nitric oxide synthase, is an important cell signaling molecule that is crucial for many physiological functions such as neuronal death, neuronal survival, synaptic plasticity, and vascular homeostasis. This diffusible gaseous compound functions as an effector or second messenger in many intercellular communications and/or cell signaling pathways. Protein S-nitrosylation is a posttranslational modification that involves the covalent attachment of an NO group to the thiol side chain of select cysteine residues on target proteins. This process is thought to be very important for the regulation of cell death, cell survival, and gene expression in the central nervous system (CNS). However, there have been few reports on the role of protein S-nitrosylation in CNS disorders. Here, we briefly review specific examples of S-nitrosylation, with particular emphasis on its functions in neuronal cell death and survival. An understanding of the role and mechanisms underlying the effects of protein S-nitrosylation on neurodegenerative/neuroprotective events may reveal a novel therapeutic strategy for rescuing neurons in neurodegenerative diseases.
一氧化氮(NO)是由一氧化氮合酶产生的,它是一种重要的细胞信号分子,对于许多生理功能至关重要,如神经元死亡、神经元存活、突触可塑性和血管内稳态。这种可扩散的气态化合物在许多细胞间通讯和/或细胞信号通路中充当效应物或第二信使。蛋白质 S-亚硝基化是一种翻译后修饰,涉及将 NO 基团共价连接到靶蛋白上特定半胱氨酸残基的巯基侧链上。这一过程被认为对中枢神经系统(CNS)中细胞死亡、细胞存活和基因表达的调节非常重要。然而,关于蛋白质 S-亚硝基化在中枢神经系统疾病中的作用的报道很少。在这里,我们简要回顾了 S-亚硝基化的具体例子,特别强调了它在神经元细胞死亡和存活中的作用。了解蛋白质 S-亚硝基化对神经退行性/神经保护事件的作用和机制可能会揭示一种新的治疗策略,以挽救神经退行性疾病中的神经元。