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对神经退行性变说“不”:S-亚硝基化在神经退行性疾病中的作用

Say NO to neurodegeneration: role of S-nitrosylation in neurodegenerative disorders.

作者信息

Chung Kenny K K

机构信息

Department of Biochemistry, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, SAR China.

出版信息

Neurosignals. 2006;15(6):307-13. doi: 10.1159/000109071. Epub 2007 Sep 27.

Abstract

Nitric oxide (NO) is an important signaling molecule that controls a wide range of biological processes. One of the signaling mechanisms of NO is through the S-nitrosylation of cysteine residues on proteins. S-nitrosylation is now regarded as an important redox signaling mechanism in the regulation of different cellular and physiological functions. However, deregulation of S-nitrosylation has also been linked to various human diseases such as neurodegenerative disorders. Nitrosative stress has long been considered as a major mediator in the development of neurodegeneration, but the molecular mechanism of how NO can contribute to neurodegeneration is not completely clear. Early studies suggested that nitration of proteins, which can induce protein aggregation might contribute to the neurodegenerative process. However, several recent studies suggest that S-nitrosylation of proteins that are important for neuronal survival contributes substantially in the development of various neurodegenerative disorders. Thus, in-depth understanding of the mechanism of neurodegeneration in relation to S-nitrosylation will be critical for the development of therapeutic treatment against these neurodegenerative diseases.

摘要

一氧化氮(NO)是一种重要的信号分子,可控制广泛的生物过程。NO的信号传导机制之一是通过蛋白质上半胱氨酸残基的S-亚硝基化。S-亚硝基化现在被认为是调节不同细胞和生理功能的重要氧化还原信号传导机制。然而,S-亚硝基化的失调也与各种人类疾病有关,如神经退行性疾病。长期以来,亚硝化应激一直被认为是神经退行性变发展的主要介质,但NO如何导致神经退行性变的分子机制尚不完全清楚。早期研究表明,可诱导蛋白质聚集的蛋白质硝化可能有助于神经退行性过程。然而,最近的几项研究表明,对神经元存活很重要的蛋白质的S-亚硝基化在各种神经退行性疾病的发展中起了重要作用。因此,深入了解与S-亚硝基化相关的神经退行性变机制对于开发针对这些神经退行性疾病的治疗方法至关重要。

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