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调控 HDAC6 活性控制氧化应激损伤的机制研究进展。

Advances in the Mechanistic Study of the Control of Oxidative Stress Injury by Modulating HDAC6 Activity.

机构信息

Department of Pathophysiology, Guangdong Medical University, Dongguan, 523808, China.

The Third Affiliated Hospital of Guangdong Medical University, Fo Shan, 528000, Guangdong, China.

出版信息

Cell Biochem Biophys. 2023 Mar;81(1):127-139. doi: 10.1007/s12013-022-01125-w. Epub 2023 Feb 7.

Abstract

Oxidative stress is defined as an injury resulting from a disturbance in the dynamic equilibrium of the redox environment due to the overproduction of active/radical oxygen exceeding the antioxidative ability of the body. This is a key step in the development of various diseases. Oxidative stress is modulated by different factors and events, including the modification of histones, which are the cores of nucleosomes. Histone modification includes acetylation and deacetylation of certain amino acid residues; this process is catalyzed by different enzymes. Histone deacetylase 6 (HDAC6) is a unique deacetylating protease that also catalyzes the deacetylation of different nonhistone substrates to regulate various physiologic processes. The intimate relationship between HDAC6 and oxidative stress has been demonstrated by different studies. The present paper aims to summarize the data obtained from a mechanistic study of HDAC6 and oxidative stress to guide further investigations on mechanistic characterization and drug development.

摘要

氧化应激被定义为由于活性/自由基氧的过度产生超过了身体的抗氧化能力,导致氧化还原环境的动态平衡紊乱而引起的损伤。这是各种疾病发展的关键步骤。氧化应激受到不同因素和事件的调节,包括组蛋白的修饰,组蛋白是核小体的核心。组蛋白修饰包括某些氨基酸残基的乙酰化和去乙酰化;这个过程是由不同的酶催化的。组蛋白去乙酰化酶 6(HDAC6)是一种独特的去乙酰化蛋白酶,也催化不同的非组蛋白底物的去乙酰化,以调节各种生理过程。不同的研究已经证明了 HDAC6 与氧化应激之间的密切关系。本文旨在总结从 HDAC6 和氧化应激的机制研究中获得的数据,以指导对机制特征和药物开发的进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9063/9925596/e67db7fe898b/12013_2022_1125_Fig1_HTML.jpg

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