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脂质过氧化产物在自噬调控中的作用。

Lipid peroxidation products' role in autophagy regulation.

机构信息

Department of Analytical Chemistry, Medical University of Bialystok, Kilinskiego 1, 15-069, Bialystok, Poland.

Department of Analytical Chemistry, Medical University of Bialystok, Kilinskiego 1, 15-069, Bialystok, Poland.

出版信息

Free Radic Biol Med. 2024 Feb 20;212:375-383. doi: 10.1016/j.freeradbiomed.2024.01.001. Epub 2024 Jan 4.

DOI:10.1016/j.freeradbiomed.2024.01.001
PMID:38182071
Abstract

Autophagy, which is responsible for removing damaged molecules, prevents their accumulation in cells, thus maintaining intracellular homeostasis. It is also responsible for removing the effects of oxidative stress, so its activation takes place during increased reactive oxygen species (ROS) generation and lipid peroxidation. Therefore, the aim of this review was to summarize all the available knowledge about the effect of protein modifications by lipid peroxidation products on autophagy activation and the impact of this interaction on the functioning of cells. This review shows that reactive aldehydes (including 4-hydroxynonenal and malondialdehyde), either directly or by the formation of adducts with autophagic proteins, can activate or prevent autophagy, depending on their concentration. This effect relates not only to the initial stages of autophagy, when 4-hydroxynonenal and malondialdehyde affect the levels of proteins involved in autophagy initiation and phagophore formation, but also to the final stage, degradation, when reactive aldehydes, by binding to the active center of cathepsins, inactivate their proteolytic functions. Moreover, this review also shows how little research exists on analyzing the impact of lipid peroxidation products and their protein adducts on autophagy. Such knowledge could be used in the therapy of diseases related to autophagy disorders.

摘要

自噬负责清除受损分子,防止它们在细胞内积累,从而维持细胞内的平衡。它还负责清除氧化应激的影响,因此其激活发生在活性氧(ROS)生成和脂质过氧化增加时。因此,本综述的目的是总结关于脂质过氧化产物对自噬激活的蛋白修饰作用的所有现有知识,以及这种相互作用对细胞功能的影响。本综述表明,反应性醛(包括 4-羟基壬烯醛和丙二醛),无论是直接作用还是通过与自噬蛋白形成加合物的方式,都可以根据其浓度激活或阻止自噬。这种效应不仅与自噬的初始阶段有关,此时 4-羟基壬烯醛和丙二醛影响参与自噬起始和吞噬泡形成的蛋白质水平,而且与最终阶段有关,即降解,此时反应性醛通过与组织蛋白酶的活性中心结合,使它们的蛋白水解功能失活。此外,本综述还表明,关于分析脂质过氧化产物及其蛋白加合物对自噬的影响的研究还很少。这些知识可用于治疗与自噬紊乱相关的疾病。

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