Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA; Biological Chemistry Department, University of Michigan Medical School, Ann Arbor, MI, USA.
Trends Biochem Sci. 2024 Sep;49(9):761-774. doi: 10.1016/j.tibs.2024.07.001. Epub 2024 Aug 21.
Loss of protein homeostasis (proteostasis) is a common hallmark of aging and age-associated diseases. Considered as the guardian of proteostasis, the proteostasis network (PN) acts to preserve the functionality of proteins during their lifetime. However, its activity declines with age, leading to disease manifestation. While reactive oxygen species (ROS) were traditionally considered culprits in this process, recent research challenges this view. While harmful at high concentrations, moderate ROS levels protect the cell against age-mediated onset of proteotoxicity by activating molecular chaperones, stress response pathways, and autophagy. This review explores the nuanced roles of ROS in proteostasis and discusses the most recent findings regarding the redox regulation of the PN and its potential in extending healthspan and delaying age-related pathologies.
蛋白质稳态(proteostasis)的丧失是衰老和与年龄相关疾病的共同标志。作为蛋白质稳态的守护者,蛋白质稳态网络(PN)在蛋白质的整个生命周期中发挥作用,以维持其功能。然而,随着年龄的增长,其活性会下降,导致疾病的发生。虽然活性氧(ROS)在传统上被认为是这一过程的罪魁祸首,但最近的研究挑战了这一观点。虽然在高浓度时有害,但适度的 ROS 水平通过激活分子伴侣、应激反应途径和自噬来保护细胞免受由年龄介导的蛋白质毒性的影响。本综述探讨了 ROS 在蛋白质稳态中的细微作用,并讨论了关于 PN 的氧化还原调节及其在延长健康寿命和延缓与年龄相关的病理方面的最新发现。