Laboratory of Protein Metabolism, Graduate School of Pharmaceutical Sciences, the University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 1130033, Japan.
J Biochem. 2024 Apr 29;175(5):473-480. doi: 10.1093/jb/mvae016.
Aging is a major risk factor for many diseases. Recent studies have shown that age-related disruption of proteostasis leads to the accumulation of abnormal proteins and that dysfunction of the two major intracellular proteolytic pathways, the ubiquitin-proteasome pathway, and the autophagy-lysosome pathway, is largely responsible for this process. Conversely, it has been shown that activation of these proteolytic pathways may contribute to lifespan extension and suppression of pathological conditions, making it a promising intervention for anti-aging. This review provides an overview of the important role of intracellular protein degradation in aging and summarizes how the disruption of proteostasis is involved in age-related diseases.
衰老是许多疾病的主要危险因素。最近的研究表明,与年龄相关的蛋白质稳态破坏导致异常蛋白质的积累,而两条主要的细胞内蛋白水解途径,即泛素-蛋白酶体途径和自噬-溶酶体途径的功能障碍,在很大程度上对此过程负责。相反,已经表明这些蛋白水解途径的激活可能有助于延长寿命和抑制病理状况,使其成为一种有前途的抗衰老干预措施。本综述提供了细胞内蛋白质降解在衰老中的重要作用概述,并总结了蛋白质稳态破坏如何参与与年龄相关的疾病。