Farout Luc, Friguet Bertrand
Laboratoire de Biologie et Biochimie Cellulaire du Vieillissement, Université Denis Diderot-Paris 7, Paris, France.
Antioxid Redox Signal. 2006 Jan-Feb;8(1-2):205-16. doi: 10.1089/ars.2006.8.205.
Damage to cellular components by reactive oxygen species is believed to be an important factor contributing to the aging process. Likewise, the progressive failure of maintenance and repair is believed to be a major cause of biological aging. Cellular aging is characterized by the accumulation of oxidatively modified proteins, a process that results, at least in part, from impaired protein turnover. Indeed, oxidized protein buildup with age may be due to increased protein damage, decreased elimination of oxidized protein (i.e., repair and degradation), or a combination of both mechanisms. Since the proteasome has been implicated in both general protein turnover and the removal of oxidized protein, the fate of the proteasome during aging has recently received considerable attention, and evidence has been provided for impaired proteasome function with age in different cellular systems. The present review will mainly address age-related changes in proteasome structure and function in relation to the impact of oxidative stress on the proteasome and the accumulation of oxidized protein. Knowledge of molecular mechanisms involved in the decline of proteasome function during aging and in oxidative stress is expected to provide new insight that will be useful in defining antiaging strategies aimed at preserving this critical function.
活性氧对细胞成分的损伤被认为是导致衰老过程的一个重要因素。同样,维持和修复功能的逐渐衰退被认为是生物衰老的主要原因。细胞衰老的特征是氧化修饰蛋白质的积累,这一过程至少部分是由于蛋白质周转受损所致。事实上,随着年龄增长氧化蛋白质的积累可能是由于蛋白质损伤增加、氧化蛋白质清除减少(即修复和降解)或这两种机制共同作用的结果。由于蛋白酶体与一般蛋白质周转以及氧化蛋白质的清除都有关联,因此蛋白酶体在衰老过程中的命运最近受到了相当多的关注,并且已有证据表明在不同细胞系统中蛋白酶体功能会随着年龄增长而受损。本综述将主要探讨蛋白酶体结构和功能与年龄相关的变化,以及氧化应激对蛋白酶体的影响和氧化蛋白质的积累。了解衰老过程中以及氧化应激下蛋白酶体功能下降所涉及的分子机制,有望提供新的见解,这将有助于制定旨在维持这一关键功能的抗衰老策略。