线粒体自噬在衰老标志中的作用。

IF 2.2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Jie Wen, Tingyu Pan, Hongyan Li, Haixia Fan, Jinhua Liu, Zhiyou Cai, Bin Zhao
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引用次数: 0

摘要

经过科学的仔细研究,衰老被广泛地定义为涉及大多数生物体的功能随时间的下降。细胞病变的时间依赖性增加通常是衰老的普遍触发因素,而线粒体功能障碍是衰老的标志。功能失调的线粒体通过线粒体自噬(一种选择性的巨噬)被识别和去除。生物生成和清除减少导致的线粒体损伤增加可能会促进衰老过程。本文的主要目的是详细说明线粒体自噬对衰老的影响,并强调线粒体自噬与其他衰老迹象之间的关系,包括饮食限制、端粒缩短、表观遗传改变和蛋白质失衡。关于这些元素对衰老的影响的证据仍然有限。尽管人们对线粒体自噬与衰老之间关系的理解已经期待已久,但分析这种关系的细节仍然是衰老研究的主要挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of mitophagy in the hallmarks of aging.

Aging, subjected to scientific scrutiny, is extensively defined as a time-dependent decline in functions that involves the majority of organisms. The time-dependent accretion of cellular lesions is generally a universal trigger of aging, while mitochondrial dysfunction is a sign of aging. Dysfunctional mitochondria are identified and removed by mitophagy, a selective form of macroautophagy. Increased mitochondrial damage resulting from reduced biogenesis and clearance may promote the aging process. The primary purpose of this paper is to illustrate in detail the effects of mitophagy on aging and emphasize the associations between mitophagy and other signs of aging, including dietary restriction, telomere shortening, epigenetic alterations, and protein imbalance. The evidence regarding the effects of these elements on aging is still limited. And although the understanding of relationship between mitophagy and aging has been long-awaited, to analyze details of such a relationship remains the main challenge in aging studies.

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来源期刊
Journal of Biomedical Research
Journal of Biomedical Research MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
4.60
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0.00%
发文量
69
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