New insights into the role of mitochondria in aging: mitochondrial dynamics and more

线粒体分裂 线粒体融合 生物 线粒体 细胞生物学 DNAJA3公司 线粒体DNA 自噬 程序性细胞死亡 细胞代谢 细胞 细胞凋亡 遗传学 基因
作者
Arnold Y. Seo,Anna‐Maria Joseph,Debapriya Dutta,Judy C.Y. Hwang,John P. Aris,Christiaan Leeuwenburgh
出处
期刊:Journal of Cell Science [The Company of Biologists]
卷期号:123 (15): 2533-2542 被引量:473
标识
DOI:10.1242/jcs.070490
摘要

A decline in mitochondrial function plays a key role in the aging process and increases the incidence of age-related disorders. A deeper understanding of the intricate nature of mitochondrial dynamics, which is described as the balance between mitochondrial fusion and fission, has revealed that functional and structural alterations in mitochondrial morphology are important factors in several key pathologies associated with aging. Indeed, a recent wave of studies has demonstrated the pleiotropic role of fusion and fission proteins in numerous cellular processes, including mitochondrial metabolism, redox signaling, the maintenance of mitochondrial DNA and cell death. Additionally, mitochondrial fusion and fission, together with autophagy, have been proposed to form a quality-maintenance mechanism that facilitates the removal of damaged mitochondria from the cell, a process that is particularly important to forestall aging. Thus, dysfunctional regulation of mitochondrial dynamics might be one of the intrinsic causes of mitochondrial dysfunction, which contributes to oxidative stress and cell death during the aging process. In this Commentary, we discuss recent studies that have converged at a consensus regarding the involvement of mitochondrial dynamics in key cellular processes, and introduce a possible link between abnormal mitochondrial dynamics and aging.

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