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衰老及衰老相关疾病的线粒体基础

The Mitochondrial Basis of Aging and Age-Related Disorders.

作者信息

Srivastava Sarika

机构信息

Virginia Tech Carilion Research Institute, 2 Riverside Circle, Roanoke, VA 24016, USA,

出版信息

Genes (Basel). 2017 Dec 19;8(12):398. doi: 10.3390/genes8120398.

DOI:10.3390/genes8120398
PMID:29257072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5748716/
Abstract

Aging is a natural phenomenon characterized by progressive decline in tissue and organ function leading to increased risk of disease and mortality. Among diverse factors that contribute to human aging, the mitochondrial dysfunction has emerged as one of the key hallmarks of aging process and is linked to the development of numerous age-related pathologies including metabolic syndrome, neurodegenerative disorders, cardiovascular diseases and cancer. Mitochondria are central in the regulation of energy and metabolic homeostasis, and harbor a complex quality control system that limits mitochondrial damage to ensure mitochondrial integrity and function. The intricate regulatory network that balances the generation of new and removal of damaged mitochondria forms the basis of aging and longevity. Here, I will review our current understanding on how mitochondrial functional decline contributes to aging, including the role of somatic mitochondrial DNA (mtDNA) mutations, reactive oxygen species (ROS), mitochondrial dynamics and quality control pathways. I will further discuss the emerging evidence on how dysregulated mitochondrial dynamics, mitochondrial biogenesis and turnover mechanisms contribute to the pathogenesis of age-related disorders. Strategies aimed to enhance mitochondrial function by targeting mitochondrial dynamics, quality control, and mitohormesis pathways might promote healthy aging, protect against age-related diseases, and mediate longevity.

摘要

衰老 是一种自然现象,其特征是组织和器官功能逐渐衰退,导致疾病风险和死亡率增加。在导致人类衰老的多种因素中,线粒体功能障碍已成为衰老过程的关键标志之一,并与包括代谢综合征、神经退行性疾病、心血管疾病和癌症在内的众多与年龄相关的病理发展有关。线粒体在能量和代谢稳态的调节中起着核心作用,并拥有一个复杂的质量控制系统,该系统限制线粒体损伤以确保线粒体的完整性和功能。平衡新线粒体生成与受损线粒体清除的复杂调控网络构成了衰老和长寿的基础。在此,我将回顾我们目前对线粒体功能衰退如何导致衰老的理解,包括体细胞线粒体DNA(mtDNA)突变、活性氧(ROS)、线粒体动力学和质量控制途径的作用。我还将进一步讨论有关线粒体动力学失调、线粒体生物发生和周转机制如何导致与年龄相关疾病发病的新证据。旨在通过靶向线粒体动力学、质量控制和线粒体应激反应途径来增强线粒体功能的策略可能会促进健康衰老、预防与年龄相关的疾病并延长寿命。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/562d/5748716/8e65d827a639/genes-08-00398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/562d/5748716/758f974ab210/genes-08-00398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/562d/5748716/8e65d827a639/genes-08-00398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/562d/5748716/758f974ab210/genes-08-00398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/562d/5748716/8e65d827a639/genes-08-00398-g002.jpg

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