Sestrin2是疾病和衰老过程中线粒体应激反应的中心调节因子

IF 12.5 1区 医学 Q1 CELL BIOLOGY
Ivo F. Machado , Carlos M. Palmeira , Anabela P. Rolo
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引用次数: 0

摘要

线粒体为细胞功能提供大部分能量,并协调许多细胞通路。它们的动态特性使它们能够适应压力和细胞代谢需求,从而确保细胞稳态的保存。正常线粒体功能的丧失损害细胞存活,并与许多疾病的发展和衰老有关。尽管暴露于持续或严重的应激对细胞有不利影响,但轻度线粒体应激可增强线粒体功能,并可能通过线粒体适应性反应延长健康寿命。在过去的几十年里,sestrin2 (SESN2)已经成为应激反应的关键调节因子。例如,SESN2响应基因毒性、氧化和代谢应激,促进细胞防御与应激相关的损伤。在这里,我们关注最近的研究结果,这些发现表明SESN2是线粒体应激适应的协调者,它参与了综合应激反应、线粒体生物发生和线粒体自噬。此外,我们还讨论了SESN2在调节运动的健康益处及其对骨骼肌、肝脏和心脏损伤以及衰老的影响中的整体作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sestrin2 is a central regulator of mitochondrial stress responses in disease and aging
Mitochondria supply most of the energy for cellular functions and coordinate numerous cellular pathways. Their dynamic nature allows them to adjust to stress and cellular metabolic demands, thus ensuring the preservation of cellular homeostasis. Loss of normal mitochondrial function compromises cell survival and has been implicated in the development of many diseases and in aging. Although exposure to continuous or severe stress has adverse effects on cells, mild mitochondrial stress enhances mitochondrial function and potentially extends health span through mitochondrial adaptive responses. Over the past few decades, sestrin2 (SESN2) has emerged as a pivotal regulator of stress responses. For instance, SESN2 responds to genotoxic, oxidative, and metabolic stress, promoting cellular defense against stress-associated damage. Here, we focus on recent findings that establish SESN2 as an orchestrator of mitochondrial stress adaptation, which is supported by its involvement in the integrated stress response, mitochondrial biogenesis, and mitophagy. Additionally, we discuss the integral role of SESN2 in mediating the health benefits of exercise as well as its impact on skeletal muscle, liver and heart injury, and aging.
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来源期刊
Ageing Research Reviews
Ageing Research Reviews 医学-老年医学
CiteScore
19.80
自引率
2.30%
发文量
216
审稿时长
55 days
期刊介绍: With the rise in average human life expectancy, the impact of ageing and age-related diseases on our society has become increasingly significant. Ageing research is now a focal point for numerous laboratories, encompassing leaders in genetics, molecular and cellular biology, biochemistry, and behavior. Ageing Research Reviews (ARR) serves as a cornerstone in this field, addressing emerging trends. ARR aims to fill a substantial gap by providing critical reviews and viewpoints on evolving discoveries concerning the mechanisms of ageing and age-related diseases. The rapid progress in understanding the mechanisms controlling cellular proliferation, differentiation, and survival is unveiling new insights into the regulation of ageing. From telomerase to stem cells, and from energy to oxyradical metabolism, we are witnessing an exciting era in the multidisciplinary field of ageing research. The journal explores the cellular and molecular foundations of interventions that extend lifespan, such as caloric restriction. It identifies the underpinnings of manipulations that extend lifespan, shedding light on novel approaches for preventing age-related diseases. ARR publishes articles on focused topics selected from the expansive field of ageing research, with a particular emphasis on the cellular and molecular mechanisms of the aging process. This includes age-related diseases like cancer, cardiovascular disease, diabetes, and neurodegenerative disorders. The journal also covers applications of basic ageing research to lifespan extension and disease prevention, offering a comprehensive platform for advancing our understanding of this critical field.
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