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The NAD(+)/Sirtuin Pathway Modulates Longevity through Activation of Mitochondrial UPR and FOXO Signaling.NAD(+)/Sirtuin 通路通过激活线粒体 UPRE 和 FOXO 信号来调节寿命。
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ROS are required for mouse spermatogonial stem cell self-renewal.ROS 对于小鼠精原干细胞自我更新是必需的。
Cell Stem Cell. 2013 Jun 6;12(6):774-86. doi: 10.1016/j.stem.2013.04.001.
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Pheromone sensing regulates Caenorhabditis elegans lifespan and stress resistance via the deacetylase SIR-2.1.信息素感应通过去乙酰化酶 SIR-2.1 调节秀丽隐杆线虫的寿命和应激抗性。
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Life-span extension from hypoxia in Caenorhabditis elegans requires both HIF-1 and DAF-16 and is antagonized by SKN-1.秀丽隐杆线虫中的缺氧延长寿命需要 HIF-1 和 DAF-16,并且受到 SKN-1 的拮抗。
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线粒体细胞生物学适应:通过增加活性氧(ROS)水平来促进健康和寿命。

Mitohormesis: Promoting Health and Lifespan by Increased Levels of Reactive Oxygen Species (ROS).

机构信息

Energy Metabolism Laboratory, ETH Zürich (Swiss Federal Institute of Technology Zurich), Schwerzenbach/Zürich, CH 8603, Switzerland; ; Dept. of Human Nutrition, Institute of Nutrition, University of Jena, Jena D-07743, Germany.

Dept. of Human Nutrition, Institute of Nutrition, University of Jena, Jena D-07743, Germany.

出版信息

Dose Response. 2014 Jan 31;12(2):288-341. doi: 10.2203/dose-response.13-035.Ristow. eCollection 2014 May.

DOI:10.2203/dose-response.13-035.Ristow
PMID:24910588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4036400/
Abstract

Increasing evidence indicates that reactive oxygen species (ROS), consisting of superoxide, hydrogen peroxide, and multiple others, do not only cause oxidative stress, but rather may function as signaling molecules that promote health by preventing or delaying a number of chronic diseases, and ultimately extend lifespan. While high levels of ROS are generally accepted to cause cellular damage and to promote aging, low levels of these may rather improve systemic defense mechanisms by inducing an adaptive response. This concept has been named mitochondrial hormesis or mitohormesis. We here evaluate and summarize more than 500 publications from current literature regarding such ROS-mediated low-dose signaling events, including calorie restriction, hypoxia, temperature stress, and physical activity, as well as signaling events downstream of insulin/IGF-1 receptors, AMP-dependent kinase (AMPK), target-of-rapamycin (TOR), and lastly sirtuins to culminate in control of proteostasis, unfolded protein response (UPR), stem cell maintenance and stress resistance. Additionally, consequences of interfering with such ROS signals by pharmacological or natural compounds are being discussed, concluding that particularly antioxidants are useless or even harmful.

摘要

越来越多的证据表明,活性氧(ROS),包括超氧阴离子、过氧化氢和其他多种物质,不仅会导致氧化应激,还可能作为信号分子发挥作用,通过预防或延缓多种慢性疾病来促进健康,并最终延长寿命。虽然通常认为高水平的 ROS 会导致细胞损伤并促进衰老,但低水平的 ROS 可能通过诱导适应性反应来改善全身防御机制。这一概念被称为线粒体应激或线粒体适应。我们在这里评估并总结了来自当前文献的 500 多篇关于这种 ROS 介导的低剂量信号事件的出版物,包括热量限制、缺氧、温度应激和体育活动,以及胰岛素/IGF-1 受体、AMP 依赖的激酶(AMPK)、雷帕霉素靶蛋白(TOR)下游的信号事件,以及最后是控制蛋白质稳态、未折叠蛋白反应(UPR)、干细胞维持和应激抗性的沉默调节蛋白。此外,还讨论了通过药理学或天然化合物干扰这种 ROS 信号的后果,得出的结论是,特别是抗氧化剂不仅无用,甚至可能有害。