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Mitochondria, reactive oxygen species, and chronological aging: A message from yeast

期刊

EXPERIMENTAL GERONTOLOGY
卷 46, 期 11, 页码 847-852

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exger.2011.08.007

关键词

Chronological lifespan; Mitochondrial theory of aging; Mitohormesis; Hormetic ROS; Oxidative phosphotylation; Target of rapamycin; Reactive oxygen species; Saccharomyces cerevisiae

资金

  1. [P01ES-011163]

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As a major intracellular source of reactive oxygen species (ROS), mitochondria are involved in aging and lifespan regulation. Using the yeast chronological aging model, researchers have identified conserved signaling pathways that affect lifespan by modulating mitochondrial functions. Caloric restriction and a genetic mimetic with reduced target of rapamycin signaling globally upregulate the mitochondrial proteome and respiratory functions. Recent discoveries support the notion that an altered mitochondrial proteome induces mitohormesis. Mitohormesis involves a variety of ROS during several growth stages and extends lifespan in yeast and other organisms. Here we recap recent advances in understanding of ROS as signals that decelerate chronological aging in yeast. We also discuss parallels between yeast and worm hypoxic signaling. In sum, this mini-review covers mitochondrial regulation by nutrient-sensing pathways and the complex underlying interactions of ROS, metabolic pathways, and chronological aging. (C) 2011 Elsevier Inc. All rights reserved.

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