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Overexpression of Atg5 in mice activates autophagy and extends lifespan

机译:Atg5在小鼠中的过表达激活自噬并延长寿命

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Autophagy has been implicated in the ageing process, but whether autophagy activation extends lifespan in mammals is unknown. Here we show that ubiquitous overexpression of Atg5, a protein essential for autophagosome formation, extends median lifespan of mice by 17.2%. We demonstrate that moderate overexpression of Atg5 in mice enhances autophagy, and that Atg5 transgenic mice showed anti-ageing phenotypes, including leanness, increased insulin sensitivity and improved motor function. Furthermore, mouse embryonic fibroblasts cultured from Atg5 transgenic mice are more tolerant to oxidative damage and cell death induced by oxidative stress, and this tolerance was reversible by treatment with an autophagy inhibitor. Our observations suggest that the leanness and lifespan extension in Atg5 transgenic mice may be the result of increased autophagic activity.
机译:自噬与衰老过程有关,但是自噬激活是否能延长哺乳动物的寿命尚不清楚。在这里,我们显示普遍存在的Atg5过表达(一种自噬体形成所必需的蛋白质)将小鼠的中位寿命延长了17.2%。我们证明了Atg5在小鼠中的过度表达会增强自噬,并且Atg5转基因小鼠表现出抗衰老的表型,包括瘦肉,增加的胰岛素敏感性和改善的运动功能。此外,从Atg5转基因小鼠培养的小鼠胚胎成纤维细胞更能耐受氧化应激引起的氧化损伤和细胞死亡,并且通过自噬抑制剂治疗可逆转这种耐受性。我们的观察结果表明,Atg5转基因小鼠的瘦度和寿命延长可能是自噬活性增强的结果。

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