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Atg5 在小鼠中的过表达激活自噬并延长寿命。

Overexpression of Atg5 in mice activates autophagy and extends lifespan.

机构信息

Global Research Laboratory, School of Biological Sciences/Bio-MAX Institute, Seoul National University, Seoul 151-747, Korea.

出版信息

Nat Commun. 2013;4:2300. doi: 10.1038/ncomms3300.

Abstract

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.

摘要

自噬作用与衰老过程有关,但自噬激活是否能延长哺乳动物的寿命尚不清楚。在这里,我们表明,Atg5(一种对于自噬体形成必不可少的蛋白质)的广泛过表达可使小鼠的中位寿命延长 17.2%。我们证明了 Atg5 在小鼠中的适度过表达可增强自噬作用,并且 Atg5 转基因小鼠表现出抗老化表型,包括消瘦、增加胰岛素敏感性和改善运动功能。此外,从 Atg5 转基因小鼠中培养的小鼠胚胎成纤维细胞对氧化应激诱导的氧化损伤和细胞死亡更具耐受性,并且这种耐受性可通过自噬抑制剂的处理而逆转。我们的观察结果表明,Atg5 转基因小鼠的消瘦和寿命延长可能是自噬活性增加的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b2/3753544/35d504cfd2a9/ncomms3300-f1.jpg

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