An AMPK-FOXO pathway mediates longevity induced by a novel method of dietary restriction in C-elegans

被引:604
作者
Greer, Eric L.
Dowlatshahi, Dara
Banko, Max R.
Villen, Judit
Hoang, Kimmi
Blanchard, Daniel
Gygi, Steven P.
Brunet, Anne [1 ]
机构
[1] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Canc Biol Program, Stanford, CA 94305 USA
[3] Stanford Univ, Biol Sci Grad Program, Stanford, CA 94305 USA
[4] Stanford Univ, Neurosci Program, Stanford, CA 94305 USA
[5] Harvard Med Sch, Dept Cell Biol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.cub.2007.08.047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Dietary restriction (DR) is the most effective environmental intervention to extend lifespan in a wide range of species. However, the molecular mechanisms underlying the benefits of DR on longevity are still poorly characterized. AMP-activated protein kinase (AMPK) is activated by a decrease in energy levels, raising the possibility that AMPK might mediate lifespan extension by DR. Results: By using a novel DR assay that we developed and validated in C. elegans, we find that AMPK is required for this DR method to extend lifespan and delay age-dependent decline. We find that AMPK exerts its effects in part via the FOXO transcription factor DAF-16. FOXO/DAF-16 is necessary for the beneficial effects of this DR method on lifespan. Expression of an active version of AMPK in worms increases stress resistance and extends longevity in a FOXO/DAF-16-dependent manner. Lastly, we find that AMPK activates FOXO/DAF-16-dependent transcription and phosphorylates FOXO/DAF-16 at previously unidentified sites, suggesting a possible direct mechanism of regulation of FOXO/DAF-16 by AMPK. Conclusions: Our study shows that an energy-sensing AMPK-FOXO pathway mediates the lifespan extension induced by a novel method of dietary restriction in C. elegans.
引用
收藏
页码:1646 / 1656
页数:11
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