ATP合酶
生物
秀丽隐杆线虫
柠檬酸循环
生物化学
自噬
新陈代谢
蛋白质亚单位
三磷酸腺苷
细胞生物学
代谢物
酶
α-酮戊二酸
线粒体
基因
细胞凋亡
作者
R Chin,Xudong Fu,Melody Y. Pai,Laurent Vergnes,Heejun Hwang,Gang Deng,Simon Diep,Brett Lomenick,Vijaykumar S. Meli,Gabriela C. Monsalve,Eileen Hu,Stephen A. Whelan,Jennifer X. Wang,Gwanghyun Jung,Gregory M. Solis,Farbod Fazlollahi,Chitrada Kaweeteerawat,Austin Quach,Mahta Nili,Abby S. Krall
出处
期刊:Nature
[Nature Portfolio]
日期:2014-05-13
卷期号:510 (7505): 397-401
被引量:552
摘要
Metabolism and ageing are intimately linked. Compared with ad libitum feeding, dietary restriction consistently extends lifespan and delays age-related diseases in evolutionarily diverse organisms. Similar conditions of nutrient limitation and genetic or pharmacological perturbations of nutrient or energy metabolism also have longevity benefits. Recently, several metabolites have been identified that modulate ageing; however, the molecular mechanisms underlying this are largely undefined. Here we show that α-ketoglutarate (α-KG), a tricarboxylic acid cycle intermediate, extends the lifespan of adult Caenorhabditis elegans. ATP synthase subunit β is identified as a novel binding protein of α-KG using a small-molecule target identification strategy termed drug affinity responsive target stability (DARTS). The ATP synthase, also known as complex V of the mitochondrial electron transport chain, is the main cellular energy-generating machinery and is highly conserved throughout evolution. Although complete loss of mitochondrial function is detrimental, partial suppression of the electron transport chain has been shown to extend C. elegans lifespan. We show that α-KG inhibits ATP synthase and, similar to ATP synthase knockdown, inhibition by α-KG leads to reduced ATP content, decreased oxygen consumption, and increased autophagy in both C. elegans and mammalian cells. We provide evidence that the lifespan increase by α-KG requires ATP synthase subunit β and is dependent on target of rapamycin (TOR) downstream. Endogenous α-KG levels are increased on starvation and α-KG does not extend the lifespan of dietary-restricted animals, indicating that α-KG is a key metabolite that mediates longevity by dietary restriction. Our analyses uncover new molecular links between a common metabolite, a universal cellular energy generator and dietary restriction in the regulation of organismal lifespan, thus suggesting new strategies for the prevention and treatment of ageing and age-related diseases.
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