Calorie restriction extends Saccharomyces cerevisiae lifespan by increasing respiration

被引:824
作者
Lin, SJ
Kaeberlein, M
Andalis, AA
Sturtz, LA
Defossez, PA
Culotta, VC
Fink, GR
Guarente, L
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[3] Johns Hopkins Univ, Sch Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/nature00829
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Calorie restriction (CR) extends lifespan in a wide spectrum of organisms and is the only regimen known to lengthen the lifespan of mammals(1-4). We established a model of CR in budding yeast Saccharomyces cerevisiae. In this system, lifespan can be extended by limiting glucose or by reducing the activity of the glucose-sensing cyclic-AMP-dependent kinase (PKA)(5). Lifespan extension in a mutant with reduced PKA activity requires Sir2 and NAD (nicotinamide adenine dinucleotide)(5). In this study we explore how CR activates Sir2 to extend lifespan. Here we show that the shunting of carbon metabolism toward the mitochondrial tricarboxylic acid cycle and the concomitant increase in respiration play a central part in this process. We discuss how this metabolic strategy may apply to CR in animals.
引用
收藏
页码:344 / 348
页数:5
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