A role for the transcriptional coactivator PGC-1α in muscle refueling

被引:202
作者
Wende, Adam R.
Schaeffer, Paul J.
Parker, Glendon J.
Zechner, Christoph
Han, Dong-Ho
Chen, May M.
Hancock, Chad R.
Lehman, John J.
Huss, Janice M.
McClain, Donald A.
Holloszy, John O.
Kelly, Daniel P.
机构
[1] Washington Univ, Sch Med, Cardiovasc Res Ctr, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[5] Univ Utah, Sch Med, Vet Affairs Med Ctr, Salt Lake City, UT 84112 USA
[6] Univ Utah, Sch Med, Div Endocrinol, Salt Lake City, UT 84112 USA
关键词
D O I
10.1074/jbc.M707006200
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
The transcriptional coactivator peroxisome proliferator-activated receptor gamma coactivator-1 alpha(PGC-1 alpha) has been identified as an inducible regulator of mitochondrial function. Skeletal muscle PGC-1 alpha expression is induced post-exercise. Therefore, we sought to determine its role in the regulation of muscle fuel metabolism. Studies were performed using conditional, muscle-specific, PGC-1 alpha gain-of-function and constitutive, generalized, loss-of-function mice. Forced expression of PGC-1 alpha increased muscle glucose uptake concomitant with augmentation of glycogen stores, a metabolic response similar to post-exercise recovery. Induction of muscle PGC-1 alpha expression prevented muscle glycogen depletion during exercise. Conversely, PGC-1 alpha-deficient animals exhibited reduced rates of muscle glycogen repletion post-exercise. PGC-1 alpha was shown to increase muscle glycogen stores via several mechanisms including stimulation of glucose import, suppression of glycolytic flux, and by down-regulation of the expression of glycogen phosphorylase and its activating kinase, phosphorylase kinase alpha. These findings identify PGC-1 alpha as a critical regulator of skeletal muscle fuel stores.
引用
收藏
页码:36642 / 36651
页数:10
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