A PGC-1α Isoform Induced by Resistance Training Regulates Skeletal Muscle Hypertrophy

被引:559
作者
Ruas, Jorge L. [1 ]
White, James P. [1 ]
Rao, Rajesh R. [1 ]
Kleiner, Sandra [1 ]
Brannan, Kevin T. [1 ]
Harrison, Brooke C. [2 ]
Greene, Nicholas P. [3 ]
Wu, Jun [1 ]
Estall, Jennifer L. [1 ]
Irving, Brian A. [4 ]
Lanza, Ian R. [4 ]
Rasbach, Kyle A. [1 ]
Okutsu, Mitsuharu [3 ]
Nair, K. Sreekumaran [4 ]
Yan, Zhen [3 ]
Leinwand, Leslie A. [2 ]
Spiegelman, Bruce M. [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Cell Biol, Boston, MA 02115 USA
[2] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
[3] Univ Virginia, Dept Med, Charlottesville, VA 22908 USA
[4] Mayo Clin, Div Endocrinol, Endocrine Res Unit, Rochester, MN 55905 USA
关键词
TRANSCRIPTIONAL COACTIVATOR PGC-1-ALPHA; MICE; GROWTH; MASS; HOMEOSTASIS; EXPRESSION; PROTECTS; ATROPHY; FIBERS; DRIVES;
D O I
10.1016/j.cell.2012.10.050
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
PGC-1 alpha is a transcriptional coactivator induced by exercise that gives muscle many of the best known adaptations to endurance-type exercise but has no effects on muscle strength or hypertrophy. We have identified a form of PGC-1 alpha (PGC-1 alpha 4) that results from alternative promoter usage and splicing of the primary transcript. PGC-1 alpha 4 is highly expressed in exercised muscle but does not regulate most known PGC-1 alpha targets such as the mitochondrial OXPHOS genes. Rather, it specifically induces IGF1 and represses myostatin, and expression of PGC-1 alpha 4 in vitro and in vivo induces robust skeletal muscle hypertrophy. Importantly, mice with skeletal muscle-specific transgenic expression of PGC-1 alpha 4 show increased muscle mass and strength and dramatic resistance to the muscle wasting of cancer cachexia. Expression of PGC-1 alpha 4 is preferentially induced in mouse and human muscle during resistance exercise. These studies identify a PGC-1 alpha protein that regulates and coordinates factors involved in skeletal muscle hypertrophy.
引用
收藏
页码:1319 / 1331
页数:13
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