Skeletal muscle fiber-type switching, exercise intolerance, and myopathy in PGC-1α muscle-specific knock-out animals

被引:511
作者
Handschin, Christoph
Chin, Sherry
Li, Ping
Liu, Fenfen
Maratos-Flier, Eleftheria
LeBrasseur, Nathan K.
Yan, Zhen
Spiegelman, Bruce M.
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Univ Zurich, Inst Physiol, CH-8057 Zurich, Switzerland
[3] Univ Zurich, Zurich Ctr Integrat Human Physiol, CH-8057 Zurich, Switzerland
[4] Duke Univ, Med Ctr, Dept Med, Durham, NC 27704 USA
[5] Beth Israel Deaconess Med Ctr, Dept Med, Div Endocrinol Diabet & Metab, Boston, MA 02215 USA
[6] Harvard Univ, Sch Med, Boston, MA 02215 USA
[7] Boston Univ, Sch Med, Diabet & Metab Unit, Boston, MA 02118 USA
关键词
D O I
10.1074/jbc.M704817200
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) is a key integrator of neuromuscular activity in skeletal muscle. Ectopic expression of PGC-1 alpha in muscle results in increased mitochondrial number and function as well as an increase in oxidative, fatigue-resistant muscle fibers. Whole body PGC-1 alpha knock-out mice have a very complex phenotype but do not have a marked skeletal muscle phenotype. We thus analyzed skeletal muscle-specific PGC-1 alpha knock-out mice to identify a specific role for PGC-1 alpha in skeletal muscle function. These mice exhibit a shift from oxidative type I and IIa toward type IIx and IIb muscle fibers. Moreover, skeletal muscle-specific PGC-1 alpha knock-out animals have reduced endurance capacity and exhibit fiber damage and elevated markers of inflammation following treadmill running. Our data demonstrate a critical role for PGC-1 alpha in maintenance of normal fiber type composition and of muscle fiber integrity following exertion.
引用
收藏
页码:30014 / 30021
页数:8
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