Exercise stimulates Pgc-1α transcription in skeletal muscle through activation of the p38 MAPK pathway

被引:559
作者
Akimoto, T [1 ]
Pohnert, SC [1 ]
Li, P [1 ]
Zhang, M [1 ]
Gumbs, C [1 ]
Rosenberg, PB [1 ]
Williams, RS [1 ]
Yan, Z [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Med, Div Cardiol, Durham, NC 27704 USA
关键词
D O I
10.1074/jbc.M408862200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Peroxisome proliferator-activated receptor gamma co-activator 1 alpha (PGC-1 alpha) promotes mitochondrial biogenesis and slow fiber formation in skeletal muscle. We hypothesized that activation of the p38 mitogen-activated protein kinase ( MAPK) pathway in response to increased muscle activity stimulated Pgc-1 alpha gene transcription as part of the mechanisms for skeletal muscle adaptation. Here we report that a single bout of voluntary running induced a transient increase of Pgc-1 alpha mRNA expression in mouse plantaris muscle, concurrent with an activation of the p38 MAPK pathway. Activation of the p38 MAPK pathway in cultured C2C12 myocytes stimulated Pgc-1 alpha promoter activity, which could be blocked by the specific inhibitors of p38, SB203580 and SB202190, or a dominant negative p38. Furthermore, the p38-mediated increase in Pgc-1 alpha promoter activity was enhanced by increased expression of the downstream transcription factor ATF2 and completely blocked by ATF2 Delta N, a dominant negative ATF2. Skeletal muscle-specific expression of a constitutively active activator of p38, MKK6E, in transgenic mice resulted in enhanced Pgc-1 alpha and cytochrome oxidase IV protein expression in fast-twitch skeletal muscles. These findings suggest that contractile activity-induced activation of the p38 MAPK pathway promotes Pgc-1 alpha gene expression and skeletal muscle adaptation.
引用
收藏
页码:19587 / 19593
页数:7
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