Muscle regeneration in the prolonged absence of myostatin

被引:162
|
作者
Wagner, KR
Liu, XS
Chang, XL
Allen, RE
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21287 USA
[3] Univ Arizona, Dept Anim Sci, Muscle Biol Grp, Tucson, AZ 85721 USA
关键词
aging; muscular dystrophy;
D O I
10.1073/pnas.0408729102
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
Myostatin is an endogenous inhibitor of muscle conserved across diverse species. In the absence of myostatin, there is massive muscle growth in mice, cattle, and humans. Previous studies in the mdx mouse model of muscular dystrophy demonstrate that inhibiting myostatin attenuates several features of dystrophic muscle. These findings have encouraged the development of human therapies to block myostatin. However, little is known of the long-term effects on muscle of myostatin blockade. To evaluate potential sequelae from the prolonged absence of myostatin, senescent myostatin null (mstn(-/-)) mice were studied. Senescent mstn(-/-) mice continue to have normal muscle with increased mass and strength relative to controls. Muscles of senescent mstn(-/-) mice regenerate robustly from both chronic and acute injury. Early markers of regeneration are enhanced in the absence of myostatin, suggesting a mechanism for the attenuation of dystrophic features found in mdx mice lacking myostatin.
引用
收藏
页码:2519 / 2524
页数:6
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