Propeptide-Mediated Inhibition of Myostatin Increases Muscle Mass Through Inhibiting Proteolytic Pathways in Aged Mice

被引:18
作者
Collins-Hooper, Henry [1 ]
Sartori, Roberta [2 ]
Macharia, Raymond [3 ]
Visanuvimol, Korntip [1 ]
Foster, Keith [1 ]
Matsakas, Antonios [4 ]
Flasskamp, Hannah [1 ]
Ray, Steve [5 ]
Dash, Philip R. [1 ]
Sandri, Marco [2 ]
Patel, Ketan [1 ]
机构
[1] Univ Reading, Sch Biol Sci, Reading RG6 6UB, Berks, England
[2] Univ Padua, Venetian Inst Mol Med, I-35100 Padua, Italy
[3] Univ London Royal Vet Coll, London NW1 0TU, England
[4] Univ Hull, Kingston Upon Hull HU6 7RX, N Humberside, England
[5] Nat Biosci, Reading, Berks, England
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2014年 / 69卷 / 09期
基金
英国生物技术与生命科学研究理事会;
关键词
Muscle; Myostatin; Aging; Mouse; Sarcopenia; SKELETAL-MUSCLE; FIBER-TYPE; AUTOPHAGY; GENE; GROWTH; HYPERTROPHY; SARCOPENIA; MECHANISMS; EXPRESSION; INDUCTION;
D O I
10.1093/gerona/glt170
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Mammalian aging is accompanied by a progressive loss of skeletal muscle, a process called sarcopenia. Myostatin, a secreted member of the transforming growth factor-beta family of signaling molecules, has been shown to be a potent inhibitor of muscle growth. Here, we examined whether muscle growth could be promoted in aged animals by antagonizing the activity of myostatin through the neutralizing activity of the myostatin propeptide. We show that a single injection of an AAV8 virus expressing the myostatin propeptide induced an increase in whole body weights and all muscles examined within 7 weeks of treatment. Our cellular studies demonstrate that muscle enlargement was due to selective fiber type hypertrophy, which was accompanied by a shift toward a glycolytic phenotype. Our molecular investigations elucidate the mechanism underpinning muscle hypertrophy by showing a decrease in the expression of key genes that control ubiquitin-mediated protein breakdown. Most importantly, we show that the hypertrophic muscle that develops as a consequence of myostatin propeptide in aged mice has normal contractile properties. We suggest that attenuating myostatin signaling could be a very attractive strategy to halt and possibly reverse age-related muscle loss.
引用
收藏
页码:1049 / 1059
页数:11
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