Myonuclear Domain Flexibility Challenges Rigid Assumptions on Satellite Cell Contribution to Skeletal Muscle Fiber Hypertrophy

被引:70
作者
Murach, Kevin A. [1 ,2 ]
Englund, Davis A. [1 ,2 ]
Dupont-Versteegden, Esther E. [1 ,2 ]
McCarthy, John J. [1 ,3 ]
Peterson, Charlotte A. [1 ,2 ]
机构
[1] Univ Kentucky, Coll Hlth Sci, Ctr Muscle Biol, Lexington, KY 40506 USA
[2] Univ Kentucky, Coll Hlth Sci, Dept Rehabil Sci, Lexington, KY 40506 USA
[3] Univ Kentucky, Coll Med, Dept Physiol, Lexington, KY USA
基金
美国国家卫生研究院;
关键词
myonuclei; Type; 2; fibers; muscle damage; muscle regeneration; Pax7-DTA; ISSUES LIMIT INTERPRETATION; DEPLETION; ADULT; SIZE; YOUNG; EXPRESSION; GROWTH; MASS; TRANSCRIPTION; ADAPTATIONS;
D O I
10.3389/fphys.2018.00635
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Satellite cell-mediated myonuclear accretion is thought to be required for skeletal muscle fiber hypertrophy, and even drive hypertrophy by preceding growth. Recent studies in humans and rodents provide evidence that challenge this axiom. Specifically, Type 2 muscle fibers reliably demonstrate a substantial capacity to hypertrophy in the absence of myonuclear accretion, challenging the notion of a tightly regulated myonuclear domain (i.e., area that each myonucleus transcriptionally governs). In fact, a "myonuclear domain ceiling", or upper limit of transcriptional output per nucleus to support hypertrophy, has yet to be identified. Satellite cells respond to muscle damage, and also play an important role in extracellular matrix remodeling during loading-induced hypertrophy. We postulate that robust satellite cell activation and proliferation in response to mechanical loading is largely for these purposes. Future work will aim to elucidate the mechanisms by which Type 2 fibers can hypertrophy without additional myonuclei, the extent to which Type 1 fibers can grow without myonuclear accretion, and whether a true myonuclear domain ceiling exists.
引用
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页数:7
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