Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis

被引:647
作者
Braun, Thomas [1 ]
Gautel, Mathias [2 ,3 ]
机构
[1] Max Planck Inst Heart & Lung Res, Dept Cardiac Dev & Remodelling, D-61231 Bad Nauheim, Germany
[2] Kings Coll London, Randall Div Cell & Mol Biophys, London SE1 1UL, England
[3] New Hunts House, Div Cardiovasc, Muscle Signalling & Dev Sect, London SE1 1UL, England
基金
英国医学研究理事会;
关键词
SERUM RESPONSE FACTOR; DEPENDENT CARDIAC-HYPERTROPHY; NEURAL CREST CELLS; SIGNALING PATHWAYS; PROGENITOR CELLS; MYF5; EXPRESSION; GENE-EXPRESSION; FIBER-TYPE; MYOBLAST DIFFERENTIATION; SATELLITE CELL;
D O I
10.1038/nrm3118
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Skeletal muscle is the dominant organ system in locomotion and energy metabolism. Postnatal muscle grows and adapts largely by remodelling pre-existing fibres, whereas embryonic muscle grows by the proliferation of myogenic cells. Recently, the genetic hierarchies of the myogenic transcription factors that control vertebrate muscle development - by myoblast proliferation, migration, fusion and functional adaptation into fast-twitch and slow- twitch fibres - have become clearer. The transcriptional mechanisms controlling postnatal hypertrophic growth, remodelling and functional differentiation redeploy myogenic factors in concert with serum response factor (SRF), JUNB and forkhead box protein O3A (FOXO3A). It has also emerged that there is extensive post-transcriptional regulation by microRNAs in development and postnatal remodelling.
引用
收藏
页码:349 / 361
页数:13
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