Noncoding RNAs as epigenetic mediators of skeletal muscle regeneration

被引:21
作者
Sohi, Gurjeev [1 ]
Dilworth, Francis Jeffrey [1 ,2 ]
机构
[1] Ottawa Hosp Res Inst, Sprott Ctr Stem Cell Res, Regenerat Med Program, Ottawa, ON K1H 8L6, Canada
[2] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON K1N 6N5, Canada
基金
加拿大健康研究院;
关键词
differentiation; epigenetics; gene expression; lncRNAs; miRNAs; MyoD; myogenesis; myoMiRs; satellite cells; skeletal muscle; SATELLITE CELL ACTIVATION; MESSENGER-RNA; GENE-EXPRESSION; STRESS GRANULES; SERIAL ANALYSIS; DOWN-REGULATION; DIFFERENTIATION; MICRORNA; CHROMATIN; PROLIFERATION;
D O I
10.1111/febs.13170
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Skeletal muscle regeneration is a well-characterized biological process in which resident adult stem cells must undertake a series of cell-fate decisions to ensure efficient repair of the damaged muscle fibers while also maintaining the stem cell niche. Satellite cells, the main stem cell contributing to the repaired muscle fiber, are maintained in a quiescent state in healthy muscle. Upon injury, the satellite cells become activated, and proliferate to expand the muscle progenitor cell population before returning to the quiescent state or differentiating to become myofibers. Importantly, the determination of cell fate is controlled at the epigenetic level in response to environmental cues. In this review, we discuss our current understanding of the role played by noncoding RNAs (both miRNAs and long-noncoding RNAs) in the epigenetic control of muscle regeneration.
引用
收藏
页码:1630 / 1646
页数:17
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