Regulation and phylogeny of skeletal muscle regeneration

被引:182
作者
Baghdadi, Meryem B. [1 ,2 ,3 ]
Tajbakhsh, Shahragim [1 ,2 ]
机构
[1] Inst Pasteur, CNRS URA 3738, Dept Dev & Stem Cell Biol, Stem Cells & Dev, 25 Rue Dr Roux, F-75015 Paris, France
[2] Inst Pasteur, CNRS UMR 3738, F-75015 Paris, France
[3] Univ Paris 06, Sorbonne Univ, UPMC, IFD ED 515, 4 Pl Jussieu, F-75252 Paris, France
基金
欧洲研究理事会;
关键词
Skeletal muscle; Regeneration; Stem cells; Evolution; Quiescence; Injury; LONG NONCODING RNA; SATELLITE CELLS CONTRIBUTE; STEM-CELLS; SELF-RENEWAL; IN-VITRO; PROGENITOR CELLS; NULL MUTATION; MOUSE MODEL; DISTINCT; MACROPHAGES;
D O I
10.1016/j.ydbio.2017.07.026
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
One of the most fascinating questions in regenerative biology is why some animals can regenerate injured structures while others cannot. Skeletal muscle has a remarkable capacity to regenerate even after repeated traumas, yet limited information is available on muscle repair mechanisms and how they have evolved. For decades, the main focus in the study of muscle regeneration was on muscle stem cells, however, their interaction with their progeny and stromal cells is only starting to emerge, and this is crucial for successful repair and re-establishment of homeostasis after injury. In addition, numerous murine injury models are used to investigate the regeneration process, and some can lead to discrepancies in observed phenotypes. This review addresses these issues and provides an overview of some of the main regulatory cellular and molecular players involved in skeletal muscle repair.
引用
收藏
页码:200 / 209
页数:10
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