Sources for skeletal muscle repair: from satellite cells to reprogramming

被引:27
|
作者
Sirabella, Dario [1 ]
De Angelis, Luciana [2 ]
Berghella, Libera [3 ,4 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
[2] Univ Roma La Sapienza, DAHFMO, Unit Histol & Med Embryol, I-00161 Rome, Italy
[3] IRCCS Fdn S Lucia, I-00143 Rome, Italy
[4] HudsonAlpha Inst Biotechnol, Huntsville, AL 35806 USA
关键词
Skeletal muscle repair; Satellite cells; Reprogramming; PLURIPOTENT STEM-CELLS; HUMAN ADIPOSE-TISSUE; BONE-MARROW; DYSTROPHIN EXPRESSION; MUSCULAR-DYSTROPHY; PROGENITOR CELLS; IN-VIVO; CARDIAC MESOANGIOBLASTS; RESTORE DYSTROPHIN; SELF-RENEWAL;
D O I
10.1007/s13539-012-0098-y
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
Skeletal muscle regeneration is the process that ensures tissue repair after damage by injury or in degenerative diseases such as muscular dystrophy. Satellite cells, the adult skeletal muscle progenitor cells, are commonly considered to be the main cell type involved in skeletal muscle regeneration. Their mechanism of action in this process is extensively characterized. However, evidence accumulated in the last decade suggests that other cell types may participate in skeletal muscle regeneration. Although their actual contribution to muscle formation and regeneration is still not clear; if properly manipulated, these cells may become new suitable and powerful sources for cell therapy of skeletal muscle degenerative diseases. Mesoangioblasts, vessel associated stem/progenitor cells with high proliferative, migratory and myogenic potential, are very good candidates for clinical applications and are already in clinical experimentation. In addition, pluripotent stem cells are very promising sources for regeneration of most tissues, including skeletal muscle. Conditions such as muscle cachexia or aging that severely alter homeostasis may be counteracted by transplantation of donor and/or recruitment and activation of resident muscle stem/progenitor cells. Advantages and limitations of different cell therapy approaches will be discussed.
引用
收藏
页码:125 / 136
页数:12
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