细胞生物学
脂肪生成
生物
骨骼肌
心肌细胞
祖细胞
内化
肌发生
干细胞
再生(生物学)
间质细胞
内科学
内分泌学
受体
间充质干细胞
癌症研究
生物化学
医学
作者
Marc Beltrà,Fabrizio Pin,Domiziana Costamagna,Robin Duelen,Alessandra Renzini,Riccardo Ballarò,Lorena Garcia‐Castillo,Ambra Iannuzzi,Viviana Moresi,Dario Coletti,Maurilio Sampaolesi,Fabio Penna,Paola Costelli
出处
期刊:iScience
[Cell Press]
日期:2022-11-01
卷期号:25 (11): 105480-105480
被引量:9
标识
DOI:10.1016/j.isci.2022.105480
摘要
Skeletal muscle repair is accomplished by satellite cells (MuSCs) in cooperation with interstitial stromal cells (ISCs), but the relationship between the function of these cells and the metabolic state of myofibers remains unclear. This study reports an altered proportion of MuSCs and ISCs (including adipogenesis-regulatory cells; Aregs) induced by the transgenic overexpression of peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) in the myofibers (MCK-PGC-1α mice). Although PGC-1α-driven increase of MuSCs does not accelerate muscle regeneration, myogenic progenitors isolated from MCK-PGC-1α mice and transplanted into intact and regenerating muscles are more prone to fuse with recipient myofibers than those derived from wild-type donors. Moreover, both young and aged MCK-PGC-1α animals exhibit reduced perilipin-positive areas when challenged with an adipogenic stimulus, demonstrating low propensity to accumulate adipocytes within the muscle. Overall, these results unveil that increased PGC-1α expression in the myofibers favors pro-myogenic and anti-adipogenic cell populations in the skeletal muscle.
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