Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle

被引:1028
作者
Uezumi, Akiyoshi [1 ]
Fukada, So-ichiro [2 ]
Yamamoto, Naoki [3 ]
Takeda, Shin'ichi [4 ]
Tsuchida, Kunihiro [1 ]
机构
[1] Fujita Hlth Univ, Div Therapies Intractable Dis, Inst Comprehens Med Sci, Aichi 4701192, Japan
[2] Osaka Univ, Grad Sch Pharmaceut Sci, Dept Immunol, Suita, Osaka 5650871, Japan
[3] Fujita Hlth Univ, Lab Mol Biol & Histochem, Joint Res Lab, Aichi 4701192, Japan
[4] Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Mol Therapy, Kodaira, Tokyo 1878502, Japan
关键词
GROWTH-FACTOR; INSULIN-RESISTANCE; STEM-CELLS; RECEPTOR; DIFFERENTIATION; POPULATION; ALPHA; REGENERATION; PURIFICATION; FIBROBLASTS;
D O I
10.1038/ncb2014
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
Ectopic fat deposition in skeletal muscle is closely associated with several disorders, however, the origin of these adipocytes is not clear, nor is the mechanism of their formation. Satellite cells function as adult muscle stem cells but are proposed to possess multipotency. Here, we identify PDGFR alpha(+) mesenchymal progenitors as being distinct from satellite cells and located in the muscle interstitium. We show that, of the muscle-derived cell populations, only PDGFRa+ cells show efficient adipogenic differentiation both in vitro and in vivo. Reciprocal transplantation between regenerating and degenerating muscles, and co-culture experiments revealed that adipogenesis of PDGFR alpha(+) cells is strongly inhibited by the presence of satellite cell-derived myofibres. These results suggest that PDGFR alpha(+) mesenchymal progenitors are the major contributor to ectopic fat cell formation in skeletal muscle, and emphasize that interaction between muscle cells and PDGFRa+ mesenchymal progenitors, not the fate decision of satellite cells, has a considerable impact on muscle homeostasis.
引用
收藏
页码:143 / U116
页数:25
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