骨骼肌
肌发生
内分泌学
内科学
生物
肌肉肥大
FGF21型
肌生成抑制素
成纤维细胞生长因子
FGF19型
P70-S6激酶1
PI3K/AKT/mTOR通路
细胞生物学
医学
信号转导
受体
作者
Bérengère Benoit,Emmanuelle Meugnier,Martina Castelli,Stéphanie Chanon,Aurélie Vieille‐Marchiset,Christine Durand,Nadia Bendridi,Sandra Pesenti,Pierre‐Axel Monternier,Anne‐Cécile Durieux,Damien Freyssenet,Jennifer Rieusset,Étienne Lefai,Hubert Vidal,Jérôme Ruzzin
出处
期刊:Nature Medicine
[Springer Nature]
日期:2017-06-26
卷期号:23 (8): 990-996
被引量:170
摘要
The endocrine-derived hormone fibroblast growth factor (FGF) 19 has recently emerged as a potential target for treating metabolic disease. Given that skeletal muscle is a key metabolic organ, we explored the role of FGF19 in that tissue. Here we report a novel function of FGF19 in regulating skeletal muscle mass through enlargement of muscle fiber size, and in protecting muscle from atrophy. Treatment with FGF19 causes skeletal muscle hypertrophy in mice, while physiological and pharmacological doses of FGF19 substantially increase the size of human myotubes in vitro. These effects were not elicited by FGF21, a closely related endocrine FGF member. Both in vitro and in vivo, FGF19 stimulates the phosphorylation of the extracellular-signal-regulated protein kinase 1/2 (ERK1/2) and the ribosomal protein S6 kinase (S6K1), an mTOR-dependent master regulator of muscle cell growth. Moreover, mice with a skeletal-muscle-specific genetic deficiency of β-Klotho (KLB), an obligate co-receptor for FGF15/19 (refs. 2,3), were unresponsive to the hypertrophic effect of FGF19. Finally, in mice, FGF19 ameliorates skeletal muscle atrophy induced by glucocorticoid treatment or obesity, as well as sarcopenia. Taken together, these findings provide evidence that the enterokine FGF19 is a novel factor in the regulation of skeletal muscle mass, and that it has therapeutic potential for the treatment of muscle wasting.
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