Wnt7a-Fzd7 signalling directly activates the Akt/mTOR anabolic growth pathway in skeletal muscle

被引:184
作者
von Maltzahn, Julia [1 ]
Bentzinger, C. Florian [1 ]
Rudnicki, Michael A. [1 ,2 ,3 ]
机构
[1] Ottawa Hosp Res Inst, Sprott Ctr Stem Cell Res, Ottawa, ON K1H 8L6, Canada
[2] Univ Ottawa, Dept Med, Ottawa, ON K1H 8M5, Canada
[3] Ottawa Hosp Res Inst, Regenerat Med Program, Ottawa, ON K1H 8L6, Canada
基金
加拿大健康研究院; 美国国家卫生研究院; 瑞士国家科学基金会;
关键词
TUMOR-NECROSIS-FACTOR; SATELLITE STEM-CELLS; MYOGENIC DIFFERENTIATION; INSULIN-RESISTANCE; CANCER CACHEXIA; FACTOR-I; KINASE; HYPERTROPHY; INHIBITION; MECHANISMS;
D O I
10.1038/ncb2404
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Wnt7a signals through its receptor Fzd7 to activate the planar-cell-polarity pathway and drive the symmetric expansion of satellite stem cells resulting in enhanced repair of skeletal muscle. In differentiated myofibres, we observed that Wnt7a binding to Fzd7 directly activates the Akt/mTOR growth pathway, thereby inducing myofibre hypertrophy. Notably, the Fzd7 receptor complex was associated with G alpha(s) and PI(3)K and these components were required for Wnt7a to activate the Akt/mTOR growth pathway in myotubes. Wnt7a-Fzd7 activation of this pathway was completely independent of IGF-receptor activation. Together, these experiments demonstrate that Wnt7a-Fzd7 activates distinct pathways at different developmental stages during myogenic lineage progression, and identify a non-canonical anabolic signalling pathway for Wnt7a and its receptor Fzd7 in skeletal muscle.
引用
收藏
页码:186 / 191
页数:6
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