Sprott Center for Stem Cell Research, Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8L6, Canada.
Nat Cell Biol. 2011 Dec 18;14(2):186-91. doi: 10.1038/ncb2404.
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 Gα(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.
Wnt7a 通过其受体 Fzd7 发出信号,激活平面细胞极性通路,并驱动卫星干细胞的对称扩张,从而增强骨骼肌的修复。在分化的肌纤维中,我们观察到 Wnt7a 与 Fzd7 的结合直接激活了 Akt/mTOR 生长通路,从而诱导肌纤维肥大。值得注意的是,Fzd7 受体复合物与 Gα(s)和 PI(3)K 相关联,并且这些成分对于 Wnt7a 在肌管中激活 Akt/mTOR 生长通路是必需的。Wnt7a-Fzd7 对该通路的激活完全独立于 IGF 受体的激活。总之,这些实验表明,Wnt7a-Fzd7 在成肌谱系进展的不同发育阶段激活不同的通路,并确定了 Wnt7a 和其受体 Fzd7 在骨骼肌中的非经典合成代谢信号通路。