Wnt/尾-catenin signaling changes C2C12 myoblast proliferation and differentiation by inducing Id3 expression

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• 作者：Long Zhang¹ ; Songting Shi¹ ; Juan Zhang ; Fangfang Zhou ; Peter ten Dijke ; ^{p.ten_dijke@lumc.nl}
• 关键词：Wnt/尾-catenin ; Id3 ; Cell proliferation ; Myoblast
• 刊名：Biochemical and Biophysical Research Communications
• 出版年：2012
• 期刊代码：159_0006291x
• 类别：bio
• 出版时间：2 March, 2012
• 卷：419
• 期：1
• 页码：83-88
• 文件大小：788 K

摘要

Canonical Wnt signaling plays important roles in regulating cell proliferation and differentiation. In this study, we report that inhibitor of differentiation (Id)3 is a Wnt-inducible gene in mouse C2C12 myoblasts. Wnt3a induced Id3 expression in a 尾-catenin-dependent manner. Bone morphogenetic protein (BMP) also potently induced Id3 expression. However, Wnt-induced Id3 expression occurred independent of the BMP/Smad pathway. Functional studies showed that Id3 depletion in C2C12 cells impaired Wnt3a-induced cell proliferation and alkaline phosphatase activity, an early marker of osteoblast cells. Id3 depletion elevated myogenin induction during myogenic differentiation and partially impaired Wnt3a suppressed myogenin expression in C2C12 cells. These results suggest that Id3 is an important Wnt/尾-catenin induced gene in myoblast cell fate determination.