C2C12型
肌发生
Wnt信号通路
丹麦克朗
细胞生物学
下调和上调
葛兰素史克-3
连环素
异位表达
生物
信号转导
小RNA
心肌细胞
连环蛋白
糖原合酶
GSK3B公司
细胞生长
化学
细胞培养
生物化学
磷酸化
遗传学
基因
作者
Lin Mi,Youlei Li,Qiangling Zhang,Chen Zhao,Ying Peng,Gongshe Yang,Xueli Zheng
标识
DOI:10.1139/bcb-2014-0079
摘要
MicroRNAs (miRNAs) are novel and potent regulators in myogenesis. However, the molecular mechanisms that many miRNAs regulate myoblast proliferation and differentiation which are largely unknown. Here, we found that miR-139-5p increased during C2C12 myoblast proliferation, while presenting an inverse trend during C2C12 myoblast differentiation. Flow cytometry and EdU incorporation assay showed that miR-139-5p slowed down the growth of C2C12 cells. Additional study demonstrated that ectopic introduction of miR-139-5p into C2C12 cells blocked myoblast differentiation. Importantly, we demonstrated for the first time that Wnt1, which is associated with the Wnt/β-catenin signaling pathway, was a direct target of miR-139-5p. Moreover, we found that the expression level of Wnt1 was suppressed significantly (p < 0.01) by miR-139-5p, which triggered inhibition of Wnt/β-catenin signaling through upregulation of glycogen synthase kinase 3 beta (GSK-3β; p < 0.05) and downregulation of p-GSK-3β (p < 0.01), β-catenin (p < 0.05), and nuclear β-catenin (p < 0.01). Taken together, these results suggest that miR-139-5p is an important negative regulator in myogenesis through blocking the Wnt1-mediated Wnt/β-catenin signaling pathway.
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