miR-142-3p promotes osteoblast differentiation by modulating Wnt signaling

被引:80
|
作者
Hu, Weihua [1 ]
Ye, Yaping [1 ]
Zhang, Weikai [1 ]
Wang, Jiang [1 ]
Chen, Anmin [1 ]
Guo, Fengjing [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Orthoped, Wuhan 430030, Peoples R China
关键词
miR-142-3p; Wnt; APC; osteoblast; differentiation; STEM-CELLS; MICRORNA-142-3P; REGULATORS; EXPRESSION;
D O I
10.3892/mmr.2012.1207
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Canonical Wnt signaling is critical for the control of osteoblast differentiation in human mesenchymal stem cells. MicroRNAs (miRs) are essential regulators of cell differentiation by post-transcriptional regulation of target gene expression. The aim of the present study was to investigate the molecular mechanism by which miR-142-3p promotes osteoblastic differentiation. using the human fetal osteoblastic 1.19 (hFOB1.19), real-time PCR and western blot analysis. Results showed an increased expression of miR-142-3p during osteoblast differentiation in the mesenchymal precursor cell line, hFOB1.19. In addition, the ectopic overexpression of miR-142-3p promoted hFOB1.19 differentiation, whereas the inhibition of miR-142-3p repressed differentiation. The expression of miR-142-3p was positively correlated with P-catenin, an important protein in Wnt signaling. The adenomatous polyposis coli (APC) gene was a direct target of miR-142-3p, whereby miR-142-3p promoted Wnt signaling through inhibition of APC, leading to accumulation and nuclear translocation of p-catenin. Therefore, miR-142-3p may be an essential mediator of osteoblast differentiation and a new therapeutic strategy for osteogenesis disorders.
引用
收藏
页码:689 / 693
页数:5
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