Chinese Journal of Tissue Engineering Research ›› 2013, Vol. 17 ›› Issue (28): 5108-5112.doi: 10.3969/j.issn.2095-4344.2013.28.002

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miR-376b-3p promotes Runx2-induced early osteogenic differentiation of C2C12 cells

Geng Qian-qian1, Yu Shou-he1, Zhang Yue1, 2, Wang Hong-mei1, Sun Fen-yong1, 2   

  1. 1Institute of Bioengineering, Jinan University, Guangzhou  510632, Guangdong Province, China;
    2Tenth People’s Hospital of Tongji University, Shanghai  200072, China
  • Online:2013-07-09 Published:2013-07-09
  • Contact: Sun Fen-yong, Doctor, Doctoral supervisor, Institute of Bioengineering, Jinan University, Guangzhou, 510632, Guangdong Province, China; Tenth People’s Hospital of Tongji University, Shanghai 200072, China sunfenyong@263.net
  • About author:Geng Qian-qian, Master, Institute of Bioengineering, Jinan University, Guangzhou 510632, Guangdong Province, China mimiqianqian@126.com
  • Supported by:

    the National Natural Science Foundation of China, No. 81071524*

Abstract:

BACKGROUND: The transcription factor Runx2 is the key factor that regulates osteogenic differention and bone development. It has been reported that the C2C12 mesenchymal cells can be induced to differentiate into osteoblasts by Runx2 overexpression, but the molecular mechanism of induction is still largely unclear.

OBJECTIVE: To investigate the role of the members of the miR-376 family during Runx2-induced osteogenic differentiation in C2C12 cells.

METHODS: The expression of the members of the miR-376 family was detected by real-time quantitative PCR at different time points using C2C12/Runx2Dox sub-line with conditional Runx2 expression. In miR-376b-3p-transfected C2C12/Runx2Dox cells, the expression of osteoblast markers, such as alkaline phosphatase and osteocalcin, was detected by real-time quantitative PCR, and the alkaline phosphatase activity was also examined by alkaline phosphatase staining. The putative miR-376b-3p targets were commonly predicted by online tools (miRanda, miRWalk and TargetScan). The functional classification of these putative targets was performed by DAVID Bioinformatics Resources database.

RESULTS AND CONCLUSION: The expression of miR-376b-3p was significantly increased during Runx2-induced osteogenic differentiation of C2C12 cells, but the expression of other members was not changed. Transfection of miR-376b-3p mimic upregulated alkaline phosphatase expression, but had no effect on osteocalcin expression. The alkaline phosphatase activity was also increased by transfection of miR-376b-3p. The functional classification of miR-376b-3p putative targets showed that miR-376b-3p is involved in the skeleton development, indicating the role of miR-376b-3p in osteoblast differentiation. Taken together, these results suggest that Runx2promotes early osteogenic differentiation in C2C12 cells by regulating the expression of genes related to osteogenic differentiation through upregulation of miR-376b-3p.

Key words: tissue construction, bone tissue construction, Runx2, C2C12 cells, miR-376b-3p, osteogenic differentiation, doxycycline, National Natural Science Foundation of China

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