Huang Ke, Fu Jingshu, Zhou Wei, Li Wei, Dong Shiwu, Yu Shengpeng, Hu Zongkai, Wang Huaqing, Xie Zhao
National & Regional United Engineering Laboratory of Tissue Engineering, Department of Orthopaedics, Southwest Hospital, Third Military Medical University, Chongqing, China.
Department of Biomedical Materials Science, School of Biomedical Engineering, Third Military Medical University, Chongqing 400038, China.
Biochimie. 2014 Jul;102:47-55. doi: 10.1016/j.biochi.2014.02.005. Epub 2014 Feb 20.
Differentiation of mesenchymal stem cells (MSCs) into a specific lineage is firmly and precisely regulated via crucial transcription factors and signaling cascades, but the accurate mechanisms still need to be revealed. MicroRNAs (miRNA) negativity regulates the target mRNA protein synthesis to regulate various kinds of biological processes. In the present study we investigate miRNAs mediated regulatory mechanisms of osteoblastic differentiation in C3H10T1/2 cells and we identified that the level of miR-125b expression was obviously decreased compared with undifferentiated ones during differentiation process. Subsequently, dual-luciferase reporter gene assay data demonstrated that miR-125b targets a putative binding site in the 3'-UTR of Cbfβ gene, a key transcription factor for osteogenesis. We observed over and interferential expression of miR-125b down-regulate for Cbfβ protein in C3H10T1/2 cells and the over-expression decrease the mRNA levels of three osteoblastic marker genes, alkaline phosphatase (ALP), osteocalcin (OCN), osteopontin (OPN) by BMP-2-induced, whereas, anti-miR-125b increased the expression of these marker genes and hence up-regulated mRNA levels of Cbfβ. It is concluded from the result that miR-125b is a key regulatory factor of osteoblastic differentiation by directly targeting Cbfβ and indirectly acting on Runx2 at an early stage osteoblastic differentiation.
间充质干细胞(MSCs)向特定谱系的分化通过关键转录因子和信号级联反应受到严格且精确的调控,但其确切机制仍有待揭示。微小RNA(miRNA)通过负向调控靶mRNA的蛋白质合成来调节各种生物学过程。在本研究中,我们探究了miRNA介导的C3H10T1/2细胞成骨分化调控机制,并且我们发现在分化过程中,与未分化细胞相比,miR-125b的表达水平明显降低。随后,双荧光素酶报告基因检测数据表明,miR-125b靶向成骨关键转录因子Cbfβ基因3'-UTR中的一个假定结合位点。我们观察到,在C3H10T1/2细胞中,miR-125b的过表达和干扰表达下调了Cbfβ蛋白,并且过表达降低了BMP-2诱导的三个成骨标记基因碱性磷酸酶(ALP)、骨钙素(OCN)、骨桥蛋白(OPN)的mRNA水平,而抗miR-125b则增加了这些标记基因的表达,从而上调了Cbfβ的mRNA水平。从结果得出结论,miR-125b是成骨分化的关键调控因子,它通过直接靶向Cbfβ并在成骨分化早期间接作用于Runx2来发挥作用。