Ohgawara Toshihiro, Kubota Satoshi, Kawaki Harumi, Kondo Seiji, Eguchi Takanori, Kurio Naito, Aoyama Eriko, Sasaki Akira, Takigawa Masaharu
Department of Biochemistry and Molecular Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, 700-8525, Japan.
FEBS Lett. 2009 Mar 18;583(6):1006-10. doi: 10.1016/j.febslet.2009.02.025. Epub 2009 Feb 20.
We searched for miRNAs that were down-regulated in chondrocytic cells and predicted to target CCN2/connective tissue growth factor (CCN2/CTGF) that promotes endochondral ossification. Among them, expression of miR-18a was most strongly repressed in chondrocytic cells. Reporter gene analysis confirmed the functionality of an miR-18a target in the 3'-untranslated region of Ccn2 mRNA, which was predicted in silico. Indeed, introduction of miR-18a efficiently repressed the CCN2 production from chondrocytic cells. Finally, transfected miR-18a significantly repressed the mature chondrocytic phenotype. Our present study revealed a regulatory role for miR-18a in chondrocytic differentiation through CCN2.
我们寻找了在软骨细胞中表达下调且预测可靶向促进软骨内成骨的CCN2/结缔组织生长因子(CCN2/CTGF)的微小RNA(miRNA)。其中,miR-18a在软骨细胞中的表达受到的抑制最为强烈。报告基因分析证实了计算机预测的Ccn2 mRNA 3'-非翻译区中miR-18a靶标的功能。实际上,导入miR-18a可有效抑制软骨细胞产生CCN2。最后,转染的miR-18a显著抑制了成熟软骨细胞表型。我们目前的研究揭示了miR-18a通过CCN2在软骨细胞分化中的调节作用。