Department of Orthopedics, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan.
Proc Natl Acad Sci U S A. 2009 Dec 8;106(49):20794-9. doi: 10.1073/pnas.0909311106. Epub 2009 Nov 20.
Growing evidence shows that microRNAs (miRNAs) regulate various developmental and homeostatic events in vertebrates and invertebrates. Osteoblast differentiation is a key step in proper skeletal development and acquisition of bone mass; however, the physiological role of non-coding small RNAs, especially miRNAs, in osteoblast differentiation remains elusive. Here, through comprehensive analysis of miRNAs expression during osteoblast differentiation, we show that miR-206, previously viewed as a muscle-specific miRNA, is a key regulator of this process. miR-206 was expressed in osteoblasts, and its expression decreased over the course of osteoblast differentiation. Overexpression of miR-206 in osteoblasts inhibited their differentiation, and conversely, knockdown of miR-206 expression promoted osteoblast differentiation. In silico analysis and molecular experiments revealed connexin 43 (Cx43), a major gap junction protein in osteoblasts, as a target of miR-206, and restoration of Cx43 expression in miR-206-expressing osteoblasts rescued them from the inhibitory effect of miR-206 on osteoblast differentiation. Finally, transgenic mice expressing miR-206 in osteoblasts developed a low bone mass phenotype due to impaired osteoblast differentiation. Our data show that miRNA is a regulator of osteoblast differentiation.
越来越多的证据表明,微小 RNA(miRNAs)在脊椎动物和无脊椎动物中调节各种发育和内稳态事件。成骨细胞分化是骨骼正常发育和获得骨量的关键步骤;然而,非编码小 RNA(尤其是 miRNAs)在成骨细胞分化中的生理作用仍不清楚。在这里,我们通过对成骨细胞分化过程中 miRNAs 表达的综合分析,表明先前被视为肌肉特异性 miRNA 的 miR-206 是该过程的关键调节因子。miR-206 在成骨细胞中表达,并在成骨细胞分化过程中表达降低。在成骨细胞中过表达 miR-206 抑制其分化,反之,下调 miR-206 的表达则促进成骨细胞分化。计算机分析和分子实验表明,间隙连接蛋白 43(Cx43),成骨细胞中的主要间隙连接蛋白,是 miR-206 的靶标,在表达 miR-206 的成骨细胞中恢复 Cx43 的表达,可挽救 miR-206 对成骨细胞分化的抑制作用。最后,在成骨细胞中表达 miR-206 的转基因小鼠由于成骨细胞分化受损而表现出低骨量表型。我们的数据表明,miRNA 是成骨细胞分化的调节因子。