首页> 外文期刊>International journal of molecular medicine >miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells
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miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells

机译:miR-21通过激活鼠类多系细胞中的BMP9 / Smad信号通路在成骨分化中与BMP9协同作用

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Bone morphogenetic proteins?(BMPs), particularly BMP9, have been shown to promote the osteogenic differentiation of murine multilineage cells?(MMCs) and to promote bone formation in bone diseases; however, the mechanisms involved remain poorly understood. MicroRNAs (miRNAs or miRs) have been proven to regulate mesenchymal stem cell?(MSC) differentiation. In this study, we identified a novel mechanism that unravels the functional axis of a key miRNA (miR-21) which contributes to BMP9?induced osteogenic differentiation. We screened differentially expressed miRNAs in MMCs during BMP9?induced osteogenic differentiation and found that miR-21 was significantly upregulated by BMP9 during the osteogenesis of MMCs. Furthermore, miR-21 was confirmed to promote the osteogenic differentiation of the MMCs by suppressing Smad7, which negatively regulates the osteogenic differentiation of MMCs. The upregulation of miR-21 may promote the osteogenic differentiation of MMCs in synergy with BMP9. The findings of our study revealed a novel function of miR-21, and suggest that the overexpression of miR-21 contributes to bone formation by promoting BMP9?induced osteogenic differentiation. Our data may provide a molecular basis for the development of novel therapeutic strategies to treat bone diseases, such as osteoporosis and other inflammatory bone diseases.
机译:骨形态发生蛋白(BMPs),特别是BMP9,已被证明能促进鼠多系细胞(MMCs)的成骨分化并促进骨骼疾病中的骨形成。但是,所涉及的机制仍然知之甚少。 MicroRNA(miRNA或miRs)已被证明可调节间充质干细胞(MSC)的分化。在这项研究中,我们确定了一种新的机制,可以揭示关键的miRNA(miR-21)的功能轴,该功能有助于BMP9?诱导的成骨分化。我们在BMP9诱导的成骨分化过程中筛选了MMCs中差异表达的miRNA,发现在MMC的成骨过程中BMP9显着上调了miR-21。此外,证实miR-21通过抑制Smad7促进MMC的成骨分化,而Smad7负调控MMC的成骨分化。 miR-21的上调可能与BMP9协同促进MMC的成骨分化。我们研究的结果揭示了miR-21的新功能,并暗示miR-21的过表达通过促进BMP9?诱导的成骨分化来促进骨形成。我们的数据可能为开发治疗骨质疏松症和其他炎症性骨病等骨病的新型治疗策略提供分子基础。

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