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MiR-144-3p regulates osteogenic differentiation and proliferation of murine mesenchymal stem cells by specifically targeting Smad4

机译:MiR-144-3p通过特异性靶向Smad4调节鼠间充质干细胞的成骨分化和增殖

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Despite extensive research on osteoblast differentiation and proliferation in mesenchymal stem cells (MSCs), the accurate mechanism remains to be further elucidated. MicroRNAs have been reported to be key regulators of osteoblast differentiation and proliferation. Here, we found that miR-144-3p is down-regulated during osteoblast differentiation of C3H10T1/2 cells. Overexpression of miR-144-3p inhibited osteogenic differentiation, whereas inhibition of miR-144-3p reversed this process. Furthermore, miR-144-3p inhibited the proliferation of C3H10T1/2 cells by arresting cells at the G0/G1 phase. Results from bioinformatics analysis, luciferase assay and western blotting demonstrated that miR-144-3p directly targeted Smad4. Additionally, Smad4 knockdown blocks the effects of miR-144-3p inhibitor. Therefore, we conclude that miR-144-3p negatively regulates osteogenic differentiation and proliferation of C3H10T1/2 cells by targeting Smad4.
机译:尽管对间充质干细胞(MSCs)中成骨细胞的分化和增殖进行了广泛的研究,但其确切机制仍有待进一步阐明。据报道,微小RNA是成骨细胞分化和增殖的关键调节剂。在这里,我们发现miR-144-3p在C3H10T1 / 2细胞的成骨细胞分化过程中被下调。 miR-144-3p的过表达抑制成骨分化,而miR-144-3p的抑制则逆转了这一过程。此外,miR-144-3p通过将细胞停在G0 / G1期来抑制C3H10T1 / 2细胞的增殖。生物信息学分析,荧光素酶测定和蛋白质印迹的结果表明,miR-144-3p直接靶向Smad4。此外,Smad4组合式阻断miR-144-3p抑制剂的作用。因此,我们得出的结论是,miR-144-3p通过靶向Smad4负调控C3H10T1 / 2细胞的成骨分化和增殖。

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