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Synergistic Effects of BMP9 and miR-548d-5p on Promoting Osteogenic Differentiation of Mesenchymal Stem Cells

机译:BMP9和miR-548d-5p对促进间充质干细胞成骨分化的协同作用

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摘要

Various stimulators have been reported to promote MSC osteogenic differentiation via different pathways such as bone morphogenetic protein 9 (BMP9) through influencing COX-2 and miR-548d-5p through targeting peroxisome proliferator-activated receptor-γ (PPARγ). Whether synergistic effects between BMP9 and miR-548d-5p existed in promoting osteogenesis from MSCs was unclear. In the study, the potential synergistic effects of BMP9 and miR-548d-5p on human MSC differentiation were investigated. Osteogenic differentiation of MSCs treated with BMP9 or miR-548d-5p was detected with multimodality of methods. The results demonstrated that BMP9 and miR-548d-5p significantly influenced COX-2 and PPARγ, respectively. BMP9 also influenced the expression of PPARγ, but no significant effect of miR-548d-5p on COX-2 was observed. When BMP9 and miR-548d-5p were combined, more potent effects on both COX-2 and PPARγ were observed than BMP9 or miR-548d-5p alone. Consistently, osteogenic analysis at different timepoints demonstrated that osteogenic genes, ALP activity, calcium deposition, OPN protein, and matrix mineralization were remarkably upregulated by BMP9/miR-548d-5p compared with BMP9 or miR-548d-5p alone, indicating the synergetic effects of BMP9 and miR-548d-5p on osteogenic differentiation of MSCs. Our study demonstrated that regulating different osteogenic regulators may be an effective strategy to promote bone tissue regeneration for bone defects.
机译:据报道,各种刺激物通过靶向过氧化物酶体增殖物激活受体-γ(PPARγ),通过影响COX-2和miR-548d-5p的不同途径,通过不同的途径促进MSC成骨分化,例如骨形态发生蛋白9(BMP9)。 BMP9和miR-548d-5p之间在促进MSCs成骨方面是否存在协同作用尚不清楚。在这项研究中,研究了BMP9和miR-548d-5p对人MSC分化的潜在协同作用。采用多模式方法检测了用BMP9或miR-548d-5p处理的MSC的成骨分化。结果表明,BMP9和miR-548d-5p分别显着影响COX-2和PPARγ。 BMP9也影响PPARγ的表达,但未观察到miR-548d-5p对COX-2的显着影响。当BMP9和miR-548d-5p结合使用时,与单独使用BMP9或miR-548d-5p相比,对COX-2和PPARγ的作用更强。一致地,在不同时间点的成骨分析表明,与单独使用BMP9或miR-548d-5p相比,BMP9 / miR-548d-5p显着上调了成骨基因,ALP活性,钙沉积,OPN蛋白和基质矿化,表明了协同作用BMP9和miR-548d-5p对MSCs成骨分化的影响我们的研究表明,调节不同的成骨调节剂可能是促进骨缺损的骨组织再生的有效策略。

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