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Titanium with Nanotopography Drives Mesenchymal Stem Cells to Osteoblast Differentiation through miR-4448, -4708 and -4773 Downregulation

机译:钛具有纳米形貌通过miR-4448,-4708和-4773下调驱动间充质干细胞向成骨细胞分化

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The results showed that the Ti with nanotopography directs hMSCs differentiation toward the osteoblast lineage. In addition, we have identified 3 miRs that target SMADs and play critical role in the osteoinductive effect of this nanotopography on hMSCs. By downregulating miR-4448, -4708, and 4773, Ti with nanotopography attenuates SMAD1 and SMAD4 degradation, intensifying BMP-2 signal transduction, which stimulates osteoblast differentiation. This novel mechanism involving a miR-SMAD-BMP-2 network in the nanotopography-mediated osteoblast differentiation is a major step for developing Ti surface modifications to modulate the osseointegration process.
机译:结果表明,具有纳米形貌的Ti将hMSCs的分化导向成骨细胞谱系。此外,我们已经确定了靶向SMAD的3个miR,并且在该纳米形貌对hMSC的骨诱导作用中起着关键作用。通过下调miR-4448,-4708和4773,具有纳米形貌的Ti可以减弱SMAD1和SMAD4的降解,从而增强BMP-2信号转导,从而刺激成骨细胞的分化。在纳米形貌介导的成骨细胞分化中涉及miR-SMAD-BMP-2网络的这一新机制是开发Ti表面修饰以调节骨整合过程的重要步骤。

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