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首页> 外文期刊>Stem cells international >Foxc2 and BMP2 Induce Osteogenic/Odontogenic Differentiation and Mineralization of Human Stem Cells from Apical Papilla
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Foxc2 and BMP2 Induce Osteogenic/Odontogenic Differentiation and Mineralization of Human Stem Cells from Apical Papilla

机译:Foxc2和BMP2诱导根尖乳头的人干细胞成骨/成牙分化和矿化。

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As a transcription factor regulated by bone morphogenetic protein 2 (BMP2), Forkhead c2 (Foxc2) plays a pivot role in osteogenesis/odontogenesis. However, the role of Foxc2 and BMP2 in regulating osteo-/odontogenic differentiation and mineralization of stem cells from apical papilla (SCAP) is still uncertain. In this research, overexpression of Foxc2 gene significantly improved the proliferation of SCAP four days and eight days after transfection, but overexpression of both Foxc2 and BMP2 genes significantly inhibited the proliferation of SCAP eight days after transfection. RT-qPCR and western blot results indicated that SCAP-Foxc2-BMP2 significantly upregulated osteo-/odontogenic genes and proteins at most of the time points in SCAP after transfection. Moreover, SCAP-Foxc2-BMP2 formed notably more alkaline phosphatase-positive and alizarin red-positive mineralized nodules than other three group cells sixteen days after transfection. In conclusion, our findings revealed that Foxc2 and BMP2 synergistically promoted osteo-/odontogenic differentiation and mineralization of SCAP in vitro.
机译:作为受骨形态发生蛋白2(BMP2)调控的转录因子,叉头c2(Foxc2)在成骨/成牙作用中起着关键作用。然而,Foxc2和BMP2在调节根尖乳头(SCAP)干细胞的骨/牙源性分化和矿化中的作用仍然不确定。在这项研究中,Foxc2基因的过表达显着改善了转染后4天和8天SCAP的增殖,但Foxc2和BMP2基因的过表达均显着抑制了转染后8天SCAP的增殖。 RT-qPCR和蛋白质印迹结果表明,SCAP-Foxc2-BMP2在转染后的大多数时间都显着上调了骨/牙源性基因和蛋白质。此外,转染十六天后,SCAP-Foxc2-BMP2形成的碱性磷酸酶阳性和茜素红阳性矿化结节明显多于其他三组细胞。总之,我们的发现表明,Foxc2和BMP2在体外协同促进SCAP的骨/牙源性分化和矿化。

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