Zhang Wen, Zhang Xiaolei, Li Junyuan, Zheng Jianmao, Hu Xiaoli, Xu Meng, Mao Xueli, Ling Junqi
Guangdong Province Key Laboratory of Stomatology, Guanghua School and Hospital of Stomatology, Sun Yat-sen University, Guangzhou, Guangdong 510055, China.
The Medical Centre of Stomatology, The 1st Affiliated Hospital of Jinan University, Guangzhou 510630, China.
Stem Cells Int. 2018 Jul 25;2018:2363917. doi: 10.1155/2018/2363917. eCollection 2018.
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 .
作为一种受骨形态发生蛋白2(BMP2)调控的转录因子,叉头框c2(Foxc2)在成骨/牙胚发生中起关键作用。然而,Foxc2和BMP2在调节根尖乳头干细胞(SCAP)的成骨/牙源性分化及矿化方面的作用仍不明确。在本研究中,Foxc2基因过表达在转染后4天和8天显著促进了SCAP的增殖,但Foxc2和BMP2基因同时过表达在转染后8天显著抑制了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点显著上调了SCAP中的成骨/牙源性基因和蛋白质。此外,转染16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,我们的研究结果表明,Foxc2和BMP2协同促进了SCAP的成骨/牙源性分化及矿化。