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MicroRNA-27 promotes the differentiation of odontoblastic cell by targeting APC and activating Wnt/β-catenin signaling

机译:MicroRNA-27通过靶向APC并激活Wnt /β-catenin信号传导来促进牙本质成骨细胞的分化

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摘要

MicroRNAs (miRNAs) play an essential role in regulating cell differentiation either by inhibiting mRNA translation or by inducing its degradation. However, the role of miRNAs in odontoblastic cell differentaion is largely unknown. In the present study, we demonstrate that the expression of miR-27 was significantly increased during MDPC-23 odontoblastic cell differentiation. Furthermore, the up-regulation of miR-27 promotes the differentiation of MDPC-23 odontoblastic cells and accelerates mineralization without cell proliferation. In addition, our results of target gene prediction revealed that the mRNA of adenomatous polyposis coli (APC) associated with Wnt/β-catenin signaling pathway has miR-27 binding site in the its 3' UTR and is suppressed by miR-27. Subsequentially, the down-regulated APC by miR-27 triggered the activation of Wnt/β-catenin signaling through accumulation of β-catenin in the nucleus. Our data suggest that miR-27 promotes MDPC-23 odontoblastic cell differentiation by targeting APC and activating Wnt/β-catenin signaling. Therefore, miR-27 might be considered a critical candidate as an odontoblastic differentiation molecular target for the development of miRNA based therapeutic agents in the dental medicine.
机译:微小RNA(miRNA)通过抑制mRNA翻译或诱导其降解在调节细胞分化中起着至关重要的作用。然而,miRNA在成牙本质细胞分化中的作用尚不清楚。在本研究中,我们证明了在MDPC-23牙胚细胞分化过程中miR-27的表达显着增加。此外,miR-27的上调促进了MDPC-23牙核母细胞的分化,并加速了矿化作用而没有细胞增殖。此外,我们的靶基因预测结果表明,与Wnt /β-catenin信号通路相关的腺瘤性息肉病大肠杆菌(APC)的mRNA在其3'UTR中具有miR-27结合位点,并被miR-27抑制。随后,miR-27对APC的下调触发了Wnt /β-catenin信号在细胞核中的积累,从而激活了Wnt /β-catenin信号。我们的数据表明,miR-27通过靶向APC并激活Wnt /β-catenin信号传导来促进MDPC-23牙胚细胞的分化。因此,miR-27可能被认为是牙科医学中基于miRNA的治疗剂开发的齿质分化分子靶标的关键候选物。

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