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Periodontal Ligament Stem Cells Modulate Root Resorption of Human Primary Teeth via Runx2 Regulating RANKL/OPG System

机译:牙周膜干细胞通过Runx2调节RANKL / OPG系统调节人乳牙的根吸收

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摘要

Physiological primary teeth exfoliation is a normal phenomenon during teeth development. However, retained primary teeth can often be observed in the patients with cleidocranial dysplasia (CCD) caused by mutation of Runx2. The potential regulative mechanism is still unknown. In the present study, periodontal ligament stem cells (PDLSCs) were derived from different resorbed stages of primary teeth and permanent teeth from normal patients and primary teeth from CCD patient. The proliferative, osteogenic and osteoclast-inductive capacities of PDLSCs from each group were detected. We demonstrated here that the proliferative ability of PDLSCs was reduced while the osteogenic and the osteoclast-inductive capacity of PDLSCs were enhanced during root resorption. The results also showed that PDLSCs from permanent teeth and CCD patient expressed low level of Runx2 and RANKL while high level of OPG. However, expression of Runx2 and RANKL were increased while expression of OPG was decreased in PDLSCs derived from resorbed teeth. Furthermore, Runx2 regulating the expression of RANKL and OPG and the osteoclast-inductive capacity of PDLSCs were confirmed by gain or loss of function assay. These data suggest that PDLSCs promote osteoclast differentiation via Runx2 upregulating RANKL and downregulating OPG, leading to enhanced root resorption that results in physiological exfoliation of primary teeth.
机译:生理性乳牙脱落是牙齿发育过程中的正常现象。但是,由于Runx2突变引起的颅骨发育不良(CCD)患者通常可以观察到保留的乳牙。潜在的调节机制仍然未知。在本研究中,牙周膜干细胞(PDLSCs)来自正常患者的乳牙和恒牙以及CCD患者的乳牙的不同吸收阶段。检测了每组中PDLSC的增殖,成骨和破骨细胞诱导能力。我们在这里证明了PDLSCs的增殖能力降低,而在根吸收过程中PDLSCs的成骨能力和破骨细胞诱导能力得到增强。结果还显示,来自恒牙和CCD患者的PDLSCs的Runx2和RANKL的水平较低,而OPG的水平较高。然而,Runx2和RANKL的表达增加,而OPG的表达在源自吸收牙齿的PDLSC中降低。此外,通过获得或丧失功能测定证实了调节RANKL和OPG表达的PDxSC的Runx2和破骨细胞诱导能力。这些数据表明PDLSC通过Runx2上调RANKL和下调OPG促进破骨细胞分化,从而导致牙根吸收增强,从而导致乳牙的生理脱落。

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