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Effect of orthodontic forces on the osteogenic differentiation of human periodontal ligament stem cells

机译:正畸力对人牙周膜干细胞成骨分化的影响

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p class="global-para-14" pThe purpose of this study was to evaluate the effects of orthodontic forces (OF) on the proliferation and differentiation of human periodontal ligament stem cells (hPDLSCs). The experimental sample consisted of 6 premolars extracted from 2 patients. After application of OF for 1 month, the hPDLSCs were separated from the primary cultured PDL cells using magnetic-activated cell sorting. The cell proliferation rate was assessed using a 3-[45-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide assay. The hPDLSCs were cultured in osteogenic medium, and the osteogenic differentiation was analyzed on day 7 and 14 using alkaline phosphatase staining and reverse transcription polymerase chain reaction analyses. The gene expression level of osteogenic markers and angiogenic markers were measured and normalized. The results showed that the application of OF increased the proliferation rates, the expression of osteogenic factors, and the expression of angiogenic factors of hPDLSCs. These findings suggest that OF can serve as a potent positive modulator of proliferation and osteogenic differentiation of hPDLSCs./p /p
机译:class =“ global-para-14”> >本研究的目的是评估正畸力(OF)对人牙周膜干细胞(hPDLSCs)增殖和分化的影响。实验样品包括从2例患者中提取的6个前磨牙。在应用OF 1个月后,使用磁激活细胞分选法将hPDLSC与原代培养的PDL细胞分离。使用3- [45-二甲基噻唑-2-基] -2,5-二苯基溴化四氮唑测定法评估细胞增殖速率。 hPDLSCs在成骨培养基中培养,并在第7天和第14天使用碱性磷酸酶染色和逆转录聚合酶链反应分析分析成骨分化。测量并标准化成骨标记和血管生成标记的基因表达水平。结果表明,OF的应用增加了hPDLSCs的增殖速率,成骨因子的表达和血管生成因子的表达。这些发现提示OF可以作为hPDLSCs增殖和成骨分化的有效正调节剂。

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