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首页> 外文期刊>Journal of Dental Sciences >High concentrations of calcium suppress osteogenic differentiation of human periodontal ligament stem cells in?vitro
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High concentrations of calcium suppress osteogenic differentiation of human periodontal ligament stem cells in?vitro

机译:高浓度钙抑制人牙周韧带干细胞的骨质发生分化

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Background/purposePeriodontal ligament stem cells (PDLSCs)-based regeneration therapy has received attention for its potential alternative applications in hard tissue and tooth. However, the environmental diversity of oral cavity that regulates PDLSCs differentiation has made it difficult to develop. Therefore, we investigated how high calcium concentrations in the oral environment influence osteogenic differentiation of human PDLSCs (hPDLSCs).Materials and methodshPDLSCs collected from human molars were isolated and cultured with CaCl2. First, multi lineage differentiation potentials to osteogenic, chondrogenic, and adipogenic cells were investigated. Then, the effects of CaCl2on both alkaline phosphatase (ALP) activity and bone mineralization were analyzed and the expression of mRNA and protein for osteogenic marker was explored. Further, luciferase assay was performed to evaluate CaCl2could regulate the transcriptional activity on osteogenic differentiation in hPDLSCsResultsCaCl2treatment at normal to high concentrations showed similar suppression of ALP activity, while mineralized nodule formation was decreased by CaCl2treatment dose-dependently without affecting proliferation or cytotoxicity in hPDLSCs. We also observed that CaCl2treatment repressed the mRNA expression and protein abundance of osteogenic genes and transcriptional factors. Notably, repression of the Runx2 level was significant, and CaCl2treatment inhibited Runx2-mediated transcriptional activity on the osteoblast-specific element (OSE) and ALP promoters.ConclusionHigh concentrations of calcium negatively regulate osteogenic differentiation of hPDLSCs, by repressing osteogenic gene expressions and transcriptional activity. Therefore, these conditions may be applicable to determine the physiologically appropriate concentration of calcium.
机译:背景/ putposeperiodontal韧带干细胞(PDLSCs)基于硬组织和牙齿的潜在替代应用受到关注。然而,调节PDLSCS分化的口腔的环境多样性使得难以发展。因此,我们调查了口腔环境中的高钙浓度如何影响人PDLSCs(HPDLSCs)的骨质发生分化。与人臼齿收集的材料和方法分离,并用CaCl 2培养。首先,研究了对骨质发生,软骨形成和脂肪细胞的多谱系分化电位。然后,分析了CaCl2ON碱性磷酸酶(ALP)活性和骨矿化的影响,探讨了骨质发生标记的mRNA和蛋白质的表达。此外,进行荧光素酶测定以评估CaCl2could在正常到高浓度下调节HPDLSCsresultscacl2中的转录活性在HPDLSCsresultscacl2中的转录活性显示出类似的ALP活性的抑制,而CaCl2处理剂量依赖性降低矿化结节形成而不会影响HPDLSC中的增殖或细胞毒性。我们还观察到CaCl2Treatment抑制了骨质发生基因和转录因子的mRNA表达和蛋白质。值得注意的是,RUNX2水平的抑制是显着的,CaCl2治疗抑制了对成骨细胞特异性元素(OSE)和ALP启动子的Runx2介导的转录活性。结论高浓度,通过抑制成骨基因表达和转录活性调节HPDLSC的骨质发生分化。因此,这些条件可能适用于确定生理学上适当的钙浓度。

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