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The Effect of Commercially Available Endodontic Cements and Biomaterials on Osteogenic Differentiation of Dental Pulp Pluripotent-Like Stem Cells

机译:市售牙髓骨水泥和生物材料对牙髓多能干细胞成骨分化的影响

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摘要

The aim of this study is to compare the osteogenic differentiation capacity of the dental pulp pluripotent-like stem cells (DPPSCs) using conditional media pretreated with ProRoot-MTA, Biodentine (BD) or the newly manufactured pure Portland cement Med-PZ (MZ). DPPSCs, isolated from human third molars, are the most relevant cell model to draw conclusions about the role of biomaterials on dental tissue regeneration. Cytotoxicity, alkaline phosphatase (ALP) activity, and calcium deposition analysis were evaluated at different differentiation time points. Gene expression of key osteogenic markers (RUNX2, Collagen I and Osteocalcin) was determined by qRT-PCR analysis. The osteogenic capacity of cells cultured in conditioned media prepared from MZ or MTA cements was comparable. BD conditioned media supported cell proliferation but failed to induce osteogenesis. Relative to controls and other cements, high osteogenic gene expression was observed in cultures pre-treated with the novel endodontic cement MZ. In conclusion, the in vitro behavior of a MZ- endodontic cement was evaluated, showing similar enhanced cell proliferation compared to other commercially available cements but with an enhanced osteogenic capacity with prospective potential as a novel cement for endodontic treatments.
机译:这项研究的目的是比较使用ProRoot-MTA,Biodentine(BD)或新生产的纯硅酸盐水泥Med-PZ(MZ)预处理的条件培养基对牙髓多能样干细胞(DPPSC)的成骨分化能力。 。从人类第三颗磨牙中分离出的DPPSC是最相关的细胞模型,可得出有关生物材料在牙齿组织再生中的作用的结论。在不同的分化时间点评估细胞毒性,碱性磷酸酶(ALP)活性和钙沉积分析。通过qRT-PCR分析确定关键成骨标记物(RUNX2,胶原蛋白I和骨钙蛋白)的基因表达。在由MZ或MTA水泥制备的条件培养基中培养的细胞的成骨能力是可比的。 BD条件培养基支持细胞增殖,但不能诱导成骨。相对于对照组和其他骨水泥,在用新型牙髓骨水泥MZ预处理的培养物中观察到了高成骨基因表达。总之,评价了MZ-牙髓牙本质水泥的体外行为,与其他市售牙骨水泥相比,显示出相似的增强的细胞增殖,但具有增强的成骨能力,具有作为牙髓治疗新水泥的潜力。

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