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Effects of Different Calcium Silicate Cements on the Inflammatory Response and Odontogenic Differentiation of Lipopolysaccharide-Stimulated Human Dental Pulp Stem Cells

机译:不同硅酸钙水泥对脂多糖刺激人牙髓干细胞炎性反应和牙源性分化的影响

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摘要

This study aimed to analyze the effects of different calcium silicate cements (CSCs) on the inflammatory response and odontogenic differentiation of lipopolysaccharide-stimulated human dental pulp stem cells. Human dental pulp stem cells (hDPSCs) were stimulated with lipopolysaccharide (LPS) to induce inflammation. These LPS-induced dental pulp stem cells (LDPSCs) were cultured with ProRoot MTA, Biodentine, Retro MTA, and Dycal. Cell viability was evaluated using the Cell Counting Kit-8 assay. Interleukin (IL)-6, IL-8, and transforming growth factor (TGF)-β1 cytokine levels were assessed using the enzyme-linked immunosorbent assay. The expressions of alkaline phosphatase (ALP), osteocalcin, and runt-related transcription factor 2 (RUNX2) were analyzed through real-time polymerase chain reaction. ProRoot MTA, Biodentine, and Retro MTA did not significantly decrease the cell viability of LDPSCs for up to 48 h (p < 0.05). Retro MTA significantly decreased the expression of IL-6 and IL-8 by LDPSCs. ProRoot MTA and Biodentine significantly reduced TGF-β expression by LDPSCs (p < 0.05). Regarding odontogenic differentiation, all CSCs had no effect on ALP expression but increased the production of RUNX2 at 12 h.
机译:这项研究旨在分析不同的硅酸钙水泥(CSCs)对脂多糖刺激的人牙髓干细胞的炎症反应和牙源性分化的影响。用脂多糖(LPS)刺激人牙髓干细胞(hDPSCs)以诱导炎症。将这些LPS诱导的牙髓干细胞(LDPSC)与ProRoot MTA,Biodentine,Retro MTA和Dycal培养。使用Cell Counting Kit-8测定法评估细胞活力。使用酶联免疫吸附试验评估白介素(IL)-6,IL-8和转化生长因子(TGF)-β1细胞因子水平。通过实时聚合酶链反应分析了碱性磷酸酶(ALP),骨钙素和矮子相关转录因子2(RUNX2)的表达。 ProRoot MTA,Biodentine和Retro MTA在长达48小时内均未显着降低LDPSCs的细胞活力(p <0.05)。 Retro MTA明显降低了LDPSCs的IL-6和IL-8的表达。 ProRoot MTA和Biodentine明显降低了LDPSC的TGF-β表达(p <0.05)。关于牙源性分化,所有CSC对ALP表达均无影响,但在12 h时增加了RUNX2的产生。

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