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An evaluation of the inflammatory response of lipopolysaccharide-treated primary dental pulp cells with regard to calcium silicate-based cements

机译:脂多糖处理的初级牙髓细胞对硅酸钙基水泥的炎性反应评估

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摘要

This study compared the biological changes of lipopolysaccharide (LPS)-treated dental pulp (DP) cells directly cultured on mineral trioxide aggregate (MTA) and calcium silicate (CS) cements. DP cells were treated with LPS for 24 h. Then, the LPS-treated DP cells were cultured on MTA or CS cements. Cell viability, cell death mechanism and interleukin (IL)-1β expressions were analysed. A one-way analysis of variance was used to evaluate the significance of the differences between the means. A significantly higher IL-1β expression (2.9-fold) was found for LPS-treated cells (P<0.05) compared with DP cells without LPS treatment at 24 h. Absorbance values of LPS-treated cells cultured on CS cement were higher than a tissue culture plate. A significant difference (P<0.05) in cell viability was observed between cells on CS and MTA cements 24 h after seeding. At 48 h, a high concentration of Si (5 mM) was released from MTA, which induced LPS-treated DP cell apoptosis. The present study demonstrates that CS cement is biocompatible with cultured LPS-treated DP cells. MTA stimulates inflammation in LPS-treated DP cells, which leads to greater IL-1β expression and apoptosis.
机译:这项研究比较了用脂多糖(LPS)处理的牙髓(DP)细胞在三氧化二矿骨料(MTA)和硅酸钙(CS)水泥上直接培养的生物学变化。用LPS处理DP细胞24小时。然后,将经LPS处理的DP细胞培养在MTA或CS水泥上。分析细胞活力,细胞死亡机制和白介素(IL)-1β表达。使用单向方差分析来评估均值之间差异的显着性。与未经LPS处理的DP细胞在24小时相比,经LPS处理的细胞的IL-1β表达明显更高(2.9倍)(P <0.05)。在CS水泥上培养的LPS处理的细胞的吸光度值高于组织培养板。播种后24小时,在CS和MTA水泥上的细胞之间观察到细胞活力的显着差异(P <0.05)。在48小时时,MTA释放出高浓度的Si(5 mM),这诱导了LPS处理的DP细胞凋亡。本研究表明CS水泥与培养的LPS处理的DP细胞具有生物相容性。 MTA刺激LPS处理的DP细胞中的炎症,从而导致更高的IL-1β表达和细胞凋亡。

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