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Induction of DNA double-strand breaks in primary gingival fibroblasts by exposure to dental resin composites.

机译:通过暴露于牙科树脂复合材料,在原发性牙龈成纤维细胞中诱导DNA双链断裂。

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Dental resin composites and their reactive monomers/co-monomers have been shown to elicit cytotoxic responses in human gingival fibroblasts (HGF), and their metabolic radical intermediates have the potential to attack the DNA backbone, which may induce DNA double-strand breaks (DSBs). In this study we have tested the cytotoxicity and induction of DSBs by the most common composite resin monomers/co-monomers: BisGMA, HEMA, TEGDMA, and UDMA in gingival fibroblasts using the sensitive gamma-H2AX DNA repair focus assay. Our results show increasing monomer cytotoxicities in the order of BisGMA>UDMA>TEGDMA>HEMA, an order that was also observed for their capacity to induce DSBs. BisGMA at the EC50 concentration of 0.09 mm evoked the highest rate of gamma-H2AX foci-formation that was 11-fold higher DNA DSBs as compared to the negative controls that ranged between 0.25 and 0.5gamma-H2AX foci/HGF cell. Our results for the first time show that exposure to dental resin monomers can induce DSBs in primary human oral cavity cells, which underscores their genotoxic capacity.
机译:牙科树脂复合材料及其反应性单体/共聚单体已显示出可引发人牙龈成纤维细胞(HGF)的细胞毒性反应,其代谢自由基中间体可能会攻击DNA主链,从而可能诱导DNA双链断裂(DSBs)。 )。在这项研究中,我们使用敏感的γ-H2AXDNA修复焦点测定法测试了牙龈成纤维细胞中最常见的复合树脂单体/共聚单体:BisGMA,HEMA,TEGDMA和UDMA对DSB的细胞毒性和诱导作用。我们的结果表明,单体细胞毒性以BisGMA> UDMA> TEGDMA> HEMA的顺序增加,也观察到它们诱导DSBs的能力。 ECs浓度为0.09 mm的BisGMA引起的最高的γ-H2AX灶形成速率是DNA DSB的11倍,而阴性对照的范围为0.25至0.5γ-H2AX灶/ HGF细胞。我们的结果首次显示,暴露于牙科树脂单体可以诱导人口腔细胞中的DSB,从而增强了它们的遗传毒性。

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