Schmalz G, Schweikl H, Hiller K A
Department of Operative Dentistry and Periodontology, University of Regensburg, Germany.
Eur J Oral Sci. 2000 Oct;108(5):442-8. doi: 10.1034/j.1600-0722.2000.108005442.x.
A three-dimensional human tissue model based on TR146 cells isolated from a squamous cell carcinoma of the buccal mucosa was used to test for the release of the proinflammatory molecules prostaglandin E2 (PGE2), interleukin 6 (IL-6), and interleukin 8 (IL-8) after exposure to nickel chloride (NiCl2), cobalt chloride (COCl2), palladium chloride (PdCl2), and triethylene glycol dimethacrylate (TEGDMA). These compounds have documented adverse biological effects in vitro. The release of PGE2 from the tissue culture models was inversely correlated with cell viability (MTT assay). Toxic concentrations of NiCl2 and CoCl2 induced the release of PGE2 by factors of about 200-300 compared to controls, but PdCl2 which was nontoxic enhanced PGE2 levels about 10-fold. TEGDMA, however, did not stimulate PGE2 release. None or weakly toxic concentrations of Ni and Co chloride induced IL-6 and IL-8 release by a factor of 5-10 compared to controls. The amounts of IL-6 were induced 25- to 30-fold by PdCl2 under physiological conditions, and IL-8 levels were also slightly enhanced. Nontoxic TEGDMA concentrations induced IL-6 levels 5-fold, but IL-8 amounts increased only slightly. We conclude that a steep rise of PGE2 is closely associated with cytotoxicity. On the other hand, the specific induction of IL-6 occurs at much lower concentrations. Therefore, the measurement of this cytokine may be included as another parameter in evaluating the biological activity of dental materials under nontoxic experimental conditions in vitro.
基于从颊黏膜鳞状细胞癌中分离出的TR146细胞构建的三维人体组织模型,用于检测暴露于氯化镍(NiCl2)、氯化钴(CoCl2)、氯化钯(PdCl2)和二甲基丙烯酸三乙二醇酯(TEGDMA)后促炎分子前列腺素E2(PGE2)、白细胞介素6(IL-6)和白细胞介素8(IL-8)的释放情况。这些化合物在体外已被证明具有不良生物学效应。组织培养模型中PGE2的释放与细胞活力(MTT法)呈负相关。与对照组相比,NiCl2和CoCl2的毒性浓度使PGE2的释放增加了约200 - 300倍,但无毒的PdCl2使PGE2水平提高了约10倍。然而,TEGDMA并未刺激PGE2的释放。与对照组相比,无毒或低毒浓度的镍和钴的氯化物使IL-6和IL-8的释放增加了5 - 10倍。在生理条件下,PdCl2使IL-6的量增加了25至30倍,IL-8水平也略有升高。无毒浓度的TEGDMA使IL-6水平增加了5倍,但IL-8的量仅略有增加。我们得出结论,PGE2的急剧升高与细胞毒性密切相关。另一方面,IL-6的特异性诱导发生在低得多的浓度下。因此,在体外无毒实验条件下评估牙科材料的生物活性时,该细胞因子的测量可作为另一个参数纳入其中。