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Interleukin-1 beta and interleukin-8 in healthy and inflamed dental pulps

机译:健康和发炎的牙髓中的白细胞介素-1 beta和白细胞介素8

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After aggression to the dental pulp, some cells produce cytokines in order to start and control the inflammatory process. Among these cytokines, interleukin-1 beta (IL-1β) and interleukin-8 (IL-8) emerge as important ones. OBJECTIVE: The purpose of this study was to analyze the location, distribution and concentration of these cytokines in healthy and inflamed dental pulps. MATERIAL AND METHODS: Twenty pulps, obtained from healthy third molars (n=10) and from pulpectomies (n=10) were used for the study, with half of each group used for immunohistochemistry and half for protein extraction and ELISA assays. Fibroblasts obtained from healthy dental pulps, stimulated or not by Escherichia coli lipopolysaccharide (LPS), in order to simulate aggression on the cell cultures, were also used and analyzed by ELISA for IL-1β and IL-8 as complementary information. Data obtained from immunohistochemistry were qualitatively analyzed. Data obtained from ELISA assays (tissue and cells) were statistically treated by the t-test (p<0.05). RESULTS: Immunohistochemically, it was observed that inflamed pulps were strongly stained for both cytokines in inflammatory cells, while healthy pulps were not immunolabeled. ELISA from tissues quantitatively confirmed the higher presence of both cytokines. Additionally, cultured pulp fibroblasts stimulated by LPS also produce more cytokines than the control cells. CONCLUSIONS: It may be concluded that inflamed pulps present higher amounts of IL-1β and IL-8 than healthy pulps and that pulp fibroblasts stimulated by bacterial LPS produce higher levels of IL-1β and IL-8 than the control group.
机译:侵害牙髓后,一些细胞会产生细胞因子,以启动并控制炎症过程。在这些细胞因子中,白介素-1β(IL-1β)和白介素8(IL-8)成为重要的细胞因子。目的:本研究的目的是分析健康和发炎的牙髓中这些细胞因子的位置,分布和浓度。材料与方法:从健康的第三臼齿(n = 10)和从果肉切除术(n = 10)获得的二十个纸浆用于研究,每组的一半用于免疫组织化学,一半用于蛋白质提取和ELISA分析。为了模拟对细胞培养物的侵袭,还使用了从健康牙髓中获得或未受大肠杆菌脂多糖(LPS)刺激的成纤维细胞,并通过ELISA分析了IL-1β和IL-8作为补充信息。从免疫组织化学获得的数据进行定性分析。通过t检验对从ELISA分析(组织和细胞)获得的数据进行统计学处理(p <0.05)。结果:免疫组织化学观察发现,发炎的牙髓在炎症细胞中被两种细胞因子强烈染色,而健康的牙髓未进行免疫标记。来自组织的ELISA定量证实了两种细胞因子的存在率更高。另外,LPS刺激的培养的果肉成纤维细胞也比对照细胞产生更多的细胞因子。结论:可以得出结论,发炎的牙髓的IL-1β和IL-8含量高于健康牙髓,细菌LPS刺激的牙髓成纤维细胞产生的IL-1β和IL-8水平高于对照组。

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