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首页> 外文期刊>Journal of Periodontology >Differential production of macrophage inflammatory protein-1alpha, stromal-derived factor-1, and IL-6 by human cultured periodontal ligament and gingival fibroblasts challenged with lipopolysaccharide from P. gingivalis.
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Differential production of macrophage inflammatory protein-1alpha, stromal-derived factor-1, and IL-6 by human cultured periodontal ligament and gingival fibroblasts challenged with lipopolysaccharide from P. gingivalis.

机译:人类培养的牙周膜和牙龈成纤维细胞受到来自牙龈卟啉单胞菌的脂多糖的刺激,导致巨噬细胞炎性蛋白-1α,基质衍生因子-1和IL-6的差异产生。

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摘要

BACKGROUND: Fibroblasts are considered important cells in periodontitis. When challenged by different agents, they respond through the release of cytokines that participate in the inflammatory process. The aim of this study is to evaluate and compare the expression and production of macrophage inflammatory protein (MIP)-1alpha, stromal-derived factor (SDF)-1, and interleukin (IL)-6 by human cultured periodontal ligament and gingival fibroblasts challenged with lipopolysaccharide (LPS) from Porphyromonas gingivalis. METHODS: Fibroblasts were cultured from biopsies of gingival tissue and periodontal ligament of the same donors and used on the fourth passage. After confluence in 24-well plates, the culture medium alone (control) or with 0.1 to 10 microg/ml of LPS from P. gingivalis was added to the wells, and after 1, 6, and 24 hours, the supernatant and the cells were collected and analyzed by enzyme-linked immunosorbent assay and real-time polymerase chain reaction, respectively. RESULTS: MIP-1alpha, SDF-1, and IL-6 protein production was significantly greater in gingival fibroblasts compared to periodontal ligament fibroblasts. IL-6 was upregulated in a time-dependent manner, mainly in gingival fibroblasts (P <0.05), which secreted more MIP-1alpha in the lowest concentration of LPS used (0.1 microg/ml). In contrast, a basal production of SDF-1 that was inhibited with the increase of LPS concentration was detected, especially after 24 hours (P <0.05). CONCLUSION: The distinct ability of the gingival and periodontal ligament fibroblasts to secrete MIP-1alpha, SDF-1, and IL-6 emphasizes that these cells may differently contribute to the balance of cytokines in the LPS-challenged periodontium.
机译:背景:成纤维细胞被认为是牙周炎中的重要细胞。当受到不同药剂的挑战时,它们通过参与炎症过程的细胞因子释放而作出反应。这项研究的目的是评估和比较人类培养的牙周膜和牙龈成纤维细胞对巨噬细胞炎性蛋白(MIP)-1alpha,基质衍生因子(SDF)-1和白介素(IL)-6的表达和产生与牙龈卟啉单胞菌的脂多糖(LPS)结合使用。方法:从相同供体的牙龈组织和牙周膜活检组织中培养成纤维细胞,并在第四次传代中使用。在24孔板中汇合后,将单独的培养基(对照)或含有0.1至10微克/毫升的来自齿龈假单胞菌的LPS的培养基添加到孔中,并在1、6和24小时后添加上清液和细胞分别通过酶联免疫吸附测定和实时聚合酶链反应进行分析。结果:与牙周膜成纤维细胞相比,牙龈成纤维细胞中MIP-1alpha,SDF-1和IL-6蛋白的产量明显更高。 IL-6以时间依赖性方式上调,主要是在牙龈成纤维细胞中(P <0.05),其在使用的最低LPS浓度(0.1 microg / ml)中分泌更多的MIP-1alpha。相反,检测到SDF-1的基础生成随LPS浓度的增加而受到抑制,尤其是在24小时后(P <0.05)。结论:牙龈和牙周膜成纤维细胞分泌MIP-1α,SDF-1和IL-6的独特能力强调了这些细胞可能在LPS挑战的牙周组织中平衡细胞因子。

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