首页> 外文期刊>Infection and immunity >Lipopolysaccharides of Bacteroides intermedius (Prevotella intermedia) and Bacteroides (Porphyromonas) gingivalis induce interleukin-8 gene expression in human gingival fibroblast cultures.
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Lipopolysaccharides of Bacteroides intermedius (Prevotella intermedia) and Bacteroides (Porphyromonas) gingivalis induce interleukin-8 gene expression in human gingival fibroblast cultures.

机译:中间细菌拟杆菌(中间细菌)和牙龈拟杆菌细菌(脂细菌)的脂多糖诱导人牙龈成纤维细胞培养物中白介素8基因的表达。

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Lipopolysaccharides (LPS) prepared from Bacteroides intermedius (Prevotella intermedia) and Bacteroides (Porphyromonas) gingivalis by hot phenol-water extraction induced interleukin-8 (IL-8) mRNA in normal human gingival fibroblast cultures, as demonstrated by Northern (RNA) blot analysis. IL-8 mRNA levels began to increase after a 2-h exposure, reached a maximum after 12 h, and then dropped to the unstimulated level at 48 h. IL-8 mRNA levels were also enhanced in a dose-dependent manner. By contrast, LPS specimens from various Salmonella species with S and R chemotypes and bacterial [corrected] and synthetic lipid A preparations did not increase IL-8 mRNA levels in fibroblasts. Although recombinant human IL-1 alpha induced IL-8 mRNA expression in fibroblast cultures, an antiserum to recombinant human IL-1 alpha did not decrease the IL-8 mRNA accumulation induced by B. intermedius LPS. Fibroblasts primed with natural human gamma interferon (IFN-gamma) expressed higher IL-8 mRNA levels upon stimulation with B. intermedius LPS, but not with Salmonella LPS, compared with nontreated cells. Natural human IFN-beta exhibited a similar priming effect on the fibroblasts, and antiserum to IFN-beta added to the cultures together with B. intermedius LPS decreased the IL-8 mRNA levels. Therefore, endogenous IFN-beta enhanced IL-8 mRNA production in response to B. intermedius LPS in fibroblasts.
机译:如Northern(RNA)印迹分析所示,在正常人牙龈成纤维细胞培养物中,通过热酚水提取从中间拟杆菌(Prevotella intermediaius)和牙龈拟杆菌(Porphyromonas)牙龈杆菌制备的脂多糖(LPS)诱导了白细胞介素8(IL-8)mRNA。 。 IL-2 mRNA水平在暴露2小时后开始增加,在12 h后达到最大值,然后在48 h降至未刺激水平。 IL-8 mRNA水平也以剂量依赖性方式增加。相比之下,来自不同沙门氏菌属的具有S和R化学型以及细菌[校正]和合成脂质A制剂的LPS标本不会增加成纤维细胞中IL-8 mRNA的水平。尽管重组人IL-1α诱导了成纤维细胞培养物中IL-8 mRNA的表达,但针对重组人IL-1α的抗血清并没有减少中间芽孢杆菌LPS诱导的IL-8 mRNA积累。与未经处理的细胞相比,用中间人双歧杆菌LPS刺激但用沙门氏菌LPS刺激的天然人γ干扰素(IFN-γ)引发的成纤维细胞表达更高的IL-8 mRNA水平。天然人IFN-β对成纤维细胞表现出类似的启动作用,并且与中间芽孢杆菌LPS一起添加到培养物中的IFN-β抗血清降低了IL-8 mRNA水平。因此,内源性IFN-β在成纤维细胞中响应中间芽孢杆菌LPS增强了IL-8 mRNA的产生。

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