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The effect of an interleukin receptor antagonist (IL-1ra) on colonocyte eicosanoid release

机译:白介素受体拮抗剂(IL-1ra)对结肠细胞类花生酸释放的影响

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摘要

We investigated whether an interleukin 1 receptor antagonist (IL-1ra) altered cellular release of prostanoids and leukotrienes in a transformed colonic cell line (CACO-2) in the presence of proinflammatory stimuli. Cellular inflammation was induced by treatment with lipopolysaccharide (LPS) or the cytokine, interleukin 1 beta (IL-1β). In a separate set of experiments, cells were pretreated with IL-1ra prior to exposure to LPS or IL-1β. Prostaglandin E2 and leukotriene B4 (LTB4) levels were quantified by ELISA assays. Both LPS and IL-1β exposure were noted to stimulate cellular PGE2 release, a response which was significantly inhibited by IL-1ra treatment. Either stimulant when administered alone failed to stimulate release of LTB4. When administered after IL-1ra pretreatment however, both stimuli caused a significant increase in LTB4 release. These results suggest that a cytokine receptor antagonist can selectively influence eicosanoid production in this cell line. Furthermore, this study suggests that a IL-1ra may have a future clinical role in the treatment of inflammatory disorders of the colon which are intimately linked to enhanced eicosanoid synthesis.
机译:我们调查了白细胞介素1受体拮抗剂(IL-1ra)是否在促炎性刺激存在的情况下改变了转化结肠细胞系(CACO-2)中前列腺素和白三烯的细胞释放。通过用脂多糖(LPS)或细胞因子白介素1β(IL-1β)治疗诱导细胞炎症。在另一组实验中,在暴露于LPS或IL-1β之前,先用IL-1ra预处理细胞。前列腺素E2和白三烯B4(LTB4)的水平通过ELISA分析进行定量。 LPS和IL-1β暴露均可刺激细胞PGE2释放,IL-1ra治疗可显着抑制这种反应。单独施用时,两种刺激剂均不能刺激LTB4的释放。但是,在IL-1ra预处理后给药时,两种刺激都会导致LTB4释放显着增加。这些结果表明,细胞因子受体拮抗剂可以选择性地影响该细胞系中类花生酸的产生。此外,这项研究表明,IL-1ra可能在结肠炎性疾病的治疗中具有未来的临床作用,这些疾病与增强的类花生酸合成密切相关。

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