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Interleukin-13 but Not Indomethacin Increases Cysteinyl-Leukotriene Synthesis in Human Lung Macrophages

机译:白介素13而不是吲哚美辛增加人肺巨噬细胞中的半胱氨酸-白三烯合成。

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摘要

Aspirin-exacerbated respiratory disease (AERD) is associated with constitutively elevated synthesis of bronchoconstrictor cysteinyl-leukotrienes, associated with increased expression of leukotriene (LT)C4 synthase and Th2 cytokines and airway eosinophilia. We examined whether interleukin-13 can increase LTC4 synthase gene transcription and cysteinyl-leukotriene synthesis in macrophages isolated from resected human lung tissue and whether an NSAID (indomethacin) can trigger further cysteinyl-leukotriene synthesis in these cells. Overnight culture of human lung macrophages with IL-13 (10 ng/mL) increased spontaneous and ionophore-stimulated production of cysteinyl-leukotrienes by 42% (P = 0.02) and 52% (P = 0.005), respectively, as quantified by enzyme immunoassays, but PCR gene transcription assays did not demonstrate an effect on LTC4S mRNA. The addition of indomethacin (100 μM) did not modulate cysteinyl-leukotriene production in either IL-13-treated or untreated macrophages. We conclude that while IL-13 enhances cysteinyl-leukotriene synthesis in human lung macrophages, it does not replicate the enhanced LTC4 synthase expression observed in the AERD lung nor confer sensitivity to NSAIDs.
机译:阿司匹林加剧的呼吸道疾病(AERD)与支气管收缩半胱氨酸-白三烯的组成合成升高,白三烯(LT)C4合酶和Th2细胞因子的表达增加以及气道嗜酸性粒细胞增多有关。我们检查了白细胞介素13是否可以增加从切除的人肺组织分离的巨噬细胞中LTC4合酶基因的转录和半胱氨酰-白三烯的合成,以及NSAID(吲哚美辛)是否可以触发这些细胞中进一步的半胱氨酸-白三烯的合成。通过酶定量,用IL-13(10μng/ mL)过夜培养人肺巨噬细胞,自发和离子载体刺激的半胱氨酰-白三烯生成分别增加了42%(P = 0.02)和52%(P = 0.005)。免疫测定,但PCR基因转录测定未证明对LTC4S mRNA有影响。吲哚美辛(100μm)的添加不能调节经IL-13处理或未经处理的巨噬细胞中半胱氨酰-白三烯的产生。我们得出的结论是,尽管IL-13增强了人类肺巨噬细胞中的半胱氨酰-白三烯合成,但它并未复制在AERD肺中观察到的增强的LTC4合酶表达,也不赋予对NSAIDs的敏感性。

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