中性粒细胞弹性蛋白酶通过Toll样受体4上调白细胞介素-8。

Neutrophil elastase up-regulates interleukin-8 via toll-like receptor 4.

作者信息

Devaney James M, Greene Catherine M, Taggart Clifford C, Carroll Tomás P, O'Neill Shane J, McElvaney Noel G

机构信息

Respiratory Research, Department of Medicine, RCSI Education and Research Centre, Smurfit Building, Beaumont Hospital, Dublin 9, Ireland.

出版信息

FEBS Lett. 2003 Jun 5;544(1-3):129-32. doi: 10.1016/s0014-5793(03)00482-4.

Abstract

Cystic fibrosis is characterised in the lungs by high levels of neutrophil elastase (NE). NE induces interleukin-8 (IL-8) expression via an IL-1 receptor-associated kinase signalling pathway. Here, we show that these events involve the cell surface membrane bound toll-like receptor 4 (TLR4). We demonstrate that human embryonic kidney (HEK)293 cells transfected with a TLR4 cDNA (HEK-TLR4) express TLR4 mRNA and protein and induce IL-8 promoter activity in response to NE. Treatment of both HEK-TLR4 and human bronchial epithelial cells with NE decreases TLR4 protein expression. Furthermore, a TLR4 neutralising antibody abrogates NE-induced IL-8 production, and induces tolerance to a secondary lipopolysaccharide stimulus. These data implicate TLR4 in NE induced IL-8 expression in bronchial epithelium.

摘要

囊性纤维化在肺部的特征是中性粒细胞弹性蛋白酶(NE)水平升高。NE通过白细胞介素-1受体相关激酶信号通路诱导白细胞介素-8(IL-8)表达。在此,我们表明这些事件涉及细胞表面膜结合的Toll样受体4(TLR4)。我们证明,用TLR4 cDNA转染的人胚肾(HEK)293细胞(HEK-TLR4)表达TLR4 mRNA和蛋白,并在对NE的反应中诱导IL-8启动子活性。用NE处理HEK-TLR4和人支气管上皮细胞均会降低TLR4蛋白表达。此外,TLR4中和抗体可消除NE诱导的IL-8产生,并诱导对二次脂多糖刺激的耐受性。这些数据表明TLR4参与NE诱导的支气管上皮细胞中IL-8的表达。

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