FEBS Letters · 2003 · 238 citations · 24 references
Life SciencesCell BiologyImmunologyImmunopathologyInflammationInnate ImmunityCytokine BiologyCytokine RegulationInflammatory Cell ResponsesInflammatory SignalingInnate Immune Signaling PathwaysToll-like ReceptorsCell Surface Toll-like ReceptorsLipopolysaccharide-mediated PathogenesisNeutrophil PhysiologyToll-like Receptor SignalingToll-like Receptor Signaling PathwaysToll-like Receptor-mediated Cytokine InductionToll-like Receptors In Inflammation
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.
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