Francesca Sposito, Sarah Northey, Amandine Charras, Paul S. McNamara, Christian M. Hedrich
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引用次数: 0
摘要
雾化高渗盐水(3-7%)通常用于增加慢性呼吸道疾病和/或病毒感染患者的粘液纤毛清除率。然而,盐浓度的改变可能会导致炎症反应。本研究的目的是调查500 mM NaCl(3%)触发人类巨噬细胞的炎症并确定所涉及的分子机制。在原代人单核细胞衍生的巨噬细胞中测量NaCl诱导的焦下垂、IL-1β、IL-18和ASC斑点释放。用重组IL-1受体拮抗剂anakinra或NLRP3抑制剂MCC950处理不影响NaCl介导的炎症小体组装。NLRP1表达的下调,而不是NLRP3和NLRC4的下调,减少了NaCl诱导的焦下垂、促炎细胞因子和人类THP-1衍生巨噬细胞的ASC斑点释放。这项研究的数据表明,3%NaCl诱导的人类巨噬细胞炎症反应依赖于NLRP1和炎症小体组装。除了吸入高渗盐水外,靶向炎症可能对炎症性气道疾病患者有益。
Hypertonic saline induces inflammation in human macrophages through the NLRP1 inflammasome
Nebulized hypertonic saline (3–7%) is commonly used to increase mucociliary clearance in patients with chronic airway disease and/or virus infections. However, altered salt concentrations may contribute to inflammatory responses. The aim of this study was to investigate whether 500 mM NaCl (3%) triggers inflammation in human macrophages and identify the molecular mechanisms involved. NaCl-induced pyroptosis, IL-1β, IL-18 and ASC speck release were measured in primary human monocyte-derived macrophages. Treatment with the recombinant IL-1 receptor antagonist anakinra or the NLRP3 inhibitor MCC950 did not affect NaCl-mediated inflammasome assembly. Knock-down of NLRP1 expression, but not of NLRP3 and NLRC4, reduced NaCl-induced pyroptosis, pro-inflammatory cytokine and ASC speck release from human THP-1-derived macrophages. Data from this study suggest that 3% NaCl-induced inflammatory responses in human macrophages depend on NLRP1 and inflammasome assembly. Targeting inflammation in addition to inhalation with hypertonic saline may benefit patients with inflammatory airway disease.
期刊介绍:
Genes & Immunity emphasizes studies investigating how genetic, genomic and functional variations affect immune cells and the immune system, and associated processes in the regulation of health and disease. It further highlights articles on the transcriptional and posttranslational control of gene products involved in signaling pathways regulating immune cells, and protective and destructive immune responses.