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Role of the NOD1/NF-kappa B pathway on bovine neutrophil responses to crude lipopolysaccharide

机译:NOD1 /NF-κB途径在牛中性粒细胞对粗脂多糖反应中的作用

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Cytosolic nucleotide oligomerisation domain (NOD)-like receptors play an important role in host defence against infection. Reduced NOD1 expression has been observed in dysfunctional neutrophils derived from periparturient cattle known to be most susceptible to coliform mastitis. However, whether impairment of NOD1 suppresses the immune responses of bovine neutrophils during bacterial infections remains unknown. Crude (phenol extracted) lipopolysaccharide (cLPS), which often contains other immunostimulatory molecules, including NOD1 agonist, is known to induce almost the whole bacterial response. This study was conducted to explore the role of NOD1uclear factor (NF)-kappa B pathway in the cytokine and functional responses of bovine neutrophils challenged with Escherichia coil-derived cLPS. Freshly isolated blood neutrophils from healthy heifers were pre-incubated for 2 h with ML130, a selective inhibitor of NOD1/NF-kappa B pathway. Cells were then exposed to cLPS for additional 4 h. Inhibition of the NOD1/NF-kappa B pathway resulted in a decrease in cLPS-induced phosphorylation of the inhibitor of NF-kappa B alpha (I kappa B alpha) in neutrophils. Impairment of the NOD1/NF-kappa B pathway tended to down-regulate mRNA levels of pro-inflammatory cytokines interleukin (IL)-1 beta and tumour necrosis factor (TNF)-alpha, chemokines IL-8 and C-X-C motif ligand 2 (CXCL2), and adhesion molecules CD11b and CD62L, in cLPS-challenged cells. Functional analyses showed that blocking the NOD1/NF-kappa B pathway inhibited neutrophil migration and phagocytic killing capacity, and promoted neutrophil death upon cLPS stimulation. The data presented here demonstrate that activation of NOD1/NF-kappa B pathway contributes to the functional responses of neutrophils to cLPS. (C) 2016 Elsevier Ltd. All rights reserved.
机译:胞质核苷酸寡聚域(NOD)样受体在宿主防御感染中起着重要作用。在来自产程障碍牛的机能障碍的中性粒细胞中,NOD1的表达降低,已知这种病的中性粒细胞对大肠菌群乳腺炎最敏感。然而,NOD1损伤是否抑制细菌感染期间牛中性粒细胞的免疫反应仍是未知的。粗(酚提取的)脂多糖(cLPS)通常包含其他免疫刺激分子,包括NOD1激动剂,已知可诱导几乎整个细菌反应。进行了这项研究,以探讨NOD1 /核因子(NF)-κB通路在牛嗜中性粒细胞受到大肠杆菌诱导的cLPS攻击的细胞因子和功能反应中的作用。将来自健康小母牛的新鲜分离出的血液中性粒细胞与ML130(一种NOD1 /NF-κB途径的选择性抑制剂)预先孵育2小时。然后将细胞暴露于cLPS 4小时。 NOD1 /NF-κB通路的抑制导致嗜中性粒细胞中cLPS诱导的NF-κBα(IκBα)抑制剂的磷酸化降低。 NOD1 /NF-κB通路的损伤倾向于下调促炎性细胞因子白介素(IL)-1和肿瘤坏死因子(TNF)-α,趋化因子IL-8和CXC基序配体2(CXCL2 ),以及受cLPS攻击的细胞中的粘附分子CD11b和CD62L。功能分析表明,阻断NOD1 /NF-κB通路可抑制中性粒细胞迁移和吞噬杀伤能力,并促进cLPS刺激后中性粒细胞死亡。此处提供的数据表明,NOD1 /NF-κB途径的激活有助于嗜中性粒细胞对cLPS的功能反应。 (C)2016 Elsevier Ltd.保留所有权利。

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