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首页> 外文期刊>Scientific reports. >NOD2 dependent neutrophil recruitment is required for early protective immune responses against infectious Litomosoides sigmodontis L3 larvae
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NOD2 dependent neutrophil recruitment is required for early protective immune responses against infectious Litomosoides sigmodontis L3 larvae

机译:需要NOD2依赖性中性粒细胞募集才能对感染性Litomosoides sigmodontis L3幼虫进行早期保护性免疫应答

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摘要

Nucleotide-binding oligomerization domain-containing protein 2 (NOD2) recognizes muramyl dipeptide (MDP) of bacterial cell walls, triggering NFκB-induced pro-inflammation. As most human pathogenic filariae contain Wolbachia endobacteria that synthesize the MDP-containing cell wall precursor lipid II, NOD2's role during infection with the rodent filaria Litomosoides sigmodontis was investigated. In NFκB reporter-cells, worm-extract containing Wolbachia induced NOD2 and NOD1. NOD2-deficient mice infected with L. sigmodontis had significantly more worms than wildtype controls early in infection. Increased worm burden was not observed after subcutaneous infection, suggesting that protective NOD2-dependent immune responses occur within the skin. Flow cytometry demonstrated that neutrophil recruitment to the skin was impaired in NOD2(-/-) mice after intradermal injection of third stage larvae (L3), and blood neutrophil numbers were reduced after L. sigmodontis infection. PCR array supported the requirement of NOD2 for recruitment of neutrophils to the skin, as genes associated with neutrophil recruitment and activation were downregulated in NOD2(-/-) mice after intradermal L3 injection. Neutrophil depletion before L. sigmodontis infection increased worm recovery in wildtype mice, confirming that neutrophils are essential against invading L3 larvae. This study indicates that NOD-like receptors are implemented in first-line protective immune responses against filarial nematodes.
机译:含有核苷酸结合的寡聚化域的蛋白质2(NOD2)识别细菌细胞壁的muramyl二肽(MDP),从而触发NFκB诱导的促炎症反应。由于大多数人类致病丝虫都含有能够合成含有MDP的细胞壁前体脂质II的Wolbachia内细菌,因此研究了NOD2在啮齿类丝虫Litomosoides sigmodontis感染过程中的作用。在NFκB报告细胞中,含有Wolbachia的蠕虫提取物诱导了NOD2和NOD1。在感染早期,感染Sigmodontis的NOD2缺陷型小鼠的蠕虫比野生型对照明显多。皮下感染后未观察到蠕虫负担增加,表明保护性NOD2依赖性免疫反应在皮肤内发生。流式细胞仪表明,在皮内注射三级幼虫(L3)后,NOD2(-/-)小鼠中性粒细胞向皮肤的募集受到损害,而感染乙状结肠炎沙门氏菌后血液中性粒细胞数量减少。 PCR阵列支持NOD2将嗜中性白细胞募集到皮肤的需求,因为皮内注射L3后NOD2(-/-)小鼠中与嗜中性白细胞募集和激活相关的基因被下调。 Sigmodontis感染前嗜中性白细胞的消耗增加了野生型小鼠的蠕虫恢复率,这证明嗜中性白细胞对入侵L3幼虫是必不可少的。这项研究表明,在针对丝虫线虫的一线保护性免疫反应中,实现了NOD样受体。

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