首页> 外文期刊>American journal of clinical and experimental immunology >Blockade of IL-1R signaling diminishes Paneth cell depletion and Toxoplasma gondii induced ileitis in mice
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Blockade of IL-1R signaling diminishes Paneth cell depletion and Toxoplasma gondii induced ileitis in mice

机译:IL-1R信号传导的阻断减少了Paneth细胞耗竭和弓形虫诱导的回肠炎

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Interleukin 1 is a critical inflammatory mediator and involved in host defense to several pathogens. Oral T. gondii infection causes lethal ileitis in C57BL/6 (BL6) mice and serves to investigate the mechanisms of acute intestinal inflammation. Here we show that IL-1 is expressed upon oral T. gondii (76K strain) infection in the small intestine and mediates ileitis as IL-1R1 deficient mice have reduced neutrophil recruitment in the lamina propria, parasite invasion, inflammatory lesions and enhanced survival as compared to BL6 infected control mice. Protection in the absence of IL-1R1 signaling was associated with reduced IFN-γ expression and preserved Paneth cells, while these cells were eliminated in infected BL6 mice. Furthermore, blockade of IL-1 by IL-1β antibody attenuated inflammation in BL6 mice. In conclusion, IL-1 signaling contributes to the inflammatory response with increase IFN-γ expression and Paneth cell depletion upon oral T. gondii infection.
机译:白介素1是一种关键的炎症介质,参与宿主对几种病原体的防御。口腔弓形虫感染可导致C57BL / 6(BL6)小鼠致命性回肠炎,可用于研究急性肠道炎症的机制。在这里,我们显示IL-1在口服小肠弓形虫(76K株)感染后表达,并介导回肠炎,因为IL-1R1缺陷型小鼠的固有层中性粒细胞募集减少,寄生虫入侵,炎性病变和存活率提高。与感染BL6的对照小鼠相比。没有IL-1R1信号传导时的保护作用与IFN-γ表达减少和Paneth细胞保存有关,而在感染的BL6小鼠中这些细胞被清除了。此外,IL-1β抗体对IL-1的阻滞减弱了BL6小鼠的炎症。总之,口服刚地弓形虫感染后,IL-1信号转导通过增加IFN-γ表达和Paneth细胞耗竭促进炎症反应。

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