首页> 美国卫生研究院文献>American Journal of Physiology - Lung Cellular and Molecular Physiology >Bioengineering the Lung: Molecules Materials Matrix Morphology and Mechanics: Atg7 deficiency impairs host defense against Klebsiella pneumoniae by impacting bacterial clearance survival and inflammatory responses in mice
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Bioengineering the Lung: Molecules Materials Matrix Morphology and Mechanics: Atg7 deficiency impairs host defense against Klebsiella pneumoniae by impacting bacterial clearance survival and inflammatory responses in mice

机译:肺的生物工程:分子材料基质形态和力学:Atg7缺乏症通过影响小鼠的细菌清除率存活率和炎症反应而损害宿主抵抗肺炎克雷伯菌的防御能力

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摘要

Klebsiella pneumoniae (Kp) is a Gram-negative bacterium that can cause serious infections in humans. Autophagy-related gene 7 (Atg7) has been implicated in certain bacterial infections; however, the role of Atg7 in macrophage-mediated immunity against Kp infection has not been elucidated. Here we showed that Atg7 expression was significantly increased in murine alveolar macrophages (MH-S) upon Kp infection, indicating that Atg7 participated in host defense. Knocking down Atg7 with small-interfering RNA increased bacterial burdens in MH-S cells. Using cell biology assays and whole animal imaging analysis, we found that compared with wild-type mice atg7 knockout (KO) mice exhibited increased susceptibility to Kp infection, with decreased survival rates, decreased bacterial clearance, and intensified lung injury. Moreover, Kp infection induced excessive proinflammatory cytokines and superoxide in the lung of atg7 KO mice. Similarly, silencing Atg7 in MH-S cells markedly increased expression levels of proinflammatory cytokines. Collectively, these findings reveal that Atg7 offers critical resistance to Kp infection by modulating both systemic and local production of proinflammatory cytokines.
机译:肺炎克雷伯氏菌(Kp)是一种革兰氏阴性细菌,可引起人类严重感染。自噬相关基因7(Atg7)与某些细菌感染有关。但是,尚未阐明Atg7在巨噬细胞介导的针对Kp感染的免疫中的作用。在这里,我们显示在Kp感染后,鼠肺泡巨噬细胞(MH-S)中Atg7表达显着增加,表明Atg7参与了宿主防御。用小干扰RNA敲低Atg7增加了MH-S细胞中的细菌负担。使用细胞生物学分析和整个动物成像分析,我们发现与野生型小鼠相比,atg7基因敲除(KO)小鼠对Kp感染的敏感性更高,存活率降低,细菌清除率降低,并且肺损伤加剧。此外,Kp感染在atg7 KO小鼠的肺中诱导了过量的促炎细胞因子和超氧化物。同样,在MH-S细胞中沉默Atg7会明显增加促炎细胞因子的表达水平。这些发现共同表明,Atg7通过调节促炎性细胞因子的全身和局部产生,对Kp感染提供了关键的抵抗力。

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