首页> 美国卫生研究院文献>PLoS Pathogens >Production of Extracellular Traps against Aspergillus fumigatus In Vitro and in Infected Lung Tissue Is Dependent on Invading Neutrophils and Influenced by Hydrophobin RodA
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Production of Extracellular Traps against Aspergillus fumigatus In Vitro and in Infected Lung Tissue Is Dependent on Invading Neutrophils and Influenced by Hydrophobin RodA

机译:体外和在感染的肺组织中针对烟曲霉的细胞外诱集的产生取决于入侵的中性粒细胞并受疏水蛋白RodA的影响

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摘要

Aspergillus fumigatus is the most important airborne fungal pathogen causing life-threatening infections in immunocompromised patients. Macrophages and neutrophils are known to kill conidia, whereas hyphae are killed mainly by neutrophils. Since hyphae are too large to be engulfed, neutrophils possess an array of extracellular killing mechanisms including the formation of neutrophil extracellular traps (NETs) consisting of nuclear DNA decorated with fungicidal proteins. However, until now NET formation in response to A. fumigatus has only been demonstrated in vitro, the importance of neutrophils for their production in vivo is unclear and the molecular mechanisms of the fungus to defend against NET formation are unknown. Here, we show that human neutrophils produce NETs in vitro when encountering A. fumigatus. In time-lapse movies NET production was a highly dynamic process which, however, was only exhibited by a sub-population of cells. NETosis was maximal against hyphae, but reduced against resting and swollen conidia. In a newly developed mouse model we could then demonstrate the existence and measure the kinetics of NET formation in vivo by 2-photon microscopy of Aspergillus-infected lungs. We also observed the enormous dynamics of neutrophils within the lung and their ability to interact with and phagocytose fungal elements in situ. Furthermore, systemic neutrophil depletion in mice almost completely inhibited NET formation in lungs, thus directly linking the immigration of neutrophils with NET formation in vivo. By using fungal mutants and purified proteins we demonstrate that hydrophobin RodA, a surface protein making conidia immunologically inert, led to reduced NET formation of neutrophils encountering Aspergillus fungal elements. NET-dependent killing of Aspergillus-hyphae could be demonstrated at later time-points, but was only moderate. Thus, these data establish that NET formation occurs in vivo during host defence against A. fumigatus, but suggest that it does not play a major role in killing this fungus. Instead, NETs may have a fungistatic effect and may prevent further spreading.
机译:烟曲霉是最重要的空气传播真菌病原体,可在免疫功能低下的患者中造成威胁生命的感染。已知巨噬细胞和嗜中性粒细胞杀死分生孢子,而菌丝主要被嗜中性粒细胞杀死。由于菌丝太大而无法被吞噬,中性粒细胞具有一系列细胞外杀伤机制,包括形成由装饰有杀真菌蛋白的核DNA组成的中性粒细胞外陷阱(NETs)。但是,到目前为止,仅在体外证明了响应于烟曲霉的NET形成,中性粒细胞对其在体内产生的重要性尚不清楚,并且真菌抵御NET形成的分子机制尚不清楚。在这里,我们显示人类嗜中性粒细胞在遇到烟曲霉时会在体外产生NETs。在延时电影中,NET的生产是一个高度动态的过程,但是,仅通过细胞亚群才能表现出来。 NETosis对菌丝最大,但对休息和分生孢子虫减少。在新开发的小鼠模型中,我们然后可以通过2-光子显微镜观察曲霉菌感染的肺部,来证明体内NET的存在并测量其动力学。我们还观察到了肺内嗜中性粒细胞的巨大动态,以及它们与原位吞噬作用和吞噬真菌成分的能力。此外,小鼠体内系统性中性粒细胞耗竭几乎完全抑制了肺中NET的形成,因此直接将中性粒细胞的迁移与体内NET形成联系起来。通过使用真菌突变体和纯化的蛋白质,我们证明了疏水蛋白RodA(一种使分生孢子具有免疫惰性的表面蛋白)可减少遇到曲霉属真菌元素的嗜中性粒细胞的NET形成。 NET依赖的杀灭曲霉菌的杀伤力可以在以后的时间点得到证实,但只是中等程度。因此,这些数据确定了NET的形成是在宿主对烟曲霉的防御过程中在体内发生的,但是表明它在杀死这种真菌中没有主要作用。相反,NET可能具有抑菌作用,并可能阻止进一步扩散。

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