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实时体内成像显示中性粒细胞能够直接从脑血管系统清除新型隐球菌。

Real-time in vivo imaging reveals the ability of neutrophils to remove Cryptococcus neoformans directly from the brain vasculature.

作者信息

Zhang Mingshun, Sun Donglei, Liu Gongguan, Wu Hui, Zhou Hong, Shi Meiqing

机构信息

*Division of Immunology, Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, College Park, Maryland, USA; and Department of Immunology, Nanjing Medical University, Nanjing, Jiangsu, China.

*Division of Immunology, Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, College Park, Maryland, USA; and Department of Immunology, Nanjing Medical University, Nanjing, Jiangsu, China

出版信息

J Leukoc Biol. 2016 Mar;99(3):467-73. doi: 10.1189/jlb.4AB0715-281R. Epub 2015 Oct 1.

Abstract

Although neutrophils are typically the first immune cells attracted to an infection site, little is known about how neutrophils dynamically interact with invading pathogens in vivo. Here, with the use of intravital microscopy, we demonstrate that neutrophils migrate to the arrested Cryptococcus neoformans, a leading agent to cause meningoencephalitis, in the brain microvasculature. Following interactions with C. neoformans, neutrophils were seen to internalize the organism and then circulate back into the bloodstream, resulting in a direct removal of the organism from the endothelial surface before its transmigration into the brain parenchyma. C. neoformans infection led to enhanced expression of adhesion molecules macrophage 1 antigen on neutrophils and ICAM-1 on brain endothelial cells. Depletion of neutrophils enhanced the brain fungal burden. Complement C3 was critically involved in the recognition of C. neoformans by neutrophils and subsequent clearance of the organism from the brain. Together, our finding of the direct removal of C. neoformans by neutrophils from its arrested site may represent a novel mechanism of host defense in the brain, in addition to the known, direct killing of microorganisms at the infection sites. These data are the first to characterize directly the dynamic interactions of leukocytes with a microbe in the brain of a living animal.

摘要

尽管中性粒细胞通常是最早被吸引到感染部位的免疫细胞,但对于中性粒细胞在体内如何与入侵病原体动态相互作用却知之甚少。在此,我们利用活体显微镜技术证明,中性粒细胞会迁移至大脑微血管中停滞的新型隐球菌(一种导致脑膜脑炎的主要病原体)处。与新型隐球菌相互作用后,可见中性粒细胞将该病原体内化,然后循环回到血液中,从而在病原体迁移至脑实质之前直接将其从内皮表面清除。新型隐球菌感染导致中性粒细胞上的黏附分子巨噬细胞1抗原和脑内皮细胞上的细胞间黏附分子-1(ICAM-1)表达增强。中性粒细胞的耗竭增加了脑部真菌负荷。补体C3在中性粒细胞识别新型隐球菌以及随后从脑中清除该病原体的过程中起关键作用。总之,我们发现中性粒细胞可直接从其停滞部位清除新型隐球菌,这可能代表了大脑中宿主防御的一种新机制,此外还有已知的在感染部位直接杀死微生物的机制。这些数据首次直接描述了活体动物大脑中白细胞与微生物的动态相互作用。

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