慢性肉芽肿性疾病
生物
斑马鱼
微生物学
吞噬作用
NADPH氧化酶
肉芽肿
免疫学
吞噬细胞
病菌
巨噬细胞
结核分枝杆菌
海洋分枝杆菌
肺结核
呼吸爆发
分枝杆菌
活性氧
细菌
病理
细胞生物学
基因
医学
体外
生物化学
遗传学
作者
Chao Yang,C.J. Cambier,J. Muse Davis,Christopher Hall,Philip S. Crosier,Lalita Ramakrishnan
标识
DOI:10.1016/j.chom.2012.07.009
摘要
Neutrophils are typically the first responders in host defense against invading pathogens, which they destroy by both oxidative and nonoxidative mechanisms. However, despite a longstanding recognition of neutrophil presence at disease sites in tuberculosis, their role in defense against mycobacteria is unclear. Here we exploit the genetic tractability and optical transparency of zebrafish to monitor neutrophil behavior and its consequences during infection with Mycobacterium marinum, a natural fish pathogen. In contrast to macrophages, neutrophils do not interact with mycobacteria at initial infection sites. Neutrophils are subsequently recruited to the nascent granuloma in response to signals from dying infected macrophages within the granuloma, which they phagocytose. Some neutrophils then rapidly kill the internalized mycobacteria through NADPH oxidase-dependent mechanisms. Our results provide a mechanistic link to the observed patterns of neutrophils in human tuberculous granulomas and the susceptibility of humans with chronic granulomatous disease to mycobacterial infection.
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