Davis J Muse, Clay Hilary, Lewis Jessica L, Ghori Nafisa, Herbomel Philippe, Ramakrishnan Lalita
Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.
Immunity. 2002 Dec;17(6):693-702. doi: 10.1016/s1074-7613(02)00475-2.
Infection of vertebrate hosts with pathogenic Mycobacteria, the agents of tuberculosis, produces granulomas, highly organized structures containing differentiated macrophages and lymphocytes, that sequester the pathogen. Adult zebrafish are naturally susceptible to tuberculosis caused by Mycobacterium marinum. Here, we exploit the optical transparency of zebrafish embryos to image the events of M. marinum infection in vivo. Despite the fact that the embryos do not yet have lymphocytes, infection leads to the formation of macrophage aggregates with pathological hallmarks of granulomas and activation of previously identified granuloma-specific Mycobacterium genes. Thus, Mycobacterium-macrophage interactions can initiate granuloma formation solely in the context of innate immunity. Strikingly, infection can redirect normal embryonic macrophage migration, even recruiting macrophages seemingly committed to their developmentally dictated tissue sites.
脊椎动物宿主感染致病性分枝杆菌(结核病的病原体)会产生肉芽肿,这是一种高度组织化的结构,包含分化的巨噬细胞和淋巴细胞,可隔离病原体。成年斑马鱼对海分枝杆菌引起的结核病自然易感。在此,我们利用斑马鱼胚胎的光学透明性对海分枝杆菌感染的体内过程进行成像。尽管胚胎尚未拥有淋巴细胞,但感染会导致巨噬细胞聚集体的形成,这些聚集体具有肉芽肿的病理特征,并激活先前鉴定出的肉芽肿特异性分枝杆菌基因。因此,分枝杆菌与巨噬细胞的相互作用可仅在先天免疫的背景下引发肉芽肿形成。令人惊讶的是,感染可改变正常胚胎巨噬细胞的迁移方向,甚至招募看似已定向迁移至其发育规定组织部位的巨噬细胞。