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CLARITY and PACT-based imaging of adult zebrafish and mouse for whole-animal analysis of infections

机译:清晰和基于PACT的成年斑马鱼和小鼠成像用于感染的全动物分析

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Visualization of infection and the associated host response has been challenging in adult vertebrates. Owing to their transparency, zebrafish larvae have been used to directly observe infection in vivo ; however, such larvae have not yet developed a functional adaptive immune system. Cells involved in adaptive immunity mature later and have therefore been difficult to access optically in intact animals. Thus, the study of many aspects of vertebrate infection requires dissection of adult organs or ex vivo isolation of immune cells. Recently, CLARITY and PACT (passive clarity technique) methodologies have enabled clearing and direct visualization of dissected organs. Here, we show that these techniques can be applied to image host-pathogen interactions directly in whole animals. CLARITY and PACT-based clearing of whole adult zebrafish and Mycobacterium tuberculosis -infected mouse lungs enables imaging of mycobacterial granulomas deep within tissue to a depth of more than 1?mm. Using established transgenic lines, we were able to image normal and pathogenic structures and their surrounding host context at high resolution. We identified the three-dimensional organization of granuloma-associated angiogenesis, an important feature of mycobacterial infection, and characterized the induction of the cytokine tumor necrosis factor (TNF) within the granuloma using an established fluorescent reporter line. We observed heterogeneity in TNF induction within granuloma macrophages, consistent with an evolving view of the tuberculous granuloma as a non-uniform, heterogeneous structure. Broad application of this technique will enable new understanding of host-pathogen interactions in situ .
机译:在成年脊椎动物中,感染的可视化和相关的宿主反应一直是具有挑战性的。由于它们的透明性,斑马鱼的幼虫已经被用来直接观察体内的感染。然而,这种幼虫尚未发展出功能性的适应性免疫系统。参与适应性免疫的细胞稍后会成熟,因此在完整动物中很难以光学方式进入。因此,对脊椎动物感染的许多方面的研究需要解剖成年器官或离体分离免疫细胞。最近,CLARITY和PACT(被动清晰度技术)方法已使清除和解剖器官的直接可视化成为可能。在这里,我们证明了这些技术可以直接应用于整只动物中的宿主-病原体相互作用图像。对整个成年斑马鱼和结核分枝杆菌感染的小鼠肺进行清晰和基于PACT的清除,可对组织内深至超过1?mm的分枝杆菌肉芽肿进行成像。使用已建立的转基因品系,我们能够以高分辨率对正常和病原体结构及其周围宿主环境进行成像。我们确定了与肉芽肿相关的血管生成的三维组织,这是分枝杆菌感染的重要特征,并使用已建立的荧光报告基因,表征了肉芽肿中细胞因子肿瘤坏死因子(TNF)的诱导。我们观察到肉芽肿巨噬细胞内TNF诱导的异质性,与结核性肉芽肿作为不均匀,异质结构的进化观点相一致。该技术的广泛应用将使人们对原位-病原体相互作用有了新的认识。

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