Rojas Alison M, Shiau Celia E
Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, United States.
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, United States.
Bio Protoc. 2021 Apr 5;11(7):e3978. doi: 10.21769/BioProtoc.3978.
Creating a robust and controlled infection model is imperative for studying the innate immune response. Leveraging the particular strengths of the zebrafish model system, such as optical transparency, development, and large clutch size, allows for the development of methods that yield consistent and reproducible results. We created a robust model for activation of innate immunity by microinjecting bacterial particles or live bacteria into larval zebrafish, unlike previous studies which largely restricted such manipulations to embryonic stages of zebrafish. The ability to introduce stimuli locally or systemically at larval stages provides significant advantages to examine host response in more mature tissues as well as the possibility to interrogate adaptive immunity at older larval stages. This protocol describes two distinct modes of microinjection to introduce lipopolysaccharide (LPS) or bacteria into the living larval zebrafish: one localized to the brain, and another into the bloodstream via the caudal vein plexus.
建立一个强大且可控的感染模型对于研究先天免疫反应至关重要。利用斑马鱼模型系统的独特优势,如光学透明性、发育过程和大量的卵,能够开发出产生一致且可重复结果的方法。我们通过将细菌颗粒或活细菌显微注射到斑马鱼幼体中,创建了一个强大的先天免疫激活模型,这与之前的研究不同,之前的研究大多将此类操作局限于斑马鱼的胚胎阶段。在幼体阶段局部或全身引入刺激的能力,为在更成熟的组织中检查宿主反应提供了显著优势,同时也为在较老的幼体阶段研究适应性免疫提供了可能性。本方案描述了两种不同的显微注射模式,用于将脂多糖(LPS)或细菌引入活的斑马鱼幼体:一种定位于脑,另一种通过尾静脉丛注入血液。