Curado Silvia, Stainier Didier Y R, Anderson Ryan M
Department of Biochemistry and Biophysics, Program in Developmental Biology, Liver Center, Diabetes Center and the Cardiovascular Research Institute, University of California, San Francisco, San Francisco, California 94158-2324, USA.
Nat Protoc. 2008;3(6):948-54. doi: 10.1038/nprot.2008.58.
Ablation studies are used to elucidate cell lineage relationships, developmental roles for specific cells during embryogenesis and mechanisms of tissue regeneration. Previous chemical and genetic approaches to directed cell ablation have been hampered by poor specificity, limited efficacy, irreversibility, hypersensitivity to promoter leakiness, restriction to proliferating cells, slow inducibility or complex genetics. Here, we provide a step-by-step protocol for a hybrid chemical-genetic cell ablation method in zebrafish that, by combining spatial and temporal control, is cell-type specific, inducible, reversible, rapid and scaleable. Bacterial Nitroreductase (NTR) is used to catalyze the reduction of the innocuous prodrug metrodinazole (Mtz), thereby producing a cytotoxic product that induces cell death. Based on this principle, NTR is expressed in transgenic zebrafish using a tissue-specific promoter. Subsequent exposure to Mtz by adding it to the media induces cell death exclusively within NTR(+) cells. This approach can be applied to regeneration studies, as removing Mtz by washing permits tissue recovery. Using this protocol, cell ablation can be achieved in 12-72 h, depending on the transgenic line used, and recovery initiates within the following 24 h.
消融研究用于阐明细胞谱系关系、胚胎发育过程中特定细胞的发育作用以及组织再生机制。以往用于定向细胞消融的化学和遗传方法存在特异性差、疗效有限、不可逆性、对启动子渗漏高度敏感、仅限于增殖细胞、诱导缓慢或遗传学复杂等问题。在此,我们提供了一种斑马鱼杂交化学-遗传细胞消融方法的详细方案,该方法通过结合空间和时间控制,具有细胞类型特异性、可诱导、可逆、快速且可扩展的特点。细菌硝基还原酶(NTR)用于催化无害前药甲硝唑(Mtz)的还原,从而产生诱导细胞死亡的细胞毒性产物。基于这一原理,NTR在转基因斑马鱼中使用组织特异性启动子进行表达。随后通过将Mtz添加到培养基中使其暴露,仅在NTR(+)细胞内诱导细胞死亡。这种方法可应用于再生研究,因为通过冲洗去除Mtz可使组织恢复。使用该方案,根据所使用的转基因品系,可在12 - 72小时内实现细胞消融,并且在接下来的24小时内开始恢复。