Cheong Sek-Shir, Luis Tiago C, Hind Matthew, Dean Charlotte H
National Heart and Lung Institute (NHLI), Imperial College London, London, UK.
Centre for Inflammatory Diseases, Department of Immunology and Inflammation, Imperial College London, London, UK.
Bio Protoc. 2024 Apr 20;14(8):e4980. doi: 10.21769/BioProtoc.4980.
Precision-cut lung slices (PCLS), ex vivo 3D lung tissue models, have been widely used for various applications in lung research. PCLS serve as an excellent intermediary between in vitro and in vivo models because they retain all resident cell types within their natural niche while preserving the extracellular matrix environment. This protocol describes the TReATS (TAT-Cre recombinase-mediated floxed allele modification in tissue slices) method that enables rapid and efficient gene modification in PCLS derived from adult floxed animals. Here, we present detailed protocols for the TReATS method, consisting of two simple steps: PCLS generation and incubation in a TAT-Cre recombinase solution. Subsequent validation of gene modification involves live staining and imaging of PCLS, quantitative real-time PCR, and cell viability assessment. This four-day protocol eliminates the need for complex Cre-breeding, circumvents issues with premature lethality related to gene mutation, and significantly reduces the use of animals. The TReATS method offers a simple and reproducible solution for gene modification in complex ex vivo tissue-based models, accelerating the study of gene function, disease mechanisms, and the discovery of drug targets. Key features • Achieve permanent ex vivo gene modifications in complex tissue-based models within four days. • Highly adaptable gene modification method that can be applied to induce gene deletion or activation. • Allows simple Cre dosage testing in a controlled ex vivo setting with the advantage of using PCLS generated from the same animal as . • With optimisation, this method can be applied to precision-cut tissue slices of other organs.
精密切割肺切片(PCLS),即离体三维肺组织模型,已广泛应用于肺研究的各种应用中。PCLS作为体外和体内模型之间的优秀中介,因为它们在保留天然微环境中所有驻留细胞类型的同时,还保留了细胞外基质环境。本方案描述了TReATS(组织切片中TAT-Cre重组酶介导的floxed等位基因修饰)方法,该方法能够在源自成年floxed动物的PCLS中实现快速有效的基因修饰。在这里,我们介绍了TReATS方法的详细方案,包括两个简单步骤:PCLS生成和在TAT-Cre重组酶溶液中孵育。随后的基因修饰验证包括PCLS的活染色和成像、定量实时PCR以及细胞活力评估。这个为期四天的方案消除了复杂的Cre育种需求,规避了与基因突变相关的过早致死问题,并显著减少了动物的使用。TReATS方法为基于复杂离体组织的模型中的基因修饰提供了一种简单且可重复的解决方案,加速了基因功能、疾病机制的研究以及药物靶点的发现。关键特性 • 在四天内实现基于复杂组织的模型中的永久性离体基因修饰。 • 高度适应性强的基因修饰方法,可用于诱导基因缺失或激活。 • 允许在可控的离体环境中进行简单的Cre剂量测试,其优点是使用来自同一动物的PCLS。 • 经过优化,该方法可应用于其他器官的精密切割组织切片。