Investigating Murine CD4 T Cell Differentiation Using CRISPR-Cas9 Ribonucleoprotein Complex-mediated Gene Ablation.

IF 1.2 4区 综合性期刊 Q3 MULTIDISCIPLINARY SCIENCES
Jillian K Perry, Pamela L Schwartzberg, Dominic P Golec
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引用次数: 0

Abstract

The widespread accessibility of clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 technology has made gene targeting in primary cells a routine method for evaluating gene function in T cells. Given the cost and limited availability of knockout (KO) mouse strains, testing preliminary hypotheses involving gene function in T cells can be prohibitive using gene-targeted animal models. However, using commercially available resources, including predesigned guide RNAs (gRNAs), researchers can conveniently generate gene-targeted naïve T cells that can be used for T cell activation and differentiation studies. Here we outline a protocol for using nucleofection-delivered CRISPR-Cas9 ribonucleoprotein complexes (RNPs) to efficiently generate gene KO murine naïve CD4 T cells that can be used to evaluate gene function in CD4 T cell differentiation, in vitro. Isolation of naïve CD4 T cells from mouse secondary lymphoid organs, followed by nucleofection with Cas9-gRNA complexes ensures gene KO is initiated before downstream T cell activation, offering a strategic advantage over retroviral-mediated gRNA delivery, which typically requires preactivation of T cells, preventing the evaluation of effects in naïve T cells. Furthermore, this nucleofection-based method bypasses potential developmental issues associated with gene KO animals. Following Cas9-gRNA delivery, we describe protocols for studying CD4 T cell differentiation into Th1, Th2, Th17, and Treg lineages using in vitro polarization. In addition, this protocol is adaptable to using gene-targeted CD4 or CD8 T cells for numerous downstream applications, including other T cell activation studies in vitro and adoptive transfer studies in vivo. The use of CRISPR-Cas9 methods has streamlined our ability to evaluate gene function in T cells and allows for the routine KO of many genes of interest, freeing researchers from limitations associated with studying gene KO animals.

利用CRISPR-Cas9核糖核蛋白复合物介导的基因消融研究小鼠CD4 T细胞分化
聚集规则间隔短回文重复(CRISPR)-Cas9技术的广泛应用使得原代细胞中的基因靶向成为评估T细胞中基因功能的常规方法。考虑到敲除(KO)小鼠品系的成本和有限的可用性,使用基因靶向动物模型测试涉及T细胞中基因功能的初步假设可能是禁止的。然而,利用商业上可获得的资源,包括预先设计的引导rna (gRNAs),研究人员可以方便地生成基因靶向naïve T细胞,可用于T细胞激活和分化研究。在这里,我们概述了一种使用核转染CRISPR-Cas9核糖核蛋白复合物(RNPs)高效生成基因KO小鼠naïve CD4 T细胞的方案,该方案可用于体外评估CD4 T细胞分化中的基因功能。从小鼠次级淋巴器官中分离naïve CD4 T细胞,然后用Cas9-gRNA复合物进行核感染,确保基因KO在下游T细胞激活之前被启动,这比逆转录病毒介导的gRNA递送具有战略优势,后者通常需要T细胞的预激活,从而阻止了naïve T细胞效应的评估。此外,这种基于细胞核的方法绕过了与基因KO动物相关的潜在发育问题。在Cas9-gRNA传递后,我们描述了使用体外极化研究CD4 T细胞分化为Th1、Th2、Th17和Treg谱系的方案。此外,该方案适用于使用基因靶向CD4或CD8 T细胞进行许多下游应用,包括其他体外T细胞活化研究和体内过继转移研究。CRISPR-Cas9方法的使用简化了我们在T细胞中评估基因功能的能力,并允许对许多感兴趣的基因进行常规KO,使研究人员摆脱了与研究基因KO动物相关的限制。
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来源期刊
Jove-Journal of Visualized Experiments
Jove-Journal of Visualized Experiments MULTIDISCIPLINARY SCIENCES-
CiteScore
2.10
自引率
0.00%
发文量
992
期刊介绍: JoVE, the Journal of Visualized Experiments, is the world''s first peer reviewed scientific video journal. Established in 2006, JoVE is devoted to publishing scientific research in a visual format to help researchers overcome two of the biggest challenges facing the scientific research community today; poor reproducibility and the time and labor intensive nature of learning new experimental techniques.
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