Aix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy, Marseille, France.
Centre de Recherche en Transplantation et Immunologie UMR1064, INSERM Université de Nantes, Nantes, France.
Front Immunol. 2020 Mar 3;11:216. doi: 10.3389/fimmu.2020.00216. eCollection 2020.
Single-cell RNA sequencing (scRNA-seq) allows the identification, characterization, and quantification of cell types in a tissue. When focused on B and T cells of the adaptive immune system, scRNA-seq carries the potential to track the clonal lineage of each analyzed cell through the unique rearranged sequence of its antigen receptor (BCR or TCR, respectively) and link it to the functional state inferred from transcriptome analysis. Here we introduce FB5P-seq, a FACS-based 5'-end scRNA-seq method for cost-effective, integrative analysis of transcriptome and paired BCR or TCR repertoire in phenotypically defined B and T cell subsets. We describe in detail the experimental workflow and provide a robust bioinformatics pipeline for computing gene count matrices and reconstructing repertoire sequences from FB5P-seq data. We further present two applications of FB5P-seq for the analysis of human tonsil B cell subsets and peripheral blood antigen-specific CD4 T cells. We believe that our novel integrative scRNA-seq method will be a valuable option to study rare adaptive immune cell subsets in immunology research.
单细胞 RNA 测序(scRNA-seq)允许鉴定、描述和量化组织中的细胞类型。当专注于适应性免疫系统的 B 细胞和 T 细胞时,scRNA-seq 有可能通过其抗原受体(分别为 BCR 或 TCR)的独特重排序列来跟踪每个分析细胞的克隆谱系,并将其与从转录组分析推断出的功能状态联系起来。在这里,我们介绍了 FB5P-seq,这是一种基于流式细胞术的 5'端 scRNA-seq 方法,用于在表型定义的 B 和 T 细胞亚群中进行经济高效的转录组和配对 BCR 或 TCR 库的综合分析。我们详细描述了实验工作流程,并提供了一个强大的生物信息学管道,用于从 FB5P-seq 数据计算基因计数矩阵和重建库序列。我们进一步介绍了 FB5P-seq 在分析人扁桃体 B 细胞亚群和外周血抗原特异性 CD4 T 细胞中的两个应用。我们相信,我们的新型综合 scRNA-seq 方法将是研究免疫学研究中罕见的适应性免疫细胞亚群的一个有价值的选择。