Department of Biotechnology, Tokyo University of Agriculture and Technology, 2-24-16, Naka-cho Koganei, Tokyo 184-8588, Japan.
Biotechnol Bioeng. 2010 Jun 1;106(2):311-8. doi: 10.1002/bit.22663.
The antigen specificity of cytotoxic T cells, provided by T-cell receptors (TCRs), plays a central role in human autoimmune diseases, infection, and cancer. As the TCR repertoire is unique in individual cytotoxic T cells, a strategy to analyze its gene rearrangement at the single-cell level is required. In this study, we applied a high-density microcavity array enabling target cell screening of several thousands of single cells for identification of functional TCR-beta gene repertoires specific to melanoma (gp100) and cytomegalovirus (CMV) antigens. T cells expressing TCRs with the ability to recognize fluorescent-labeled antigen peptide tetramers were isolated by using a micromanipulator under microscopy. Regularly arranged cells on the microcavity array eased detection and isolation of target single cells from a polyclonal T-cell population. The isolated single cells were then directly utilized for RT-PCR. By sequencing the amplified PCR products, antigen-specific TCR-beta repertoires for gp100 and human cytomegalovirus antigens were successfully identified at the single-cell level. This simple, accurate, and cost-effective technique for single-cell analysis has further potential as a valuable and widely applicable tool for studies on gene screening and expression analyses of various kinds of cells.
细胞毒性 T 细胞的抗原特异性由 T 细胞受体 (TCRs) 提供,在人类自身免疫性疾病、感染和癌症中发挥着核心作用。由于 TCR 库在个体细胞毒性 T 细胞中是独特的,因此需要一种在单细胞水平上分析其基因重排的策略。在这项研究中,我们应用了高密度微腔阵列,能够对数千个单细胞进行靶细胞筛选,以鉴定针对黑色素瘤 (gp100) 和巨细胞病毒 (CMV) 抗原的特异性细胞毒性 TCR-β基因库。通过在显微镜下使用微操作器,分离出能够识别荧光标记抗原肽四聚体的表达 TCR 的 T 细胞。在微腔阵列上规则排列的细胞便于从多克隆 T 细胞群体中检测和分离目标单细胞。然后直接将分离的单细胞用于 RT-PCR。通过对扩增的 PCR 产物进行测序,成功地在单细胞水平上鉴定了针对 gp100 和人巨细胞病毒抗原的特异性 TCR-β库。这种简单、准确、具有成本效益的单细胞分析技术具有进一步的潜力,可作为一种有价值的、广泛适用的工具,用于各种细胞的基因筛选和表达分析研究。