TCR-β Repertoire Analysis of Antigen-Specific Single T Cells Using a High-Density Microcavity Array

被引:12
作者
Arakaki, Atsushi [1 ]
Ooya, Kaori [1 ]
Akiyama, Yasuto [2 ]
Hosokawa, Masahito [1 ]
Komiyama, Masaru [2 ]
Iizuka, Akira [2 ]
Yamaguchi, Ken [2 ]
Matsunaga, Tadashi [1 ]
机构
[1] Tokyo Univ Agr & Technol, Dept Biotechnol, Koganei, Tokyo 1848588, Japan
[2] Shizuoka Canc Ctr, Res Inst, Div Immunotherapy, Nagaizumi, Shizuoka 4118777, Japan
基金
日本学术振兴会;
关键词
microarray analytical devices; single-cell; T-cell receptor beta genes; T-cell antigen receptor specificity; gene expression analysis; GENE-EXPRESSION; CLONES; MICROMESH; SELECTION; KINETICS;
D O I
10.1002/bit.22663
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. Biotechnol. Bioeng. 2010;106: 311-318. (C) 2010 Wiley Periodicals, Inc.
引用
收藏
页码:311 / 318
页数:8
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