GFP-specific CD8 T cells enable targeted cell depletion and visualization of T-cell interactions

被引:425
作者
Agudo, Judith [1 ]
Ruzo, Albert [1 ]
Park, Eun Sook [1 ]
Sweeney, Robert [1 ]
Kana, Veronika [2 ]
Wu, Meng [1 ]
Zhao, Yong [1 ]
Egli, Dieter [3 ]
Merad, Miriam [2 ,4 ,5 ]
Brown, Brian D. [1 ,4 ,5 ,6 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
[3] New York Stem Cell Fdn, Res Inst, New York, NY USA
[4] Icahn Sch Med Mt Sinai, Mt Sinai Immunol Inst, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
[6] Icahn Sch Med Mt Sinai, Diabet Obes & Metab Inst, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
CENTRAL-NERVOUS-SYSTEM; RECEPTOR TRANSGENIC MICE; IN-VIVO; EXPRESSION; TOLERANCE; MICROGLIA; MONOCYTES; DELETION; LINEAGE; TISSUE;
D O I
10.1038/nbt.3386
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 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
There are numerous cell types with scarcely understood functions, whose interactions with the immune system are not well characterized. To facilitate their study, we generated a mouse bearing enhanced green fluorescent protein (EGFP)-specific CD8(+) T cells. Transfer of the T cells into EGFP reporter animals can be used to kill EGFP-expressing cells, allowing selective depletion of desired cell types, or to interrogate T-cell interactions with specific populations. Using this system, we eliminate a rare EGFP-expressing cell type in the heart and demonstrate its role in cardiac function. We also show that naive T cells are recruited into the mouse brain by antigen-expressing microglia, providing evidence of an immune surveillance pathway in the central nervous system. The just EGFP death-inducing (Jedi) T cells enable visualization of a T-cell antigen. They also make it possible to utilize hundreds of existing EGFP-expressing mice, tumors, pathogens and other tools, to study T-cell interactions with many different cell types, to model disease states and to determine the functions of poorly characterized cell populations.
引用
收藏
页码:1287 / +
页数:8
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