细胞生物学
生物
CD8型
T细胞
免疫系统
细胞毒性T细胞
抗原提呈细胞
电池类型
细胞
抗原
小胶质细胞
绿色荧光蛋白
免疫学
体外
遗传学
炎症
基因
作者
Judith Agudo,Albert Ruzo,Eun Sook Park,Robert E. Sweeney,Veronika Kana,Meng Wu,Yong Zhao,Dieter Egli,Miriam Mérad,Brian D. Brown
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.
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