CCR7-mediated migration of developing thymocytes to the medulla is essential for negative selection to tissue-restricted antigens

被引:96
|
作者
Nitta, Takeshi [1 ]
Nitta, Sachiko [1 ]
Lei, Yu [1 ]
Lipp, Martin [2 ]
Takahama, Yousuke [1 ]
机构
[1] Univ Tokushima, Div Expt Immunol, Inst Genome Res, Tokushima 7708503, Japan
[2] Max Delbruck Ctr Mol Med, Dept Mol Tumor Genet & Imunogenet, D-13092 Berlin, Germany
关键词
chemokine; self-tolerance; thymic medulla; thymic epithelial cell; POSITIVELY SELECTED THYMOCYTES; THYMIC EPITHELIAL-CELLS; CLONAL DELETION; T-CELLS; EXPRESSION; RECEPTOR; AIRE; TOLERANCE; CD4;
D O I
10.1073/pnas.0906956106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Immature double-positive thymocytes are generated in the thymic cortex, and on positive selection, are induced to differentiate into mature single-positive thymocytes and relocate to the medulla. CCR7 is pivotal for cortex-to-medulla migration of positively selected thymocytes, and CCR7-mediated migration to the medulla is essential for establishing central tolerance, thereby, preventing tissue-specific autoimmunity. However, it was unclear how CCR7-mediated migration to the medulla affects the establishment of self-tolerance. Here, we show that the deletion of thymocytes specific for insulin-promoter-driven tissue-restricted antigens (TRAs) is significantly impaired in CCR7- or CCR7-ligand-deficient mice. These results indicate that CCR7-mediated migration to the medulla contributes to the negative selection of TRA-reactive thymocytes.
引用
收藏
页码:17129 / 17133
页数:5
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