Thymic origin of intestinal αβ T cells revealed by fate mapping of RORγt+ cells

被引:408
作者
Eberl, G
Littman, DR
机构
[1] NYU, Sch Med, Mol Pathogenesis Program, New York, NY 10016 USA
[2] NYU, Sch Med, Skirball Inst Biomol Med, Howard Hughes Med Inst, New York, NY 10016 USA
关键词
D O I
10.1126/science.1096472
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
Intestinal intraepithelial T lymphocytes (IELs) are likely to play a key role in host mucosal immunity and, unlike other T cells, have been proposed to differentiate from local precursors rather than from thymocytes. We show here that IELs expressing the alphabeta T cell receptor are derived from precursors that express RORgammat, an orphan nuclear hormone receptor detected only in immature CD4(+) CD8(+) thymocytes, fetal lymphoid tissue-inducer (LTi) cells, and LTi-like cells in crypto-patches within the adult intestinal lamina propria. Using cell fate mapping, we found that all intestinal alphabeta T cells are progeny of CD4(+) CD8(+) thymocytes, indicating that the adult intestine is not a significant site for alphabeta T cell development. Our results suggest that intestinal RORgammat(+) cells are local organizers of mucosal lymphoid tissue.
引用
收藏
页码:248 / 251
页数:4
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