Themis, a T cell-specific protein important for late thymocyte development

被引:118
|
作者
Lesourne, Renaud [1 ]
Uehara, Shoji [1 ]
Lee, Jan [1 ]
Song, Ki-Duk [1 ]
Li, LiQi [1 ]
Pinkhasov, Julia [1 ]
Zhang, Yongqing [2 ]
Weng, Nan-Ping [3 ]
Wildt, Kathryn F. [4 ]
Wang, Lie [4 ]
Bosselut, Remy [4 ]
Love, Paul E. [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Lab Mammalian Genes & Dev, Bethesda, MD USA
[2] NIMH, Intramural Res Program, DNA Array Unit, Bethesda, MD 20892 USA
[3] NIA, Immunol Lab, Bethesda, MD 20892 USA
[4] NCI, Lab Immune Cell Biol, NIH, Bethesda, MD 20892 USA
关键词
CD4-CD8 LINEAGE COMMITMENT; POSITIVE SELECTION SIGNALS; IN-VIVO; CORECEPTOR EXPRESSION; TRANSCRIPTION FACTORS; DIFFERENTIATION; CD4; TCR; RECEPTOR; THYMUS;
D O I
10.1038/ni.1768
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During positive selection, thymocytes transition through a stage during which T cell antigen receptor (TCR) signaling controls CD4-versus-CD8 lineage 'choice' and subsequent maturation. Here we describe a previously unknown T cell-specific protein, Themis, that serves a distinct function during this stage. In Themis(-/-) mice, thymocyte selection was impaired and the number of transitional CD4(+)CD8(int) thymocytes as well as CD4(+) or CD8(+) single-positive thymocytes was lower. Notably, although we detected no overt TCR-proximal signaling deficiencies, Themis(-/-) CD4(+)CD8(int) thymocytes showed developmental defects consistent with attenuated signaling that were reversible by TCR stimulation. Our results identify Themis as a critical component of the T cell developmental program and suggest that Themis functions to sustain and/or integrate signals required for proper lineage commitment and maturation.
引用
收藏
页码:840 / U53
页数:9
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