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Sustained Expression of Pre-TCR Induced β-Catenin in Post-β-Selection Thymocytes Blocks T Cell Development
被引:15
作者:
Xu, Mai
Sharma, Archna
Hossain, M. Zulfiquer
Wiest, David L.
[2
]
Sen, Jyoti Misra
[1
]
机构:
[1] NIA, Lymphocyte Dev Unit, Immunol Lab, NIH,Biomed Res Ctr, Baltimore, MD 21224 USA
[2] Fox Chase Canc Ctr, Div Basic Sci, Philadelphia, PA 19111 USA
基金:
美国国家卫生研究院;
关键词:
ROR-GAMMA-T;
TRANSCRIPTION FACTORS;
POSITIVE SELECTION;
RECEPTOR;
SIGNALS;
DIFFERENTIATION;
CHAIN;
PROLIFERATION;
SURVIVAL;
CYCLE;
D O I:
10.4049/jimmunol.182.2.759
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Pre-TCR and IL-7R signals regulate beta-selection of thymocytes and then must be down-regulated for further development. However, the molecular events that control down-regulation remain unknown. We and others have previously shown that beta-catenin in cooperation with TCF regulates beta-selection. In this paper, we demonstrate that beta-catenin expression is stringently regulated by intrathymic signals, it is expressed at the highest levels in the pre-TCR signaled thymocytes, and is down-regulated in post-beta-selection thymocytes. Pre-TCR-induced beta-catenin regulates initial stages of pre-TCR signaling including expression of early growth response (Egr) genes but must be down-regulated to express ROR gamma t, which is essential for maturation to the CD4(+)CD8(+) double positive (DP) stage. Sustained expression of beta-catenin results in the generation of IL-7R-, Egr-, and TGF beta-expressing pre-DP thymocytes that are blocked in development. These data are consistent with a model in which post-beta-selection, pre-TCR-induced beta-catenin expression must return to background levels for efficient transition to the DP stage. The Journal of Immunology, 2009, 182: 759-765.
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页码:759 / 765
页数:7
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