T cell receptor γ gene regulatory sequences prevent the function of a novel TCRγ/pTα pre-T cell receptor

被引:37
作者
Kang, JS
Fehling, HJ
Laplace, C
Malissen, M
Cado, D
Raulet, DH
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Canc Res Lab, Div Immunol, Berkeley, CA 94720 USA
[3] Basel Inst Immunol, CH-4005 Basel, Switzerland
[4] CNRS, INSERM, Ctr Immunol, F-13288 Marseille 9, France
关键词
D O I
10.1016/S1074-7613(00)80576-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Expression of a TCR gamma transgene in RAG-1(-/-) mice resulted in the development of a limited number of CD4(+)CD8(+) (DP) thymocytes. In vivo treatments with anti-TCR gamma antibody enhanced the number of DP thymocytes, demonstrating that TCR gamma chains were expressed on the cell surface in the absence of delta, alpha, or beta chains. Mutations in pT alpha or CD3 epsilon genes abolished transgene-induced DP cell development, indicating that TCR gamma can associate with pT alpha and CD3 to form a novel pre-TCR. With a transgene containing additional regulatory sequences, TCR gamma expression was downregulated in DP cells, and little DP cell development occurred. Thus, the function of the endogenous TCR gamma/pT alpha is limited by the transcriptional down-regulation of TCR gamma genes that normally accompanies DP cell development.
引用
收藏
页码:713 / 721
页数:9
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