Domains of the TCR beta-chain required for early thymocyte development

被引:28
|
作者
Jacobs, H
Iacomini, J
vandeVen, M
Tonegawa, S
Berns, A
机构
[1] NETHERLANDS CANC INST,DIV MOL GENET,NL-1066 CX AMSTERDAM,NETHERLANDS
[2] MIT,DEPT BIOL,CAMBRIDGE,MA 02139
[3] MIT,HOWARD HUGHES MED INST,CTR CANC RES,CAMBRIDGE,MA 02139
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 1996年 / 184卷 / 05期
关键词
D O I
10.1084/jem.184.5.1833
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The T cell receptor beta (TCR beta) chain controls the developmental transition from CD4(-)CD8(-) to CD4(+)8(+) thymocytes. We show that the extracellular constant region and the transmembrane region, but not the variable domain or cytoplasmic tail of the TCR beta chain are required for this differentiation step. TCR beta mutant chains lacking the cytoplasmic tail can be found at the cell surface both in functional TCR/CD3 complexes and in a GPI-anchored monomeric form indicating that the cytoplasmic tail of the TCR beta chain functions as an ER retention signal. The concordance between cell surface expression of the mutant chains as TCR/CD3 complexes and their capacity to mediate thymocyte differentiation supports the CD3 mediated feedback model in which preTCR/CD3 complexes control the developmental transition from CD4(-)CD8(-) to CD4(+)CD8(+) thymocytes.
引用
收藏
页码:1833 / 1843
页数:11
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