The cytoplasmic domain of CD4 promotes the development of CD4 lineage T cells

被引:124
作者
Itano, A
Salmon, P
Kioussis, D
Tolaini, M
Corbella, P
Robey, E
机构
[1] UNIV CALIF BERKELEY, DEPT MOLEC & CELL BIOL, DIV IMMUNOL, BERKELEY, CA 94720 USA
[2] NATL INST MED RES, DIV MOL IMMUNOL, LONDON NW7 1AA, ENGLAND
关键词
D O I
10.1084/jem.183.3.731
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymocytes must bind major histocompatibility complex (MHC) proteins on thymic epithelial cells in order to mature into either CD8(+) cytotoxic T cells or CD4(+) helper T cells. Thymic precursors express both CD8 and CD4, and it has been suggested that the intracellular signals generated by CD8 or CD4 binding to class I or II MHC, respectively, might influence the fate of uncommitted cells. Here we test the notion that intracellular signaling by CD4 directs the development of thymocytes to a CD4 lineage. A hybrid protein consisting of the CD8 extracellular and transmembrane domains and the cytoplasmic domain of CD4 (CD884) should bind class I MHC but deliver a CD4 intracellular signal. We find that expression of a hybrid CD884 protein in thymocytes of transgenic mice leads to the development of large numbers of class I MHC-specific, CD4 lineage T cells. We discuss these results in terms of current models for CD4 and CD8 lineage commitment.
引用
收藏
页码:731 / 741
页数:11
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