MHC class II-specific T cells can develop in the CD8 lineage when CD4 is absent

被引:200
作者
Matechak, EO
Killeen, N
Hedrick, SM
Fowlkes, BJ
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT MICROBIOL,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,DEPT IMMUNOL,SAN FRANCISCO,CA 94143
[3] UNIV CALIF SAN FRANCISCO,DEPT BIOCHEM,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,DEPT BIOPHYS,SAN FRANCISCO,CA 94143
[5] UNIV CALIF SAN DIEGO,DEPT BIOL,LA JOLLA,CA 92093
[6] UNIV CALIF SAN DIEGO,CTR CANC,LA JOLLA,CA 92093
关键词
RECEPTOR TRANSGENIC MICE; ANTIGEN RECEPTOR; THYMOCYTE DEVELOPMENT; IMMATURE THYMOCYTES; NEGATIVE SELECTION; THYMIC SELECTION; DEFICIENT MICE; LYMPHOCYTES; EXPRESSION; MOLECULES;
D O I
10.1016/S1074-7613(00)80247-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The generation of mature CD4 T cells from CD4(+)CD8(+) precursor thymocytes usually requires corecognition of class II MHC by a TCR and CD4, while the production of mature CD8 T cells requires corecognition of class I MHC by a TCR and CD8. To assess the role of the CD4 coreceptor in development and lineage commitment, we generated CD4-deficient mice expressing a transgenic class Ii-specific TCR. Surprisingly, in the absence of CD4 a large number of T cells mature, but these cells appear in the CD8 lineage. Thus, when CD4 is present, the majority of immature T cells with this class Ii-specific TCR choose the CD4 lineage but develop in the CD8 pathway when CD4 is absent. The results indicate that even for TCRs that are not dependent on coreceptor for MHC recognition, the coreceptor can influence the lineage choice. These findings are considered in terms of a quantitative signaling model for CD4/CD8 lineage commitment.
引用
收藏
页码:337 / 347
页数:11
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