Receptor signals and nuclear events in CD4 and CD8 T cell lineage commitment

被引:23
作者
Laky, K [1 ]
Fowkes, BJ [1 ]
机构
[1] NIAID, Cellular & Mol Immunol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.coi.2005.02.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MHC specificity in positive selection is a major determinant in the CD4/CD8 T cell lineage decision. Previous studies support the view that quantitative differences in T cell receptor (TCR) signaling in immature CD4(+)CD8(+) double positive thymocytes leads to an instructive bias in CD4/CD8 T cell lineage commitment that must be re-inforced in subsequent selection steps to ensure that MHC-restricted antigen recognition is linked to appropriate effector functions in mature T cells. Recent work has further defined the TCR signaling pathways involved in this process, but a major effort has been made to identify transcription factors and other regulators of CID4 and CD8 T cell lineage commitment. Methods and screens for detecting changes in gene expression, associated with TCR signaling in positive selection and lineage determination, are starting to provide a better understanding of these complex developmental processes.
引用
收藏
页码:116 / 121
页数:6
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