The Journal of Experimental Medicine · 1996 · 143 citations · 39 references
Life SciencesDevelopmental BiologyImmunologyCell DifferentiationCell Fate SpecificationCellular ImmunologyImmune Cell DifferentiationMajor Histocompatibility ComplexT Cell BiologyT Cell DevelopmentT Cell DifferentiationThymic DevelopmentCd4 Positive T Cell DifferentiationCd4 Positive T CellsMhc Class I MoleculesT Helper CellsThymic DifferentiationThymic T Cell DevelopmentTransgenic MiceTransmembrane Domains
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.
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Mice lacking MHC class II molecules
Dominic Cosgrove, David W. Gray, Andrée Dierich et al. · Cell · 1991 · 850 citations · Full text
Peripheral Selection of the T Cell Repertoire
Bénédita Rocha, Harald von Boehmer · Science · 1991 · 657 citations