Positive selection of T cells begins with TCR alpha beta(lo) thymic progenitors. Here, we show that the most efficient TCR(lo) progenitors are c-kit(+) with intermediate levels of CD4 and CD8 (DPint). Positive selection of DPint TCR(lo) c-kit(+) cells results in TCR(med) CD69(+) c-kit(+) transitional intermediates that show increased TCRV beta frequencies to selecting superantigen (SAg) that are committed to the CD4 or CD8 pathway. The cells on the c-kit(+) maturation pathway maintain Bcl-2 expression. Most DPint c-kit(+) progenitors fail positive selection, and become DPhi c-kit(+) cells that lose Bcl-2 expression. Some DPhi c-kit blast cells can be salvaged to produce mature single-positive (SP) cells. DPint c-kit(+) maturation to SP cells can occur in <12 hr in vitro on thymic stromal monolayers.
机构:Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Building 4
FOWLKES, BJ
SCHWEIGHOFFER, E
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机构:Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Building 4
机构:Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Building 4
FOWLKES, BJ
SCHWEIGHOFFER, E
论文数: 0引用数: 0
h-index: 0
机构:Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Building 4