Author/Authors :
Yoko Fujimoto، نويسنده , , Lili Tu، نويسنده , , Ann S. Miller، نويسنده , , Cheryl Bock، نويسنده , , Manabu Fujimoto، نويسنده , , Carolyn Doyle، نويسنده , , Douglas A. Steeber، نويسنده , , Thomas F. Tedder، نويسنده ,
Abstract :
T lymphocyte selection and lineage commitment in the thymus requires multiple signals. Herein, CD4+ T cell generation required engagement of CD83, a surface molecule expressed by thymic epithelial and dendritic cells. CD83-deficient (CD83−/−) mice had a specific block in CD4+ single-positive thymocyte development without increased CD4+CD8+ double- or CD8+ single-positive thymocytes. This resulted in a selective 75%–90% reduction in peripheral CD4+ T cells, predominantly within the naive subset. Wild-type thymocytes and bone marrow stem cells failed to differentiate into mature CD4+ T cells when transferred into CD83−/− mice, while CD83−/− thymocytes and stem cells developed normally in wild-type mice. Thereby, CD83 expression represents an additional regulatory component for CD4+ T cell development in the thymus.