Epidermal Growth Factor Modulates Fetal Thymocyte Growth and Differentiation

In the present study, we used the fetal organ culture (FTOC) technique in order to study a putative effect of epidermal growth factor (EGF) on the thymus ontogeny. Functional EGF receptors and more recently the EGF molecule itself, respectively, on the membrane of epithelial components of thymic stroma and on a few thymocytes in adult thymus, had been reported in the literature. We could observe a dose-dependent decrease in cellularity and a progressive retention of thymocytes in the double-negative (CD4(-)/CD8(-)) stage of differentiation when exogenous EGF was added. Epidermal growth factor interfered with both fetal stroma growth and thymocyte development at a precise moment, that is, in the passage from double-negative to the double-positive (CD4(+)/CD8(+)) stage. After a 7-day FTOC in the presence of EGF, most cells recovered were Thy-1.2(+), c-kit(+), TSA1(-/int), CD3(-), and one of CD44(high)/CD25(int), CD44(-)/CD25(int), or CD44(-)/CD25(-). Some developed into γδTCR(+) cells with a mature (CD3(+)) phenotype, but not into αβTCR(+) thymocytes. It seems that EGF addition makes the cultures "nonpermissible" for αβTCR(+) thymocyte generation. We report here the presence of a high Mr "EGF-like" molecule on the membrane of fetal thymocytes, which role in the observed effects is under investigation. Further biochemical characterization of this molecule is still required, because its presence was only evidenced on the basis of its antigenicity.