Thymic epithelium is involved in negative selection, but its precise r
ole in selecting the CD4 T cell repertoire remains elusive. By using t
wo transgenic mice, we have investigated how medullary thymic epitheli
um (mTE) and bone marrow (BM)-derived cells contribute to tolerance of
CD4 T cells to nuclear beta-galactosidase (beta-gal). CD4 T cells wer
e not tolerant when beta-gal was expressed in thymic BM-derived cells.
In contrast, CD4 T cells of mice expressing beta-gal in mTE were tole
rized. Tolerance resulted from presentation of endogenous beta-gal by
mTE cells but not from cross-priming. mTE cells presented nuclear beta
-gal to a Th clone in vitro, while thymic dendritic cells did not. The
data indicate that mTE but not thymic BM-derived cells can use a MHC
class II endogenous presentation pathway to induce tolerance to nuclea
r proteins.