Bone marrow derived cells (dendritic cells, macrophages and B cells) a
re involved in antigen presentation and T cell tolerance. However, the
precise functions of each cell type remain unclear. To determine the
role of macrophages we produced transgenic mice expressing I-E molecul
es only on macrophages, by introducing the hybrid gene containing the
colony stimulating factor-1 (CSF-1) receptor promoter region and the s
tructural gene encoding E(alpha)d into C57BL/6 mice. In these mice I-E
restricted antigen presentation and T cell priming were impaired. Wit
h respect to T cell tolerance, I-E reactive T cells were anergized but
not clonally deleted. These results clearly demonstrate that macropha
ges by themselves are defective in efficient I-E restricted antigen pr
esentation, so that T cells exposed to antigens expressed on macrophag
es are led to anergy.