| Literature DB >> 8241051 |
T Miyazaki1, G Suzuki, K Yamamura.
Abstract
Bone marrow derived cells (dendritic cells, macrophages and B cells) are 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 molecules only on macrophages, by introducing the hybrid gene containing the colony stimulating factor-1 (CSF-1) receptor promoter region and the structural gene encoding E alpha d into C57BL/6 mice. In these mice I-E restricted antigen presentation and T cell priming were impaired. With respect to T cell tolerance, I-E reactive T cells were anergized but not clonally deleted. These results clearly demonstrate that macrophages by themselves are defective in efficient I-E restricted antigen presentation, so that T cells exposed to antigens expressed on macrophages are led to anergy.Entities:
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Year: 1993 PMID: 8241051 DOI: 10.1093/intimm/5.9.1023
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823