Abstract
Thymic T cell development is controlled by T cell receptor (TCR)-major histocompatibility complex (MHC) interactions, whereas a further dependence of peripheral mature T cells on TCR-MHC contact has not been described so far. To study this question, CD4 T cell survival was surveyed in mice lacking MHC class II expression and in mice expressing MHC class II exclusively on dendritic cells. Since neither of these mice positively select CD4 T cells in the thymus, they were grafted with MHC class II-positive embryonic thymic tissue, which had been depleted of bone marrow derived cells. Although the thymus grafts in both hosts were repopulated with host origin thymocytes of identical phenotype and numbers, an accumulation of CD4+ T cells in peripheral lymphoid organs could only be observed in mice expressing MHC class II on dendritic cells, but not in mice that were completely MHC class II deficient. As assessed by histology, the accumulating peripheral CD4 T cells were found to be in close contact with MHC class II+ dendritic cells, suggesting that CD4 T cells need peripheral MHC class II expression for survival and that class II+ dendritic cells might play an important role for the longevity of CD4 T cells.
MeSH Terms
Animals
CD11 Antigens/genetics
CD4-Positive T-Lymphocytes/cytology,immunology
Cell Communication/immunology
Cell Differentiation/immunology
Cell Movement/genetics,immunology
Cell Survival/immunology
Dendritic Cells/immunology,metabolism
Fetus
Histocompatibility Antigens Class II/biosynthesis,genetics
Lymph Nodes/cytology,immunology
Lymphoid Tissue/immunology
Mice
Mice, Inbred C57BL
Mice, Inbred DBA
Mice, Transgenic
Regeneration/immunology
Thymus Gland/transplantation
Chemicals
CD11 Antigens
Histocompatibility Antigens Class II
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Brocker T
Basel Institute for Immunology, Switzerland. BROCKER@bii.ch
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