Abstract
CD83 is a member of the Ig superfamily expressed primarily by mature dendritic cells (DCs). In mice, CD83 expression by thymic stromal cells regulates CD4+ T cell development, with CD83-/- mice demonstrating dramatic reductions in both thymus and peripheral CD4+ T cells. In this study, CD83 expression was also found to affect MHC class II antigen expression within the thymus and periphery. CD83 deficiency reduced cell-surface class II antigen expression by 25-50% on splenic B cells and DCs, thymic epithelial cells and peritoneal macrophages. Reduced class II expression was a stable and intrinsic property that resulted from increased internalization of class II from the surface of CD83-/- B cells. Otherwise, class II antigen transcription, intracellular expression, heterodimer structure, antigen processing and antigen presentation were normal. Reduced class II antigen expression was not the primary cause of the CD83-/- phenotype since thymocyte and peripheral T cell development was normal in class II+/- mice. Comparable blocks in CD4+ thymocyte development were also observed in CD83-/- and CD83-/-class II+/- littermates. TCR and CD69 expression patterns in CD83-/- mice further suggested that double-positive thymocytes proceed through the class II-dependent stages of positive selection in the absence of CD83. These studies further emphasize a role for CD83 in lymphocyte development and immune regulation and reveal an unexpected role for CD83 expression in influencing cell-surface MHC class II turnover.
Original language | English |
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Pages (from-to) | 977-992 |
Number of pages | 16 |
Journal | International Immunology |
Volume | 19 |
Issue number | 8 |
DOIs | |
State | Published - Aug 2007 |
Externally published | Yes |
Keywords
- B cell
- CD83
- Cell surface expression
- MHC class II
- Turnover