Abstract
Interaction of Ag-loaded dendritic cells with Ag-specific CD4 T cells induces the formation of long tubular class II MHC-positive compartments that polarize toward the T cell. We show involvement of a Toll-like receptor-mediated signal in this unusual form of intracellular class II MHC trafficking. First, wild-type dendritic cells loaded with LPS-free Ag failed to show formation of class II-positive tubules upon Ag-specific T cell engagement, but did so upon supplementation of the Ag with low concentrations of LPS. Second, Ag-loaded myeloid differentiation factor 88 -deficient dendritic cells failed to form these tubules upon interaction with T cells, regardless of the presence of LPS. Finally, inclusion of a cell-permeable peptide that blocks TNFR-associated factor 6 function, downstream of myeloid differentiation factor N, blocked T cell-dependent tubulation. A Toll-like receptor-dependent signal is thus required to allow Ag-loaded dendritic cells to respond to T cell contact by formation of extended endosomal compartments. This activation does not result in massive translocation of class II MHC molecules to the cell surface.
| Original language | English |
|---|---|
| Pages (from-to) | 4081-4088 |
| Number of pages | 8 |
| Journal | Journal of Immunology |
| Volume | 171 |
| Issue number | 8 |
| Publication status | Published - 15 Oct 2003 |
Keywords
- INVARIANT CHAIN DEGRADATION
- ANTIGEN PRESENTATION
- DEFECTIVE INTERLEUKIN-1
- LYSOSOMAL COMPARTMENTS
- INFLAMMATORY STIMULI
- FAMILY-MEMBER
- COMPLEX
- TRANSPORT
- MYD88
- DISTINCT
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