Immature dendritic cells (DCs) sample their environment for antigens and after stimulation present peptide associated with major histocompatibility complex class II (MHC II) to naive T cells. We have studied the intracellular trafficking of MHC II in cultured DCs. In immature cells, the majority of MHC II was stored intracellularly at the internal vesicles of multivesicular bodies (MVBs). In contrast, DM, an accessory molecule required for peptide loading, was located predominantly at the limiting membrane of MVBs. After stimulation, the internal vesicles carrying MHC II were transferred to the limiting membrane of the MVB, bringing MHC II and DM to the same membrane domain. Concomitantly, the MVBs transformed into long tubular organelles that extended into the periphery of the cells. Vesicles that were formed at the tips of these tubules nonselectively incorporated MHC II and DM and presumably mediated transport to the plasma membrane. We propose that in maturing DCs, the reorganization of MVBs is fundamental for the timing of MHC II antigen loading and transport to the plasma membrane.
Reorganization of multivesicular bodies regulates MHC class II antigen presentation by dendritic cells
M. Kleijmeer and G. Ramm contributed equally to this work.
Abbreviations used in this paper: CIIV, class II vesicle; DAB, diaminobenzidine; DC, dendritic cell; Ii, invariant chain; LPS, lipopolysaccharide; MHC II, major histocompatibility complex class II; MIIC, MHC II–enriched compartment; MVB, multivesicular body.
Monique Kleijmeer, Georg Ramm, Danita Schuurhuis, Janice Griffith, Maria Rescigno, Paola Ricciardi-Castagnoli, Alexander Y. Rudensky, Ferry Ossendorp, Cornelis J.M. Melief, Willem Stoorvogel, Hans J. Geuze; Reorganization of multivesicular bodies regulates MHC class II antigen presentation by dendritic cells . J Cell Biol 1 October 2001; 155 (1): 53–64. doi: https://doi.org/10.1083/jcb.200103071
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