Reorganization of multivesicular bodies regulates MHC class II antigen presentation by dendritic cells

被引:235
作者
Kleijmeer, M
Ramm, G
Schuurhuis, D
Griffith, J
Rescigno, M
Ricciardi-Castagnoli, P
Rudensky, AY
Ossendorp, F
Melief, CJM
Stoorvogel, W
Geuze, HJ
机构
[1] Univ Med Ctr, Inst Biomembranes, Dept Cell Biol, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr, Ctr Biomed Genet, NL-3584 CX Utrecht, Netherlands
[3] Leiden Univ, Med Ctr, Dept Immunohaematol & Blood Transfus, NL-2300 RC Leiden, Netherlands
[4] Univ Milano Bicocca, Dept Biosci & Biotechnol, I-20126 Milan, Italy
[5] Univ Washington, Sch Med, Howard Hughes Med Inst, Seattle, WA 98195 USA
关键词
antigen presentation; dendritic cells; endosomes; lysosomes; major histocompatibility complex;
D O I
10.1083/jcb.200103071
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
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.
引用
收藏
页码:53 / 63
页数:11
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