Transport of peptide-MHC class II complexes in developing dendritic cells

Science. 2000 Apr 21;288(5465):522-7. doi: 10.1126/science.288.5465.522.

Abstract

Major histocompatibility complex class II (MHC II) molecules capture peptides within the endocytic pathway to generate T cell receptor (TCR) ligands. Immature dendritic cells (DCs) sequester intact antigens in lysosomes, processing and converting antigens into peptide-MHC II complexes upon induction of DC maturation. The complexes then accumulate in distinctive, nonlysosomal MHC II+ vesicles that appear to migrate to the cell surface. Although the vesicles exclude soluble lysosomal contents and antigen-processing machinery, many contain MHC I and B7 costimulatory molecules. After arrival at the cell surface, the MHC and costimulatory molecules remain clustered. Thus, transport of peptide-MHC II complexes by DCs not only accomplishes transfer from late endocytic compartments to the plasma membrane, but does so in a manner that selectively concentrates TCR ligands and costimulatory molecules for T cell contact.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal
  • Antigen Presentation*
  • Antigens, CD / immunology
  • Antigens, CD / metabolism
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • B7-2 Antigen
  • Biological Transport
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Cell Membrane / immunology
  • Cell Membrane / metabolism
  • Cells, Cultured
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism*
  • Endocytosis
  • Endosomes / immunology
  • Endosomes / metabolism
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class I / metabolism
  • Histocompatibility Antigens Class II / immunology
  • Histocompatibility Antigens Class II / metabolism*
  • Kinetics
  • Ligands
  • Lipopolysaccharides / immunology
  • Lysosomes / immunology
  • Lysosomes / metabolism
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred C3H
  • Muramidase / immunology
  • Muramidase / metabolism*
  • Peptide Fragments / immunology
  • Peptide Fragments / metabolism*
  • Receptors, Antigen, T-Cell / metabolism
  • Thiazoles / pharmacology
  • Thiazolidines

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • B7-2 Antigen
  • Bridged Bicyclo Compounds, Heterocyclic
  • Cd86 protein, mouse
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • I-Ak antigen
  • I-E-antigen
  • Ligands
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • Peptide Fragments
  • Receptors, Antigen, T-Cell
  • Thiazoles
  • Thiazolidines
  • hen egg lysozyme peptide (46-61)
  • Muramidase
  • latrunculin B