Cytoplasmic tail-dependent localization of CD1b antigen-presenting molecules to MIICs

Science. 1996 Jul 19;273(5273):349-52. doi: 10.1126/science.273.5273.349.

Abstract

CD1 proteins have been implicated as antigen-presenting molecules for T cell-mediated immune responses, but their intracellular localization and trafficking remain uncharacterized. CD1b, a member of this family that presents microbial lipid antigens of exogenous origin, was found to localize to endocytic compartments that included the same specialized subset of endosomes in which major histocompatibility complex (MHC) class II molecules are proposed to bind endocytosed antigens. Unlike MHC class II molecules, which traffic to antigen-loading endosomal compartments [MHC class II compartments (MIICs)] primarily as a consequence of their association with the invariant chain, localization of CD1b to these compartments was dependent on a tyrosine-based motif in its own cytoplasmic tail.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Antigens, CD1 / analysis
  • Antigens, CD1 / chemistry
  • Antigens, CD1 / metabolism*
  • B-Lymphocytes
  • Base Sequence
  • Cell Compartmentation
  • Cell Line
  • Cell Membrane / immunology
  • Coated Pits, Cell-Membrane / immunology
  • Endocytosis
  • Endosomes / immunology*
  • Endosomes / ultrastructure
  • HLA-D Antigens / analysis
  • HeLa Cells
  • Histocompatibility Antigens Class II / analysis
  • Histocompatibility Antigens Class II / metabolism*
  • Humans
  • Microscopy, Immunoelectron
  • Molecular Sequence Data
  • Monocytes / immunology
  • Transfection

Substances

  • Antigens, CD1
  • H2-M antigens
  • HLA-D Antigens
  • HLA-DM antigens
  • Histocompatibility Antigens Class II