CD4 raft association and signaling regulate molecular clustering at the immunological synapse site

J Immunol. 2004 May 15;172(10):5887-92. doi: 10.4049/jimmunol.172.10.5887.

Abstract

T cell activation is associated with the partitioning of TCRs and other signaling proteins, forming an immunological synapse. This study demonstrates a novel function for the CD4 coreceptor in regulating molecular clustering at the immunological synapse site. We show using transgenic mouse and retroviral reconstitution studies that CD4 is required for TCR/protein kinase C (PKC) theta clustering. Specifically, we demonstrate that CD4 palmitoylation sequences are required for TCR/PKCtheta raft association and subsequent clustering, indicating a particular role for raft-associated CD4 molecules in regulating immune synapse organization. Although raft association of CD4 is necessary, it is not sufficient to mediate clustering, as cytoplasmic tail deletion mutants are able to localize to rafts, but are unable to mediate TCR/PKCtheta clustering, indicating an additional requirement for CD4 signaling. These studies suggest that CD4 coreceptor function is regulated not only through its known signaling function, but also by posttranslational lipid modifications which regulate localization of CD4 in lipid rafts.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CD4 Antigens / chemistry
  • CD4 Antigens / genetics
  • CD4 Antigens / metabolism
  • CD4 Antigens / physiology*
  • Cytochromes c / immunology
  • Cytochromes c / metabolism
  • Cytoplasm / genetics
  • Cytoplasm / immunology
  • Cytoplasm / metabolism
  • Isoenzymes / metabolism
  • Kinetics
  • Membrane Microdomains / immunology*
  • Membrane Microdomains / metabolism*
  • Mice
  • Mice, Inbred A
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Molecular Sequence Data
  • Moths
  • Palmitic Acid / metabolism
  • Peptide Fragments / immunology
  • Peptide Fragments / metabolism
  • Protein Kinase C / metabolism
  • Protein Kinase C-theta
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / metabolism*
  • Signal Transduction / genetics
  • Signal Transduction / immunology*
  • T-Lymphocyte Subsets / enzymology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism*
  • Th1 Cells / enzymology
  • Th1 Cells / immunology
  • Th1 Cells / metabolism

Substances

  • CD4 Antigens
  • Isoenzymes
  • Peptide Fragments
  • Receptors, Antigen, T-Cell
  • Palmitic Acid
  • Cytochromes c
  • Prkcq protein, mouse
  • Protein Kinase C
  • Protein Kinase C-theta