Cbl-b is a negative regulator of receptor clustering and raft aggregation in T cells

Immunity. 2000 Oct;13(4):463-73. doi: 10.1016/s1074-7613(00)00046-7.

Abstract

Stimulation of T cells via the antigen and costimulatory receptors leads to the organization of a supramolecular activation cluster called the immune synapse. We report that loss of the molecular adaptor Cbl-b in T cells frees antigen receptor-triggered receptor clustering, lipid raft aggregation, and sustained tyrosine phosphorylation from the requirement for CD28 costimulation. Introduction of the cbl-b mutation into a vav1-/- background relieved the functional defects of vav1-/- T cells and caused spontaneous autoimmunity. Wiscott Aldrich Syndrome protein (WASP) was found to be essential for deregulated proliferation and membrane receptor reorganization of cbl-b mutant T cells. Antigen receptor-triggered Ca2+ mobilization, cytokine production, and receptor clustering can be genetically uncoupled in cbl-b mutant T cells. Thus, Cbl-b functions as a negative regulator of receptor clustering and raft aggregation in T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Animals
  • Autoimmune Diseases / genetics
  • Calcium Signaling / genetics
  • Calcium Signaling / immunology
  • Carrier Proteins / genetics
  • Carrier Proteins / physiology*
  • Cell Cycle Proteins*
  • Cytotoxicity, Immunologic / genetics
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Down-Regulation / genetics
  • Down-Regulation / immunology*
  • Enzyme Activation / genetics
  • Enzyme Activation / immunology
  • Genetic Complementation Test
  • Humans
  • Interleukin-2 / biosynthesis
  • Lymphocyte Activation / genetics
  • Lymphoproliferative Disorders / genetics
  • Membrane Microdomains / genetics
  • Membrane Microdomains / immunology*
  • Membrane Microdomains / metabolism*
  • Mice
  • Mice, Knockout
  • NFATC Transcription Factors
  • Nuclear Proteins*
  • Phosphoproteins / deficiency
  • Phosphoproteins / genetics
  • Phosphoproteins / physiology*
  • Phosphorylation
  • Proteins / genetics
  • Proteins / physiology
  • Proto-Oncogene Proteins / deficiency
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / physiology
  • Proto-Oncogene Proteins c-cbl
  • Proto-Oncogene Proteins c-vav
  • Receptor Aggregation / genetics
  • Receptor Aggregation / immunology*
  • Receptors, Antigen, T-Cell / metabolism
  • Receptors, Antigen, T-Cell / physiology
  • T-Lymphocytes / enzymology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism*
  • T-Lymphocytes, Cytotoxic / immunology
  • T-Lymphocytes, Cytotoxic / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcriptional Activation / immunology
  • Tyrosine / metabolism
  • Ubiquitin-Protein Ligases*
  • Wiskott-Aldrich Syndrome / genetics
  • Wiskott-Aldrich Syndrome / immunology
  • Wiskott-Aldrich Syndrome Protein
  • cdc42 GTP-Binding Protein / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • Cblb protein, mouse
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Interleukin-2
  • NFATC Transcription Factors
  • Nuclear Proteins
  • Phosphoproteins
  • Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-vav
  • Receptors, Antigen, T-Cell
  • Transcription Factors
  • VAV1 protein, human
  • Vav1 protein, mouse
  • WAS protein, human
  • Was protein, mouse
  • Wiskott-Aldrich Syndrome Protein
  • Tyrosine
  • CBLB protein, human
  • Proto-Oncogene Proteins c-cbl
  • Ubiquitin-Protein Ligases
  • cdc42 GTP-Binding Protein