CD3ε recruits Numb to promote TCR degradation

Int Immunol. 2016 Mar;28(3):127-37. doi: 10.1093/intimm/dxv060. Epub 2015 Oct 27.

Abstract

Modulation of TCR signaling upon ligand binding is achieved by changes in the equilibrium between TCR degradation, recycling and synthesis; surprisingly, the molecular mechanism of such an important process is not fully understood. Here, we describe the role of a new player in the mediation of TCR degradation: the endocytic adaptor Numb. Our data show that Numb inhibition leads to abnormal intracellular distribution and defective TCR degradation in mature T lymphocytes. In addition, we find that Numb simultaneously binds to both Cbl and a site within CD3ε that overlaps with the Nck binding site. As a result, Cbl couples specifically to the CD3ε chain to mediate TCR degradation. The present study unveils a novel role of Numb that lies at the heart of TCR signaling initiation and termination.

Keywords: T-cell activation; T-cell differentiation; T-cell receptor; lymphocyte signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • CD3 Complex / metabolism*
  • HEK293 Cells
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Transgenic
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Oncogene Proteins / metabolism
  • Protein Binding / genetics
  • Protein Transport / genetics
  • Proteolysis*
  • Proto-Oncogene Proteins c-cbl / metabolism
  • Receptors, Antigen, T-Cell / metabolism*
  • Sequence Deletion / genetics
  • T-Lymphocytes / physiology*

Substances

  • Adaptor Proteins, Signal Transducing
  • CD3 Complex
  • Cd3e protein, mouse
  • Membrane Proteins
  • Nck protein
  • Nerve Tissue Proteins
  • Numb protein, mouse
  • Oncogene Proteins
  • Receptors, Antigen, T-Cell
  • Proto-Oncogene Proteins c-cbl
  • Cbl protein, mouse