The Cbl family and other ubiquitin ligases: destructive forces in control of antigen receptor signaling

Immunity. 2004 Jul;21(1):7-17. doi: 10.1016/j.immuni.2004.06.012.

Abstract

Regulation of tyrosine kinase-mediated cellular activation through antigen receptors is of great biological and practical significance. The evolutionarily conserved Cbl family ubiquitin ligases have emerged as key negative regulators of activated tyrosine kinase-coupled receptors, and their impaired function switches a normal immune response into autoimmunity. Cbl proteins facilitate the ubiquitinylation of activated tyrosine kinases and other signaling proteins and of the signaling chains of receptors themselves; monoubiquitin tag promotes sorting of activated receptors and associated proteins into internal vesicles of the multivesicular body, facilitating their lysosomal degradation, whereas polyubiquitin tag promotes proteasomal degradation. Notably, increased expression of Cbl proteins and other ubiquitin ligases is a component of anergic signaling program in T cells. Thus, controlled destruction of the signaling apparatus has emerged as a key to fine-tuning antigen receptor signaling. Further studies of this pathway are likely to elucidate the pathogenesis of autoimmune diseases and offer new therapeutic targets.

Publication types

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

MeSH terms

  • Animals
  • Immune Tolerance
  • Mice
  • Mice, Knockout
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins c-cbl
  • Receptors, Antigen / physiology*
  • Receptors, Antigen, T-Cell / physiology
  • Signal Transduction*
  • Ubiquitin-Protein Ligases / physiology*
  • src-Family Kinases / physiology

Substances

  • Proto-Oncogene Proteins
  • Receptors, Antigen
  • Receptors, Antigen, T-Cell
  • Proto-Oncogene Proteins c-cbl
  • Ubiquitin-Protein Ligases
  • src-Family Kinases
  • CBL protein, human