p75 neurotrophin receptor reduces ligand-induced Trk receptor ubiquitination and delays Trk receptor internalization and degradation

EMBO Rep. 2005 Oct;6(10):936-41. doi: 10.1038/sj.embor.7400503.

Abstract

Target-derived neurotrophins regulate neuronal survival and growth by interacting with cell-surface tyrosine kinase receptors. The p75 neurotrophin receptor (p75 NTR) is coexpressed with Trk receptors in long-range projection neurons, in which it facilitates neurotrophin binding to Trk and enhances Trk activity. Here, we show that TrkA and TrkB receptors undergo robust ligand-dependent ubiquitination that is dependent on activation of the endogenous Trk activity of the receptors. Coexpression of p75 NTR attenuated ubiquitination of TrkA and TrkB and delayed nerve growth factor-induced TrkA receptor internalization and receptor degradation. These results indicate that p75 NTR may prolong cell-surface Trk-dependent signalling events by negatively regulating receptor ubiquitination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / pharmacology
  • Cells, Cultured
  • Electrophoresis, Polyacrylamide Gel
  • Humans
  • Immunoblotting
  • Immunoprecipitation
  • Nerve Growth Factor / pharmacology
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism
  • PC12 Cells
  • Rats
  • Receptor, Nerve Growth Factor / metabolism*
  • Receptor, trkA / metabolism*
  • Receptor, trkB / metabolism*
  • Signal Transduction / physiology
  • Transfection
  • Ubiquitin / metabolism*

Substances

  • Brain-Derived Neurotrophic Factor
  • Receptor, Nerve Growth Factor
  • Ubiquitin
  • Nerve Growth Factor
  • Receptor, trkA
  • Receptor, trkB