Protein-tyrosine phosphatase 1B (PTP1B) is a novel regulator of central brain-derived neurotrophic factor and tropomyosin receptor kinase B (TrkB) signaling

J Biol Chem. 2014 Nov 14;289(46):31682-31692. doi: 10.1074/jbc.M114.603621. Epub 2014 Oct 6.

Abstract

Neuronal protein-tyrosine phosphatase 1B (PTP1B) deficiency in mice results in enhanced leptin signaling and protection from diet-induced obesity; however, whether additional signaling pathways in the brain contribute to the metabolic effects of PTP1B deficiency remains unclear. Here, we show that the tropomyosin receptor kinase B (TrkB) receptor is a direct PTP1B substrate and implicate PTP1B in the regulation of the central brain-derived neurotrophic factor (BDNF) signaling. PTP1B interacts with activated TrkB receptor in mouse brain and human SH-SY5Y neuroblastoma cells. PTP1B overexpression reduces TrkB phosphorylation and activation of downstream signaling pathways, whereas PTP1B inhibition augments TrkB signaling. Notably, brains of Ptpn1(-/-) mice exhibit enhanced TrkB phosphorylation, and Ptpn1(-/-) mice are hypersensitive to central BDNF-induced increase in core temperature. Taken together, our findings demonstrate that PTP1B is a novel physiological regulator of TrkB and that enhanced BDNF/TrkB signaling may contribute to the beneficial metabolic effects of PTP1B deficiency.

Keywords: Brain-derived Neurotrophic Factor (BDNF); Hypothalamus; Metabolism; Phosphotyrosine Signaling; Receptor Tyrosine Kinase; Signal Transduction; Tyrosine-Protein Phosphatase (Tyrosine Phosphatase).

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cell Line, Tumor
  • Gene Expression Regulation, Enzymologic*
  • Humans
  • Hypothalamus / metabolism
  • Male
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neurons / metabolism
  • Phosphorylation
  • Protein Binding
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / metabolism*
  • Protein-Tyrosine Kinases / metabolism*
  • Receptor, trkB
  • Signal Transduction
  • Temperature

Substances

  • Brain-Derived Neurotrophic Factor
  • Membrane Glycoproteins
  • Protein-Tyrosine Kinases
  • Receptor, trkB
  • tropomyosin-related kinase-B, human
  • PTPN1 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1