K-252b selectively potentiates cellular actions and trk tyrosine phosphorylation mediated by neurotrophin-3

J Neurochem. 1992 Aug;59(2):715-22. doi: 10.1111/j.1471-4159.1992.tb09427.x.

Abstract

K-252b, a protein kinase inhibitor, has been shown earlier to inhibit nerve growth factor actions on cholinergic neurons of the basal forebrain. In the present study, K-252b was found to prevent trophic actions of two other neurotrophins, brain-derived neurotrophic factor, and neurotrophin-3, on central cholinergic and dopaminergic neurons, peripheral sensory neurons, and PC12 pheochromocytoma cells, when used at greater than 2 microM concentration. Comparable actions of nonneurotrophin growth factors were not affected. Surprisingly, at 0.1-100 nM, K-252b selectively enhanced the trophic action of neurotrophin-3 on central cholinergic neurons, peripheral sensory neurons, and PC12 cells. In PC12 cells, K-252b potentiated the neurotrophin-3-induced tyrosine phosphorylation of trk, a protein kinase responsible for transmitting neurotrophin signals. Of the three structurally related nerve growth factor inhibitors, K-252a, K-252b, and staurosporine, only the first two also mediated neurotrophin-3 potentiation. These findings indicate that K-252b generally and selectively potentiates the neurotrophic action of neurotrophin-3 and suggest that this action involves trk-type neurotrophin receptors.

Publication types

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

MeSH terms

  • Adrenal Gland Neoplasms / metabolism
  • Adrenal Gland Neoplasms / pathology
  • Alkaloids / pharmacology
  • Animals
  • Brain-Derived Neurotrophic Factor
  • Carbazoles / pharmacology*
  • Cells, Cultured
  • Chick Embryo
  • Dose-Response Relationship, Drug
  • Indole Alkaloids
  • Nerve Growth Factors / antagonists & inhibitors
  • Nerve Growth Factors / pharmacology*
  • Nerve Tissue Proteins / pharmacology
  • Neurons / cytology*
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons, Afferent / cytology
  • Neurons, Afferent / drug effects
  • Neurons, Afferent / metabolism
  • Neurotrophin 3
  • Pheochromocytoma / metabolism
  • Pheochromocytoma / pathology
  • Phosphorylation
  • Protein Kinase C / antagonists & inhibitors*
  • Proto-Oncogene Proteins / analysis
  • Proto-Oncogene Proteins / metabolism*
  • Rats
  • Receptor, trkA
  • Signal Transduction / physiology
  • Staurosporine
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / metabolism
  • Tumor Cells, Cultured / pathology
  • Tyrosine / analysis
  • Tyrosine / metabolism*

Substances

  • Alkaloids
  • Brain-Derived Neurotrophic Factor
  • Carbazoles
  • Indole Alkaloids
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Neurotrophin 3
  • Proto-Oncogene Proteins
  • Tyrosine
  • staurosporine aglycone
  • Receptor, trkA
  • Protein Kinase C
  • Staurosporine