Activation of a tyrosine kinase-MAPK cascade enhances the induction of long-term synaptic facilitation and long-term memory in Aplysia

Neuron. 2003 Feb 6;37(3):473-84. doi: 10.1016/s0896-6273(03)00030-8.

Abstract

Tyrosine kinases have been implicated in cellular processes thought to underlie learning and memory. Here we show that tyrosine kinases play a direct role in long-term synaptic facilitation (LTF) and long-term memory (LTM) for sensitization in Aplysia. Tyrosine kinase activity is required for serotonin-induced LTF of sensorimotor (SN-MN) synapses, and enhancement of endogenous tyrosine kinase activity facilitates the induction of LTF. These effects are mediated, at least in part, through mitogen-activated protein kinase (MAPK) activation and are blocked by transcriptional and translational inhibitors. Moreover, brain-derived neurotrophic factor (BDNF) also enhances the induction of LTF in a MAPK-dependent fashion. Finally, activation of endogenous tyrosine kinases enhances the induction of long-term memory for sensitization, and this enhancement also requires MAPK activation. Thus, tyrosine kinases, acting through MAPK, play a pivotal role in LTF and LTM formation.

Publication types

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

MeSH terms

  • Animals
  • Aplysia
  • Brain-Derived Neurotrophic Factor / pharmacology
  • Dactinomycin / pharmacology
  • Enzyme Activation / physiology
  • Long-Term Potentiation / drug effects
  • Long-Term Potentiation / physiology*
  • MAP Kinase Signaling System / physiology*
  • Memory / physiology*
  • Mitogen-Activated Protein Kinases / metabolism
  • Nucleic Acid Synthesis Inhibitors / pharmacology
  • Protein Biosynthesis / physiology
  • Protein-Tyrosine Kinases / metabolism
  • Serotonin / pharmacology
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology*
  • Transcription, Genetic / physiology

Substances

  • Brain-Derived Neurotrophic Factor
  • Nucleic Acid Synthesis Inhibitors
  • Dactinomycin
  • Serotonin
  • Protein-Tyrosine Kinases
  • Mitogen-Activated Protein Kinases