Bidirectional regulation of dendritic voltage-gated potassium channels by the fragile X mental retardation protein

Neuron. 2011 Nov 17;72(4):630-42. doi: 10.1016/j.neuron.2011.09.033.

Abstract

How transmitter receptors modulate neuronal signaling by regulating voltage-gated ion channel expression remains an open question. Here we report dendritic localization of mRNA of Kv4.2 voltage-gated potassium channel, which regulates synaptic plasticity, and its local translational regulation by fragile X mental retardation protein (FMRP) linked to fragile X syndrome (FXS), the most common heritable mental retardation. FMRP suppression of Kv4.2 is revealed by elevation of Kv4.2 in neurons from fmr1 knockout (KO) mice and in neurons expressing Kv4.2-3'UTR that binds FMRP. Moreover, treating hippocampal slices from fmr1 KO mice with Kv4 channel blocker restores long-term potentiation induced by moderate stimuli. Surprisingly, recovery of Kv4.2 after N-methyl-D-aspartate receptor (NMDAR)-induced degradation also requires FMRP, likely due to NMDAR-induced FMRP dephosphorylation, which turns off FMRP suppression of Kv4.2. Our study of FMRP regulation of Kv4.2 deepens our knowledge of NMDAR signaling and reveals a FMRP target of potential relevance to FXS.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Dendrites / physiology*
  • Fragile X Mental Retardation Protein / physiology*
  • HEK293 Cells
  • Humans
  • Long-Term Potentiation / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Potassium Channels, Voltage-Gated / physiology
  • Shal Potassium Channels / antagonists & inhibitors
  • Shal Potassium Channels / physiology*

Substances

  • Fmr1 protein, mouse
  • Potassium Channels, Voltage-Gated
  • Shal Potassium Channels
  • Fragile X Mental Retardation Protein