FMRP regulates neurotransmitter release and synaptic information transmission by modulating action potential duration via BK channels

Neuron. 2013 Feb 20;77(4):696-711. doi: 10.1016/j.neuron.2012.12.018.

Abstract

Loss of FMRP causes fragile X syndrome (FXS), but the physiological functions of FMRP remain highly debatable. Here we show that FMRP regulates neurotransmitter release in CA3 pyramidal neurons by modulating action potential (AP) duration. Loss of FMRP leads to excessive AP broadening during repetitive activity, enhanced presynaptic calcium influx, and elevated neurotransmitter release. The AP broadening defects caused by FMRP loss have a cell-autonomous presynaptic origin and can be acutely rescued in postnatal neurons. These presynaptic actions of FMRP are translation independent and are mediated selectively by BK channels via interaction of FMRP with BK channel's regulatory β4 subunits. Information-theoretical analysis demonstrates that loss of these FMRP functions causes marked dysregulation of synaptic information transmission. FMRP-dependent AP broadening is not limited to the hippocampus, but also occurs in cortical pyramidal neurons. Our results thus suggest major translation-independent presynaptic functions of FMRP that may have important implications for understanding FXS neuropathology.

Publication types

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

MeSH terms

  • Action Potentials / physiology*
  • Animals
  • Calcium / metabolism
  • Excitatory Postsynaptic Potentials / physiology
  • Fragile X Mental Retardation Protein / metabolism*
  • Fragile X Syndrome / metabolism
  • Hippocampus / metabolism
  • Large-Conductance Calcium-Activated Potassium Channels / metabolism*
  • Mice
  • Neurons / metabolism*
  • Neurotransmitter Agents / metabolism*
  • Presynaptic Terminals
  • Synaptic Transmission*

Substances

  • Fmr1 protein, mouse
  • Large-Conductance Calcium-Activated Potassium Channels
  • Neurotransmitter Agents
  • Fragile X Mental Retardation Protein
  • Calcium