Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development

Neuron. 2013 Oct 2;80(1):97-112. doi: 10.1016/j.neuron.2013.07.043. Epub 2013 Sep 12.

Abstract

Neuronal arborization is regulated by cell-autonomous and nonautonomous mechanisms including endosomal signaling via BDNF/TrkB. The endosomal Na⁺/H⁺ exchanger 6 (NHE6) is mutated in a new autism-related disorder. NHE6 functions to permit proton leak from endosomes, yet the mechanisms causing disease are unknown. We demonstrate that loss of NHE6 results in overacidification of the endosomal compartment and attenuated TrkB signaling. Mouse brains with disrupted NHE6 display reduced axonal and dendritic branching, synapse number, and circuit strength. Site-directed mutagenesis shows that the proton leak function of NHE6 is required for neuronal arborization. We find that TrkB receptor colocalizes to NHE6-associated endosomes. TrkB protein and phosphorylation are reduced in NHE6 mutant neurons in response to BDNF signaling. Finally, exogenous BDNF rescues defects in neuronal arborization. We propose that NHE6 mutation leads to circuit defects that are in part due to impoverished neuronal arborization that may be treatable by enhanced TrkB signaling.

Publication types

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

MeSH terms

  • Animals
  • Brain / metabolism
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cells, Cultured
  • Dendrites / physiology
  • Endosomes / genetics
  • Endosomes / metabolism*
  • Mice
  • Mice, Knockout
  • Nerve Net / metabolism*
  • Neurogenesis / genetics
  • Neurogenesis / physiology
  • Neurons / metabolism*
  • Receptor, trkB / genetics*
  • Receptor, trkB / metabolism
  • Signal Transduction* / physiology
  • Sodium-Hydrogen Exchangers / genetics*
  • Sodium-Hydrogen Exchangers / metabolism

Substances

  • Brain-Derived Neurotrophic Factor
  • NHE6 protein, mouse
  • Sodium-Hydrogen Exchangers
  • Receptor, trkB