APC conditional knock-out mouse is a model of infantile spasms with elevated neuronal β-catenin levels, neonatal spasms, and chronic seizures

Neurobiol Dis. 2017 Feb;98:149-157. doi: 10.1016/j.nbd.2016.11.002. Epub 2016 Nov 13.

Abstract

Infantile spasms (IS) are a catastrophic childhood epilepsy syndrome characterized by flexion-extension spasms during infancy that progress to chronic seizures and cognitive deficits in later life. The molecular causes of IS are poorly defined. Genetic screens of individuals with IS have identified multiple risk genes, several of which are predicted to alter β-catenin pathways. However, evidence linking malfunction of β-catenin pathways and IS is lacking. Here, we show that conditional deletion in mice of the adenomatous polyposis coli gene (APC cKO), the major negative regulator of β-catenin, leads to excessive β-catenin levels and multiple salient features of human IS. Compared with wild-type littermates, neonatal APC cKO mice exhibit flexion-extension motor spasms and abnormal high-amplitude electroencephalographic discharges. Additionally, the frequency of excitatory postsynaptic currents is increased in layer V pyramidal cells, the major output neurons of the cerebral cortex. At adult ages, APC cKOs display spontaneous electroclinical seizures. These data provide the first evidence that malfunctions of APC/β-catenin pathways cause pathophysiological changes consistent with IS. Our findings demonstrate that the APC cKO is a new genetic model of IS, provide novel insights into molecular and functional alterations that can lead to IS, and suggest novel targets for therapeutic intervention.

Keywords: Cortex; Epilepsy; Infantile spasms; Wnt signaling; β-Catenin.

MeSH terms

  • Adenomatous Polyposis Coli Protein / deficiency*
  • Adenomatous Polyposis Coli Protein / genetics
  • Animals
  • Animals, Newborn
  • Cerebral Cortex / growth & development
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology
  • Disease Models, Animal*
  • Electroencephalography
  • Excitatory Postsynaptic Potentials / physiology
  • Female
  • Humans
  • Infant
  • Male
  • Mice, Knockout
  • Movement / physiology
  • Neurons / metabolism*
  • Neurons / pathology
  • Phenotype
  • Seizures / metabolism*
  • Seizures / pathology
  • Signal Transduction
  • Spasms, Infantile / metabolism*
  • Spasms, Infantile / pathology
  • Tissue Culture Techniques
  • beta Catenin / metabolism*

Substances

  • Adenomatous Polyposis Coli Protein
  • CTNNB1 protein, mouse
  • adenomatous polyposis coli protein, mouse
  • beta Catenin