A human Dravet syndrome model from patient induced pluripotent stem cells

Mol Brain. 2013 May 2:6:19. doi: 10.1186/1756-6606-6-19.

Abstract

Background: Dravet syndrome is a devastating infantile-onset epilepsy syndrome with cognitive deficits and autistic traits caused by genetic alterations in SCN1A gene encoding the α-subunit of the voltage-gated sodium channel Na(v)1.1. Disease modeling using patient-derived induced pluripotent stem cells (iPSCs) can be a powerful tool to reproduce this syndrome's human pathology. However, no such effort has been reported to date. We here report a cellular model for DS that utilizes patient-derived iPSCs.

Results: We generated iPSCs from a Dravet syndrome patient with a c.4933C>T substitution in SCN1A, which is predicted to result in truncation in the fourth homologous domain of the protein (p.R1645*). Neurons derived from these iPSCs were primarily GABAergic (>50%), although glutamatergic neurons were observed as a minor population (<1%). Current-clamp analyses revealed significant impairment in action potential generation when strong depolarizing currents were injected.

Conclusions: Our results indicate a functional decline in Dravet neurons, especially in the GABAergic subtype, which supports previous findings in murine disease models, where loss-of-function in GABAergic inhibition appears to be a main driver in epileptogenesis. Our data indicate that patient-derived iPSCs may serve as a new and powerful research platform for genetic disorders, including the epilepsies.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials
  • Adult
  • Cell Differentiation
  • Epilepsies, Myoclonic / pathology*
  • Epilepsies, Myoclonic / physiopathology
  • Female
  • Genes, Reporter / genetics
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / pathology*
  • Infant
  • Lentivirus / metabolism
  • Models, Biological*
  • NAV1.1 Voltage-Gated Sodium Channel / metabolism
  • Neurons / metabolism
  • Neurons / pathology
  • Parvalbumins / genetics
  • Parvalbumins / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Real-Time Polymerase Chain Reaction
  • Young Adult

Substances

  • NAV1.1 Voltage-Gated Sodium Channel
  • Parvalbumins
  • RNA, Messenger