Hyperexcitable phenotypes in iPSC-derived neurons from patients with 15q11-q13 duplication syndrome, a genetic form of autism

Fink, J. J.; Schreiner, J. D.; Bloom, J. E.; Baker, D. S.; Robinson, T. M.; Lieberman, R.; Loew, L. M.; Chamberlain, S. J.; Levine, E.

doi:10.1101/286336

bioRxiv · 10.1101/286336

Hyperexcitable phenotypes in iPSC-derived neurons from patients with 15q11-q13 duplication syndrome, a genetic form of autism

Fink, J. J.·Schreiner, J. D.·Bloom, J. E.·Baker, D. S.·Robinson, T. M.·Lieberman, R.·Loew, L. M.·Chamberlain, S. J.·Levine, E.

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Abstract

Chromosome 15q11-q13 duplication syndrome (Dup15q) is a neurogenetic disorder caused by duplications of the maternal copy of this region. In addition to hypotonia, motor deficits, and language impairments, Dup15q patients commonly meet the criteria for autism spectrum disorder (ASD) and have a high prevalence of seizures. Here, we explored mechanisms of hyperexcitability in neurons derived from induced pluripotent stem cell (iPSC) lines from Dup15q patients. Maturation of resting membrane potential in Dup15q-derived neurons was similar to neurons from unaffected control subjects, but Dup15q neurons had delayed action potential maturation and increased synaptic event frequency and amplitude. Dup15q neurons also showed impairments in activity-dependent synaptic plasticity and homeostatic synaptic scaling. Finally, Dup15q neurons showed an increased frequency of spontaneous action potential firing compared to control neurons, in part due to disruption of KCNQ2 channels. Together these data point to multiple mechanisms underlying hyperexcitability that may provide new targets for the treatment of seizures and other phenotypes associated with Dup15q.

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Fink, J. J., Schreiner, J. D., Bloom, J. E., Baker, D. S., Robinson, T. M., Lieberman, R., Loew, L. M., Chamberlain, S. J., Levine, E.. 2018-03-21. Hyperexcitable phenotypes in iPSC-derived neurons from patients with 15q11-q13 duplication syndrome, a genetic form of autism. https://doi.org/10.1101/286336

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