Neurobiology of DiseaseNeurosciencePeer-reviewed journal article
Electrophysiological signatures of a developmental delay in a stem cell model of KCNQ2 developmental and epileptic encephalopathy
Filip Rosa, Stephan TheissiD, Susanne Krepp, Heidi Loeffler, Dulini C. Mendis, Stefanie KlingensteiniD, Stefan LiebauiD, Sarah WeckhuyseniD, Michael AlberiD, Steven PetrouiD, Holger LercheiD, Snezana MaljeviciD, Thomas V. WuttkeiD
Abstract
BackgroundKCNQ2, encoding KV7.2 ion channels, has emerged as one of the prominent genes causing early onset seizures with developmental delay (KCNQ2 developmental and epileptic encephalopathy; KCNQ2-DEE). KCNQ2 de novo loss-of-function (LOF) and associated neuronal hyperexcitability have been accepted as mechanisms contributing to seizures. To investigate the developmental impact of KCNQ2 LOF, we generated patient iPSC-derived models for two previously reported de novo variants, p.(Arg325Gly) and p.(Gly315Arg), linked to severe congenital DEE. MethodsFunctional investigation of the two variants was initially performed in Xenopus laevis oocyte system. Patient-derived iPSC lines were differentiated using NGN2- and embryoid body-based protocols yielding neurons roughly corresponding to mid- and mid-late gestational stages, respectively. KV7- mediated M-current, passive neuronal properties, action potential generation and spontaneous oscillatory network activities were analysed with whole-cell patch clamping. FindingsStudied KCNQ2 variants showed LOF with a dominant-negative effect in the heterologous system. Reduced M-currents in patient iPSC-derived neurons corroborated a LOF as the main pathomechanism. Interestingly, this led to the reduced neuronal firing of the early neurons and to a disruption of complex oscillatory activity, with significantly reduced duration and amplitude of these events in patient iPSC-derived neurons. InterpretationWe provide experimental evidence for changing roles of the M-current throughout development and place disease variant-mediated M-current reduction in the context of the neuronal maturation in the prenatal brain. Based on the reduced neuronal firing and disrupted oscillatory activity seen in patient iPSC-derived neurons, we propose that a delayed/impaired maturation of neuronal and network properties underlies KCNQ-DEE caused by LOF variants.
- organism: human
- assay: electronic health records
- research focus: cell type annotation
- approach: experimental assay
- Citations
- 5
- FWCI
- 2.68
- Field percentile
- top 10%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Time-limited alterations in cortical activity of a Knock-in mice model of KCNQ2-related Developmental and Epileptic Encephalopathy
Najoua Biba, Hélène Becq, … Laurent Aniksztejn·The Journal of PhysiologyPeer-reviewed·Apr 7, 2022
- Machine Learning Resolves Functional Phenotypes and Therapeutic Responses in KCNQ2 Developmental Epileptic Encephalopathy iPSC Models
Dina Simkin, Syed M.A. Wafa, … Evangelos Kiskinis·bioRxiv·Jul 26, 2025
- Kv7.2 Loss-of-Function Causes Early Hyperexcitability and Network Remodeling
Nina Dirkx, Mark D. Kaji, … Sarah Weckhuysen·bioRxiv·Jul 22, 2025
- Impaired M-current in KCNQ2 Encephalopathy Evokes Dyshomeostatic Modulation of Excitability
Dina Simkin, Timothy J. Searl, … Evangelos Kiskinis·bioRxiv·Sep 22, 2020
- Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy
Timothy J Abreo, Emma C. Thompson, … Edward C. Cooper·eLifePeer-reviewed·Jan 6, 2025
- CONSTITUTIVE OPENING OF THE Kv7.2 PORE ACTIVATION GATE CAUSES KCNQ2-DEVELOPMENTAL ENCEPHALOPATHY
Mario Nappi, Giulio Alberini, … Maurizio Taglialatela·Proceedings of the National Academy of SciencesPeer-reviewed·Nov 27, 2024