Literature DB >> 32968789

Variant-specific changes in persistent or resurgent sodium current in SCN8A-related epilepsy patient-derived neurons.

Andrew M Tidball1, Luis F Lopez-Santiago2, Yukun Yuan2, Trevor W Glenn1, Joshua L Margolis1, J Clayton Walker1, Emma G Kilbane1, Christopher A Miller3, E Martina Bebin4,5, M Scott Perry6, Lori L Isom1,2,7, Jack M Parent1,8.   

Abstract

Missense variants in the SCN8A voltage-gated sodium channel gene are linked to early-infantile epileptic encephalopathy type 13, also known as SCN8A-related epilepsy. These patients exhibit a wide spectrum of intractable seizure types, severe developmental delay, movement disorders, and elevated risk of sudden unexpected death in epilepsy. The mechanisms by which SCN8A variants lead to epilepsy are poorly understood, although heterologous expression systems and mouse models have demonstrated altered sodium current properties. To investigate these mechanisms using a patient-specific model, we generated induced pluripotent stem cells from three patients with missense variants in SCN8A: p.R1872>L (Patient 1); p.V1592>L (Patient 2); and p.N1759>S (Patient 3). Using small molecule differentiation into excitatory neurons, induced pluripotent stem cell-derived neurons from all three patients displayed altered sodium currents. Patients 1 and 2 had elevated persistent current, while Patient 3 had increased resurgent current compared to controls. Neurons from all three patients displayed shorter axon initial segment lengths compared to controls. Further analyses focused on one of the patients with increased persistent sodium current (Patient 1) and the patient with increased resurgent current (Patient 3). Excitatory cortical neurons from both patients had prolonged action potential repolarization. Using doxycycline-inducible expression of the neuronal transcription factors neurogenin 1 and 2 to synchronize differentiation of induced excitatory cortical-like neurons, we investigated network activity and response to pharmacotherapies. Both small molecule differentiated and induced patient neurons displayed similar abnormalities in action potential repolarization. Patient induced neurons showed increased burstiness that was sensitive to phenytoin, currently a standard treatment for SCN8A-related epilepsy patients, or riluzole, an FDA-approved drug used in amyotrophic lateral sclerosis and known to block persistent and resurgent sodium currents, at pharmacologically relevant concentrations. Patch-clamp recordings showed that riluzole suppressed spontaneous firing and increased the action potential firing threshold of patient-derived neurons to more depolarized potentials. Two of the patients in this study were prescribed riluzole off-label. Patient 1 had a 50% reduction in seizure frequency. Patient 3 experienced an immediate and dramatic seizure reduction with months of seizure freedom. An additional patient with a SCN8A variant in domain IV of Nav1.6 (p.V1757>I) had a dramatic reduction in seizure frequency for several months after starting riluzole treatment, but then seizures recurred. Our results indicate that patient-specific neurons are useful for modelling SCN8A-related epilepsy and demonstrate SCN8A variant-specific mechanisms. Moreover, these findings suggest that patient-specific neuronal disease modelling offers a useful platform for discovering precision epilepsy therapies.
© The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  developmental and epileptic encephalopathy; epileptogenesis; genetic epilepsy; induced pluripotent stem cell; voltage-gated sodium channel

Year:  2020        PMID: 32968789     DOI: 10.1093/brain/awaa247

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  16 in total

1.  NBI-921352, a first-in-class, NaV1.6 selective, sodium channel inhibitor that prevents seizures in Scn8a gain-of-function mice, and wild-type mice and rats.

Authors:  J P Johnson; Thilo Focken; Kuldip Khakh; Parisa Karimi Tari; Celine Dube; Samuel J Goodchild; Jean-Christophe Andrez; Girish Bankar; David Bogucki; Kristen Burford; Elaine Chang; Sultan Chowdhury; Richard Dean; Gina de Boer; Shannon Decker; Christoph Dehnhardt; Mandy Feng; Wei Gong; Michael Grimwood; Abid Hasan; Angela Hussainkhel; Qi Jia; Stephanie Lee; Jenny Li; Sophia Lin; Andrea Lindgren; Verner Lofstrand; Janette Mezeyova; Rostam Namdari; Karen Nelkenbrecher; Noah Gregory Shuart; Luis Sojo; Shaoyi Sun; Matthew Taron; Matthew Waldbrook; Diana Weeratunge; Steven Wesolowski; Aaron Williams; Michael Wilson; Zhiwei Xie; Rhena Yoo; Clint Young; Alla Zenova; Wei Zhang; Alison J Cutts; Robin P Sherrington; Simon N Pimstone; Raymond Winquist; Charles J Cohen; James R Empfield
Journal:  Elife       Date:  2022-03-02       Impact factor: 8.140

2.  SCN8A epileptic encephalopathy mutations display a gain-of-function phenotype and divergent sensitivity to antiepileptic drugs.

Authors:  Qian-Bei Guo; Li Zhan; Hai-Yan Xu; Zhao-Bing Gao; Yue-Ming Zheng
Journal:  Acta Pharmacol Sin       Date:  2022-07-27       Impact factor: 7.169

Review 3.  Rational Small Molecule Treatment for Genetic Epilepsies.

Authors:  Ethan M Goldberg
Journal:  Neurotherapeutics       Date:  2021-08-24       Impact factor: 6.088

Review 4.  Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progress.

Authors:  Juliet K Knowles; Ingo Helbig; Cameron S Metcalf; Laura S Lubbers; Lori L Isom; Scott Demarest; Ethan M Goldberg; Alfred L George; Holger Lerche; Sarah Weckhuysen; Vicky Whittemore; Samuel F Berkovic; Daniel H Lowenstein
Journal:  Epilepsia       Date:  2022-07-17       Impact factor: 6.740

5.  Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity.

Authors:  Stefania Scalise; Clara Zannino; Valeria Lucchino; Michela Lo Conte; Luana Scaramuzzino; Pierangelo Cifelli; Tiziano D'Andrea; Katiuscia Martinello; Sergio Fucile; Eleonora Palma; Antonio Gambardella; Gabriele Ruffolo; Giovanni Cuda; Elvira Immacolata Parrotta
Journal:  Biomedicines       Date:  2022-05-05

6.  Hyperexcitability and Pharmacological Responsiveness of Cortical Neurons Derived from Human iPSCs Carrying Epilepsy-Associated Sodium Channel Nav1.2-L1342P Genetic Variant.

Authors:  Zhefu Que; Maria I Olivero-Acosta; Jingliang Zhang; Muriel Eaton; Anke M Tukker; Xiaoling Chen; Jiaxiang Wu; Junkai Xie; Tiange Xiao; Kyle Wettschurack; Layan Yunis; J Marshall Shafer; James A Schaber; Jean-Christophe Rochet; Aaron B Bowman; Chongli Yuan; Zhuo Huang; Chang-Deng Hu; Darci J Trader; William C Skarnes; Yang Yang
Journal:  J Neurosci       Date:  2021-10-29       Impact factor: 6.709

Review 7.  Screening Platforms for Genetic Epilepsies-Zebrafish, iPSC-Derived Neurons, and Organoids.

Authors:  Aleksandr Shcheglovitov; Randall T Peterson
Journal:  Neurotherapeutics       Date:  2021-09-30       Impact factor: 6.088

Review 8.  'Channeling' therapeutic discovery for epileptic encephalopathy through iPSC technologies.

Authors:  Dina Simkin; Christina Ambrosi; Kelly A Marshall; Luis A Williams; Jordyn Eisenberg; Mennat Gharib; Graham T Dempsey; Alfred L George; Owen B McManus; Evangelos Kiskinis
Journal:  Trends Pharmacol Sci       Date:  2022-05       Impact factor: 17.638

Review 9.  Sodium channelopathies in neurodevelopmental disorders.

Authors:  Miriam H Meisler; Sophie F Hill; Wenxi Yu
Journal:  Nat Rev Neurosci       Date:  2021-02-02       Impact factor: 34.870

Review 10.  Clinical and therapeutic significance of genetic variation in the GRIN gene family encoding NMDARs.

Authors:  Tim A Benke; Kristen Park; Ilona Krey; Chad R Camp; Rui Song; Amy J Ramsey; Hongjie Yuan; Stephen F Traynelis; Johannes Lemke
Journal:  Neuropharmacology       Date:  2021-09-22       Impact factor: 5.250

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.