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http://hdl.handle.net/2445/185597
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DC Field | Value | Language |
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dc.contributor.author | Simkin, Dina | - |
dc.contributor.author | Marshall, Kelly A. | - |
dc.contributor.author | Vanoye, Carlos G. | - |
dc.contributor.author | Desai, Reshma R. | - |
dc.contributor.author | Bustos, Bernabe I. | - |
dc.contributor.author | Piyevsky, Brandon N. | - |
dc.contributor.author | Ortega Cano, Juan Alberto | - |
dc.contributor.author | Forrest, Marc | - |
dc.contributor.author | Robertson, Gabriella L. | - |
dc.contributor.author | Penzes, Peter | - |
dc.contributor.author | Laux, Linda C. | - |
dc.contributor.author | Lubbe, Steven J. | - |
dc.contributor.author | Millichap, John J. | - |
dc.contributor.author | George Jr, Alfred L. | - |
dc.contributor.author | Kiskinis, Evangelos | - |
dc.date.accessioned | 2022-05-13T15:34:48Z | - |
dc.date.available | 2022-05-13T15:34:48Z | - |
dc.date.issued | 2021-02-05 | - |
dc.identifier.issn | 2050-084X | - |
dc.identifier.uri | http://hdl.handle.net/2445/185597 | - |
dc.description.abstract | Mutations in KCNQ2, which encodes a pore-forming K+ channel subunit responsible for neuronal M-current, cause neonatal epileptic encephalopathy, a complex disorder presenting with severe early-onset seizures and impaired neurodevelopment. The condition is exceptionally difficult to treat, partially because the effects of KCNQ2 mutations on the development and function of human neurons are unknown. Here, we used induced pluripotent stem cells (iPSCs) and gene editing to establish a disease model and measured the functional properties of differentiated excitatory neurons. We find that patient iPSC-derived neurons exhibit faster action potential repolarization, larger post-burst afterhyperpolarization and a functional enhancement of Ca2+-activated K+ channels. These properties, which can be recapitulated by chronic inhibition of M-current in control neurons, facilitate a burst-suppression firing pattern that is reminiscent of the interictal electroencephalography pattern in patients. Our findings suggest that dyshomeostatic mechanisms compound KCNQ2 loss-of-function leading to alterations in the neurodevelopmental trajectory of patient iPSC-derived neurons. | - |
dc.format.extent | 32 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | eLife Sciences | - |
dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.7554/eLife.64434 | - |
dc.relation.ispartof | eLife, 2021 | - |
dc.relation.uri | https://doi.org/10.7554/eLife.64434 | - |
dc.rights | cc-by (c) Simkin, Dina et al., 2021 | - |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | - |
dc.source | Articles publicats en revistes (Patologia i Terapèutica Experimental) | - |
dc.subject.classification | Canals de potassi | - |
dc.subject.classification | Neurones | - |
dc.subject.classification | Cèl·lules mare | - |
dc.subject.classification | Malalties neonatals | - |
dc.subject.other | Potassium channels | - |
dc.subject.other | Neurons | - |
dc.subject.other | Stem cells | - |
dc.subject.other | Neonatal diseases | - |
dc.title | Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.identifier.idgrec | 713968 | - |
dc.date.updated | 2022-05-13T15:34:48Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
dc.identifier.pmid | 33544076 | - |
Appears in Collections: | Articles publicats en revistes (Patologia i Terapèutica Experimental) |
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File | Description | Size | Format | |
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713968.pdf | 5.18 MB | Adobe PDF | View/Open |
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