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dc.contributor.authorMartínez, A.L.
dc.contributor.authorBrea Floriani, José Manuel
dc.contributor.authorDomínguez Medina, Eduardo
dc.contributor.authorVarela, M.J.
dc.contributor.authorAllegue Toscano, Catarina
dc.contributor.authorCruz Guerrero, Raquel
dc.contributor.authorMonroy, X.
dc.contributor.authorMerlos, M.
dc.contributor.authorBurgueño, J.
dc.contributor.authorCarracedo Ávarez, Ángel
dc.contributor.authorLoza García, María Isabel
dc.date.accessioned2025-08-25T12:39:59Z
dc.date.available2025-08-25T12:39:59Z
dc.date.issued2022
dc.identifier.citationMartínez AL, Brea J, Domínguez E, Varela MJ, Allegue C, Cruz R, et al. Identification of Sodium Transients Through NaV1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons. Frontiers in Cellular Neuroscience. 2022;16.
dc.identifier.issn1662-5102
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/6276b6482c3d9944cd36d7a4*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20488
dc.description.abstractNeuronal differentiation is a complex process through which newborn neurons acquire the morphology of mature neurons and become excitable. We employed a combination of functional and transcriptomic approaches to deconvolute and identify key regulators of the differentiation process of a DRG neuron-derived cell line, and we focused our study on the NaV1.5 ion channel (encoded by Scn5a) as a channel involved in the acquisition of DRG neuronal features. Overexpression of Scn5a enhances the acquisition of neuronal phenotypic features and increases the KCl-elicited hyperexcitability response in a DRG-derived cell line. Moreover, pharmacologic inhibition of the NaV1.5 channel during differentiation hinders the acquisition of phenotypic features of neuronal cells and the hyperexcitability increase in response to changes in the extracellular medium ionic composition. Taken together, these data highlight the relevance of sodium transients in regulating the neuronal differentiation process in a DRG neuron-derived cell line.en
dc.description.sponsorshipThis work was supported by the Joint R&D Unit Esteve-USC (IN853A-2014-08), co-financed by the Galician Innovation Agency and the Spanish Ministry of Economy and Competitiveness (MINECO) within the framework of the Spanish Strategy of Innovation in Galicia, and by the Phenopain project (RTC-2015-4207-1) of the RETOS-COLABORACION program of the MINECO, co-financed by the European Union through the European Regional Development Fund (ERDF). AM received a predoctoral fellowship from the FPU program (Spanish Ministry of Education, Culture and Sports).en
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleIdentification of Sodium Transients Through NaV1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons*
dc.typeArticleen
dc.authorsophosMartínez, M. I. A. L.
dc.authorsophosBrea, J.
dc.authorsophosDomínguez, E.
dc.authorsophosVarela, M. J.
dc.authorsophosAllegue, C.
dc.authorsophosCruz, R.
dc.authorsophosMonroy, X.
dc.authorsophosMerlos, M.
dc.authorsophosBurgueño, J.
dc.authorsophosCarracedo, Á
dc.authorsophosLoza
dc.identifier.doi10.3389/fncel.2022.816325
dc.identifier.sophos6276b6482c3d9944cd36d7a4
dc.issue.numbernull
dc.journal.titleFrontiers in Cellular Neuroscience*
dc.page.initialnull
dc.relation.projectIDJoint R&D Unit Esteve-USC [IN853A-2014-08]; Galician Innovation Agency; Spanish Ministry of Economy and Competitiveness (MINECO); Phenopain project of the RETOS-COLABORACION program of the MINECO [RTC-2015-4207-1]; European Union through the European Regional Development Fund (ERDF); FPU program (Spanish Ministry of Education, Culture and Sports)
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fncel.2022.816325/pdf;https://www.frontiersin.org/journals/cellular-neuroscience/articles/10.3389/fncel.2022.816325/pdfes
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Santiagoes
dc.subject.keywordIDISes
dc.subject.keywordFPGMXes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number16


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