Cargando…
Identification of Sodium Transients Through Na(V)1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons
Neuronal 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-d...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018981/ https://www.ncbi.nlm.nih.gov/pubmed/35465610 http://dx.doi.org/10.3389/fncel.2022.816325 |
_version_ | 1784689145733447680 |
---|---|
author | Martínez, Antón L. Brea, José Domínguez, Eduardo Varela, María J. Allegue, Catarina Cruz, Raquel Monroy, Xavier Merlos, Manuel Burgueño, Javier Carracedo, Ángel Loza, María Isabel |
author_facet | Martínez, Antón L. Brea, José Domínguez, Eduardo Varela, María J. Allegue, Catarina Cruz, Raquel Monroy, Xavier Merlos, Manuel Burgueño, Javier Carracedo, Ángel Loza, María Isabel |
author_sort | Martínez, Antón L. |
collection | PubMed |
description | Neuronal 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 Na(V)1.5 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 Na(V)1.5 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. |
format | Online Article Text |
id | pubmed-9018981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90189812022-04-21 Identification of Sodium Transients Through Na(V)1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons Martínez, Antón L. Brea, José Domínguez, Eduardo Varela, María J. Allegue, Catarina Cruz, Raquel Monroy, Xavier Merlos, Manuel Burgueño, Javier Carracedo, Ángel Loza, María Isabel Front Cell Neurosci Neuroscience Neuronal 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 Na(V)1.5 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 Na(V)1.5 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. Frontiers Media S.A. 2022-04-06 /pmc/articles/PMC9018981/ /pubmed/35465610 http://dx.doi.org/10.3389/fncel.2022.816325 Text en Copyright © 2022 Martínez, Brea, Domínguez, Varela, Allegue, Cruz, Monroy, Merlos, Burgueño, Carracedo and Loza. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Martínez, Antón L. Brea, José Domínguez, Eduardo Varela, María J. Allegue, Catarina Cruz, Raquel Monroy, Xavier Merlos, Manuel Burgueño, Javier Carracedo, Ángel Loza, María Isabel Identification of Sodium Transients Through Na(V)1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons |
title | Identification of Sodium Transients Through Na(V)1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons |
title_full | Identification of Sodium Transients Through Na(V)1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons |
title_fullStr | Identification of Sodium Transients Through Na(V)1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons |
title_full_unstemmed | Identification of Sodium Transients Through Na(V)1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons |
title_short | Identification of Sodium Transients Through Na(V)1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons |
title_sort | identification of sodium transients through na(v)1.5 channels as regulators of differentiation in immortalized dorsal root ganglia neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018981/ https://www.ncbi.nlm.nih.gov/pubmed/35465610 http://dx.doi.org/10.3389/fncel.2022.816325 |
work_keys_str_mv | AT martinezantonl identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT breajose identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT dominguezeduardo identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT varelamariaj identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT alleguecatarina identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT cruzraquel identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT monroyxavier identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT merlosmanuel identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT burguenojavier identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT carracedoangel identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons AT lozamariaisabel identificationofsodiumtransientsthroughnav15channelsasregulatorsofdifferentiationinimmortalizeddorsalrootganglianeurons |