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Electrophysiological Properties of Adult Zebrafish Oligodendrocyte Progenitor Cells

Low remyelination efficiency after spinal cord injury (SCI) is a major restraint to successful axonal and functional regeneration in mammals. In contrast, adult zebrafish can: (i) regenerate oligodendrocytes and myelin sheaths within 2 weeks post lesion; (ii) re-grow axonal projections across the le...

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Autores principales: Tsata, Vasiliki, Kroehne, Volker, Reinhardt, Susanne, El-Armouche, Ali, Brand, Michael, Wagner, Michael, Reimer, Michell M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473327/
https://www.ncbi.nlm.nih.gov/pubmed/31031593
http://dx.doi.org/10.3389/fncel.2019.00102
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author Tsata, Vasiliki
Kroehne, Volker
Reinhardt, Susanne
El-Armouche, Ali
Brand, Michael
Wagner, Michael
Reimer, Michell M.
author_facet Tsata, Vasiliki
Kroehne, Volker
Reinhardt, Susanne
El-Armouche, Ali
Brand, Michael
Wagner, Michael
Reimer, Michell M.
author_sort Tsata, Vasiliki
collection PubMed
description Low remyelination efficiency after spinal cord injury (SCI) is a major restraint to successful axonal and functional regeneration in mammals. In contrast, adult zebrafish can: (i) regenerate oligodendrocytes and myelin sheaths within 2 weeks post lesion; (ii) re-grow axonal projections across the lesion site and (iii) recover locomotor function within 6 weeks after spinal cord transection. However, little is known about the intrinsic properties of oligodendrocyte progenitor cells (OPCs), the remyelinating cells of the central nervous system (CNS). Here, we demonstrate that purified OPCs from the adult zebrafish spinal cord are electrically active. They functionally express voltage-gated K(+) and Na(+) channels, glutamate receptors and exhibit depolarizing, tetrodotoxin (TTX)-sensitive spikes, as previously seen in rodent and human OPCs. Furthermore, we show that the percentage of zebrafish OPCs exhibiting depolarizing spikes and Na(v)-mediated currents is lower as compared to rodent white matter OPCs, where these membrane characteristics have been shown to underlie OPC injury susceptibility. These findings imply that adult zebrafish OPCs resemble electrical properties found in mammals and represent a relevant cell type towards understanding the biology of the primary cells targeted in remyelination therapies for non-regenerative species. The in vitro platform introduced in this study could be used in the future to: (i) elucidate how membrane characteristics of zebrafish OPCs change upon injury and (ii) identify potential signaling components underlying OPC injury recognition.
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spelling pubmed-64733272019-04-26 Electrophysiological Properties of Adult Zebrafish Oligodendrocyte Progenitor Cells Tsata, Vasiliki Kroehne, Volker Reinhardt, Susanne El-Armouche, Ali Brand, Michael Wagner, Michael Reimer, Michell M. Front Cell Neurosci Neuroscience Low remyelination efficiency after spinal cord injury (SCI) is a major restraint to successful axonal and functional regeneration in mammals. In contrast, adult zebrafish can: (i) regenerate oligodendrocytes and myelin sheaths within 2 weeks post lesion; (ii) re-grow axonal projections across the lesion site and (iii) recover locomotor function within 6 weeks after spinal cord transection. However, little is known about the intrinsic properties of oligodendrocyte progenitor cells (OPCs), the remyelinating cells of the central nervous system (CNS). Here, we demonstrate that purified OPCs from the adult zebrafish spinal cord are electrically active. They functionally express voltage-gated K(+) and Na(+) channels, glutamate receptors and exhibit depolarizing, tetrodotoxin (TTX)-sensitive spikes, as previously seen in rodent and human OPCs. Furthermore, we show that the percentage of zebrafish OPCs exhibiting depolarizing spikes and Na(v)-mediated currents is lower as compared to rodent white matter OPCs, where these membrane characteristics have been shown to underlie OPC injury susceptibility. These findings imply that adult zebrafish OPCs resemble electrical properties found in mammals and represent a relevant cell type towards understanding the biology of the primary cells targeted in remyelination therapies for non-regenerative species. The in vitro platform introduced in this study could be used in the future to: (i) elucidate how membrane characteristics of zebrafish OPCs change upon injury and (ii) identify potential signaling components underlying OPC injury recognition. Frontiers Media S.A. 2019-04-12 /pmc/articles/PMC6473327/ /pubmed/31031593 http://dx.doi.org/10.3389/fncel.2019.00102 Text en Copyright © 2019 Tsata, Kroehne, Reinhardt, El-Armouche, Brand, Wagner and Reimer. http://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
Tsata, Vasiliki
Kroehne, Volker
Reinhardt, Susanne
El-Armouche, Ali
Brand, Michael
Wagner, Michael
Reimer, Michell M.
Electrophysiological Properties of Adult Zebrafish Oligodendrocyte Progenitor Cells
title Electrophysiological Properties of Adult Zebrafish Oligodendrocyte Progenitor Cells
title_full Electrophysiological Properties of Adult Zebrafish Oligodendrocyte Progenitor Cells
title_fullStr Electrophysiological Properties of Adult Zebrafish Oligodendrocyte Progenitor Cells
title_full_unstemmed Electrophysiological Properties of Adult Zebrafish Oligodendrocyte Progenitor Cells
title_short Electrophysiological Properties of Adult Zebrafish Oligodendrocyte Progenitor Cells
title_sort electrophysiological properties of adult zebrafish oligodendrocyte progenitor cells
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473327/
https://www.ncbi.nlm.nih.gov/pubmed/31031593
http://dx.doi.org/10.3389/fncel.2019.00102
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