Cargando…

CNS Hypomyelination Disrupts Axonal Conduction and Behavior in Larval Zebrafish

Myelination is essential for central nervous system (CNS) formation, health and function. As a model organism, larval zebrafish have been extensively employed to investigate the molecular and cellular basis of CNS myelination, because of their genetic tractability and suitability for non-invasive li...

Descripción completa

Detalles Bibliográficos
Autores principales: Madden, M. E., Suminaite, D., Ortiz, E., Early, J. J., Koudelka, S., Livesey, M. R., Bianco, I. H., Granato, M., Lyons, D. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570833/
https://www.ncbi.nlm.nih.gov/pubmed/34544838
http://dx.doi.org/10.1523/JNEUROSCI.0842-21.2021
_version_ 1784594899530678272
author Madden, M. E.
Suminaite, D.
Ortiz, E.
Early, J. J.
Koudelka, S.
Livesey, M. R.
Bianco, I. H.
Granato, M.
Lyons, D. A.
author_facet Madden, M. E.
Suminaite, D.
Ortiz, E.
Early, J. J.
Koudelka, S.
Livesey, M. R.
Bianco, I. H.
Granato, M.
Lyons, D. A.
author_sort Madden, M. E.
collection PubMed
description Myelination is essential for central nervous system (CNS) formation, health and function. As a model organism, larval zebrafish have been extensively employed to investigate the molecular and cellular basis of CNS myelination, because of their genetic tractability and suitability for non-invasive live cell imaging. However, it has not been assessed to what extent CNS myelination affects neural circuit function in zebrafish larvae, prohibiting the integration of molecular and cellular analyses of myelination with concomitant network maturation. To test whether larval zebrafish might serve as a suitable platform with which to study the effects of CNS myelination and its dysregulation on circuit function, we generated zebrafish myelin regulatory factor (myrf) mutants with CNS-specific hypomyelination and investigated how this affected their axonal conduction properties and behavior. We found that myrf mutant larvae exhibited increased latency to perform startle responses following defined acoustic stimuli. Furthermore, we found that hypomyelinated animals often selected an impaired response to acoustic stimuli, exhibiting a bias toward reorientation behavior instead of the stimulus-appropriate startle response. To begin to study how myelination affected the underlying circuitry, we established electrophysiological protocols to assess various conduction properties along single axons. We found that the hypomyelinated myrf mutants exhibited reduced action potential conduction velocity and an impaired ability to sustain high-frequency action potential firing. This study indicates that larval zebrafish can be used to bridge molecular and cellular investigation of CNS myelination with multiscale assessment of neural circuit function. SIGNIFICANCE STATEMENT Myelination of CNS axons is essential for their health and function, and it is now clear that myelination is a dynamic life-long process subject to modulation by neuronal activity. However, it remains unclear precisely how changes to myelination affects animal behavior and underlying action potential conduction along axons in intact neural circuits. In recent years, zebrafish have been employed to study cellular and molecular mechanisms of myelination, because of their relatively simple, optically transparent, experimentally tractable vertebrate nervous system. Here we find that changes to myelination alter the behavior of young zebrafish and action potential conduction along individual axons, providing a platform to integrate molecular, cellular, and circuit level analyses of myelination using this model.
format Online
Article
Text
id pubmed-8570833
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-85708332021-11-08 CNS Hypomyelination Disrupts Axonal Conduction and Behavior in Larval Zebrafish Madden, M. E. Suminaite, D. Ortiz, E. Early, J. J. Koudelka, S. Livesey, M. R. Bianco, I. H. Granato, M. Lyons, D. A. J Neurosci Research Articles Myelination is essential for central nervous system (CNS) formation, health and function. As a model organism, larval zebrafish have been extensively employed to investigate the molecular and cellular basis of CNS myelination, because of their genetic tractability and suitability for non-invasive live cell imaging. However, it has not been assessed to what extent CNS myelination affects neural circuit function in zebrafish larvae, prohibiting the integration of molecular and cellular analyses of myelination with concomitant network maturation. To test whether larval zebrafish might serve as a suitable platform with which to study the effects of CNS myelination and its dysregulation on circuit function, we generated zebrafish myelin regulatory factor (myrf) mutants with CNS-specific hypomyelination and investigated how this affected their axonal conduction properties and behavior. We found that myrf mutant larvae exhibited increased latency to perform startle responses following defined acoustic stimuli. Furthermore, we found that hypomyelinated animals often selected an impaired response to acoustic stimuli, exhibiting a bias toward reorientation behavior instead of the stimulus-appropriate startle response. To begin to study how myelination affected the underlying circuitry, we established electrophysiological protocols to assess various conduction properties along single axons. We found that the hypomyelinated myrf mutants exhibited reduced action potential conduction velocity and an impaired ability to sustain high-frequency action potential firing. This study indicates that larval zebrafish can be used to bridge molecular and cellular investigation of CNS myelination with multiscale assessment of neural circuit function. SIGNIFICANCE STATEMENT Myelination of CNS axons is essential for their health and function, and it is now clear that myelination is a dynamic life-long process subject to modulation by neuronal activity. However, it remains unclear precisely how changes to myelination affects animal behavior and underlying action potential conduction along axons in intact neural circuits. In recent years, zebrafish have been employed to study cellular and molecular mechanisms of myelination, because of their relatively simple, optically transparent, experimentally tractable vertebrate nervous system. Here we find that changes to myelination alter the behavior of young zebrafish and action potential conduction along individual axons, providing a platform to integrate molecular, cellular, and circuit level analyses of myelination using this model. Society for Neuroscience 2021-11-03 /pmc/articles/PMC8570833/ /pubmed/34544838 http://dx.doi.org/10.1523/JNEUROSCI.0842-21.2021 Text en Copyright © 2021 Madden et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Madden, M. E.
Suminaite, D.
Ortiz, E.
Early, J. J.
Koudelka, S.
Livesey, M. R.
Bianco, I. H.
Granato, M.
Lyons, D. A.
CNS Hypomyelination Disrupts Axonal Conduction and Behavior in Larval Zebrafish
title CNS Hypomyelination Disrupts Axonal Conduction and Behavior in Larval Zebrafish
title_full CNS Hypomyelination Disrupts Axonal Conduction and Behavior in Larval Zebrafish
title_fullStr CNS Hypomyelination Disrupts Axonal Conduction and Behavior in Larval Zebrafish
title_full_unstemmed CNS Hypomyelination Disrupts Axonal Conduction and Behavior in Larval Zebrafish
title_short CNS Hypomyelination Disrupts Axonal Conduction and Behavior in Larval Zebrafish
title_sort cns hypomyelination disrupts axonal conduction and behavior in larval zebrafish
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570833/
https://www.ncbi.nlm.nih.gov/pubmed/34544838
http://dx.doi.org/10.1523/JNEUROSCI.0842-21.2021
work_keys_str_mv AT maddenme cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish
AT suminaited cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish
AT ortize cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish
AT earlyjj cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish
AT koudelkas cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish
AT liveseymr cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish
AT biancoih cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish
AT granatom cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish
AT lyonsda cnshypomyelinationdisruptsaxonalconductionandbehaviorinlarvalzebrafish