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An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination
Myelinating oligodendrocytes are essential for central nervous system (CNS) formation and function. Their disruption is implicated in numerous neurodevelopmental, neuropsychiatric and neurodegenerative disorders. However, recent studies have indicated that oligodendrocytes may be tractable for treat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056238/ https://www.ncbi.nlm.nih.gov/pubmed/29979149 http://dx.doi.org/10.7554/eLife.35136 |
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author | Early, Jason J Marshall-Phelps, Katy LH Williamson, Jill M Swire, Matthew Kamadurai, Hari Muskavitch, Marc Lyons, David A |
author_facet | Early, Jason J Marshall-Phelps, Katy LH Williamson, Jill M Swire, Matthew Kamadurai, Hari Muskavitch, Marc Lyons, David A |
author_sort | Early, Jason J |
collection | PubMed |
description | Myelinating oligodendrocytes are essential for central nervous system (CNS) formation and function. Their disruption is implicated in numerous neurodevelopmental, neuropsychiatric and neurodegenerative disorders. However, recent studies have indicated that oligodendrocytes may be tractable for treatment of disease. In recent years, zebrafish have become well established for the study of myelinating oligodendrocyte biology and drug discovery in vivo. Here, by automating the delivery of zebrafish larvae to a spinning disk confocal microscope, we were able to automate high-resolution imaging of myelinating oligodendrocytes in vivo. From there, we developed an image analysis pipeline that facilitated a screen of compounds with epigenetic and post-translational targets for their effects on regulating myelinating oligodendrocyte number. This screen identified novel compounds that strongly promote myelinating oligodendrocyte formation in vivo. Our imaging platform and analysis pipeline is flexible and can be employed for high-resolution imaging-based screens of broad interest using zebrafish. |
format | Online Article Text |
id | pubmed-6056238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60562382018-07-25 An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination Early, Jason J Marshall-Phelps, Katy LH Williamson, Jill M Swire, Matthew Kamadurai, Hari Muskavitch, Marc Lyons, David A eLife Neuroscience Myelinating oligodendrocytes are essential for central nervous system (CNS) formation and function. Their disruption is implicated in numerous neurodevelopmental, neuropsychiatric and neurodegenerative disorders. However, recent studies have indicated that oligodendrocytes may be tractable for treatment of disease. In recent years, zebrafish have become well established for the study of myelinating oligodendrocyte biology and drug discovery in vivo. Here, by automating the delivery of zebrafish larvae to a spinning disk confocal microscope, we were able to automate high-resolution imaging of myelinating oligodendrocytes in vivo. From there, we developed an image analysis pipeline that facilitated a screen of compounds with epigenetic and post-translational targets for their effects on regulating myelinating oligodendrocyte number. This screen identified novel compounds that strongly promote myelinating oligodendrocyte formation in vivo. Our imaging platform and analysis pipeline is flexible and can be employed for high-resolution imaging-based screens of broad interest using zebrafish. eLife Sciences Publications, Ltd 2018-07-06 /pmc/articles/PMC6056238/ /pubmed/29979149 http://dx.doi.org/10.7554/eLife.35136 Text en © 2018, Early et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Early, Jason J Marshall-Phelps, Katy LH Williamson, Jill M Swire, Matthew Kamadurai, Hari Muskavitch, Marc Lyons, David A An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination |
title | An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination |
title_full | An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination |
title_fullStr | An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination |
title_full_unstemmed | An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination |
title_short | An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination |
title_sort | automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056238/ https://www.ncbi.nlm.nih.gov/pubmed/29979149 http://dx.doi.org/10.7554/eLife.35136 |
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