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Time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants

Interneuron migration involves repetitive cycles of pausing and motion that include nucleokinesis and dynamic branching of the leading process. Here, we provide a step-by-step description of how to culture and record the migration of cortical interneurons. We provide two culture models: the first in...

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Autores principales: Lepiemme, Fanny, Silva, Carla G., Nguyen, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082162/
https://www.ncbi.nlm.nih.gov/pubmed/33982012
http://dx.doi.org/10.1016/j.xpro.2021.100467
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author Lepiemme, Fanny
Silva, Carla G.
Nguyen, Laurent
author_facet Lepiemme, Fanny
Silva, Carla G.
Nguyen, Laurent
author_sort Lepiemme, Fanny
collection PubMed
description Interneuron migration involves repetitive cycles of pausing and motion that include nucleokinesis and dynamic branching of the leading process. Here, we provide a step-by-step description of how to culture and record the migration of cortical interneurons. We provide two culture models: the first includes organotypic brain slices and the second medial ganglionic eminence (MGE) explants. While organotypic brain slices provide a close-to-physiological context to analyze interneuron migration into cortical streams, MGE explants are appropriate to investigate the fine details of interneuron morphology remodeling during movement. For complete details on the use and execution of this protocol, please refer to Silva et al. (2018).
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spelling pubmed-80821622021-05-11 Time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants Lepiemme, Fanny Silva, Carla G. Nguyen, Laurent STAR Protoc Protocol Interneuron migration involves repetitive cycles of pausing and motion that include nucleokinesis and dynamic branching of the leading process. Here, we provide a step-by-step description of how to culture and record the migration of cortical interneurons. We provide two culture models: the first includes organotypic brain slices and the second medial ganglionic eminence (MGE) explants. While organotypic brain slices provide a close-to-physiological context to analyze interneuron migration into cortical streams, MGE explants are appropriate to investigate the fine details of interneuron morphology remodeling during movement. For complete details on the use and execution of this protocol, please refer to Silva et al. (2018). Elsevier 2021-04-16 /pmc/articles/PMC8082162/ /pubmed/33982012 http://dx.doi.org/10.1016/j.xpro.2021.100467 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Lepiemme, Fanny
Silva, Carla G.
Nguyen, Laurent
Time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants
title Time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants
title_full Time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants
title_fullStr Time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants
title_full_unstemmed Time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants
title_short Time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants
title_sort time lapse recording of cortical interneuron migration in mouse organotypic brain slices and explants
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082162/
https://www.ncbi.nlm.nih.gov/pubmed/33982012
http://dx.doi.org/10.1016/j.xpro.2021.100467
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