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Live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture

Microglial dynamics and interactions with nearby radial glia can be visualized in real time in embryonic mouse brain tissue using time-lapse imaging in slice culture. This live-cell imaging protocol can be used to study the morphology and activities of a number of cell types across a variety of brai...

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Detalles Bibliográficos
Autores principales: Rosin, Jessica M., Malik, Faizan, Kurrasch, Deborah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339326/
https://www.ncbi.nlm.nih.gov/pubmed/34382012
http://dx.doi.org/10.1016/j.xpro.2021.100670
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author Rosin, Jessica M.
Malik, Faizan
Kurrasch, Deborah M.
author_facet Rosin, Jessica M.
Malik, Faizan
Kurrasch, Deborah M.
author_sort Rosin, Jessica M.
collection PubMed
description Microglial dynamics and interactions with nearby radial glia can be visualized in real time in embryonic mouse brain tissue using time-lapse imaging in slice culture. This live-cell imaging protocol can be used to study the morphology and activities of a number of cell types across a variety of brain regions and developmental time points. The advantage of this brain slice culture model is that it allows for the visualization of cellular interactions and movements in real time, especially across embryogenesis. For complete details on the use and execution of this protocol, please refer to Rosin et al. (2021).
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spelling pubmed-83393262021-08-10 Live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture Rosin, Jessica M. Malik, Faizan Kurrasch, Deborah M. STAR Protoc Protocol Microglial dynamics and interactions with nearby radial glia can be visualized in real time in embryonic mouse brain tissue using time-lapse imaging in slice culture. This live-cell imaging protocol can be used to study the morphology and activities of a number of cell types across a variety of brain regions and developmental time points. The advantage of this brain slice culture model is that it allows for the visualization of cellular interactions and movements in real time, especially across embryogenesis. For complete details on the use and execution of this protocol, please refer to Rosin et al. (2021). Elsevier 2021-07-29 /pmc/articles/PMC8339326/ /pubmed/34382012 http://dx.doi.org/10.1016/j.xpro.2021.100670 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
Rosin, Jessica M.
Malik, Faizan
Kurrasch, Deborah M.
Live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture
title Live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture
title_full Live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture
title_fullStr Live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture
title_full_unstemmed Live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture
title_short Live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture
title_sort live-cell imaging of microglial interactions with radial glia in transgenic embryonic mouse brains using slice culture
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339326/
https://www.ncbi.nlm.nih.gov/pubmed/34382012
http://dx.doi.org/10.1016/j.xpro.2021.100670
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