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Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia

Most of the protocols to analyze metabolic features of cell populations from different tissues rely on in vitro cell culture conditions. Here, we present a flow-cytometry-based protocol for measuring the respiratory chain function in permeabilized mouse microglia ex vivo. We describe microglial cell...

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Detalles Bibliográficos
Autores principales: Erny, Daniel, Dokalis, Nikolaos, Mezö, Charlotte, Mossad, Omar, Blank, Thomas, Prinz, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861812/
https://www.ncbi.nlm.nih.gov/pubmed/35243376
http://dx.doi.org/10.1016/j.xpro.2022.101186
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author Erny, Daniel
Dokalis, Nikolaos
Mezö, Charlotte
Mossad, Omar
Blank, Thomas
Prinz, Marco
author_facet Erny, Daniel
Dokalis, Nikolaos
Mezö, Charlotte
Mossad, Omar
Blank, Thomas
Prinz, Marco
author_sort Erny, Daniel
collection PubMed
description Most of the protocols to analyze metabolic features of cell populations from different tissues rely on in vitro cell culture conditions. Here, we present a flow-cytometry-based protocol for measuring the respiratory chain function in permeabilized mouse microglia ex vivo. We describe microglial cell isolation, followed by analyzing complex I and II using flow cytometry. This optimized protocol requires a low input of permeabilized cells and can be applied to other ex vivo isolated cells or cells derived from cell cultures. For complete details on the use and execution of this protocol, please refer to Erny et al. (2021).
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spelling pubmed-88618122022-03-02 Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia Erny, Daniel Dokalis, Nikolaos Mezö, Charlotte Mossad, Omar Blank, Thomas Prinz, Marco STAR Protoc Protocol Most of the protocols to analyze metabolic features of cell populations from different tissues rely on in vitro cell culture conditions. Here, we present a flow-cytometry-based protocol for measuring the respiratory chain function in permeabilized mouse microglia ex vivo. We describe microglial cell isolation, followed by analyzing complex I and II using flow cytometry. This optimized protocol requires a low input of permeabilized cells and can be applied to other ex vivo isolated cells or cells derived from cell cultures. For complete details on the use and execution of this protocol, please refer to Erny et al. (2021). Elsevier 2022-02-18 /pmc/articles/PMC8861812/ /pubmed/35243376 http://dx.doi.org/10.1016/j.xpro.2022.101186 Text en © 2022 The Author(s) 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
Erny, Daniel
Dokalis, Nikolaos
Mezö, Charlotte
Mossad, Omar
Blank, Thomas
Prinz, Marco
Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia
title Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia
title_full Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia
title_fullStr Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia
title_full_unstemmed Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia
title_short Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia
title_sort flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861812/
https://www.ncbi.nlm.nih.gov/pubmed/35243376
http://dx.doi.org/10.1016/j.xpro.2022.101186
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