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High-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages

Regulation of bioenergetics and cell death are pivotal mitochondrial functions determining the responses of macrophages to infection. Here, we provide a protocol to investigate mitochondrial functions during infection of macrophages by intracellular bacteria. We describe steps for quantifying mitoch...

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Autores principales: Dramé, Mariatou, Garcia-Rodriguez, Francisco Javier, Buchrieser, Carmen, Escoll, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031535/
https://www.ncbi.nlm.nih.gov/pubmed/36933221
http://dx.doi.org/10.1016/j.xpro.2023.102175
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author Dramé, Mariatou
Garcia-Rodriguez, Francisco Javier
Buchrieser, Carmen
Escoll, Pedro
author_facet Dramé, Mariatou
Garcia-Rodriguez, Francisco Javier
Buchrieser, Carmen
Escoll, Pedro
author_sort Dramé, Mariatou
collection PubMed
description Regulation of bioenergetics and cell death are pivotal mitochondrial functions determining the responses of macrophages to infection. Here, we provide a protocol to investigate mitochondrial functions during infection of macrophages by intracellular bacteria. We describe steps for quantifying mitochondrial polarization, cell death, and bacterial infection in infected, living, human primary macrophages at the single-cell level. We also detail the use of the pathogen Legionella pneumophila as model. This protocol can be adapted to investigate mitochondrial functions in other settings. For complete details on the use and execution of this protocol, please refer to Escoll et al. (2021).(1)
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spelling pubmed-100315352023-03-23 High-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages Dramé, Mariatou Garcia-Rodriguez, Francisco Javier Buchrieser, Carmen Escoll, Pedro STAR Protoc Protocol Regulation of bioenergetics and cell death are pivotal mitochondrial functions determining the responses of macrophages to infection. Here, we provide a protocol to investigate mitochondrial functions during infection of macrophages by intracellular bacteria. We describe steps for quantifying mitochondrial polarization, cell death, and bacterial infection in infected, living, human primary macrophages at the single-cell level. We also detail the use of the pathogen Legionella pneumophila as model. This protocol can be adapted to investigate mitochondrial functions in other settings. For complete details on the use and execution of this protocol, please refer to Escoll et al. (2021).(1) Elsevier 2023-03-17 /pmc/articles/PMC10031535/ /pubmed/36933221 http://dx.doi.org/10.1016/j.xpro.2023.102175 Text en © 2023 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
Dramé, Mariatou
Garcia-Rodriguez, Francisco Javier
Buchrieser, Carmen
Escoll, Pedro
High-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages
title High-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages
title_full High-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages
title_fullStr High-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages
title_full_unstemmed High-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages
title_short High-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages
title_sort high-content assay to measure mitochondrial function and bacterial vacuole size in infected human primary macrophages
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031535/
https://www.ncbi.nlm.nih.gov/pubmed/36933221
http://dx.doi.org/10.1016/j.xpro.2023.102175
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