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A redox-based characterization of human immune cell subsets by polychromatic flow cytometry

Cellular redox state determinants are traditionally studied using fluorescent microscopy and immunoblot analysis; however, no procedure has been developed for simultaneous measurement in various immune cell subsets. Here, we present a flow cytometry assay for measuring antioxidant defense systems an...

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Detalles Bibliográficos
Autores principales: Pitsillidou, Christina, Muradore, Ivan, Pontarini, Elena, Bertolotti, Milena, Roberto, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587764/
https://www.ncbi.nlm.nih.gov/pubmed/37838948
http://dx.doi.org/10.1016/j.xpro.2023.102632
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author Pitsillidou, Christina
Muradore, Ivan
Pontarini, Elena
Bertolotti, Milena
Roberto, Alessandra
author_facet Pitsillidou, Christina
Muradore, Ivan
Pontarini, Elena
Bertolotti, Milena
Roberto, Alessandra
author_sort Pitsillidou, Christina
collection PubMed
description Cellular redox state determinants are traditionally studied using fluorescent microscopy and immunoblot analysis; however, no procedure has been developed for simultaneous measurement in various immune cell subsets. Here, we present a flow cytometry assay for measuring antioxidant defense systems and reactive oxygen species simultaneously in T, B, and natural killer lymphocytes. We describe steps for preparing and treating peripheral blood mononuclear cells, surface and dye staining, cell fixation/permeabilization, and intracellular staining. We then detail machine standardization, acquisition, and analysis.
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spelling pubmed-105877642023-10-21 A redox-based characterization of human immune cell subsets by polychromatic flow cytometry Pitsillidou, Christina Muradore, Ivan Pontarini, Elena Bertolotti, Milena Roberto, Alessandra STAR Protoc Protocol Cellular redox state determinants are traditionally studied using fluorescent microscopy and immunoblot analysis; however, no procedure has been developed for simultaneous measurement in various immune cell subsets. Here, we present a flow cytometry assay for measuring antioxidant defense systems and reactive oxygen species simultaneously in T, B, and natural killer lymphocytes. We describe steps for preparing and treating peripheral blood mononuclear cells, surface and dye staining, cell fixation/permeabilization, and intracellular staining. We then detail machine standardization, acquisition, and analysis. Elsevier 2023-10-14 /pmc/articles/PMC10587764/ /pubmed/37838948 http://dx.doi.org/10.1016/j.xpro.2023.102632 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
Pitsillidou, Christina
Muradore, Ivan
Pontarini, Elena
Bertolotti, Milena
Roberto, Alessandra
A redox-based characterization of human immune cell subsets by polychromatic flow cytometry
title A redox-based characterization of human immune cell subsets by polychromatic flow cytometry
title_full A redox-based characterization of human immune cell subsets by polychromatic flow cytometry
title_fullStr A redox-based characterization of human immune cell subsets by polychromatic flow cytometry
title_full_unstemmed A redox-based characterization of human immune cell subsets by polychromatic flow cytometry
title_short A redox-based characterization of human immune cell subsets by polychromatic flow cytometry
title_sort redox-based characterization of human immune cell subsets by polychromatic flow cytometry
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587764/
https://www.ncbi.nlm.nih.gov/pubmed/37838948
http://dx.doi.org/10.1016/j.xpro.2023.102632
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