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Murine brain tumor microenvironment immunophenotyping using mass cytometry

Here, we present a mass cytometry protocol optimized to examine the phenotype of immune cells within the mouse glioma microenvironment, using a Sleeping Beauty transposon-mediated mouse glioma model. We describe antibody conjugation and titrations for analysis of immune cells. We then detail mouse b...

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Autores principales: McClellan, Brandon L., Alghamri, Mahmoud S., Thalla, Rohit, Lowenstein, Pedro R., Castro, Maria G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136353/
https://www.ncbi.nlm.nih.gov/pubmed/35634359
http://dx.doi.org/10.1016/j.xpro.2022.101357
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author McClellan, Brandon L.
Alghamri, Mahmoud S.
Thalla, Rohit
Lowenstein, Pedro R.
Castro, Maria G.
author_facet McClellan, Brandon L.
Alghamri, Mahmoud S.
Thalla, Rohit
Lowenstein, Pedro R.
Castro, Maria G.
author_sort McClellan, Brandon L.
collection PubMed
description Here, we present a mass cytometry protocol optimized to examine the phenotype of immune cells within the mouse glioma microenvironment, using a Sleeping Beauty transposon-mediated mouse glioma model. We describe antibody conjugation and titrations for analysis of immune cells. We then detail mouse brain tumor tissue collection and processing, staining, followed by data acquisition, analysis, and gating strategy. This protocol can be applied to any brain tumor-harboring mouse model. For complete details on the use and execution of this protocol, please refer to Alghamri et al. (2021).
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spelling pubmed-91363532022-05-28 Murine brain tumor microenvironment immunophenotyping using mass cytometry McClellan, Brandon L. Alghamri, Mahmoud S. Thalla, Rohit Lowenstein, Pedro R. Castro, Maria G. STAR Protoc Protocol Here, we present a mass cytometry protocol optimized to examine the phenotype of immune cells within the mouse glioma microenvironment, using a Sleeping Beauty transposon-mediated mouse glioma model. We describe antibody conjugation and titrations for analysis of immune cells. We then detail mouse brain tumor tissue collection and processing, staining, followed by data acquisition, analysis, and gating strategy. This protocol can be applied to any brain tumor-harboring mouse model. For complete details on the use and execution of this protocol, please refer to Alghamri et al. (2021). Elsevier 2022-05-25 /pmc/articles/PMC9136353/ /pubmed/35634359 http://dx.doi.org/10.1016/j.xpro.2022.101357 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
McClellan, Brandon L.
Alghamri, Mahmoud S.
Thalla, Rohit
Lowenstein, Pedro R.
Castro, Maria G.
Murine brain tumor microenvironment immunophenotyping using mass cytometry
title Murine brain tumor microenvironment immunophenotyping using mass cytometry
title_full Murine brain tumor microenvironment immunophenotyping using mass cytometry
title_fullStr Murine brain tumor microenvironment immunophenotyping using mass cytometry
title_full_unstemmed Murine brain tumor microenvironment immunophenotyping using mass cytometry
title_short Murine brain tumor microenvironment immunophenotyping using mass cytometry
title_sort murine brain tumor microenvironment immunophenotyping using mass cytometry
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136353/
https://www.ncbi.nlm.nih.gov/pubmed/35634359
http://dx.doi.org/10.1016/j.xpro.2022.101357
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