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Protocol for the isolation of mouse senescence-associated CD4(+) T cells using flow cytometry and functional assays

Senescence-associated (SA) CD4(+) T cells, which increase with age, may underlie the development of autoimmunity and chronic inflammation, but their pathological function remains understudied. Here, we present a protocol to isolate CD153(+) SA-T cells and evaluate their characteristic responses upon...

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Detalles Bibliográficos
Autores principales: Fukushima, Yuji, Minato, Nagahiro, Hattori, Masakazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400959/
https://www.ncbi.nlm.nih.gov/pubmed/37515759
http://dx.doi.org/10.1016/j.xpro.2023.102472
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author Fukushima, Yuji
Minato, Nagahiro
Hattori, Masakazu
author_facet Fukushima, Yuji
Minato, Nagahiro
Hattori, Masakazu
author_sort Fukushima, Yuji
collection PubMed
description Senescence-associated (SA) CD4(+) T cells, which increase with age, may underlie the development of autoimmunity and chronic inflammation, but their pathological function remains understudied. Here, we present a protocol to isolate CD153(+) SA-T cells and evaluate their characteristic responses upon T cell receptor stimulation. We describe steps for the isolation of CD153(+) SA-T cells using flow cytometry and in vitro culture with stimulatory antibodies against CD3, CD28, and CD153. We then detail the assessment of the proliferation capacity and cytokine production. For complete details on the use and execution of this protocol, please refer to Fukushima et al. (2022).(1)
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spelling pubmed-104009592023-08-05 Protocol for the isolation of mouse senescence-associated CD4(+) T cells using flow cytometry and functional assays Fukushima, Yuji Minato, Nagahiro Hattori, Masakazu STAR Protoc Protocol Senescence-associated (SA) CD4(+) T cells, which increase with age, may underlie the development of autoimmunity and chronic inflammation, but their pathological function remains understudied. Here, we present a protocol to isolate CD153(+) SA-T cells and evaluate their characteristic responses upon T cell receptor stimulation. We describe steps for the isolation of CD153(+) SA-T cells using flow cytometry and in vitro culture with stimulatory antibodies against CD3, CD28, and CD153. We then detail the assessment of the proliferation capacity and cytokine production. For complete details on the use and execution of this protocol, please refer to Fukushima et al. (2022).(1) Elsevier 2023-07-28 /pmc/articles/PMC10400959/ /pubmed/37515759 http://dx.doi.org/10.1016/j.xpro.2023.102472 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Fukushima, Yuji
Minato, Nagahiro
Hattori, Masakazu
Protocol for the isolation of mouse senescence-associated CD4(+) T cells using flow cytometry and functional assays
title Protocol for the isolation of mouse senescence-associated CD4(+) T cells using flow cytometry and functional assays
title_full Protocol for the isolation of mouse senescence-associated CD4(+) T cells using flow cytometry and functional assays
title_fullStr Protocol for the isolation of mouse senescence-associated CD4(+) T cells using flow cytometry and functional assays
title_full_unstemmed Protocol for the isolation of mouse senescence-associated CD4(+) T cells using flow cytometry and functional assays
title_short Protocol for the isolation of mouse senescence-associated CD4(+) T cells using flow cytometry and functional assays
title_sort protocol for the isolation of mouse senescence-associated cd4(+) t cells using flow cytometry and functional assays
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400959/
https://www.ncbi.nlm.nih.gov/pubmed/37515759
http://dx.doi.org/10.1016/j.xpro.2023.102472
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