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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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) |
format | Online Article Text |
id | pubmed-10400959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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