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Imaging and analysis on the interaction between human antigen-pulsed Vδ2 T cells and antigen-specific CD4 T cells
This protocol describes how to visualize surface protein-protein co-localization across a cell-cell interface between antigen-presenting γδ-T cells and CD4 T cells. By consolidating immunofluorescence assay, confocal microscopy and 3D imaging analysis, it enables assessment of interaction between ce...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076705/ https://www.ncbi.nlm.nih.gov/pubmed/33937873 http://dx.doi.org/10.1016/j.xpro.2021.100453 |
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author | Mo, Yufei Cheung, Allen Ka Loon Liu, Yue Liu, Li Chen, Zhiwei |
author_facet | Mo, Yufei Cheung, Allen Ka Loon Liu, Yue Liu, Li Chen, Zhiwei |
author_sort | Mo, Yufei |
collection | PubMed |
description | This protocol describes how to visualize surface protein-protein co-localization across a cell-cell interface between antigen-presenting γδ-T cells and CD4 T cells. By consolidating immunofluorescence assay, confocal microscopy and 3D imaging analysis, it enables assessment of interaction between cell surface proteins such as Δ42PD1 and TLR4 between co-cultured γδ-T and CD4 T cells. This protocol can be applied to study a surface protein of interest and its potential interaction with a target cell/protein at the cell-cell interface. For complete details on the use and execution of this profile, please refer to Mo et al. (2020). |
format | Online Article Text |
id | pubmed-8076705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80767052021-04-29 Imaging and analysis on the interaction between human antigen-pulsed Vδ2 T cells and antigen-specific CD4 T cells Mo, Yufei Cheung, Allen Ka Loon Liu, Yue Liu, Li Chen, Zhiwei STAR Protoc Protocol This protocol describes how to visualize surface protein-protein co-localization across a cell-cell interface between antigen-presenting γδ-T cells and CD4 T cells. By consolidating immunofluorescence assay, confocal microscopy and 3D imaging analysis, it enables assessment of interaction between cell surface proteins such as Δ42PD1 and TLR4 between co-cultured γδ-T and CD4 T cells. This protocol can be applied to study a surface protein of interest and its potential interaction with a target cell/protein at the cell-cell interface. For complete details on the use and execution of this profile, please refer to Mo et al. (2020). Elsevier 2021-04-14 /pmc/articles/PMC8076705/ /pubmed/33937873 http://dx.doi.org/10.1016/j.xpro.2021.100453 Text en © 2021 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 Mo, Yufei Cheung, Allen Ka Loon Liu, Yue Liu, Li Chen, Zhiwei Imaging and analysis on the interaction between human antigen-pulsed Vδ2 T cells and antigen-specific CD4 T cells |
title | Imaging and analysis on the interaction between human antigen-pulsed Vδ2 T cells and antigen-specific CD4 T cells |
title_full | Imaging and analysis on the interaction between human antigen-pulsed Vδ2 T cells and antigen-specific CD4 T cells |
title_fullStr | Imaging and analysis on the interaction between human antigen-pulsed Vδ2 T cells and antigen-specific CD4 T cells |
title_full_unstemmed | Imaging and analysis on the interaction between human antigen-pulsed Vδ2 T cells and antigen-specific CD4 T cells |
title_short | Imaging and analysis on the interaction between human antigen-pulsed Vδ2 T cells and antigen-specific CD4 T cells |
title_sort | imaging and analysis on the interaction between human antigen-pulsed vδ2 t cells and antigen-specific cd4 t cells |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076705/ https://www.ncbi.nlm.nih.gov/pubmed/33937873 http://dx.doi.org/10.1016/j.xpro.2021.100453 |
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