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Detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line
Recent data suggest that cells respond to infection by upregulating the antiviral cytokine interferon-beta (IFN-ß) in a fraction of infected cells. Approaches are thus needed to study these responses on a single-cell level rather than bulk population. Here, we describe a protocol to analyze the IFN-...
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/PMC8063907/ https://www.ncbi.nlm.nih.gov/pubmed/33912845 http://dx.doi.org/10.1016/j.xpro.2021.100436 |
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author | Hare, David N. Subapanditha, Minomi K. Mossman, Karen L. |
author_facet | Hare, David N. Subapanditha, Minomi K. Mossman, Karen L. |
author_sort | Hare, David N. |
collection | PubMed |
description | Recent data suggest that cells respond to infection by upregulating the antiviral cytokine interferon-beta (IFN-ß) in a fraction of infected cells. Approaches are thus needed to study these responses on a single-cell level rather than bulk population. Here, we describe a protocol to analyze the IFN-ß response of individual cells using flow cytometry and immunofluorescence microscopy. We show the heterogeneous IFN-ß response to inactivated Sendai virus and human cytomegalovirus, but this protocol can be adapted to other viruses. For complete details on the use and execution of this protocol, please refer to Hare et al. (2020). |
format | Online Article Text |
id | pubmed-8063907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80639072021-04-27 Detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line Hare, David N. Subapanditha, Minomi K. Mossman, Karen L. STAR Protoc Protocol Recent data suggest that cells respond to infection by upregulating the antiviral cytokine interferon-beta (IFN-ß) in a fraction of infected cells. Approaches are thus needed to study these responses on a single-cell level rather than bulk population. Here, we describe a protocol to analyze the IFN-ß response of individual cells using flow cytometry and immunofluorescence microscopy. We show the heterogeneous IFN-ß response to inactivated Sendai virus and human cytomegalovirus, but this protocol can be adapted to other viruses. For complete details on the use and execution of this protocol, please refer to Hare et al. (2020). Elsevier 2021-04-10 /pmc/articles/PMC8063907/ /pubmed/33912845 http://dx.doi.org/10.1016/j.xpro.2021.100436 Text en © 2021 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 Hare, David N. Subapanditha, Minomi K. Mossman, Karen L. Detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line |
title | Detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line |
title_full | Detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line |
title_fullStr | Detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line |
title_full_unstemmed | Detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line |
title_short | Detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line |
title_sort | detecting single cell interferon-beta production using a fluorescent reporter telomerase-immortalized human fibroblast cell line |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063907/ https://www.ncbi.nlm.nih.gov/pubmed/33912845 http://dx.doi.org/10.1016/j.xpro.2021.100436 |
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