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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-...

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Detalles Bibliográficos
Autores principales: Hare, David N., Subapanditha, Minomi K., Mossman, Karen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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).
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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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