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Detection of exogenous DNA uptake by murine dendritic cells
This protocol has been developed to measure exogenous DNA uptake by murine dendritic cells (DCs) using supernatant containing cellular debris, which allows for DNA uptake in the absence of transfection reagents. Inhibitors or antibodies that alter the process can be added, and either flow cytometry...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204794/ https://www.ncbi.nlm.nih.gov/pubmed/35719726 http://dx.doi.org/10.1016/j.xpro.2022.101464 |
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author | Celias, Daiana P. de Mingo Pulido, Álvaro Ruffell, Brian |
author_facet | Celias, Daiana P. de Mingo Pulido, Álvaro Ruffell, Brian |
author_sort | Celias, Daiana P. |
collection | PubMed |
description | This protocol has been developed to measure exogenous DNA uptake by murine dendritic cells (DCs) using supernatant containing cellular debris, which allows for DNA uptake in the absence of transfection reagents. Inhibitors or antibodies that alter the process can be added, and either flow cytometry or fluorescent microscopy can be used to measure DNA uptake. This is intended to mimic the exposure of DCs to dying cells in the tumor microenvironment or other pathological conditions of high cellular death. For complete details on the use and execution of this protocol, please refer to de Mingo Pulido et al. (2021). |
format | Online Article Text |
id | pubmed-9204794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92047942022-06-18 Detection of exogenous DNA uptake by murine dendritic cells Celias, Daiana P. de Mingo Pulido, Álvaro Ruffell, Brian STAR Protoc Protocol This protocol has been developed to measure exogenous DNA uptake by murine dendritic cells (DCs) using supernatant containing cellular debris, which allows for DNA uptake in the absence of transfection reagents. Inhibitors or antibodies that alter the process can be added, and either flow cytometry or fluorescent microscopy can be used to measure DNA uptake. This is intended to mimic the exposure of DCs to dying cells in the tumor microenvironment or other pathological conditions of high cellular death. For complete details on the use and execution of this protocol, please refer to de Mingo Pulido et al. (2021). Elsevier 2022-06-14 /pmc/articles/PMC9204794/ /pubmed/35719726 http://dx.doi.org/10.1016/j.xpro.2022.101464 Text en © 2022 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 Celias, Daiana P. de Mingo Pulido, Álvaro Ruffell, Brian Detection of exogenous DNA uptake by murine dendritic cells |
title | Detection of exogenous DNA uptake by murine dendritic cells |
title_full | Detection of exogenous DNA uptake by murine dendritic cells |
title_fullStr | Detection of exogenous DNA uptake by murine dendritic cells |
title_full_unstemmed | Detection of exogenous DNA uptake by murine dendritic cells |
title_short | Detection of exogenous DNA uptake by murine dendritic cells |
title_sort | detection of exogenous dna uptake by murine dendritic cells |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204794/ https://www.ncbi.nlm.nih.gov/pubmed/35719726 http://dx.doi.org/10.1016/j.xpro.2022.101464 |
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