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Protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media
Tumor-associated macrophages (TAMs) are key contributors to antitumor immunity. Here, we present a protocol to drive human monocyte-macrophage differentiation using tumor-derived conditioned media, followed by phenotypic and functional characterization of TAMs in vitro. We describe CD14+ cell isolat...
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/PMC9494234/ https://www.ncbi.nlm.nih.gov/pubmed/36125932 http://dx.doi.org/10.1016/j.xpro.2022.101666 |
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author | George, Samantha Georgouli, Mirella Sanz-Moreno, Victoria |
author_facet | George, Samantha Georgouli, Mirella Sanz-Moreno, Victoria |
author_sort | George, Samantha |
collection | PubMed |
description | Tumor-associated macrophages (TAMs) are key contributors to antitumor immunity. Here, we present a protocol to drive human monocyte-macrophage differentiation using tumor-derived conditioned media, followed by phenotypic and functional characterization of TAMs in vitro. We describe CD14+ cell isolation from healthy human blood, and detail the procedure to induce macrophage polarization. Finally, we outline morphological assessment of macrophages, and validation of their functional behaviors with a tumor cell killing assay. This translatable-based approach can be applied to different cancer cell types. For complete details on the use and execution of this protocol, please refer to Georgouli et al. (2019). |
format | Online Article Text |
id | pubmed-9494234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94942342022-09-23 Protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media George, Samantha Georgouli, Mirella Sanz-Moreno, Victoria STAR Protoc Protocol Tumor-associated macrophages (TAMs) are key contributors to antitumor immunity. Here, we present a protocol to drive human monocyte-macrophage differentiation using tumor-derived conditioned media, followed by phenotypic and functional characterization of TAMs in vitro. We describe CD14+ cell isolation from healthy human blood, and detail the procedure to induce macrophage polarization. Finally, we outline morphological assessment of macrophages, and validation of their functional behaviors with a tumor cell killing assay. This translatable-based approach can be applied to different cancer cell types. For complete details on the use and execution of this protocol, please refer to Georgouli et al. (2019). Elsevier 2022-09-19 /pmc/articles/PMC9494234/ /pubmed/36125932 http://dx.doi.org/10.1016/j.xpro.2022.101666 Text en © 2022 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 George, Samantha Georgouli, Mirella Sanz-Moreno, Victoria Protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media |
title | Protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media |
title_full | Protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media |
title_fullStr | Protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media |
title_full_unstemmed | Protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media |
title_short | Protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media |
title_sort | protocol to drive human monocyte-to-macrophage polarization in vitro using tumor conditioned media |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494234/ https://www.ncbi.nlm.nih.gov/pubmed/36125932 http://dx.doi.org/10.1016/j.xpro.2022.101666 |
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