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Enabling cell recovery from 3D cell culture microfluidic devices for tumour microenvironment biomarker profiling

The tumour microenvironment (TME) has recently drawn much attention due to its profound impact on tumour development, drug resistance and patient outcome. There is an increasing interest in new therapies that target the TME. Nonetheless, most established in vitro models fail to include essential cue...

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Autores principales: Virumbrales-Muñoz, María, Ayuso, Jose M., Lacueva, Alodia, Randelovic, Teodora, Livingston, Megan K., Beebe, David J., Oliván, Sara, Pereboom, Desirée, Doblare, Manuel, Fernández, Luis, Ochoa, Ignacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470149/
https://www.ncbi.nlm.nih.gov/pubmed/30996291
http://dx.doi.org/10.1038/s41598-019-42529-8
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author Virumbrales-Muñoz, María
Ayuso, Jose M.
Lacueva, Alodia
Randelovic, Teodora
Livingston, Megan K.
Beebe, David J.
Oliván, Sara
Pereboom, Desirée
Doblare, Manuel
Fernández, Luis
Ochoa, Ignacio
author_facet Virumbrales-Muñoz, María
Ayuso, Jose M.
Lacueva, Alodia
Randelovic, Teodora
Livingston, Megan K.
Beebe, David J.
Oliván, Sara
Pereboom, Desirée
Doblare, Manuel
Fernández, Luis
Ochoa, Ignacio
author_sort Virumbrales-Muñoz, María
collection PubMed
description The tumour microenvironment (TME) has recently drawn much attention due to its profound impact on tumour development, drug resistance and patient outcome. There is an increasing interest in new therapies that target the TME. Nonetheless, most established in vitro models fail to include essential cues of the TME. Microfluidics can be used to reproduce the TME in vitro and hence provide valuable insight on tumour evolution and drug sensitivity. However, microfluidics remains far from well-established mainstream molecular and cell biology methods. Therefore, we have developed a quick and straightforward collagenase-based enzymatic method to recover cells embedded in a 3D hydrogel in a microfluidic device with no impact on cell viability. We demonstrate the validity of this method on two different cell lines in a TME microfluidic model. Cells were successfully retrieved with high viability, and we characterised the different cell death mechanisms via AMNIS image cytometry in our model.
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spelling pubmed-64701492019-04-23 Enabling cell recovery from 3D cell culture microfluidic devices for tumour microenvironment biomarker profiling Virumbrales-Muñoz, María Ayuso, Jose M. Lacueva, Alodia Randelovic, Teodora Livingston, Megan K. Beebe, David J. Oliván, Sara Pereboom, Desirée Doblare, Manuel Fernández, Luis Ochoa, Ignacio Sci Rep Article The tumour microenvironment (TME) has recently drawn much attention due to its profound impact on tumour development, drug resistance and patient outcome. There is an increasing interest in new therapies that target the TME. Nonetheless, most established in vitro models fail to include essential cues of the TME. Microfluidics can be used to reproduce the TME in vitro and hence provide valuable insight on tumour evolution and drug sensitivity. However, microfluidics remains far from well-established mainstream molecular and cell biology methods. Therefore, we have developed a quick and straightforward collagenase-based enzymatic method to recover cells embedded in a 3D hydrogel in a microfluidic device with no impact on cell viability. We demonstrate the validity of this method on two different cell lines in a TME microfluidic model. Cells were successfully retrieved with high viability, and we characterised the different cell death mechanisms via AMNIS image cytometry in our model. Nature Publishing Group UK 2019-04-17 /pmc/articles/PMC6470149/ /pubmed/30996291 http://dx.doi.org/10.1038/s41598-019-42529-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Virumbrales-Muñoz, María
Ayuso, Jose M.
Lacueva, Alodia
Randelovic, Teodora
Livingston, Megan K.
Beebe, David J.
Oliván, Sara
Pereboom, Desirée
Doblare, Manuel
Fernández, Luis
Ochoa, Ignacio
Enabling cell recovery from 3D cell culture microfluidic devices for tumour microenvironment biomarker profiling
title Enabling cell recovery from 3D cell culture microfluidic devices for tumour microenvironment biomarker profiling
title_full Enabling cell recovery from 3D cell culture microfluidic devices for tumour microenvironment biomarker profiling
title_fullStr Enabling cell recovery from 3D cell culture microfluidic devices for tumour microenvironment biomarker profiling
title_full_unstemmed Enabling cell recovery from 3D cell culture microfluidic devices for tumour microenvironment biomarker profiling
title_short Enabling cell recovery from 3D cell culture microfluidic devices for tumour microenvironment biomarker profiling
title_sort enabling cell recovery from 3d cell culture microfluidic devices for tumour microenvironment biomarker profiling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470149/
https://www.ncbi.nlm.nih.gov/pubmed/30996291
http://dx.doi.org/10.1038/s41598-019-42529-8
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