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Spatiotemporal variation of endogenous cell-generated stresses within 3D multicellular spheroids

Multicellular spheroids serve as an excellent platform to study tissue behavior and tumor growth in a controlled, three-dimensional (3D) environment. While molecular and cellular studies have long used this platform to study cell behavior in 3D, only recently have studies using multicellular spheroi...

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Autores principales: Lucio, Adam A., Mongera, Alessandro, Shelton, Elijah, Chen, Renwei, Doyle, Adele M., Campàs, Otger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607343/
https://www.ncbi.nlm.nih.gov/pubmed/28931891
http://dx.doi.org/10.1038/s41598-017-12363-x
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author Lucio, Adam A.
Mongera, Alessandro
Shelton, Elijah
Chen, Renwei
Doyle, Adele M.
Campàs, Otger
author_facet Lucio, Adam A.
Mongera, Alessandro
Shelton, Elijah
Chen, Renwei
Doyle, Adele M.
Campàs, Otger
author_sort Lucio, Adam A.
collection PubMed
description Multicellular spheroids serve as an excellent platform to study tissue behavior and tumor growth in a controlled, three-dimensional (3D) environment. While molecular and cellular studies have long used this platform to study cell behavior in 3D, only recently have studies using multicellular spheroids shown an important role for the mechanics of the microenvironment in a wide range of cellular processes, including during tumor progression. Despite the well-established relevance of mechanical cues to cell behavior and the numerous studies on mechanics using 2D cell culture systems, the spatial and temporal variations in endogenous cellular forces within growing multicellular aggregates remain unknown. Using cell-sized oil droplets with controlled physicochemical properties as force transducers in mesenchymal cell aggregates, we show that the magnitude of cell-generated stresses varies only weakly with spatial location within the spherical aggregate, but it increases considerably over time during aggregate compaction and growth. Moreover, our results indicate that the temporal increase in cellular stresses is due to increasing cell pulling forces transmitted via integrin-mediated cell adhesion, consistent with the need for larger intercellular pulling forces to compact cell aggregates.
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spelling pubmed-56073432017-10-04 Spatiotemporal variation of endogenous cell-generated stresses within 3D multicellular spheroids Lucio, Adam A. Mongera, Alessandro Shelton, Elijah Chen, Renwei Doyle, Adele M. Campàs, Otger Sci Rep Article Multicellular spheroids serve as an excellent platform to study tissue behavior and tumor growth in a controlled, three-dimensional (3D) environment. While molecular and cellular studies have long used this platform to study cell behavior in 3D, only recently have studies using multicellular spheroids shown an important role for the mechanics of the microenvironment in a wide range of cellular processes, including during tumor progression. Despite the well-established relevance of mechanical cues to cell behavior and the numerous studies on mechanics using 2D cell culture systems, the spatial and temporal variations in endogenous cellular forces within growing multicellular aggregates remain unknown. Using cell-sized oil droplets with controlled physicochemical properties as force transducers in mesenchymal cell aggregates, we show that the magnitude of cell-generated stresses varies only weakly with spatial location within the spherical aggregate, but it increases considerably over time during aggregate compaction and growth. Moreover, our results indicate that the temporal increase in cellular stresses is due to increasing cell pulling forces transmitted via integrin-mediated cell adhesion, consistent with the need for larger intercellular pulling forces to compact cell aggregates. Nature Publishing Group UK 2017-09-20 /pmc/articles/PMC5607343/ /pubmed/28931891 http://dx.doi.org/10.1038/s41598-017-12363-x Text en © The Author(s) 2017 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
Lucio, Adam A.
Mongera, Alessandro
Shelton, Elijah
Chen, Renwei
Doyle, Adele M.
Campàs, Otger
Spatiotemporal variation of endogenous cell-generated stresses within 3D multicellular spheroids
title Spatiotemporal variation of endogenous cell-generated stresses within 3D multicellular spheroids
title_full Spatiotemporal variation of endogenous cell-generated stresses within 3D multicellular spheroids
title_fullStr Spatiotemporal variation of endogenous cell-generated stresses within 3D multicellular spheroids
title_full_unstemmed Spatiotemporal variation of endogenous cell-generated stresses within 3D multicellular spheroids
title_short Spatiotemporal variation of endogenous cell-generated stresses within 3D multicellular spheroids
title_sort spatiotemporal variation of endogenous cell-generated stresses within 3d multicellular spheroids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607343/
https://www.ncbi.nlm.nih.gov/pubmed/28931891
http://dx.doi.org/10.1038/s41598-017-12363-x
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