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Dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures
Understanding how forces orchestrate tissue formation requires technologies to map internal tissue stress at cellular length scales. Here, we develop ultrasoft mechanosensors that visibly deform under less than 10 Pascals of cell-generated stress. By incorporating these mechanosensors into multicell...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329783/ https://www.ncbi.nlm.nih.gov/pubmed/30635553 http://dx.doi.org/10.1038/s41467-018-07967-4 |
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author | Lee, Wontae Kalashnikov, Nikita Mok, Stephanie Halaoui, Ruba Kuzmin, Elena Putnam, Andrew J. Takayama, Shuichi Park, Morag McCaffrey, Luke Zhao, Ruogang Leask, Richard L. Moraes, Christopher |
author_facet | Lee, Wontae Kalashnikov, Nikita Mok, Stephanie Halaoui, Ruba Kuzmin, Elena Putnam, Andrew J. Takayama, Shuichi Park, Morag McCaffrey, Luke Zhao, Ruogang Leask, Richard L. Moraes, Christopher |
author_sort | Lee, Wontae |
collection | PubMed |
description | Understanding how forces orchestrate tissue formation requires technologies to map internal tissue stress at cellular length scales. Here, we develop ultrasoft mechanosensors that visibly deform under less than 10 Pascals of cell-generated stress. By incorporating these mechanosensors into multicellular spheroids, we capture the patterns of internal stress that arise during spheroid formation. We experimentally demonstrate the spontaneous generation of a tensional ‘skin’, only a few cell layers thick, at the spheroid surface, which correlates with activation of mechanobiological signalling pathways, and balances a compressive stress profile within the tissue. These stresses develop through cell-driven mechanical compaction at the tissue periphery, and suggest that the tissue formation process plays a critically important role in specifying mechanobiological function. The broad applicability of this technique should ultimately provide a quantitative basis to design tissues that leverage the mechanical activity of constituent cells to evolve towards a desired form and function. |
format | Online Article Text |
id | pubmed-6329783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63297832019-01-15 Dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures Lee, Wontae Kalashnikov, Nikita Mok, Stephanie Halaoui, Ruba Kuzmin, Elena Putnam, Andrew J. Takayama, Shuichi Park, Morag McCaffrey, Luke Zhao, Ruogang Leask, Richard L. Moraes, Christopher Nat Commun Article Understanding how forces orchestrate tissue formation requires technologies to map internal tissue stress at cellular length scales. Here, we develop ultrasoft mechanosensors that visibly deform under less than 10 Pascals of cell-generated stress. By incorporating these mechanosensors into multicellular spheroids, we capture the patterns of internal stress that arise during spheroid formation. We experimentally demonstrate the spontaneous generation of a tensional ‘skin’, only a few cell layers thick, at the spheroid surface, which correlates with activation of mechanobiological signalling pathways, and balances a compressive stress profile within the tissue. These stresses develop through cell-driven mechanical compaction at the tissue periphery, and suggest that the tissue formation process plays a critically important role in specifying mechanobiological function. The broad applicability of this technique should ultimately provide a quantitative basis to design tissues that leverage the mechanical activity of constituent cells to evolve towards a desired form and function. Nature Publishing Group UK 2019-01-11 /pmc/articles/PMC6329783/ /pubmed/30635553 http://dx.doi.org/10.1038/s41467-018-07967-4 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 Lee, Wontae Kalashnikov, Nikita Mok, Stephanie Halaoui, Ruba Kuzmin, Elena Putnam, Andrew J. Takayama, Shuichi Park, Morag McCaffrey, Luke Zhao, Ruogang Leask, Richard L. Moraes, Christopher Dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures |
title | Dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures |
title_full | Dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures |
title_fullStr | Dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures |
title_full_unstemmed | Dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures |
title_short | Dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures |
title_sort | dispersible hydrogel force sensors reveal patterns of solid mechanical stress in multicellular spheroid cultures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329783/ https://www.ncbi.nlm.nih.gov/pubmed/30635553 http://dx.doi.org/10.1038/s41467-018-07967-4 |
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