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Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion

Observation and analysis of cancer cell behaviour in 3D environment is essential for full understanding of the mechanisms of cancer cell invasion. However, label-free imaging of live cells in 3D conditions is optically more challenging than in 2D. Quantitative phase imaging provided by coherence con...

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Autores principales: Tolde, Ondřej, Gandalovičová, Aneta, Křížová, Aneta, Veselý, Pavel, Chmelík, Radim, Rosel, Daniel, Brábek, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089916/
https://www.ncbi.nlm.nih.gov/pubmed/30104699
http://dx.doi.org/10.1038/s41598-018-30408-7
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author Tolde, Ondřej
Gandalovičová, Aneta
Křížová, Aneta
Veselý, Pavel
Chmelík, Radim
Rosel, Daniel
Brábek, Jan
author_facet Tolde, Ondřej
Gandalovičová, Aneta
Křížová, Aneta
Veselý, Pavel
Chmelík, Radim
Rosel, Daniel
Brábek, Jan
author_sort Tolde, Ondřej
collection PubMed
description Observation and analysis of cancer cell behaviour in 3D environment is essential for full understanding of the mechanisms of cancer cell invasion. However, label-free imaging of live cells in 3D conditions is optically more challenging than in 2D. Quantitative phase imaging provided by coherence controlled holographic microscopy produces images with enhanced information compared to ordinary light microscopy and, due to inherent coherence gate effect, enables observation of live cancer cells’ activity even in scattering milieu such as the 3D collagen matrix. Exploiting the dynamic phase differences method, we for the first time describe dynamics of differences in cell mass distribution in 3D migrating mesenchymal and amoeboid cancer cells, and also demonstrate that certain features are shared by both invasion modes. We found that amoeboid fibrosarcoma cells’ membrane blebbing is enhanced upon constriction and is also occasionally present in mesenchymally invading cells around constricted nuclei. Further, we demonstrate that both leading protrusions and leading pseudopods of invading fibrosarcoma cells are defined by higher cell mass density. In addition, we directly document bundling of collagen fibres by protrusions of mesenchymal fibrosarcoma cells. Thus, such a non-invasive microscopy offers a novel insight into cellular events during 3D invasion.
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spelling pubmed-60899162018-08-17 Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion Tolde, Ondřej Gandalovičová, Aneta Křížová, Aneta Veselý, Pavel Chmelík, Radim Rosel, Daniel Brábek, Jan Sci Rep Article Observation and analysis of cancer cell behaviour in 3D environment is essential for full understanding of the mechanisms of cancer cell invasion. However, label-free imaging of live cells in 3D conditions is optically more challenging than in 2D. Quantitative phase imaging provided by coherence controlled holographic microscopy produces images with enhanced information compared to ordinary light microscopy and, due to inherent coherence gate effect, enables observation of live cancer cells’ activity even in scattering milieu such as the 3D collagen matrix. Exploiting the dynamic phase differences method, we for the first time describe dynamics of differences in cell mass distribution in 3D migrating mesenchymal and amoeboid cancer cells, and also demonstrate that certain features are shared by both invasion modes. We found that amoeboid fibrosarcoma cells’ membrane blebbing is enhanced upon constriction and is also occasionally present in mesenchymally invading cells around constricted nuclei. Further, we demonstrate that both leading protrusions and leading pseudopods of invading fibrosarcoma cells are defined by higher cell mass density. In addition, we directly document bundling of collagen fibres by protrusions of mesenchymal fibrosarcoma cells. Thus, such a non-invasive microscopy offers a novel insight into cellular events during 3D invasion. Nature Publishing Group UK 2018-08-13 /pmc/articles/PMC6089916/ /pubmed/30104699 http://dx.doi.org/10.1038/s41598-018-30408-7 Text en © The Author(s) 2018 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
Tolde, Ondřej
Gandalovičová, Aneta
Křížová, Aneta
Veselý, Pavel
Chmelík, Radim
Rosel, Daniel
Brábek, Jan
Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion
title Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion
title_full Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion
title_fullStr Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion
title_full_unstemmed Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion
title_short Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion
title_sort quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089916/
https://www.ncbi.nlm.nih.gov/pubmed/30104699
http://dx.doi.org/10.1038/s41598-018-30408-7
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