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Morphodynamic signatures of MDA-MB-231 single cells and cell doublets undergoing invasion in confined microenvironments
Cancer cell metastasis is a major factor in cancer-related mortality. During the process of metastasis, cancer cells exhibit migratory phenotypes and invade through pores in the dense extracellular matrix. However, the characterization of morphological and subcellular features of cells in similar mi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985374/ https://www.ncbi.nlm.nih.gov/pubmed/33753788 http://dx.doi.org/10.1038/s41598-021-85640-5 |
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author | Zhang, Xingjian Chan, Trevor Mak, Michael |
author_facet | Zhang, Xingjian Chan, Trevor Mak, Michael |
author_sort | Zhang, Xingjian |
collection | PubMed |
description | Cancer cell metastasis is a major factor in cancer-related mortality. During the process of metastasis, cancer cells exhibit migratory phenotypes and invade through pores in the dense extracellular matrix. However, the characterization of morphological and subcellular features of cells in similar migratory phenotypes and the effects of geometric confinement on cell morphodynamics are not well understood. Here, we investigate the phenotypes of highly aggressive MDA-MB-231 cells in single cell and cell doublet (an initial and simplified collective state) forms in confined microenvironments. We group phenotypically similar single cells and cell doublets and characterize related morphological and subcellular features. We further detect two distinct migratory phenotypes, fluctuating and non-fluctuating, within the fast migrating single cell group. In addition, we demonstrate an increase in the number of protrusions formed at the leading edge of cells after invasion through geometric confinement. Finally, we track the short and long term effects of varied degrees of confinement on protrusion formation. Overall, our findings elucidate the underlying morphological and subcellular features associated with different single cell and cell doublet phenotypes and the impact of invasion through confined geometry on cell behavior. |
format | Online Article Text |
id | pubmed-7985374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79853742021-03-25 Morphodynamic signatures of MDA-MB-231 single cells and cell doublets undergoing invasion in confined microenvironments Zhang, Xingjian Chan, Trevor Mak, Michael Sci Rep Article Cancer cell metastasis is a major factor in cancer-related mortality. During the process of metastasis, cancer cells exhibit migratory phenotypes and invade through pores in the dense extracellular matrix. However, the characterization of morphological and subcellular features of cells in similar migratory phenotypes and the effects of geometric confinement on cell morphodynamics are not well understood. Here, we investigate the phenotypes of highly aggressive MDA-MB-231 cells in single cell and cell doublet (an initial and simplified collective state) forms in confined microenvironments. We group phenotypically similar single cells and cell doublets and characterize related morphological and subcellular features. We further detect two distinct migratory phenotypes, fluctuating and non-fluctuating, within the fast migrating single cell group. In addition, we demonstrate an increase in the number of protrusions formed at the leading edge of cells after invasion through geometric confinement. Finally, we track the short and long term effects of varied degrees of confinement on protrusion formation. Overall, our findings elucidate the underlying morphological and subcellular features associated with different single cell and cell doublet phenotypes and the impact of invasion through confined geometry on cell behavior. Nature Publishing Group UK 2021-03-22 /pmc/articles/PMC7985374/ /pubmed/33753788 http://dx.doi.org/10.1038/s41598-021-85640-5 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Xingjian Chan, Trevor Mak, Michael Morphodynamic signatures of MDA-MB-231 single cells and cell doublets undergoing invasion in confined microenvironments |
title | Morphodynamic signatures of MDA-MB-231 single cells and cell doublets undergoing invasion in confined microenvironments |
title_full | Morphodynamic signatures of MDA-MB-231 single cells and cell doublets undergoing invasion in confined microenvironments |
title_fullStr | Morphodynamic signatures of MDA-MB-231 single cells and cell doublets undergoing invasion in confined microenvironments |
title_full_unstemmed | Morphodynamic signatures of MDA-MB-231 single cells and cell doublets undergoing invasion in confined microenvironments |
title_short | Morphodynamic signatures of MDA-MB-231 single cells and cell doublets undergoing invasion in confined microenvironments |
title_sort | morphodynamic signatures of mda-mb-231 single cells and cell doublets undergoing invasion in confined microenvironments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985374/ https://www.ncbi.nlm.nih.gov/pubmed/33753788 http://dx.doi.org/10.1038/s41598-021-85640-5 |
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