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Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement
Little is known about how mitotic cells round against epithelial confinement. Here, we engineer micropillar arrays that subject cells to lateral mechanical confinement similar to that experienced in epithelia. If generating sufficient force to deform the pillars, rounding epithelial (MDCK) cells can...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696517/ https://www.ncbi.nlm.nih.gov/pubmed/26602832 http://dx.doi.org/10.1038/ncomms9872 |
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author | Sorce, Barbara Escobedo, Carlos Toyoda, Yusuke Stewart, Martin P. Cattin, Cedric J. Newton, Richard Banerjee, Indranil Stettler, Alexander Roska, Botond Eaton, Suzanne Hyman, Anthony A. Hierlemann, Andreas Müller, Daniel J. |
author_facet | Sorce, Barbara Escobedo, Carlos Toyoda, Yusuke Stewart, Martin P. Cattin, Cedric J. Newton, Richard Banerjee, Indranil Stettler, Alexander Roska, Botond Eaton, Suzanne Hyman, Anthony A. Hierlemann, Andreas Müller, Daniel J. |
author_sort | Sorce, Barbara |
collection | PubMed |
description | Little is known about how mitotic cells round against epithelial confinement. Here, we engineer micropillar arrays that subject cells to lateral mechanical confinement similar to that experienced in epithelia. If generating sufficient force to deform the pillars, rounding epithelial (MDCK) cells can create space to divide. However, if mitotic cells cannot create sufficient space, their rounding force, which is generated by actomyosin contraction and hydrostatic pressure, pushes the cell out of confinement. After conducting mitosis in an unperturbed manner, both daughter cells return to the confinement of the pillars. Cells that cannot round against nor escape confinement cannot orient their mitotic spindles and more likely undergo apoptosis. The results highlight how spatially constrained epithelial cells prepare for mitosis: either they are strong enough to round up or they must escape. The ability to escape from confinement and reintegrate after mitosis appears to be a basic property of epithelial cells. |
format | Online Article Text |
id | pubmed-4696517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46965172016-01-12 Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement Sorce, Barbara Escobedo, Carlos Toyoda, Yusuke Stewart, Martin P. Cattin, Cedric J. Newton, Richard Banerjee, Indranil Stettler, Alexander Roska, Botond Eaton, Suzanne Hyman, Anthony A. Hierlemann, Andreas Müller, Daniel J. Nat Commun Article Little is known about how mitotic cells round against epithelial confinement. Here, we engineer micropillar arrays that subject cells to lateral mechanical confinement similar to that experienced in epithelia. If generating sufficient force to deform the pillars, rounding epithelial (MDCK) cells can create space to divide. However, if mitotic cells cannot create sufficient space, their rounding force, which is generated by actomyosin contraction and hydrostatic pressure, pushes the cell out of confinement. After conducting mitosis in an unperturbed manner, both daughter cells return to the confinement of the pillars. Cells that cannot round against nor escape confinement cannot orient their mitotic spindles and more likely undergo apoptosis. The results highlight how spatially constrained epithelial cells prepare for mitosis: either they are strong enough to round up or they must escape. The ability to escape from confinement and reintegrate after mitosis appears to be a basic property of epithelial cells. Nature Publishing Group 2015-11-25 /pmc/articles/PMC4696517/ /pubmed/26602832 http://dx.doi.org/10.1038/ncomms9872 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Sorce, Barbara Escobedo, Carlos Toyoda, Yusuke Stewart, Martin P. Cattin, Cedric J. Newton, Richard Banerjee, Indranil Stettler, Alexander Roska, Botond Eaton, Suzanne Hyman, Anthony A. Hierlemann, Andreas Müller, Daniel J. Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement |
title | Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement |
title_full | Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement |
title_fullStr | Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement |
title_full_unstemmed | Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement |
title_short | Mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement |
title_sort | mitotic cells contract actomyosin cortex and generate pressure to round against or escape epithelial confinement |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696517/ https://www.ncbi.nlm.nih.gov/pubmed/26602832 http://dx.doi.org/10.1038/ncomms9872 |
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