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Chromatin de-condensation by switching substrate elasticity
Mechanical properties of the cellular environment are known to influence cell fate. Chromatin de-condensation appears as an early event in cell reprogramming. Whereas the ratio of euchromatin versus heterochromatin can be increased chemically, we report herein for the first time that the ratio can a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107547/ https://www.ncbi.nlm.nih.gov/pubmed/30140058 http://dx.doi.org/10.1038/s41598-018-31023-2 |
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author | Rabineau, Morgane Flick, Florence Ehlinger, Claire Mathieu, Eric Duluc, Isabelle Jung, Matthieu Senger, Bernard Kocgozlu, Leyla Schaaf, Pierre Lavalle, Philippe Freund, Jean-Noël Haikel, Youssef Vautier, Dominique |
author_facet | Rabineau, Morgane Flick, Florence Ehlinger, Claire Mathieu, Eric Duluc, Isabelle Jung, Matthieu Senger, Bernard Kocgozlu, Leyla Schaaf, Pierre Lavalle, Philippe Freund, Jean-Noël Haikel, Youssef Vautier, Dominique |
author_sort | Rabineau, Morgane |
collection | PubMed |
description | Mechanical properties of the cellular environment are known to influence cell fate. Chromatin de-condensation appears as an early event in cell reprogramming. Whereas the ratio of euchromatin versus heterochromatin can be increased chemically, we report herein for the first time that the ratio can also be increased by purely changing the mechanical properties of the microenvironment by successive 24 h-contact of the cells on a soft substrate alternated with relocation and growth for 7 days on a hard substrate. An initial contact with soft substrate caused massive SW480 cancer cell death by necrosis, whereas approximately 7% of the cells did survived exhibiting a high level of condensed chromatin (21% heterochromatin). However, four consecutive hard/soft cycles elicited a strong chromatin de-condensation (6% heterochromatin) correlating with an increase of cellular survival (approximately 90%). Furthermore, cell survival appeared to be reversible, indicative of an adaptive process rather than an irreversible gene mutation(s). This adaptation process is associated with modifications in gene expression patterns. A completely new approach for chromatin de-condensation, based only on mechanical properties of the microenvironment, without any drug mediation is presented. |
format | Online Article Text |
id | pubmed-6107547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61075472018-08-28 Chromatin de-condensation by switching substrate elasticity Rabineau, Morgane Flick, Florence Ehlinger, Claire Mathieu, Eric Duluc, Isabelle Jung, Matthieu Senger, Bernard Kocgozlu, Leyla Schaaf, Pierre Lavalle, Philippe Freund, Jean-Noël Haikel, Youssef Vautier, Dominique Sci Rep Article Mechanical properties of the cellular environment are known to influence cell fate. Chromatin de-condensation appears as an early event in cell reprogramming. Whereas the ratio of euchromatin versus heterochromatin can be increased chemically, we report herein for the first time that the ratio can also be increased by purely changing the mechanical properties of the microenvironment by successive 24 h-contact of the cells on a soft substrate alternated with relocation and growth for 7 days on a hard substrate. An initial contact with soft substrate caused massive SW480 cancer cell death by necrosis, whereas approximately 7% of the cells did survived exhibiting a high level of condensed chromatin (21% heterochromatin). However, four consecutive hard/soft cycles elicited a strong chromatin de-condensation (6% heterochromatin) correlating with an increase of cellular survival (approximately 90%). Furthermore, cell survival appeared to be reversible, indicative of an adaptive process rather than an irreversible gene mutation(s). This adaptation process is associated with modifications in gene expression patterns. A completely new approach for chromatin de-condensation, based only on mechanical properties of the microenvironment, without any drug mediation is presented. Nature Publishing Group UK 2018-08-23 /pmc/articles/PMC6107547/ /pubmed/30140058 http://dx.doi.org/10.1038/s41598-018-31023-2 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 Rabineau, Morgane Flick, Florence Ehlinger, Claire Mathieu, Eric Duluc, Isabelle Jung, Matthieu Senger, Bernard Kocgozlu, Leyla Schaaf, Pierre Lavalle, Philippe Freund, Jean-Noël Haikel, Youssef Vautier, Dominique Chromatin de-condensation by switching substrate elasticity |
title | Chromatin de-condensation by switching substrate elasticity |
title_full | Chromatin de-condensation by switching substrate elasticity |
title_fullStr | Chromatin de-condensation by switching substrate elasticity |
title_full_unstemmed | Chromatin de-condensation by switching substrate elasticity |
title_short | Chromatin de-condensation by switching substrate elasticity |
title_sort | chromatin de-condensation by switching substrate elasticity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107547/ https://www.ncbi.nlm.nih.gov/pubmed/30140058 http://dx.doi.org/10.1038/s41598-018-31023-2 |
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