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Cyclic stretching of soft substrates induces spreading and growth

In the body, soft tissues often undergo cycles of stretching and relaxation that may affect cell behaviour without changing matrix rigidity. To determine whether transient forces can substitute for a rigid matrix, we stretched soft pillar arrays. Surprisingly, 1–5% cyclic stretching over a frequency...

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Detalles Bibliográficos
Autores principales: Cui, Yidan, Hameed, Feroz M., Yang, Bo, Lee, Kyunghee, Pan, Catherine Qiurong, Park, Sungsu, Sheetz, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346610/
https://www.ncbi.nlm.nih.gov/pubmed/25704457
http://dx.doi.org/10.1038/ncomms7333
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author Cui, Yidan
Hameed, Feroz M.
Yang, Bo
Lee, Kyunghee
Pan, Catherine Qiurong
Park, Sungsu
Sheetz, Michael
author_facet Cui, Yidan
Hameed, Feroz M.
Yang, Bo
Lee, Kyunghee
Pan, Catherine Qiurong
Park, Sungsu
Sheetz, Michael
author_sort Cui, Yidan
collection PubMed
description In the body, soft tissues often undergo cycles of stretching and relaxation that may affect cell behaviour without changing matrix rigidity. To determine whether transient forces can substitute for a rigid matrix, we stretched soft pillar arrays. Surprisingly, 1–5% cyclic stretching over a frequency range of 0.01–10 Hz caused spreading and stress fibre formation (optimum 0.1 Hz) that persisted after 4 h of stretching. Similarly, stretching increased cell growth rates on soft pillars comparative to rigid substrates. Of possible factors linked to fibroblast growth, MRTF-A (myocardin-related transcription factor-A) moved to the nucleus in 2 h of cyclic stretching and reversed on cessation; but YAP (Yes-associated protein) moved much later. Knockdown of either MRTF-A or YAP blocked stretch-dependent growth. Thus, we suggest that the repeated pulling from a soft matrix can substitute for a stiff matrix in stimulating spreading, stress fibre formation and growth.
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spelling pubmed-43466102015-03-13 Cyclic stretching of soft substrates induces spreading and growth Cui, Yidan Hameed, Feroz M. Yang, Bo Lee, Kyunghee Pan, Catherine Qiurong Park, Sungsu Sheetz, Michael Nat Commun Article In the body, soft tissues often undergo cycles of stretching and relaxation that may affect cell behaviour without changing matrix rigidity. To determine whether transient forces can substitute for a rigid matrix, we stretched soft pillar arrays. Surprisingly, 1–5% cyclic stretching over a frequency range of 0.01–10 Hz caused spreading and stress fibre formation (optimum 0.1 Hz) that persisted after 4 h of stretching. Similarly, stretching increased cell growth rates on soft pillars comparative to rigid substrates. Of possible factors linked to fibroblast growth, MRTF-A (myocardin-related transcription factor-A) moved to the nucleus in 2 h of cyclic stretching and reversed on cessation; but YAP (Yes-associated protein) moved much later. Knockdown of either MRTF-A or YAP blocked stretch-dependent growth. Thus, we suggest that the repeated pulling from a soft matrix can substitute for a stiff matrix in stimulating spreading, stress fibre formation and growth. Nature Pub. Group 2015-02-23 /pmc/articles/PMC4346610/ /pubmed/25704457 http://dx.doi.org/10.1038/ncomms7333 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
Cui, Yidan
Hameed, Feroz M.
Yang, Bo
Lee, Kyunghee
Pan, Catherine Qiurong
Park, Sungsu
Sheetz, Michael
Cyclic stretching of soft substrates induces spreading and growth
title Cyclic stretching of soft substrates induces spreading and growth
title_full Cyclic stretching of soft substrates induces spreading and growth
title_fullStr Cyclic stretching of soft substrates induces spreading and growth
title_full_unstemmed Cyclic stretching of soft substrates induces spreading and growth
title_short Cyclic stretching of soft substrates induces spreading and growth
title_sort cyclic stretching of soft substrates induces spreading and growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346610/
https://www.ncbi.nlm.nih.gov/pubmed/25704457
http://dx.doi.org/10.1038/ncomms7333
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