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The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts
Myofibroblast contraction is fundamental in the excessive tissue remodeling that is characteristic of fibrotic tissue contractures. Tissue remodeling during development of fibrosis leads to gradually increasing stiffness of the extracellular matrix. We propose that this increased stiffness positivel...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3653915/ https://www.ncbi.nlm.nih.gov/pubmed/23691248 http://dx.doi.org/10.1371/journal.pone.0064560 |
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author | Godbout, Charles Follonier Castella, Lysianne Smith, Eric A. Talele, Nilesh Chow, Melissa L. Garonna, Adriano Hinz, Boris |
author_facet | Godbout, Charles Follonier Castella, Lysianne Smith, Eric A. Talele, Nilesh Chow, Melissa L. Garonna, Adriano Hinz, Boris |
author_sort | Godbout, Charles |
collection | PubMed |
description | Myofibroblast contraction is fundamental in the excessive tissue remodeling that is characteristic of fibrotic tissue contractures. Tissue remodeling during development of fibrosis leads to gradually increasing stiffness of the extracellular matrix. We propose that this increased stiffness positively feeds back on the contractile activities of myofibroblasts. We have previously shown that cycles of contraction directly correlate with periodic intracellular calcium oscillations in cultured myofibroblasts. We analyze cytosolic calcium dynamics using fluorescent calcium indicators to evaluate the possible impact of mechanical stress on myofibroblast contractile activity. To modulate extracellular mechanics, we seeded primary rat subcutaneous myofibroblasts on silicone substrates and into collagen gels of different elastic modulus. We modulated cell stress by cell growth on differently adhesive culture substrates, by restricting cell spreading area on micro-printed adhesive islands, and depolymerizing actin with Cytochalasin D. In general, calcium oscillation frequencies in myofibroblasts increased with increasing mechanical challenge. These results provide new insight on how changing mechanical conditions for myofibroblasts are encoded in calcium oscillations and possibly explain how reparative cells adapt their contractile behavior to the stresses occurring in normal and pathological tissue repair. |
format | Online Article Text |
id | pubmed-3653915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36539152013-05-20 The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts Godbout, Charles Follonier Castella, Lysianne Smith, Eric A. Talele, Nilesh Chow, Melissa L. Garonna, Adriano Hinz, Boris PLoS One Research Article Myofibroblast contraction is fundamental in the excessive tissue remodeling that is characteristic of fibrotic tissue contractures. Tissue remodeling during development of fibrosis leads to gradually increasing stiffness of the extracellular matrix. We propose that this increased stiffness positively feeds back on the contractile activities of myofibroblasts. We have previously shown that cycles of contraction directly correlate with periodic intracellular calcium oscillations in cultured myofibroblasts. We analyze cytosolic calcium dynamics using fluorescent calcium indicators to evaluate the possible impact of mechanical stress on myofibroblast contractile activity. To modulate extracellular mechanics, we seeded primary rat subcutaneous myofibroblasts on silicone substrates and into collagen gels of different elastic modulus. We modulated cell stress by cell growth on differently adhesive culture substrates, by restricting cell spreading area on micro-printed adhesive islands, and depolymerizing actin with Cytochalasin D. In general, calcium oscillation frequencies in myofibroblasts increased with increasing mechanical challenge. These results provide new insight on how changing mechanical conditions for myofibroblasts are encoded in calcium oscillations and possibly explain how reparative cells adapt their contractile behavior to the stresses occurring in normal and pathological tissue repair. Public Library of Science 2013-05-14 /pmc/articles/PMC3653915/ /pubmed/23691248 http://dx.doi.org/10.1371/journal.pone.0064560 Text en © 2013 Godbout et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Godbout, Charles Follonier Castella, Lysianne Smith, Eric A. Talele, Nilesh Chow, Melissa L. Garonna, Adriano Hinz, Boris The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts |
title | The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts |
title_full | The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts |
title_fullStr | The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts |
title_full_unstemmed | The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts |
title_short | The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts |
title_sort | mechanical environment modulates intracellular calcium oscillation activities of myofibroblasts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3653915/ https://www.ncbi.nlm.nih.gov/pubmed/23691248 http://dx.doi.org/10.1371/journal.pone.0064560 |
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