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Mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through TGFbeta signaling
Mechanical forces between cells and extracellular matrix (ECM) influence cell shape and function. Tendons are ECM-rich tissues connecting muscles with bones that bear extreme tensional force. Analysis of transgenic zebrafish expressing mCherry driven by the tendon determinant scleraxis reveals that...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345564/ https://www.ncbi.nlm.nih.gov/pubmed/30475205 http://dx.doi.org/10.7554/eLife.38069 |
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author | Subramanian, Arul Kanzaki, Lauren Fallon Galloway, Jenna Lauren Schilling, Thomas Friedrich |
author_facet | Subramanian, Arul Kanzaki, Lauren Fallon Galloway, Jenna Lauren Schilling, Thomas Friedrich |
author_sort | Subramanian, Arul |
collection | PubMed |
description | Mechanical forces between cells and extracellular matrix (ECM) influence cell shape and function. Tendons are ECM-rich tissues connecting muscles with bones that bear extreme tensional force. Analysis of transgenic zebrafish expressing mCherry driven by the tendon determinant scleraxis reveals that tendon fibroblasts (tenocytes) extend arrays of microtubule-rich projections at the onset of muscle contraction. In the trunk, these form a dense curtain along the myotendinous junctions at somite boundaries, perpendicular to myofibers, suggesting a role as force sensors to control ECM production and tendon strength. Paralysis or destabilization of microtubules reduces projection length and surrounding ECM, both of which are rescued by muscle stimulation. Paralysis also reduces SMAD3 phosphorylation in tenocytes and chemical inhibition of TGFβ signaling shortens tenocyte projections. These results suggest that TGFβ, released in response to force, acts on tenocytes to alter their morphology and ECM production, revealing a feedback mechanism by which tendons adapt to tension. |
format | Online Article Text |
id | pubmed-6345564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63455642019-01-28 Mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through TGFbeta signaling Subramanian, Arul Kanzaki, Lauren Fallon Galloway, Jenna Lauren Schilling, Thomas Friedrich eLife Cell Biology Mechanical forces between cells and extracellular matrix (ECM) influence cell shape and function. Tendons are ECM-rich tissues connecting muscles with bones that bear extreme tensional force. Analysis of transgenic zebrafish expressing mCherry driven by the tendon determinant scleraxis reveals that tendon fibroblasts (tenocytes) extend arrays of microtubule-rich projections at the onset of muscle contraction. In the trunk, these form a dense curtain along the myotendinous junctions at somite boundaries, perpendicular to myofibers, suggesting a role as force sensors to control ECM production and tendon strength. Paralysis or destabilization of microtubules reduces projection length and surrounding ECM, both of which are rescued by muscle stimulation. Paralysis also reduces SMAD3 phosphorylation in tenocytes and chemical inhibition of TGFβ signaling shortens tenocyte projections. These results suggest that TGFβ, released in response to force, acts on tenocytes to alter their morphology and ECM production, revealing a feedback mechanism by which tendons adapt to tension. eLife Sciences Publications, Ltd 2018-11-26 /pmc/articles/PMC6345564/ /pubmed/30475205 http://dx.doi.org/10.7554/eLife.38069 Text en © 2018, Subramanian et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Subramanian, Arul Kanzaki, Lauren Fallon Galloway, Jenna Lauren Schilling, Thomas Friedrich Mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through TGFbeta signaling |
title | Mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through TGFbeta signaling |
title_full | Mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through TGFbeta signaling |
title_fullStr | Mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through TGFbeta signaling |
title_full_unstemmed | Mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through TGFbeta signaling |
title_short | Mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through TGFbeta signaling |
title_sort | mechanical force regulates tendon extracellular matrix organization and tenocyte morphogenesis through tgfbeta signaling |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345564/ https://www.ncbi.nlm.nih.gov/pubmed/30475205 http://dx.doi.org/10.7554/eLife.38069 |
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