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Cellular homeostatic tension and force transmission measured in human engineered tendon

Tendons transmit contractile muscular force to bone to produce movement, and it is believed cells can generate endogenous forces on the extracellular matrix to maintain tissue homeostasis. However, little is known about the direct mechanical measurement of cell-matrix interaction in cell-generated h...

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Autores principales: Giannopoulos, Antonis, Svensson, Rene B., Heinemeier, Katja M., Schjerling, Peter, Kadler, Karl E., Holmes, David F., Kjaer, Michael, Peter Magnusson, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135935/
https://www.ncbi.nlm.nih.gov/pubmed/30100218
http://dx.doi.org/10.1016/j.jbiomech.2018.07.032
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author Giannopoulos, Antonis
Svensson, Rene B.
Heinemeier, Katja M.
Schjerling, Peter
Kadler, Karl E.
Holmes, David F.
Kjaer, Michael
Peter Magnusson, S.
author_facet Giannopoulos, Antonis
Svensson, Rene B.
Heinemeier, Katja M.
Schjerling, Peter
Kadler, Karl E.
Holmes, David F.
Kjaer, Michael
Peter Magnusson, S.
author_sort Giannopoulos, Antonis
collection PubMed
description Tendons transmit contractile muscular force to bone to produce movement, and it is believed cells can generate endogenous forces on the extracellular matrix to maintain tissue homeostasis. However, little is known about the direct mechanical measurement of cell-matrix interaction in cell-generated human tendon constructs. In this study we examined if cell-generated force could be detected and quantified in engineered human tendon constructs, and if glycosaminoglycans (GAGs) contribute to tendon force transmission. Following de-tensioning of the tendon constructs it was possible to quantify an endogenous re-tensioning. Further, it was demonstrated that the endogenous re-tensioning response was markedly blunted after interference with the cytoskeleton (inhibiting non-muscle myosin-dependent cell contraction by blebbistatin), which confirmed that re-tensioning was cell generated. When the constructs were elongated and held at a constant length a stress relaxation response was quantified, and removing 27% of the GAG content of tendon did not alter the relaxation behavior, which indicates that GAGs do not play a meaningful role in force transmission within this system.
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spelling pubmed-61359352018-09-19 Cellular homeostatic tension and force transmission measured in human engineered tendon Giannopoulos, Antonis Svensson, Rene B. Heinemeier, Katja M. Schjerling, Peter Kadler, Karl E. Holmes, David F. Kjaer, Michael Peter Magnusson, S. J Biomech Article Tendons transmit contractile muscular force to bone to produce movement, and it is believed cells can generate endogenous forces on the extracellular matrix to maintain tissue homeostasis. However, little is known about the direct mechanical measurement of cell-matrix interaction in cell-generated human tendon constructs. In this study we examined if cell-generated force could be detected and quantified in engineered human tendon constructs, and if glycosaminoglycans (GAGs) contribute to tendon force transmission. Following de-tensioning of the tendon constructs it was possible to quantify an endogenous re-tensioning. Further, it was demonstrated that the endogenous re-tensioning response was markedly blunted after interference with the cytoskeleton (inhibiting non-muscle myosin-dependent cell contraction by blebbistatin), which confirmed that re-tensioning was cell generated. When the constructs were elongated and held at a constant length a stress relaxation response was quantified, and removing 27% of the GAG content of tendon did not alter the relaxation behavior, which indicates that GAGs do not play a meaningful role in force transmission within this system. Elsevier Science 2018-09-10 /pmc/articles/PMC6135935/ /pubmed/30100218 http://dx.doi.org/10.1016/j.jbiomech.2018.07.032 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Giannopoulos, Antonis
Svensson, Rene B.
Heinemeier, Katja M.
Schjerling, Peter
Kadler, Karl E.
Holmes, David F.
Kjaer, Michael
Peter Magnusson, S.
Cellular homeostatic tension and force transmission measured in human engineered tendon
title Cellular homeostatic tension and force transmission measured in human engineered tendon
title_full Cellular homeostatic tension and force transmission measured in human engineered tendon
title_fullStr Cellular homeostatic tension and force transmission measured in human engineered tendon
title_full_unstemmed Cellular homeostatic tension and force transmission measured in human engineered tendon
title_short Cellular homeostatic tension and force transmission measured in human engineered tendon
title_sort cellular homeostatic tension and force transmission measured in human engineered tendon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135935/
https://www.ncbi.nlm.nih.gov/pubmed/30100218
http://dx.doi.org/10.1016/j.jbiomech.2018.07.032
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