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Tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales
Cardiomyocytes generate force for the contraction of the heart to pump blood into the lungs and body. At the same time, they are exquisitely tuned to the mechanical environment and react to e.g. changes in cell and extracellular matrix stiffness or altered stretching due to reduced ejection fraction...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553672/ https://www.ncbi.nlm.nih.gov/pubmed/34765044 http://dx.doi.org/10.1007/s12551-021-00837-2 |
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author | Swiatlowska, Pamela Iskratsch, Thomas |
author_facet | Swiatlowska, Pamela Iskratsch, Thomas |
author_sort | Swiatlowska, Pamela |
collection | PubMed |
description | Cardiomyocytes generate force for the contraction of the heart to pump blood into the lungs and body. At the same time, they are exquisitely tuned to the mechanical environment and react to e.g. changes in cell and extracellular matrix stiffness or altered stretching due to reduced ejection fraction in heart disease, by adapting their cytoskeleton, force generation and cell mechanics. Both mechanical sensing and cell mechanical adaptations are multiscale processes. Receptor interactions with the extracellular matrix at the nanoscale will lead to clustering of receptors and modification of the cytoskeleton. This in turn alters mechanosensing, force generation, cell and nuclear stiffness and viscoelasticity at the microscale. Further, this affects cell shape, orientation, maturation and tissue integration at the microscale to macroscale. A variety of tools have been developed and adapted to measure cardiomyocyte receptor-ligand interactions and forces or mechanics at the different ranges, resulting in a wealth of new information about cardiomyocyte mechanobiology. Here, we take stock at the different tools for exploring cardiomyocyte mechanosensing and cell mechanics at the different scales from the nanoscale to microscale and macroscale. |
format | Online Article Text |
id | pubmed-8553672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-85536722021-11-10 Tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales Swiatlowska, Pamela Iskratsch, Thomas Biophys Rev Review Cardiomyocytes generate force for the contraction of the heart to pump blood into the lungs and body. At the same time, they are exquisitely tuned to the mechanical environment and react to e.g. changes in cell and extracellular matrix stiffness or altered stretching due to reduced ejection fraction in heart disease, by adapting their cytoskeleton, force generation and cell mechanics. Both mechanical sensing and cell mechanical adaptations are multiscale processes. Receptor interactions with the extracellular matrix at the nanoscale will lead to clustering of receptors and modification of the cytoskeleton. This in turn alters mechanosensing, force generation, cell and nuclear stiffness and viscoelasticity at the microscale. Further, this affects cell shape, orientation, maturation and tissue integration at the microscale to macroscale. A variety of tools have been developed and adapted to measure cardiomyocyte receptor-ligand interactions and forces or mechanics at the different ranges, resulting in a wealth of new information about cardiomyocyte mechanobiology. Here, we take stock at the different tools for exploring cardiomyocyte mechanosensing and cell mechanics at the different scales from the nanoscale to microscale and macroscale. Springer Berlin Heidelberg 2021-09-05 /pmc/articles/PMC8553672/ /pubmed/34765044 http://dx.doi.org/10.1007/s12551-021-00837-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Swiatlowska, Pamela Iskratsch, Thomas Tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales |
title | Tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales |
title_full | Tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales |
title_fullStr | Tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales |
title_full_unstemmed | Tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales |
title_short | Tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales |
title_sort | tools for studying and modulating (cardiac muscle) cell mechanics and mechanosensing across the scales |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553672/ https://www.ncbi.nlm.nih.gov/pubmed/34765044 http://dx.doi.org/10.1007/s12551-021-00837-2 |
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