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Imaging methods in mechanosensing: a historical perspective and visions for the future

Over the past three decades, as mechanobiology has become a distinct area of study, researchers have developed novel imaging tools to discover the pathways of biomechanical signaling. Early work with substrate engineering and particle tracking demonstrated the importance of cell–extracellular matrix...

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Detalles Bibliográficos
Autores principales: Lavrenyuk, Kirill, Conway, Daniel, Dahl, Kris Noel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108522/
https://www.ncbi.nlm.nih.gov/pubmed/33788578
http://dx.doi.org/10.1091/mbc.E20-10-0671
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author Lavrenyuk, Kirill
Conway, Daniel
Dahl, Kris Noel
author_facet Lavrenyuk, Kirill
Conway, Daniel
Dahl, Kris Noel
author_sort Lavrenyuk, Kirill
collection PubMed
description Over the past three decades, as mechanobiology has become a distinct area of study, researchers have developed novel imaging tools to discover the pathways of biomechanical signaling. Early work with substrate engineering and particle tracking demonstrated the importance of cell–extracellular matrix interactions on the cell cycle as well as the mechanical flux of the intracellular environment. Most recently, tension sensor approaches allowed directly measuring tension in cell–cell and cell–substrate interactions. We retrospectively analyze how these various optical techniques progressed the field and suggest our vision forward for a unified theory of cell mechanics, mapping cellular mechanosensing, and novel biomedical applications for mechanobiology.
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spelling pubmed-81085222021-07-04 Imaging methods in mechanosensing: a historical perspective and visions for the future Lavrenyuk, Kirill Conway, Daniel Dahl, Kris Noel Mol Biol Cell Articles Over the past three decades, as mechanobiology has become a distinct area of study, researchers have developed novel imaging tools to discover the pathways of biomechanical signaling. Early work with substrate engineering and particle tracking demonstrated the importance of cell–extracellular matrix interactions on the cell cycle as well as the mechanical flux of the intracellular environment. Most recently, tension sensor approaches allowed directly measuring tension in cell–cell and cell–substrate interactions. We retrospectively analyze how these various optical techniques progressed the field and suggest our vision forward for a unified theory of cell mechanics, mapping cellular mechanosensing, and novel biomedical applications for mechanobiology. The American Society for Cell Biology 2021-04-19 /pmc/articles/PMC8108522/ /pubmed/33788578 http://dx.doi.org/10.1091/mbc.E20-10-0671 Text en © 2021 Lavrenyuk et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Articles
Lavrenyuk, Kirill
Conway, Daniel
Dahl, Kris Noel
Imaging methods in mechanosensing: a historical perspective and visions for the future
title Imaging methods in mechanosensing: a historical perspective and visions for the future
title_full Imaging methods in mechanosensing: a historical perspective and visions for the future
title_fullStr Imaging methods in mechanosensing: a historical perspective and visions for the future
title_full_unstemmed Imaging methods in mechanosensing: a historical perspective and visions for the future
title_short Imaging methods in mechanosensing: a historical perspective and visions for the future
title_sort imaging methods in mechanosensing: a historical perspective and visions for the future
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108522/
https://www.ncbi.nlm.nih.gov/pubmed/33788578
http://dx.doi.org/10.1091/mbc.E20-10-0671
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