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Light-sheet photonic force optical coherence elastography for high-throughput quantitative 3D micromechanical imaging
Quantitative characterisation of micro-scale mechanical properties of the extracellular matrix (ECM) and dynamic cell-ECM interactions can significantly enhance fundamental discoveries and their translational potential in the rapidly growing field of mechanobiology. However, quantitative 3D imaging...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203576/ https://www.ncbi.nlm.nih.gov/pubmed/35710790 http://dx.doi.org/10.1038/s41467-022-30995-0 |
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author | Lin, Yuechuan Leartprapun, Nichaluk Luo, Justin C. Adie, Steven G. |
author_facet | Lin, Yuechuan Leartprapun, Nichaluk Luo, Justin C. Adie, Steven G. |
author_sort | Lin, Yuechuan |
collection | PubMed |
description | Quantitative characterisation of micro-scale mechanical properties of the extracellular matrix (ECM) and dynamic cell-ECM interactions can significantly enhance fundamental discoveries and their translational potential in the rapidly growing field of mechanobiology. However, quantitative 3D imaging of ECM mechanics with cellular-scale resolution and dynamic monitoring of cell-mediated changes to pericellular viscoelasticity remain a challenge for existing mechanical characterisation methods. Here, we present light-sheet photonic force optical coherence elastography (LS-pfOCE) to address this need by leveraging a light-sheet for parallelised, non-invasive, and localised mechanical loading. We demonstrate the capabilities of LS-pfOCE by imaging the micromechanical heterogeneity of fibrous collagen matrices and perform live-cell imaging of cell-mediated ECM micromechanical dynamics. By providing access to 4D spatiotemporal variations in the micromechanical properties of 3D biopolymer constructs and engineered cellular systems, LS-pfOCE has the potential to drive new discoveries in mechanobiology and contribute to the development of novel biomechanics-based clinical diagnostics and therapies. |
format | Online Article Text |
id | pubmed-9203576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92035762022-06-18 Light-sheet photonic force optical coherence elastography for high-throughput quantitative 3D micromechanical imaging Lin, Yuechuan Leartprapun, Nichaluk Luo, Justin C. Adie, Steven G. Nat Commun Article Quantitative characterisation of micro-scale mechanical properties of the extracellular matrix (ECM) and dynamic cell-ECM interactions can significantly enhance fundamental discoveries and their translational potential in the rapidly growing field of mechanobiology. However, quantitative 3D imaging of ECM mechanics with cellular-scale resolution and dynamic monitoring of cell-mediated changes to pericellular viscoelasticity remain a challenge for existing mechanical characterisation methods. Here, we present light-sheet photonic force optical coherence elastography (LS-pfOCE) to address this need by leveraging a light-sheet for parallelised, non-invasive, and localised mechanical loading. We demonstrate the capabilities of LS-pfOCE by imaging the micromechanical heterogeneity of fibrous collagen matrices and perform live-cell imaging of cell-mediated ECM micromechanical dynamics. By providing access to 4D spatiotemporal variations in the micromechanical properties of 3D biopolymer constructs and engineered cellular systems, LS-pfOCE has the potential to drive new discoveries in mechanobiology and contribute to the development of novel biomechanics-based clinical diagnostics and therapies. Nature Publishing Group UK 2022-06-16 /pmc/articles/PMC9203576/ /pubmed/35710790 http://dx.doi.org/10.1038/s41467-022-30995-0 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lin, Yuechuan Leartprapun, Nichaluk Luo, Justin C. Adie, Steven G. Light-sheet photonic force optical coherence elastography for high-throughput quantitative 3D micromechanical imaging |
title | Light-sheet photonic force optical coherence elastography for high-throughput quantitative 3D micromechanical imaging |
title_full | Light-sheet photonic force optical coherence elastography for high-throughput quantitative 3D micromechanical imaging |
title_fullStr | Light-sheet photonic force optical coherence elastography for high-throughput quantitative 3D micromechanical imaging |
title_full_unstemmed | Light-sheet photonic force optical coherence elastography for high-throughput quantitative 3D micromechanical imaging |
title_short | Light-sheet photonic force optical coherence elastography for high-throughput quantitative 3D micromechanical imaging |
title_sort | light-sheet photonic force optical coherence elastography for high-throughput quantitative 3d micromechanical imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203576/ https://www.ncbi.nlm.nih.gov/pubmed/35710790 http://dx.doi.org/10.1038/s41467-022-30995-0 |
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