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Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies

The central goals of mechanobiology are to understand how cells generate force and how they respond to environmental mechanical stimuli. A full picture of these processes requires high-resolution, volumetric imaging with time-correlated force measurements. Here we present an instrument that combines...

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Autores principales: Nelsen, E., Hobson, C. M., Kern, M. E., Hsiao, J. P., O’Brien III, E. T., Watanabe, T., Condon, B. M., Boyce, M., Grinstein, S., Hahn, K. M., Falvo, M. R., Superfine, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234992/
https://www.ncbi.nlm.nih.gov/pubmed/32424215
http://dx.doi.org/10.1038/s41598-020-65205-8
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author Nelsen, E.
Hobson, C. M.
Kern, M. E.
Hsiao, J. P.
O’Brien III, E. T.
Watanabe, T.
Condon, B. M.
Boyce, M.
Grinstein, S.
Hahn, K. M.
Falvo, M. R.
Superfine, R.
author_facet Nelsen, E.
Hobson, C. M.
Kern, M. E.
Hsiao, J. P.
O’Brien III, E. T.
Watanabe, T.
Condon, B. M.
Boyce, M.
Grinstein, S.
Hahn, K. M.
Falvo, M. R.
Superfine, R.
author_sort Nelsen, E.
collection PubMed
description The central goals of mechanobiology are to understand how cells generate force and how they respond to environmental mechanical stimuli. A full picture of these processes requires high-resolution, volumetric imaging with time-correlated force measurements. Here we present an instrument that combines an open-top, single-objective light sheet fluorescence microscope with an atomic force microscope (AFM), providing simultaneous volumetric imaging with high spatiotemporal resolution and high dynamic range force capability (10 pN – 100 nN). With this system we have captured lysosome trafficking, vimentin nuclear caging, and actin dynamics on the order of one second per single-cell volume. To showcase the unique advantages of combining Line Bessel light sheet imaging with AFM, we measured the forces exerted by a macrophage during FcɣR-mediated phagocytosis while performing both sequential two-color, fixed plane and volumetric imaging of F-actin. This unique instrument allows for a myriad of novel studies investigating the coupling of cellular dynamics and mechanical forces.
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spelling pubmed-72349922020-05-26 Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies Nelsen, E. Hobson, C. M. Kern, M. E. Hsiao, J. P. O’Brien III, E. T. Watanabe, T. Condon, B. M. Boyce, M. Grinstein, S. Hahn, K. M. Falvo, M. R. Superfine, R. Sci Rep Article The central goals of mechanobiology are to understand how cells generate force and how they respond to environmental mechanical stimuli. A full picture of these processes requires high-resolution, volumetric imaging with time-correlated force measurements. Here we present an instrument that combines an open-top, single-objective light sheet fluorescence microscope with an atomic force microscope (AFM), providing simultaneous volumetric imaging with high spatiotemporal resolution and high dynamic range force capability (10 pN – 100 nN). With this system we have captured lysosome trafficking, vimentin nuclear caging, and actin dynamics on the order of one second per single-cell volume. To showcase the unique advantages of combining Line Bessel light sheet imaging with AFM, we measured the forces exerted by a macrophage during FcɣR-mediated phagocytosis while performing both sequential two-color, fixed plane and volumetric imaging of F-actin. This unique instrument allows for a myriad of novel studies investigating the coupling of cellular dynamics and mechanical forces. Nature Publishing Group UK 2020-05-18 /pmc/articles/PMC7234992/ /pubmed/32424215 http://dx.doi.org/10.1038/s41598-020-65205-8 Text en © The Author(s) 2020 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/.
spellingShingle Article
Nelsen, E.
Hobson, C. M.
Kern, M. E.
Hsiao, J. P.
O’Brien III, E. T.
Watanabe, T.
Condon, B. M.
Boyce, M.
Grinstein, S.
Hahn, K. M.
Falvo, M. R.
Superfine, R.
Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies
title Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies
title_full Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies
title_fullStr Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies
title_full_unstemmed Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies
title_short Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies
title_sort combined atomic force microscope and volumetric light sheet system for correlative force and fluorescence mechanobiology studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234992/
https://www.ncbi.nlm.nih.gov/pubmed/32424215
http://dx.doi.org/10.1038/s41598-020-65205-8
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