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Fibronectin-based nanomechanical biosensors to map 3D surface strains in live cells and tissue

Mechanical forces are integral to cellular migration, differentiation and tissue morphogenesis; however, it has proved challenging to directly measure strain at high spatial resolution with minimal perturbation in living sytems. Here, we fabricate, calibrate, and test a fibronectin (FN)-based nanome...

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Autores principales: Shiwarski, Daniel J., Tashman, Joshua W., Tsamis, Alkiviadis, Bliley, Jaci M., Blundon, Malachi A., Aranda-Michel, Edgar, Jallerat, Quentin, Szymanski, John M., McCartney, Brooke M., Feinberg, Adam W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675982/
https://www.ncbi.nlm.nih.gov/pubmed/33208732
http://dx.doi.org/10.1038/s41467-020-19659-z
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author Shiwarski, Daniel J.
Tashman, Joshua W.
Tsamis, Alkiviadis
Bliley, Jaci M.
Blundon, Malachi A.
Aranda-Michel, Edgar
Jallerat, Quentin
Szymanski, John M.
McCartney, Brooke M.
Feinberg, Adam W.
author_facet Shiwarski, Daniel J.
Tashman, Joshua W.
Tsamis, Alkiviadis
Bliley, Jaci M.
Blundon, Malachi A.
Aranda-Michel, Edgar
Jallerat, Quentin
Szymanski, John M.
McCartney, Brooke M.
Feinberg, Adam W.
author_sort Shiwarski, Daniel J.
collection PubMed
description Mechanical forces are integral to cellular migration, differentiation and tissue morphogenesis; however, it has proved challenging to directly measure strain at high spatial resolution with minimal perturbation in living sytems. Here, we fabricate, calibrate, and test a fibronectin (FN)-based nanomechanical biosensor (NMBS) that can be applied to the surface of cells and tissues to measure the magnitude, direction, and strain dynamics from subcellular to tissue length-scales. The NMBS is a fluorescently-labeled, ultra-thin FN lattice-mesh with spatial resolution tailored by adjusting the width and spacing of the lattice from 2–100 µm. Time-lapse 3D confocal imaging of the NMBS demonstrates 2D and 3D surface strain tracking during mechanical deformation of known materials and is validated with finite element modeling. Analysis of the NMBS applied to single cells, cell monolayers, and Drosophila ovarioles highlights the NMBS’s ability to dynamically track microscopic tensile and compressive strains across diverse biological systems where forces guide structure and function.
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spelling pubmed-76759822020-11-24 Fibronectin-based nanomechanical biosensors to map 3D surface strains in live cells and tissue Shiwarski, Daniel J. Tashman, Joshua W. Tsamis, Alkiviadis Bliley, Jaci M. Blundon, Malachi A. Aranda-Michel, Edgar Jallerat, Quentin Szymanski, John M. McCartney, Brooke M. Feinberg, Adam W. Nat Commun Article Mechanical forces are integral to cellular migration, differentiation and tissue morphogenesis; however, it has proved challenging to directly measure strain at high spatial resolution with minimal perturbation in living sytems. Here, we fabricate, calibrate, and test a fibronectin (FN)-based nanomechanical biosensor (NMBS) that can be applied to the surface of cells and tissues to measure the magnitude, direction, and strain dynamics from subcellular to tissue length-scales. The NMBS is a fluorescently-labeled, ultra-thin FN lattice-mesh with spatial resolution tailored by adjusting the width and spacing of the lattice from 2–100 µm. Time-lapse 3D confocal imaging of the NMBS demonstrates 2D and 3D surface strain tracking during mechanical deformation of known materials and is validated with finite element modeling. Analysis of the NMBS applied to single cells, cell monolayers, and Drosophila ovarioles highlights the NMBS’s ability to dynamically track microscopic tensile and compressive strains across diverse biological systems where forces guide structure and function. Nature Publishing Group UK 2020-11-18 /pmc/articles/PMC7675982/ /pubmed/33208732 http://dx.doi.org/10.1038/s41467-020-19659-z 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
Shiwarski, Daniel J.
Tashman, Joshua W.
Tsamis, Alkiviadis
Bliley, Jaci M.
Blundon, Malachi A.
Aranda-Michel, Edgar
Jallerat, Quentin
Szymanski, John M.
McCartney, Brooke M.
Feinberg, Adam W.
Fibronectin-based nanomechanical biosensors to map 3D surface strains in live cells and tissue
title Fibronectin-based nanomechanical biosensors to map 3D surface strains in live cells and tissue
title_full Fibronectin-based nanomechanical biosensors to map 3D surface strains in live cells and tissue
title_fullStr Fibronectin-based nanomechanical biosensors to map 3D surface strains in live cells and tissue
title_full_unstemmed Fibronectin-based nanomechanical biosensors to map 3D surface strains in live cells and tissue
title_short Fibronectin-based nanomechanical biosensors to map 3D surface strains in live cells and tissue
title_sort fibronectin-based nanomechanical biosensors to map 3d surface strains in live cells and tissue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675982/
https://www.ncbi.nlm.nih.gov/pubmed/33208732
http://dx.doi.org/10.1038/s41467-020-19659-z
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