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Three-Dimensional Reflectance Traction Microscopy

Cells in three-dimensional (3D) environments exhibit very different biochemical and biophysical phenotypes compared to the behavior of cells in two-dimensional (2D) environments. As an important biomechanical measurement, 2D traction force microscopy can not be directly extended into 3D cases. In or...

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Detalles Bibliográficos
Autores principales: Kim, Jihan, Jones, Christopher A. R., Groves, Nicholas Scott, Sun, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909212/
https://www.ncbi.nlm.nih.gov/pubmed/27304456
http://dx.doi.org/10.1371/journal.pone.0156797
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author Kim, Jihan
Jones, Christopher A. R.
Groves, Nicholas Scott
Sun, Bo
author_facet Kim, Jihan
Jones, Christopher A. R.
Groves, Nicholas Scott
Sun, Bo
author_sort Kim, Jihan
collection PubMed
description Cells in three-dimensional (3D) environments exhibit very different biochemical and biophysical phenotypes compared to the behavior of cells in two-dimensional (2D) environments. As an important biomechanical measurement, 2D traction force microscopy can not be directly extended into 3D cases. In order to quantitatively characterize the contraction field, we have developed 3D reflectance traction microscopy which combines confocal reflection imaging and partial volume correlation postprocessing. We have measured the deformation field of collagen gel under controlled mechanical stress. We have also characterized the deformation field generated by invasive breast cancer cells of different morphologies in 3D collagen matrix. In contrast to employ dispersed tracing particles or fluorescently-tagged matrix proteins, our methods provide a label-free, computationally effective strategy to study the cell mechanics in native 3D extracellular matrix.
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spelling pubmed-49092122016-07-06 Three-Dimensional Reflectance Traction Microscopy Kim, Jihan Jones, Christopher A. R. Groves, Nicholas Scott Sun, Bo PLoS One Research Article Cells in three-dimensional (3D) environments exhibit very different biochemical and biophysical phenotypes compared to the behavior of cells in two-dimensional (2D) environments. As an important biomechanical measurement, 2D traction force microscopy can not be directly extended into 3D cases. In order to quantitatively characterize the contraction field, we have developed 3D reflectance traction microscopy which combines confocal reflection imaging and partial volume correlation postprocessing. We have measured the deformation field of collagen gel under controlled mechanical stress. We have also characterized the deformation field generated by invasive breast cancer cells of different morphologies in 3D collagen matrix. In contrast to employ dispersed tracing particles or fluorescently-tagged matrix proteins, our methods provide a label-free, computationally effective strategy to study the cell mechanics in native 3D extracellular matrix. Public Library of Science 2016-06-15 /pmc/articles/PMC4909212/ /pubmed/27304456 http://dx.doi.org/10.1371/journal.pone.0156797 Text en © 2016 Kim et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kim, Jihan
Jones, Christopher A. R.
Groves, Nicholas Scott
Sun, Bo
Three-Dimensional Reflectance Traction Microscopy
title Three-Dimensional Reflectance Traction Microscopy
title_full Three-Dimensional Reflectance Traction Microscopy
title_fullStr Three-Dimensional Reflectance Traction Microscopy
title_full_unstemmed Three-Dimensional Reflectance Traction Microscopy
title_short Three-Dimensional Reflectance Traction Microscopy
title_sort three-dimensional reflectance traction microscopy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909212/
https://www.ncbi.nlm.nih.gov/pubmed/27304456
http://dx.doi.org/10.1371/journal.pone.0156797
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