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Multiparameter mechanical and morphometric screening of cells
We introduce a label-free method to rapidly phenotype and classify cells purely based on physical properties. We extract 15 biophysical parameters from cells as they deform in a microfluidic stretching flow field via high-speed microscopy and apply machine-learning approaches to discriminate differe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133672/ https://www.ncbi.nlm.nih.gov/pubmed/27910869 http://dx.doi.org/10.1038/srep37863 |
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author | Masaeli, Mahdokht Gupta, Dewal O’Byrne, Sean Tse, Henry T. K. Gossett, Daniel R. Tseng, Peter Utada, Andrew S. Jung, Hea-Jin Young, Stephen Clark, Amander T. Di Carlo, Dino |
author_facet | Masaeli, Mahdokht Gupta, Dewal O’Byrne, Sean Tse, Henry T. K. Gossett, Daniel R. Tseng, Peter Utada, Andrew S. Jung, Hea-Jin Young, Stephen Clark, Amander T. Di Carlo, Dino |
author_sort | Masaeli, Mahdokht |
collection | PubMed |
description | We introduce a label-free method to rapidly phenotype and classify cells purely based on physical properties. We extract 15 biophysical parameters from cells as they deform in a microfluidic stretching flow field via high-speed microscopy and apply machine-learning approaches to discriminate different cell types and states. When employing the full 15 dimensional dataset, the technique robustly classifies individual cells based on their pluripotency, with accuracy above 95%. Rheological and morphological properties of cells while deforming were critical for this classification. We also show the application of this method in accurate classifying cells based on their viability, drug screening and detecting populations of malignant cells in mixed samples. We show that some of the extracted parameters are not linearly independent, and in fact we reach maximum classification accuracy by using only a subset of parameters. However, the informative subsets could vary depending on cell types in the sample. This work shows the utility of an assay purely based on intrinsic biophysical properties of cells to identify changes in cell state. In addition to a label-free alternative to flow cytometry in certain applications, this work, also can provide novel intracellular metrics that would not be feasible with labeled approaches (i.e. flow cytometry). |
format | Online Article Text |
id | pubmed-5133672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51336722017-01-27 Multiparameter mechanical and morphometric screening of cells Masaeli, Mahdokht Gupta, Dewal O’Byrne, Sean Tse, Henry T. K. Gossett, Daniel R. Tseng, Peter Utada, Andrew S. Jung, Hea-Jin Young, Stephen Clark, Amander T. Di Carlo, Dino Sci Rep Article We introduce a label-free method to rapidly phenotype and classify cells purely based on physical properties. We extract 15 biophysical parameters from cells as they deform in a microfluidic stretching flow field via high-speed microscopy and apply machine-learning approaches to discriminate different cell types and states. When employing the full 15 dimensional dataset, the technique robustly classifies individual cells based on their pluripotency, with accuracy above 95%. Rheological and morphological properties of cells while deforming were critical for this classification. We also show the application of this method in accurate classifying cells based on their viability, drug screening and detecting populations of malignant cells in mixed samples. We show that some of the extracted parameters are not linearly independent, and in fact we reach maximum classification accuracy by using only a subset of parameters. However, the informative subsets could vary depending on cell types in the sample. This work shows the utility of an assay purely based on intrinsic biophysical properties of cells to identify changes in cell state. In addition to a label-free alternative to flow cytometry in certain applications, this work, also can provide novel intracellular metrics that would not be feasible with labeled approaches (i.e. flow cytometry). Nature Publishing Group 2016-12-02 /pmc/articles/PMC5133672/ /pubmed/27910869 http://dx.doi.org/10.1038/srep37863 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Masaeli, Mahdokht Gupta, Dewal O’Byrne, Sean Tse, Henry T. K. Gossett, Daniel R. Tseng, Peter Utada, Andrew S. Jung, Hea-Jin Young, Stephen Clark, Amander T. Di Carlo, Dino Multiparameter mechanical and morphometric screening of cells |
title | Multiparameter mechanical and morphometric screening of cells |
title_full | Multiparameter mechanical and morphometric screening of cells |
title_fullStr | Multiparameter mechanical and morphometric screening of cells |
title_full_unstemmed | Multiparameter mechanical and morphometric screening of cells |
title_short | Multiparameter mechanical and morphometric screening of cells |
title_sort | multiparameter mechanical and morphometric screening of cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133672/ https://www.ncbi.nlm.nih.gov/pubmed/27910869 http://dx.doi.org/10.1038/srep37863 |
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