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High-throughput monitoring of major cell functions by means of lensfree video microscopy
Quantification of basic cell functions is a preliminary step to understand complex cellular mechanisms, for e.g., to test compatibility of biomaterials, to assess the effectiveness of drugs and siRNAs, and to control cell behavior. However, commonly used quantification methods are label-dependent, a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380008/ https://www.ncbi.nlm.nih.gov/pubmed/25096726 http://dx.doi.org/10.1038/srep05942 |
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author | Kesavan, S. Vinjimore Momey, F. Cioni, O. David-Watine, B. Dubrulle, N. Shorte, S. Sulpice, E. Freida, D. Chalmond, B. Dinten, J. M. Gidrol, X. Allier, C. |
author_facet | Kesavan, S. Vinjimore Momey, F. Cioni, O. David-Watine, B. Dubrulle, N. Shorte, S. Sulpice, E. Freida, D. Chalmond, B. Dinten, J. M. Gidrol, X. Allier, C. |
author_sort | Kesavan, S. Vinjimore |
collection | PubMed |
description | Quantification of basic cell functions is a preliminary step to understand complex cellular mechanisms, for e.g., to test compatibility of biomaterials, to assess the effectiveness of drugs and siRNAs, and to control cell behavior. However, commonly used quantification methods are label-dependent, and end-point assays. As an alternative, using our lensfree video microscopy platform to perform high-throughput real-time monitoring of cell culture, we introduce specifically devised metrics that are capable of non-invasive quantification of cell functions such as cell-substrate adhesion, cell spreading, cell division, cell division orientation and cell death. Unlike existing methods, our platform and associated metrics embrace entire population of thousands of cells whilst monitoring the fate of every single cell within the population. This results in a high content description of cell functions that typically contains 25,000 – 900,000 measurements per experiment depending on cell density and period of observation. As proof of concept, we monitored cell-substrate adhesion and spreading kinetics of human Mesenchymal Stem Cells (hMSCs) and primary human fibroblasts, we determined the cell division orientation of hMSCs, and we observed the effect of transfection of siCellDeath (siRNA known to induce cell death) on hMSCs and human Osteo Sarcoma (U2OS) Cells. |
format | Online Article Text |
id | pubmed-5380008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53800082017-04-10 High-throughput monitoring of major cell functions by means of lensfree video microscopy Kesavan, S. Vinjimore Momey, F. Cioni, O. David-Watine, B. Dubrulle, N. Shorte, S. Sulpice, E. Freida, D. Chalmond, B. Dinten, J. M. Gidrol, X. Allier, C. Sci Rep Article Quantification of basic cell functions is a preliminary step to understand complex cellular mechanisms, for e.g., to test compatibility of biomaterials, to assess the effectiveness of drugs and siRNAs, and to control cell behavior. However, commonly used quantification methods are label-dependent, and end-point assays. As an alternative, using our lensfree video microscopy platform to perform high-throughput real-time monitoring of cell culture, we introduce specifically devised metrics that are capable of non-invasive quantification of cell functions such as cell-substrate adhesion, cell spreading, cell division, cell division orientation and cell death. Unlike existing methods, our platform and associated metrics embrace entire population of thousands of cells whilst monitoring the fate of every single cell within the population. This results in a high content description of cell functions that typically contains 25,000 – 900,000 measurements per experiment depending on cell density and period of observation. As proof of concept, we monitored cell-substrate adhesion and spreading kinetics of human Mesenchymal Stem Cells (hMSCs) and primary human fibroblasts, we determined the cell division orientation of hMSCs, and we observed the effect of transfection of siCellDeath (siRNA known to induce cell death) on hMSCs and human Osteo Sarcoma (U2OS) Cells. Nature Publishing Group 2014-08-06 /pmc/articles/PMC5380008/ /pubmed/25096726 http://dx.doi.org/10.1038/srep05942 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Kesavan, S. Vinjimore Momey, F. Cioni, O. David-Watine, B. Dubrulle, N. Shorte, S. Sulpice, E. Freida, D. Chalmond, B. Dinten, J. M. Gidrol, X. Allier, C. High-throughput monitoring of major cell functions by means of lensfree video microscopy |
title | High-throughput monitoring of major cell functions by means of lensfree video microscopy |
title_full | High-throughput monitoring of major cell functions by means of lensfree video microscopy |
title_fullStr | High-throughput monitoring of major cell functions by means of lensfree video microscopy |
title_full_unstemmed | High-throughput monitoring of major cell functions by means of lensfree video microscopy |
title_short | High-throughput monitoring of major cell functions by means of lensfree video microscopy |
title_sort | high-throughput monitoring of major cell functions by means of lensfree video microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380008/ https://www.ncbi.nlm.nih.gov/pubmed/25096726 http://dx.doi.org/10.1038/srep05942 |
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