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Computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth
The fine balance of growth and division is a fundamental property of the physiology of cells, and one of the least understood. Its study has been thwarted by difficulties in the accurate measurement of cell size and the even greater challenges of measuring growth of a single cell over time. We addre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959529/ https://www.ncbi.nlm.nih.gov/pubmed/33087574 http://dx.doi.org/10.1073/pnas.2002152117 |
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author | Liu, Xili Oh, Seungeun Peshkin, Leonid Kirschner, Marc W. |
author_facet | Liu, Xili Oh, Seungeun Peshkin, Leonid Kirschner, Marc W. |
author_sort | Liu, Xili |
collection | PubMed |
description | The fine balance of growth and division is a fundamental property of the physiology of cells, and one of the least understood. Its study has been thwarted by difficulties in the accurate measurement of cell size and the even greater challenges of measuring growth of a single cell over time. We address these limitations by demonstrating a computationally enhanced methodology for quantitative phase microscopy for adherent cells, using improved image processing algorithms and automated cell-tracking software. Accuracy has been improved more than twofold and this improvement is sufficient to establish the dynamics of cell growth and adherence to simple growth laws. It is also sufficient to reveal unknown features of cell growth, previously unmeasurable. With these methodological and analytical improvements, in several cell lines we document a remarkable oscillation in growth rate, occurring throughout the cell cycle, coupled to cell division or birth yet independent of cell cycle progression. We expect that further exploration with this advanced tool will provide a better understanding of growth rate regulation in mammalian cells. |
format | Online Article Text |
id | pubmed-7959529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-79595292021-03-23 Computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth Liu, Xili Oh, Seungeun Peshkin, Leonid Kirschner, Marc W. Proc Natl Acad Sci U S A Biological Sciences The fine balance of growth and division is a fundamental property of the physiology of cells, and one of the least understood. Its study has been thwarted by difficulties in the accurate measurement of cell size and the even greater challenges of measuring growth of a single cell over time. We address these limitations by demonstrating a computationally enhanced methodology for quantitative phase microscopy for adherent cells, using improved image processing algorithms and automated cell-tracking software. Accuracy has been improved more than twofold and this improvement is sufficient to establish the dynamics of cell growth and adherence to simple growth laws. It is also sufficient to reveal unknown features of cell growth, previously unmeasurable. With these methodological and analytical improvements, in several cell lines we document a remarkable oscillation in growth rate, occurring throughout the cell cycle, coupled to cell division or birth yet independent of cell cycle progression. We expect that further exploration with this advanced tool will provide a better understanding of growth rate regulation in mammalian cells. National Academy of Sciences 2020-11-03 2020-10-21 /pmc/articles/PMC7959529/ /pubmed/33087574 http://dx.doi.org/10.1073/pnas.2002152117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Liu, Xili Oh, Seungeun Peshkin, Leonid Kirschner, Marc W. Computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth |
title | Computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth |
title_full | Computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth |
title_fullStr | Computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth |
title_full_unstemmed | Computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth |
title_short | Computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth |
title_sort | computationally enhanced quantitative phase microscopy reveals autonomous oscillations in mammalian cell growth |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959529/ https://www.ncbi.nlm.nih.gov/pubmed/33087574 http://dx.doi.org/10.1073/pnas.2002152117 |
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