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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...

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Autores principales: Liu, Xili, Oh, Seungeun, Peshkin, Leonid, Kirschner, Marc W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
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.
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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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