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Quantitative Model for Ion Transport and Cytoplasm Conductivity of Chinese Hamster Ovary Cells

In mammalian cells cytoplasm ion concentrations and hence cytoplasm conductivity is an important indicator of their physiological state. Changes in the cytoplasm conductivity has been associated with physiological changes such as progression of cancer and apoptosis. In this work, a model that predic...

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Autores principales: Fazelkhah, Azita, Braasch, Katrin, Afshar, Samaneh, Salimi, Elham, Butler, Michael, Bridges, Greg, Thomson, Douglas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292909/
https://www.ncbi.nlm.nih.gov/pubmed/30546044
http://dx.doi.org/10.1038/s41598-018-36127-3
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author Fazelkhah, Azita
Braasch, Katrin
Afshar, Samaneh
Salimi, Elham
Butler, Michael
Bridges, Greg
Thomson, Douglas
author_facet Fazelkhah, Azita
Braasch, Katrin
Afshar, Samaneh
Salimi, Elham
Butler, Michael
Bridges, Greg
Thomson, Douglas
author_sort Fazelkhah, Azita
collection PubMed
description In mammalian cells cytoplasm ion concentrations and hence cytoplasm conductivity is an important indicator of their physiological state. Changes in the cytoplasm conductivity has been associated with physiological changes such as progression of cancer and apoptosis. In this work, a model that predicts the effects of physiological changes in ion transport on the cytoplasm conductivity of Chinese hamster ovary (CHO) cells is demonstrated. We determined CHO-specific model parameters, Na(+)/K(+) ATPase pumps and ion channels densities, using a flux assay approach. The obtained sodium (P(Na)), potassium (P(K)) and chloride (P(Cl)) permeability and Na(+)/K(+) ATPase pump density were estimated to be 5.6 × 10(−8) cm/s, 5.6 × 10(−8) cm/s, 3.2 × 10(−7) cm/s and 2.56 × 10(−11) mol/cm(2), respectively. The model was tested by comparing the model predictions with the experimentally determined temporal changes in the cytoplasm conductivity of Na(+)/K(+) ATPase pump inhibited CHO cells. Cells’ Na(+)/K(+) ATPase pumps were inhibited using 5 mM Ouabain and the temporal behavior of their cytoplasm conductivity was measured using dielectrophoresis cytometry. The measured results are in close agreement with the model-calculated values. This model will provide insight on the effects of processes such as apoptosis or external media ion concentration on the cytoplasm conductivity of mammalian cells.
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spelling pubmed-62929092018-12-21 Quantitative Model for Ion Transport and Cytoplasm Conductivity of Chinese Hamster Ovary Cells Fazelkhah, Azita Braasch, Katrin Afshar, Samaneh Salimi, Elham Butler, Michael Bridges, Greg Thomson, Douglas Sci Rep Article In mammalian cells cytoplasm ion concentrations and hence cytoplasm conductivity is an important indicator of their physiological state. Changes in the cytoplasm conductivity has been associated with physiological changes such as progression of cancer and apoptosis. In this work, a model that predicts the effects of physiological changes in ion transport on the cytoplasm conductivity of Chinese hamster ovary (CHO) cells is demonstrated. We determined CHO-specific model parameters, Na(+)/K(+) ATPase pumps and ion channels densities, using a flux assay approach. The obtained sodium (P(Na)), potassium (P(K)) and chloride (P(Cl)) permeability and Na(+)/K(+) ATPase pump density were estimated to be 5.6 × 10(−8) cm/s, 5.6 × 10(−8) cm/s, 3.2 × 10(−7) cm/s and 2.56 × 10(−11) mol/cm(2), respectively. The model was tested by comparing the model predictions with the experimentally determined temporal changes in the cytoplasm conductivity of Na(+)/K(+) ATPase pump inhibited CHO cells. Cells’ Na(+)/K(+) ATPase pumps were inhibited using 5 mM Ouabain and the temporal behavior of their cytoplasm conductivity was measured using dielectrophoresis cytometry. The measured results are in close agreement with the model-calculated values. This model will provide insight on the effects of processes such as apoptosis or external media ion concentration on the cytoplasm conductivity of mammalian cells. Nature Publishing Group UK 2018-12-13 /pmc/articles/PMC6292909/ /pubmed/30546044 http://dx.doi.org/10.1038/s41598-018-36127-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fazelkhah, Azita
Braasch, Katrin
Afshar, Samaneh
Salimi, Elham
Butler, Michael
Bridges, Greg
Thomson, Douglas
Quantitative Model for Ion Transport and Cytoplasm Conductivity of Chinese Hamster Ovary Cells
title Quantitative Model for Ion Transport and Cytoplasm Conductivity of Chinese Hamster Ovary Cells
title_full Quantitative Model for Ion Transport and Cytoplasm Conductivity of Chinese Hamster Ovary Cells
title_fullStr Quantitative Model for Ion Transport and Cytoplasm Conductivity of Chinese Hamster Ovary Cells
title_full_unstemmed Quantitative Model for Ion Transport and Cytoplasm Conductivity of Chinese Hamster Ovary Cells
title_short Quantitative Model for Ion Transport and Cytoplasm Conductivity of Chinese Hamster Ovary Cells
title_sort quantitative model for ion transport and cytoplasm conductivity of chinese hamster ovary cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292909/
https://www.ncbi.nlm.nih.gov/pubmed/30546044
http://dx.doi.org/10.1038/s41598-018-36127-3
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