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Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples
Cell culture of cardiac tissue analog is becoming increasingly interesting for regenerative medicine (cell therapy and tissue engineering) and is widely used for high throughput cardiotoxicity. As a cost-effective approach to rapidly discard new compounds with high toxicity risks, cardiotoxicity eva...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886216/ https://www.ncbi.nlm.nih.gov/pubmed/35242049 http://dx.doi.org/10.3389/fphys.2022.733706 |
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author | Béland, Jonathan Duverger, James Elber Comtois, Philippe |
author_facet | Béland, Jonathan Duverger, James Elber Comtois, Philippe |
author_sort | Béland, Jonathan |
collection | PubMed |
description | Cell culture of cardiac tissue analog is becoming increasingly interesting for regenerative medicine (cell therapy and tissue engineering) and is widely used for high throughput cardiotoxicity. As a cost-effective approach to rapidly discard new compounds with high toxicity risks, cardiotoxicity evaluation is firstly done in vitro requiring cells/tissue with physiological/pathological characteristics (close to in vivo properties). Studying multicellular electrophysiological and contractile properties is needed to assess drug effects. Techniques favoring process automation which could help in simplifying screening drug candidates are thus of central importance. A lot of effort has been made to ameliorate in vitro models including several in vitro platforms for engineering neonatal rat cardiac tissues. However, most of the initial evaluation is done by studying the rate of activity. In this study, we present new approaches that use the videomicroscopy video of monolayer activity to study contractile properties of beating cells in culture. Two new variables are proposed which are linked to the contraction dynamics and are dependent on the rhythm of activity. Methods for evaluation of regional synchronicity within the image field of view are also presented that can rapidly determine regions with abnormal activity or heterogeneity in contraction dynamics. |
format | Online Article Text |
id | pubmed-8886216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88862162022-03-02 Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples Béland, Jonathan Duverger, James Elber Comtois, Philippe Front Physiol Physiology Cell culture of cardiac tissue analog is becoming increasingly interesting for regenerative medicine (cell therapy and tissue engineering) and is widely used for high throughput cardiotoxicity. As a cost-effective approach to rapidly discard new compounds with high toxicity risks, cardiotoxicity evaluation is firstly done in vitro requiring cells/tissue with physiological/pathological characteristics (close to in vivo properties). Studying multicellular electrophysiological and contractile properties is needed to assess drug effects. Techniques favoring process automation which could help in simplifying screening drug candidates are thus of central importance. A lot of effort has been made to ameliorate in vitro models including several in vitro platforms for engineering neonatal rat cardiac tissues. However, most of the initial evaluation is done by studying the rate of activity. In this study, we present new approaches that use the videomicroscopy video of monolayer activity to study contractile properties of beating cells in culture. Two new variables are proposed which are linked to the contraction dynamics and are dependent on the rhythm of activity. Methods for evaluation of regional synchronicity within the image field of view are also presented that can rapidly determine regions with abnormal activity or heterogeneity in contraction dynamics. Frontiers Media S.A. 2022-02-15 /pmc/articles/PMC8886216/ /pubmed/35242049 http://dx.doi.org/10.3389/fphys.2022.733706 Text en Copyright © 2022 Béland, Duverger and Comtois. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Béland, Jonathan Duverger, James Elber Comtois, Philippe Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples |
title | Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples |
title_full | Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples |
title_fullStr | Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples |
title_full_unstemmed | Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples |
title_short | Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples |
title_sort | novel analysis method for beating cells videomicroscopy data: functional characterization of culture samples |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886216/ https://www.ncbi.nlm.nih.gov/pubmed/35242049 http://dx.doi.org/10.3389/fphys.2022.733706 |
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