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Biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials
Current platforms for in vitro drug development utilize confluent, unorganized monolayers of heart cells to study the effect on action potential propagation. However, standard cell cultures are of limited use in cardiac research, as they do not preserve important structural and functional properties...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459200/ https://www.ncbi.nlm.nih.gov/pubmed/26053434 http://dx.doi.org/10.1038/srep11067 |
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author | Trantidou, Tatiana Terracciano, Cesare M. Kontziampasis, Dimitrios Humphrey, Eleanor J. Prodromakis, Themistoklis |
author_facet | Trantidou, Tatiana Terracciano, Cesare M. Kontziampasis, Dimitrios Humphrey, Eleanor J. Prodromakis, Themistoklis |
author_sort | Trantidou, Tatiana |
collection | PubMed |
description | Current platforms for in vitro drug development utilize confluent, unorganized monolayers of heart cells to study the effect on action potential propagation. However, standard cell cultures are of limited use in cardiac research, as they do not preserve important structural and functional properties of the myocardium. Here we present a method to integrate a scaffolding technology with multi-electrode arrays and deliver a compact, off-the-shelf monitoring platform for growing biomimetic cardiac tissue. Our approach produces anisotropic cultures with conduction velocity (CV) profiles that closer resemble native heart tissue; the fastest impulse propagation is along the long axis of the aligned cardiomyocytes (CVL) and the slowest propagation is perpendicular (CVT), in contrast to standard cultures where action potential propagates isotropically (CVL ≈ CVT). The corresponding anisotropy velocity ratios (CVL/CVT = 1.38 – 2.22) are comparable with values for healthy adult rat ventricles (1.98 – 3.63). The main advantages of this approach are that (i) it provides ultimate pattern control, (ii) it is compatible with automated manufacturing steps and (iii) it is utilized through standard cell culturing protocols. Our platform is compatible with existing read-out equipment and comprises a prompt method for more reliable CV studies. |
format | Online Article Text |
id | pubmed-4459200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44592002015-06-17 Biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials Trantidou, Tatiana Terracciano, Cesare M. Kontziampasis, Dimitrios Humphrey, Eleanor J. Prodromakis, Themistoklis Sci Rep Article Current platforms for in vitro drug development utilize confluent, unorganized monolayers of heart cells to study the effect on action potential propagation. However, standard cell cultures are of limited use in cardiac research, as they do not preserve important structural and functional properties of the myocardium. Here we present a method to integrate a scaffolding technology with multi-electrode arrays and deliver a compact, off-the-shelf monitoring platform for growing biomimetic cardiac tissue. Our approach produces anisotropic cultures with conduction velocity (CV) profiles that closer resemble native heart tissue; the fastest impulse propagation is along the long axis of the aligned cardiomyocytes (CVL) and the slowest propagation is perpendicular (CVT), in contrast to standard cultures where action potential propagates isotropically (CVL ≈ CVT). The corresponding anisotropy velocity ratios (CVL/CVT = 1.38 – 2.22) are comparable with values for healthy adult rat ventricles (1.98 – 3.63). The main advantages of this approach are that (i) it provides ultimate pattern control, (ii) it is compatible with automated manufacturing steps and (iii) it is utilized through standard cell culturing protocols. Our platform is compatible with existing read-out equipment and comprises a prompt method for more reliable CV studies. Nature Publishing Group 2015-06-08 /pmc/articles/PMC4459200/ /pubmed/26053434 http://dx.doi.org/10.1038/srep11067 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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 to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Trantidou, Tatiana Terracciano, Cesare M. Kontziampasis, Dimitrios Humphrey, Eleanor J. Prodromakis, Themistoklis Biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials |
title | Biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials |
title_full | Biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials |
title_fullStr | Biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials |
title_full_unstemmed | Biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials |
title_short | Biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials |
title_sort | biorealistic cardiac cell culture platforms with integrated monitoring of extracellular action potentials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459200/ https://www.ncbi.nlm.nih.gov/pubmed/26053434 http://dx.doi.org/10.1038/srep11067 |
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