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Biomimetic cardiac tissue culture model (CTCM) to emulate cardiac physiology and pathophysiology ex vivo
There is need for a reliable in vitro system that can accurately replicate the cardiac physiological environment for drug testing. The limited availability of human heart tissue culture systems has led to inaccurate interpretations of cardiac-related drug effects. Here, we developed a cardiac tissue...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463130/ https://www.ncbi.nlm.nih.gov/pubmed/36085302 http://dx.doi.org/10.1038/s42003-022-03919-3 |
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author | Miller, Jessica M. Meki, Moustafa H. Elnakib, Ahmed Ou, Qinghui Abouleisa, Riham R. E. Tang, Xian-Liang Salama, Abou Bakr M. Gebreil, Ahmad Lin, Cindy Abdeltawab, Hisham Khalifa, Fahmi Hill, Bradford G. Abi-Gerges, Najah Bolli, Roberto El-Baz, Ayman S. Giridharan, Guruprasad A. Mohamed, Tamer M. A. |
author_facet | Miller, Jessica M. Meki, Moustafa H. Elnakib, Ahmed Ou, Qinghui Abouleisa, Riham R. E. Tang, Xian-Liang Salama, Abou Bakr M. Gebreil, Ahmad Lin, Cindy Abdeltawab, Hisham Khalifa, Fahmi Hill, Bradford G. Abi-Gerges, Najah Bolli, Roberto El-Baz, Ayman S. Giridharan, Guruprasad A. Mohamed, Tamer M. A. |
author_sort | Miller, Jessica M. |
collection | PubMed |
description | There is need for a reliable in vitro system that can accurately replicate the cardiac physiological environment for drug testing. The limited availability of human heart tissue culture systems has led to inaccurate interpretations of cardiac-related drug effects. Here, we developed a cardiac tissue culture model (CTCM) that can electro-mechanically stimulate heart slices with physiological stretches in systole and diastole during the cardiac cycle. After 12 days in culture, this approach partially improved the viability of heart slices but did not completely maintain their structural integrity. Therefore, following small molecule screening, we found that the incorporation of 100 nM tri-iodothyronine (T3) and 1 μM dexamethasone (Dex) into our culture media preserved the microscopic structure of the slices for 12 days. When combined with T3/Dex treatment, the CTCM system maintained the transcriptional profile, viability, metabolic activity, and structural integrity for 12 days at the same levels as the fresh heart tissue. Furthermore, overstretching the cardiac tissue induced cardiac hypertrophic signaling in culture, which provides a proof of concept for the ability of the CTCM to emulate cardiac stretch-induced hypertrophic conditions. In conclusion, CTCM can emulate cardiac physiology and pathophysiology in culture for an extended time, thereby enabling reliable drug screening. |
format | Online Article Text |
id | pubmed-9463130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94631302022-09-11 Biomimetic cardiac tissue culture model (CTCM) to emulate cardiac physiology and pathophysiology ex vivo Miller, Jessica M. Meki, Moustafa H. Elnakib, Ahmed Ou, Qinghui Abouleisa, Riham R. E. Tang, Xian-Liang Salama, Abou Bakr M. Gebreil, Ahmad Lin, Cindy Abdeltawab, Hisham Khalifa, Fahmi Hill, Bradford G. Abi-Gerges, Najah Bolli, Roberto El-Baz, Ayman S. Giridharan, Guruprasad A. Mohamed, Tamer M. A. Commun Biol Article There is need for a reliable in vitro system that can accurately replicate the cardiac physiological environment for drug testing. The limited availability of human heart tissue culture systems has led to inaccurate interpretations of cardiac-related drug effects. Here, we developed a cardiac tissue culture model (CTCM) that can electro-mechanically stimulate heart slices with physiological stretches in systole and diastole during the cardiac cycle. After 12 days in culture, this approach partially improved the viability of heart slices but did not completely maintain their structural integrity. Therefore, following small molecule screening, we found that the incorporation of 100 nM tri-iodothyronine (T3) and 1 μM dexamethasone (Dex) into our culture media preserved the microscopic structure of the slices for 12 days. When combined with T3/Dex treatment, the CTCM system maintained the transcriptional profile, viability, metabolic activity, and structural integrity for 12 days at the same levels as the fresh heart tissue. Furthermore, overstretching the cardiac tissue induced cardiac hypertrophic signaling in culture, which provides a proof of concept for the ability of the CTCM to emulate cardiac stretch-induced hypertrophic conditions. In conclusion, CTCM can emulate cardiac physiology and pathophysiology in culture for an extended time, thereby enabling reliable drug screening. Nature Publishing Group UK 2022-09-09 /pmc/articles/PMC9463130/ /pubmed/36085302 http://dx.doi.org/10.1038/s42003-022-03919-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Miller, Jessica M. Meki, Moustafa H. Elnakib, Ahmed Ou, Qinghui Abouleisa, Riham R. E. Tang, Xian-Liang Salama, Abou Bakr M. Gebreil, Ahmad Lin, Cindy Abdeltawab, Hisham Khalifa, Fahmi Hill, Bradford G. Abi-Gerges, Najah Bolli, Roberto El-Baz, Ayman S. Giridharan, Guruprasad A. Mohamed, Tamer M. A. Biomimetic cardiac tissue culture model (CTCM) to emulate cardiac physiology and pathophysiology ex vivo |
title | Biomimetic cardiac tissue culture model (CTCM) to emulate cardiac physiology and pathophysiology ex vivo |
title_full | Biomimetic cardiac tissue culture model (CTCM) to emulate cardiac physiology and pathophysiology ex vivo |
title_fullStr | Biomimetic cardiac tissue culture model (CTCM) to emulate cardiac physiology and pathophysiology ex vivo |
title_full_unstemmed | Biomimetic cardiac tissue culture model (CTCM) to emulate cardiac physiology and pathophysiology ex vivo |
title_short | Biomimetic cardiac tissue culture model (CTCM) to emulate cardiac physiology and pathophysiology ex vivo |
title_sort | biomimetic cardiac tissue culture model (ctcm) to emulate cardiac physiology and pathophysiology ex vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463130/ https://www.ncbi.nlm.nih.gov/pubmed/36085302 http://dx.doi.org/10.1038/s42003-022-03919-3 |
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