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Biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies
Living myocardial slices (LMS) are beating sections of intact human myocardium that maintain 3D microarchitecture and multicellularity, thereby overcoming most limitations of conventional myocardial cell cultures. We introduce a novel method to produce LMS from human atria and apply pacing modalitie...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985600/ https://www.ncbi.nlm.nih.gov/pubmed/36871094 http://dx.doi.org/10.1038/s41598-023-30688-8 |
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author | Amesz, Jorik H. de Groot, Natasja M. S. Langmuur, Sanne J. J. Azzouzi, Hamid el Tiggeloven, Vera P. C. van Rooij, Manuela M. M. M. Knops, P. Bogers, Ad J. J. C. Taverne, Yannick J. H. J. |
author_facet | Amesz, Jorik H. de Groot, Natasja M. S. Langmuur, Sanne J. J. Azzouzi, Hamid el Tiggeloven, Vera P. C. van Rooij, Manuela M. M. M. Knops, P. Bogers, Ad J. J. C. Taverne, Yannick J. H. J. |
author_sort | Amesz, Jorik H. |
collection | PubMed |
description | Living myocardial slices (LMS) are beating sections of intact human myocardium that maintain 3D microarchitecture and multicellularity, thereby overcoming most limitations of conventional myocardial cell cultures. We introduce a novel method to produce LMS from human atria and apply pacing modalities to bridge the gap between in-vitro and in-vivo atrial arrhythmia studies. Human atrial biopsies from 15 patients undergoing cardiac surgery were dissected to tissue blocks of ~ 1 cm(2) and cut to 300 µm thin LMS with a precision-cutting vibratome. LMS were placed in a biomimetic cultivation chamber, filled with standard cell culture medium, under diastolic preload (1 mN) and continuous electrical stimulation (1000 ms cycle length (CL)), resulting in 68 beating LMS. Atrial LMS refractory period was determined at 192 ± 26 ms. Fixed rate pacing with a CL of 333 ms was applied as atrial tachyarrhythmia (AT) model. This novel state-of-the-art platform for AT research can be used to investigate arrhythmia mechanisms and test novel therapies. |
format | Online Article Text |
id | pubmed-9985600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99856002023-03-06 Biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies Amesz, Jorik H. de Groot, Natasja M. S. Langmuur, Sanne J. J. Azzouzi, Hamid el Tiggeloven, Vera P. C. van Rooij, Manuela M. M. M. Knops, P. Bogers, Ad J. J. C. Taverne, Yannick J. H. J. Sci Rep Article Living myocardial slices (LMS) are beating sections of intact human myocardium that maintain 3D microarchitecture and multicellularity, thereby overcoming most limitations of conventional myocardial cell cultures. We introduce a novel method to produce LMS from human atria and apply pacing modalities to bridge the gap between in-vitro and in-vivo atrial arrhythmia studies. Human atrial biopsies from 15 patients undergoing cardiac surgery were dissected to tissue blocks of ~ 1 cm(2) and cut to 300 µm thin LMS with a precision-cutting vibratome. LMS were placed in a biomimetic cultivation chamber, filled with standard cell culture medium, under diastolic preload (1 mN) and continuous electrical stimulation (1000 ms cycle length (CL)), resulting in 68 beating LMS. Atrial LMS refractory period was determined at 192 ± 26 ms. Fixed rate pacing with a CL of 333 ms was applied as atrial tachyarrhythmia (AT) model. This novel state-of-the-art platform for AT research can be used to investigate arrhythmia mechanisms and test novel therapies. Nature Publishing Group UK 2023-03-04 /pmc/articles/PMC9985600/ /pubmed/36871094 http://dx.doi.org/10.1038/s41598-023-30688-8 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Amesz, Jorik H. de Groot, Natasja M. S. Langmuur, Sanne J. J. Azzouzi, Hamid el Tiggeloven, Vera P. C. van Rooij, Manuela M. M. M. Knops, P. Bogers, Ad J. J. C. Taverne, Yannick J. H. J. Biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies |
title | Biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies |
title_full | Biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies |
title_fullStr | Biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies |
title_full_unstemmed | Biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies |
title_short | Biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies |
title_sort | biomimetic cultivation of atrial tissue slices as novel platform for in-vitro atrial arrhythmia studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985600/ https://www.ncbi.nlm.nih.gov/pubmed/36871094 http://dx.doi.org/10.1038/s41598-023-30688-8 |
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