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Fast Optical Investigation of Cardiac Electrophysiology by Parallel Detection in Multiwell Plates
Current techniques for fast characterization of cardiac electrophysiology employ optical technologies to control and monitor action potential features of single cells or cellular monolayers placed in multiwell plates. High-speed investigation capacities are commonly achieved by serially analyzing we...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446431/ https://www.ncbi.nlm.nih.gov/pubmed/34539428 http://dx.doi.org/10.3389/fphys.2021.692496 |
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author | Credi, Caterina Balducci, Valentina Munagala, U. Cianca, C. Bigiarini, S. de Vries, Antoine A. F. Loew, Leslie M. Pavone, Francesco S. Cerbai, Elisabetta Sartiani, Laura Sacconi, Leonardo |
author_facet | Credi, Caterina Balducci, Valentina Munagala, U. Cianca, C. Bigiarini, S. de Vries, Antoine A. F. Loew, Leslie M. Pavone, Francesco S. Cerbai, Elisabetta Sartiani, Laura Sacconi, Leonardo |
author_sort | Credi, Caterina |
collection | PubMed |
description | Current techniques for fast characterization of cardiac electrophysiology employ optical technologies to control and monitor action potential features of single cells or cellular monolayers placed in multiwell plates. High-speed investigation capacities are commonly achieved by serially analyzing well after well employing fully automated fluorescence microscopes. Here, we describe an alternative cost-effective optical approach (MULTIPLE) that exploits high-power LED arrays to globally illuminate a culture plate and an sCMOS sensor for parallel detection of the fluorescence coming from multiple wells. MULTIPLE combines optical detection of action potentials using a red-shifted voltage-sensitive fluorescent dye (di-4-ANBDQPQ) with optical stimulation, employing optogenetic actuators, to ensure excitation of cardiomyocytes at constant rates. MULTIPLE was first characterized in terms of interwell uniformity of the illumination intensity and optical detection performance. Then, it was applied for probing action potential features in HL-1 cells (i.e., mouse atrial myocyte-like cells) stably expressing the blue light-activatable cation channel CheRiff. Under proper stimulation conditions, we were able to accurately measure action potential dynamics across a 24-well plate with variability across the whole plate of the order of 10%. The capability of MULTIPLE to detect action potential changes across a 24-well plate was demonstrated employing the selective K(v)11.1 channel blocker (E-4031), in a dose titration experiment. Finally, action potential recordings were performed in spontaneous beating human induced pluripotent stem cell derived cardiomyocytes following pharmacological manipulation of their beating frequency. We believe that the simplicity of the presented optical scheme represents a valid complement to sophisticated and expensive state-of-the-art optical systems for high-throughput cardiac electrophysiological investigations. |
format | Online Article Text |
id | pubmed-8446431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84464312021-09-18 Fast Optical Investigation of Cardiac Electrophysiology by Parallel Detection in Multiwell Plates Credi, Caterina Balducci, Valentina Munagala, U. Cianca, C. Bigiarini, S. de Vries, Antoine A. F. Loew, Leslie M. Pavone, Francesco S. Cerbai, Elisabetta Sartiani, Laura Sacconi, Leonardo Front Physiol Physiology Current techniques for fast characterization of cardiac electrophysiology employ optical technologies to control and monitor action potential features of single cells or cellular monolayers placed in multiwell plates. High-speed investigation capacities are commonly achieved by serially analyzing well after well employing fully automated fluorescence microscopes. Here, we describe an alternative cost-effective optical approach (MULTIPLE) that exploits high-power LED arrays to globally illuminate a culture plate and an sCMOS sensor for parallel detection of the fluorescence coming from multiple wells. MULTIPLE combines optical detection of action potentials using a red-shifted voltage-sensitive fluorescent dye (di-4-ANBDQPQ) with optical stimulation, employing optogenetic actuators, to ensure excitation of cardiomyocytes at constant rates. MULTIPLE was first characterized in terms of interwell uniformity of the illumination intensity and optical detection performance. Then, it was applied for probing action potential features in HL-1 cells (i.e., mouse atrial myocyte-like cells) stably expressing the blue light-activatable cation channel CheRiff. Under proper stimulation conditions, we were able to accurately measure action potential dynamics across a 24-well plate with variability across the whole plate of the order of 10%. The capability of MULTIPLE to detect action potential changes across a 24-well plate was demonstrated employing the selective K(v)11.1 channel blocker (E-4031), in a dose titration experiment. Finally, action potential recordings were performed in spontaneous beating human induced pluripotent stem cell derived cardiomyocytes following pharmacological manipulation of their beating frequency. We believe that the simplicity of the presented optical scheme represents a valid complement to sophisticated and expensive state-of-the-art optical systems for high-throughput cardiac electrophysiological investigations. Frontiers Media S.A. 2021-09-03 /pmc/articles/PMC8446431/ /pubmed/34539428 http://dx.doi.org/10.3389/fphys.2021.692496 Text en Copyright © 2021 Credi, Balducci, Munagala, Cianca, Bigiarini, de Vries, Loew, Pavone, Cerbai, Sartiani and Sacconi. 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 Credi, Caterina Balducci, Valentina Munagala, U. Cianca, C. Bigiarini, S. de Vries, Antoine A. F. Loew, Leslie M. Pavone, Francesco S. Cerbai, Elisabetta Sartiani, Laura Sacconi, Leonardo Fast Optical Investigation of Cardiac Electrophysiology by Parallel Detection in Multiwell Plates |
title | Fast Optical Investigation of Cardiac Electrophysiology by Parallel Detection in Multiwell Plates |
title_full | Fast Optical Investigation of Cardiac Electrophysiology by Parallel Detection in Multiwell Plates |
title_fullStr | Fast Optical Investigation of Cardiac Electrophysiology by Parallel Detection in Multiwell Plates |
title_full_unstemmed | Fast Optical Investigation of Cardiac Electrophysiology by Parallel Detection in Multiwell Plates |
title_short | Fast Optical Investigation of Cardiac Electrophysiology by Parallel Detection in Multiwell Plates |
title_sort | fast optical investigation of cardiac electrophysiology by parallel detection in multiwell plates |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446431/ https://www.ncbi.nlm.nih.gov/pubmed/34539428 http://dx.doi.org/10.3389/fphys.2021.692496 |
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