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Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes

Electrical activity and intracellular Ca(2+) transients are key features of cardiomyocytes. They can be measured using organic voltage- and Ca(2+)-sensitive dyes but their photostability and phototoxicity mean they are unsuitable for long-term measurements. Here, we investigated whether genetically...

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Autores principales: Yiangou, Loukia, Blanch-Asensio, Albert, de Korte, Tessa, Miller, Duncan C, van Meer, Berend J, Mol, Mervyn P H, van den Brink, Lettine, Brandão, Karina O, Mummery, Christine L, Davis, Richard P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9332902/
https://www.ncbi.nlm.nih.gov/pubmed/35429386
http://dx.doi.org/10.1093/stmcls/sxac029
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author Yiangou, Loukia
Blanch-Asensio, Albert
de Korte, Tessa
Miller, Duncan C
van Meer, Berend J
Mol, Mervyn P H
van den Brink, Lettine
Brandão, Karina O
Mummery, Christine L
Davis, Richard P
author_facet Yiangou, Loukia
Blanch-Asensio, Albert
de Korte, Tessa
Miller, Duncan C
van Meer, Berend J
Mol, Mervyn P H
van den Brink, Lettine
Brandão, Karina O
Mummery, Christine L
Davis, Richard P
author_sort Yiangou, Loukia
collection PubMed
description Electrical activity and intracellular Ca(2+) transients are key features of cardiomyocytes. They can be measured using organic voltage- and Ca(2+)-sensitive dyes but their photostability and phototoxicity mean they are unsuitable for long-term measurements. Here, we investigated whether genetically encoded voltage and Ca(2+) indicators (GEVIs and GECIs) delivered as modified mRNA (modRNA) into human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) would be accurate alternatives allowing measurements over long periods. These indicators were detected in hiPSC-CMs for up to 7 days after transfection and did not affect responses to proarrhythmic compounds. Furthermore, using the GEVI ASAP2f we observed action potential prolongation in long QT syndrome models, while the GECI jRCaMP1b facilitated the repeated evaluation of Ca(2+) handling responses for various tyrosine kinase inhibitors. This study demonstrated that modRNAs encoding optogenetic constructs report cardiac physiology in hiPSC-CMs without toxicity or the need for stable integration, illustrating their value as alternatives to organic dyes or other gene delivery methods for expressing transgenes.
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spelling pubmed-93329022022-07-29 Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes Yiangou, Loukia Blanch-Asensio, Albert de Korte, Tessa Miller, Duncan C van Meer, Berend J Mol, Mervyn P H van den Brink, Lettine Brandão, Karina O Mummery, Christine L Davis, Richard P Stem Cells Embryonic Stem Cells/Induced Pluripotent Stem Cells Electrical activity and intracellular Ca(2+) transients are key features of cardiomyocytes. They can be measured using organic voltage- and Ca(2+)-sensitive dyes but their photostability and phototoxicity mean they are unsuitable for long-term measurements. Here, we investigated whether genetically encoded voltage and Ca(2+) indicators (GEVIs and GECIs) delivered as modified mRNA (modRNA) into human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) would be accurate alternatives allowing measurements over long periods. These indicators were detected in hiPSC-CMs for up to 7 days after transfection and did not affect responses to proarrhythmic compounds. Furthermore, using the GEVI ASAP2f we observed action potential prolongation in long QT syndrome models, while the GECI jRCaMP1b facilitated the repeated evaluation of Ca(2+) handling responses for various tyrosine kinase inhibitors. This study demonstrated that modRNAs encoding optogenetic constructs report cardiac physiology in hiPSC-CMs without toxicity or the need for stable integration, illustrating their value as alternatives to organic dyes or other gene delivery methods for expressing transgenes. Oxford University Press 2022-04-16 /pmc/articles/PMC9332902/ /pubmed/35429386 http://dx.doi.org/10.1093/stmcls/sxac029 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Embryonic Stem Cells/Induced Pluripotent Stem Cells
Yiangou, Loukia
Blanch-Asensio, Albert
de Korte, Tessa
Miller, Duncan C
van Meer, Berend J
Mol, Mervyn P H
van den Brink, Lettine
Brandão, Karina O
Mummery, Christine L
Davis, Richard P
Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes
title Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes
title_full Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes
title_fullStr Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes
title_full_unstemmed Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes
title_short Optogenetic Reporters Delivered as mRNA Facilitate Repeatable Action Potential and Calcium Handling Assessment in Human iPSC-Derived Cardiomyocytes
title_sort optogenetic reporters delivered as mrna facilitate repeatable action potential and calcium handling assessment in human ipsc-derived cardiomyocytes
topic Embryonic Stem Cells/Induced Pluripotent Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9332902/
https://www.ncbi.nlm.nih.gov/pubmed/35429386
http://dx.doi.org/10.1093/stmcls/sxac029
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