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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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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. |
format | Online Article Text |
id | pubmed-9332902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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