Cargando…

The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) and higher throughput platforms have emerged as potential tools to advance cardiac drug safety screening. This study evaluated the use of high bandwidth photometry applied to voltage-sensitive fluorescent dyes (VSDs) to assess dru...

Descripción completa

Detalles Bibliográficos
Autores principales: Hortigon-Vinagre, M. P., Zamora, V., Burton, F. L., Green, J., Gintant, G. A., Smith, G. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139069/
https://www.ncbi.nlm.nih.gov/pubmed/27621282
http://dx.doi.org/10.1093/toxsci/kfw171
_version_ 1782472176648060928
author Hortigon-Vinagre, M. P.
Zamora, V.
Burton, F. L.
Green, J.
Gintant, G. A.
Smith, G. L.
author_facet Hortigon-Vinagre, M. P.
Zamora, V.
Burton, F. L.
Green, J.
Gintant, G. A.
Smith, G. L.
author_sort Hortigon-Vinagre, M. P.
collection PubMed
description Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) and higher throughput platforms have emerged as potential tools to advance cardiac drug safety screening. This study evaluated the use of high bandwidth photometry applied to voltage-sensitive fluorescent dyes (VSDs) to assess drug-induced changes in action potential characteristics of spontaneously active hiPSC-CM. Human iPSC-CM from 2 commercial sources (Cor.4U and iCell Cardiomyocytes) were stained with the VSD di-4-ANEPPS and placed in a specialized photometry system that simultaneously monitors 2 wavebands of emitted fluorescence, allowing ratiometric measurement of membrane voltage. Signals were acquired at 10 kHz and analyzed using custom software. Action potential duration (APD) values were normally distributed in cardiomyocytes (CMC) from both sources though the mean and variance differed significantly (APD(90): 229 ± 15 ms vs 427 ± 49 ms [mean ± SD, P < 0.01]; average spontaneous cycle length: 0.99 ± 0.02 s vs 1.47 ± 0.35 s [mean ± SD, P < 0.01], Cor.4U vs iCell CMC, respectively). The 10–90% rise time of the AP (T(rise)) was ∼6 ms and was normally distributed when expressed as 1/ [Formula: see text] in both cell preparations. Both cell types showed a rate dependence analogous to that of adult human cardiac cells. Furthermore, nifedipine, ranolazine, and E4031 had similar effects on cardiomyocyte electrophysiology in both cell types. However, ranolazine and E4031 induced early after depolarization-like events and high intrinsic firing rates at lower concentrations in iCell CMC. These data show that VSDs provide a minimally invasive, quantitative, and accurate method to assess hiPSC-CM electrophysiology and detect subtle drug-induced effects for drug safety screening while highlighting a need to standardize experimental protocols across preparations.
format Online
Article
Text
id pubmed-5139069
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-51390692016-12-07 The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Hortigon-Vinagre, M. P. Zamora, V. Burton, F. L. Green, J. Gintant, G. A. Smith, G. L. Toxicol Sci Voltage-Sensitive Dyes in Human iPSC-Derived Cardiomyocytes Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) and higher throughput platforms have emerged as potential tools to advance cardiac drug safety screening. This study evaluated the use of high bandwidth photometry applied to voltage-sensitive fluorescent dyes (VSDs) to assess drug-induced changes in action potential characteristics of spontaneously active hiPSC-CM. Human iPSC-CM from 2 commercial sources (Cor.4U and iCell Cardiomyocytes) were stained with the VSD di-4-ANEPPS and placed in a specialized photometry system that simultaneously monitors 2 wavebands of emitted fluorescence, allowing ratiometric measurement of membrane voltage. Signals were acquired at 10 kHz and analyzed using custom software. Action potential duration (APD) values were normally distributed in cardiomyocytes (CMC) from both sources though the mean and variance differed significantly (APD(90): 229 ± 15 ms vs 427 ± 49 ms [mean ± SD, P < 0.01]; average spontaneous cycle length: 0.99 ± 0.02 s vs 1.47 ± 0.35 s [mean ± SD, P < 0.01], Cor.4U vs iCell CMC, respectively). The 10–90% rise time of the AP (T(rise)) was ∼6 ms and was normally distributed when expressed as 1/ [Formula: see text] in both cell preparations. Both cell types showed a rate dependence analogous to that of adult human cardiac cells. Furthermore, nifedipine, ranolazine, and E4031 had similar effects on cardiomyocyte electrophysiology in both cell types. However, ranolazine and E4031 induced early after depolarization-like events and high intrinsic firing rates at lower concentrations in iCell CMC. These data show that VSDs provide a minimally invasive, quantitative, and accurate method to assess hiPSC-CM electrophysiology and detect subtle drug-induced effects for drug safety screening while highlighting a need to standardize experimental protocols across preparations. Oxford University Press 2016-12 2016-09-11 /pmc/articles/PMC5139069/ /pubmed/27621282 http://dx.doi.org/10.1093/toxsci/kfw171 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society of Toxicology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Voltage-Sensitive Dyes in Human iPSC-Derived Cardiomyocytes
Hortigon-Vinagre, M. P.
Zamora, V.
Burton, F. L.
Green, J.
Gintant, G. A.
Smith, G. L.
The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_full The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_fullStr The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_full_unstemmed The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_short The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_sort use of ratiometric fluorescence measurements of the voltage sensitive dye di-4-anepps to examine action potential characteristics and drug effects on human induced pluripotent stem cell-derived cardiomyocytes
topic Voltage-Sensitive Dyes in Human iPSC-Derived Cardiomyocytes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139069/
https://www.ncbi.nlm.nih.gov/pubmed/27621282
http://dx.doi.org/10.1093/toxsci/kfw171
work_keys_str_mv AT hortigonvinagremp theuseofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT zamorav theuseofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT burtonfl theuseofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT greenj theuseofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT gintantga theuseofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT smithgl theuseofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT hortigonvinagremp useofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT zamorav useofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT burtonfl useofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT greenj useofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT gintantga useofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes
AT smithgl useofratiometricfluorescencemeasurementsofthevoltagesensitivedyedi4aneppstoexamineactionpotentialcharacteristicsanddrugeffectsonhumaninducedpluripotentstemcellderivedcardiomyocytes