Human-induced pluripotent stem cell-derived cardiomyocytes have limited I for repolarization reserve as revealed by specific KCNQ1/KCNE1 blocker

Objective We investigated if there is I Ks , and if there is repolarization reserve by I Ks in human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs). Design We used a specific KCNQ1/KCNE1 channel blocker, L-000768673, with an IC 50 of 9 nM, and four hERG-specific blockers, astemizol...

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Main Authors: Haoyu Zeng, Jixin Wang, Holly Clouse, Armando Lagrutta, Frederick Sannajust
Format: Article
Language:English
Published: SAGE Publishing 2019-06-01
Series:JRSM Cardiovascular Disease
Online Access:https://doi.org/10.1177/2048004019854919
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spelling doaj-2caecd0927db476ba4b6cc8a907543b02020-11-25T03:32:22ZengSAGE PublishingJRSM Cardiovascular Disease2048-00402019-06-01810.1177/2048004019854919Human-induced pluripotent stem cell-derived cardiomyocytes have limited I for repolarization reserve as revealed by specific KCNQ1/KCNE1 blockerHaoyu ZengJixin WangHolly ClouseArmando LagruttaFrederick SannajustObjective We investigated if there is I Ks , and if there is repolarization reserve by I Ks in human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs). Design We used a specific KCNQ1/KCNE1 channel blocker, L-000768673, with an IC 50 of 9 nM, and four hERG-specific blockers, astemizole, cisapride, dofetilide, and E-4031 to investigate the issue. Results L-000768673 concentration-dependently prolonged feature point duration (FPD)―a surrogate signal of action potential duration―from 1 to 30 nM without pacing or paced at 1.2 Hz, resulting from I Ks blockade in hiPSC-CMs. At higher concentrations, the effect of L-000768673 on I Ks was mitigated by its effect on I Ca-L , resulting in shortened FPD, reduced impedance amplitude, and increased beating rate at 1 µM and above, recapitulating the self-limiting properties of L-000768673 on action potentials. All four hERG-specific blockers prolonged FPD as expected. Co-application of L-000768673 at sub-threshold (0.1 and 0.3 nM) and threshold (1 nM) concentrations failed to synergistically enhance the effects of hERG blockers on FPD prolongation, rather it showed additive effects, inconsistent with the repolarization reserve role of I Ks in mature human myocytes that enhanced I Kr response, implying a difference between hiPSC-CMs used in this study and mature human cardiomyocytes. Conclusion There was I Ks current in hiPSC-CMs, and blockade of I Ks current caused prolongation of action potential of hiPSC-CMs. However, we could not demonstrate any synergistic effects on action potential duration prolongation of hiPSC-CMs by blocking hERG current and I Ks current simultaneously, implying little or no repolarization reserve by I Ks current in hiPSC-CMs used in this study.https://doi.org/10.1177/2048004019854919
collection DOAJ
language English
format Article
sources DOAJ
author Haoyu Zeng
Jixin Wang
Holly Clouse
Armando Lagrutta
Frederick Sannajust
spellingShingle Haoyu Zeng
Jixin Wang
Holly Clouse
Armando Lagrutta
Frederick Sannajust
Human-induced pluripotent stem cell-derived cardiomyocytes have limited I for repolarization reserve as revealed by specific KCNQ1/KCNE1 blocker
JRSM Cardiovascular Disease
author_facet Haoyu Zeng
Jixin Wang
Holly Clouse
Armando Lagrutta
Frederick Sannajust
author_sort Haoyu Zeng
title Human-induced pluripotent stem cell-derived cardiomyocytes have limited I for repolarization reserve as revealed by specific KCNQ1/KCNE1 blocker
title_short Human-induced pluripotent stem cell-derived cardiomyocytes have limited I for repolarization reserve as revealed by specific KCNQ1/KCNE1 blocker
title_full Human-induced pluripotent stem cell-derived cardiomyocytes have limited I for repolarization reserve as revealed by specific KCNQ1/KCNE1 blocker
title_fullStr Human-induced pluripotent stem cell-derived cardiomyocytes have limited I for repolarization reserve as revealed by specific KCNQ1/KCNE1 blocker
title_full_unstemmed Human-induced pluripotent stem cell-derived cardiomyocytes have limited I for repolarization reserve as revealed by specific KCNQ1/KCNE1 blocker
title_sort human-induced pluripotent stem cell-derived cardiomyocytes have limited i for repolarization reserve as revealed by specific kcnq1/kcne1 blocker
publisher SAGE Publishing
series JRSM Cardiovascular Disease
issn 2048-0040
publishDate 2019-06-01
description Objective We investigated if there is I Ks , and if there is repolarization reserve by I Ks in human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs). Design We used a specific KCNQ1/KCNE1 channel blocker, L-000768673, with an IC 50 of 9 nM, and four hERG-specific blockers, astemizole, cisapride, dofetilide, and E-4031 to investigate the issue. Results L-000768673 concentration-dependently prolonged feature point duration (FPD)―a surrogate signal of action potential duration―from 1 to 30 nM without pacing or paced at 1.2 Hz, resulting from I Ks blockade in hiPSC-CMs. At higher concentrations, the effect of L-000768673 on I Ks was mitigated by its effect on I Ca-L , resulting in shortened FPD, reduced impedance amplitude, and increased beating rate at 1 µM and above, recapitulating the self-limiting properties of L-000768673 on action potentials. All four hERG-specific blockers prolonged FPD as expected. Co-application of L-000768673 at sub-threshold (0.1 and 0.3 nM) and threshold (1 nM) concentrations failed to synergistically enhance the effects of hERG blockers on FPD prolongation, rather it showed additive effects, inconsistent with the repolarization reserve role of I Ks in mature human myocytes that enhanced I Kr response, implying a difference between hiPSC-CMs used in this study and mature human cardiomyocytes. Conclusion There was I Ks current in hiPSC-CMs, and blockade of I Ks current caused prolongation of action potential of hiPSC-CMs. However, we could not demonstrate any synergistic effects on action potential duration prolongation of hiPSC-CMs by blocking hERG current and I Ks current simultaneously, implying little or no repolarization reserve by I Ks current in hiPSC-CMs used in this study.
url https://doi.org/10.1177/2048004019854919
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