Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0050641
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dc.titleHydrogen Sulfide Suppresses Outward Rectifier Potassium Currents in Human Pluripotent Stem Cell-Derived Cardiomyocytes
dc.contributor.authorWei H.
dc.contributor.authorZhang G.
dc.contributor.authorQiu S.
dc.contributor.authorLu J.
dc.contributor.authorSheng J.
dc.contributor.authorManasi
dc.contributor.authorTan G.
dc.contributor.authorWong P.
dc.contributor.authorGan S.U.
dc.contributor.authorShim W.
dc.date.accessioned2020-03-31T03:03:45Z
dc.date.available2020-03-31T03:03:45Z
dc.date.issued2012
dc.identifier.citationWei H., Zhang G., Qiu S., Lu J., Sheng J., Manasi, Tan G., Wong P., Gan S.U., Shim W. (2012). Hydrogen Sulfide Suppresses Outward Rectifier Potassium Currents in Human Pluripotent Stem Cell-Derived Cardiomyocytes. PLoS ONE 7 (11) : e50641. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0050641
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/166207
dc.description.abstractAim: Hydrogen sulfide (H2S) is a promising cardioprotective agent and a potential modulator of cardiac ion currents. Yet its cardiac effects on humans are poorly understood due to lack of functional cardiomyocytes. This study investigates electrophysiological responses of human pluripotent stem cells (hPSCs) derived cardiomyocytes towards H2S. Methods and Results: Cardiomyocytes of ventricular, atrial and nodal subtypes differentiated from H9 embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs) were electrophysiologically characterized. The effect of NaHS, a donor of H2S, on action potential (AP), outward rectifier potassium currents (IKs and IKr), L-type Ca2+ currents (ICaL) and hyperpolarization-activated inward current (If) were determined by patch-clamp electrophysiology and confocal calcium imaging. In a concentration-dependent manner, NaHS (100 to 300 ?M) consistently altered the action potential properties including prolonging action potential duration (APD) and slowing down contracting rates of ventricular-and atrial-like cardiomyocytes derived from both hESCs and hiPSCs. Moreover, inhibitions of slow and rapid IK (IKs and IKr), ICaL and If were found in NaHS treated cardiomyocytes and it could collectively contribute to the remodeling of AP properties. Conclusions: This is the first demonstration of effects of H2S on cardiac electrophysiology of human ventricular-like, atrial-like and nodal-like cardiomyocytes. It reaffirmed the inhibitory effect of H2S on ICaL and revealed additional novel inhibitory effects on If, IKs and IKr currents in human cardiomyocytes. © 2012 Wei et al.
dc.publisherPublic Library of Science
dc.sourceUnpaywall 20200320
dc.subjectcalcium channel L type
dc.subjecthydrogen sulfide
dc.subjectoutward rectifier potassium channel
dc.subjectpotassium channel
dc.subjectunclassified drug
dc.subjectarticle
dc.subjectcalcium cell level
dc.subjectcell differentiation
dc.subjectcell function
dc.subjectchannel gating
dc.subjectconcentration response
dc.subjectcontrolled study
dc.subjectembryonic stem cell
dc.subjectheart electrophysiology
dc.subjectheart muscle cell
dc.subjectheart muscle fiber membrane potential
dc.subjecthuman
dc.subjecthuman cell
dc.subjecthyperpolarization
dc.subjectmolecular imaging
dc.subjectmolecular interaction
dc.subjectpatch clamp
dc.subjectpluripotent stem cell
dc.subjectAction Potentials
dc.subjectCalcium Channel Blockers
dc.subjectCalcium Channels, L-Type
dc.subjectCell Differentiation
dc.subjectElectric Conductivity
dc.subjectEmbryonic Stem Cells
dc.subjectHeart Atria
dc.subjectHeart Ventricles
dc.subjectHumans
dc.subjectHydrogen Sulfide
dc.subjectMyocytes, Cardiac
dc.subjectPluripotent Stem Cells
dc.subjectPotassium Channel Blockers
dc.subjectPotassium Channels
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentSURGERY
dc.description.doi10.1371/journal.pone.0050641
dc.description.sourcetitlePLoS ONE
dc.description.volume7
dc.description.issue11
dc.description.pagee50641
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