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Updated: Feb 14, 2026

Model of Ischemic Heart Disease and Video-Based Comparison of Cardiomyocyte Contraction Using hiPSC-Derived Cardiomyocytes
Published on: May 5, 2020
Low Resting Membrane Potential and Low Inward Rectifier Potassium Currents Are Not Inherent Features of hiPSC-Derived
András Horváth1, Marc D Lemoine2, Alexandra Löser3
1Department of Experimental Pharmacology and Toxicology, University Medical Center Hamburg-Eppendorf, Institut für Experimentelle Pharmakologie und Toxikologie, Universitätsklinikum Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany; DZHK (German Centre for Cardiovascular Research), Partner Site Hamburg/Kiel/Lübeck, 20246 Hamburg, Germany; Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, University of Szeged, 6721 Szeged, Hungary.
Insights
Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) may not inherently have low inward rectifier potassium currents (IK1). Technical factors, not just cell type, may explain variations in resting membrane potential (RMP) in hiPSC-CM research.
Area of Science:
- Cardiology
- Stem Cell Biology
- Electrophysiology
Background:
- Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) often exhibit a less negative resting membrane potential (RMP).
- This RMP difference is frequently attributed to reduced inward rectifier potassium currents (IK1).
- Understanding ion channel function in hiPSC-CMs is crucial for their application in disease modeling and drug screening.
Purpose of the Study:
- To investigate and compare IK1 density and RMP in hiPSC-CMs cultured under different conditions.
- To directly compare hiPSC-CMs with human native atrial and ventricular cardiomyocytes.
- To identify factors contributing to observed RMP variations in hiPSC-CMs.
Main Methods:
- Measurement of IK1 and RMP in hiPSC-CMs (proprietary and commercial lines) cultured as monolayer (ML) or 3D engineered heart tissue (EHT).
- Direct comparison with cardiomyocytes from human right atrium (RA) and left ventricle (LV).
- Assessment of repolarization fraction and IK,ACh response to differentiate chamber phenotypes.
Main Results:
- IK1 density in ML- and EHT-hiPSC-CMs (proprietary line) was comparable to LV and RA CMs, respectively.
- A 2-fold lower IK1 density was observed in EHT-hiPSC-CMs from the commercial line compared to the proprietary line.
- RMP in EHT-hiPSC-CMs from both lines resembled native RA and LV CMs.
- Repolarization and IK,ACh responses indicated a predominantly ventricular phenotype in hiPSC-CMs/EHT.
- IK1 levels in hiPSC-CMs are not universally low, suggesting technical issues may influence RMP measurements.
Conclusions:
- The inherent IK1 current in hiPSC-CMs may not be as low as previously assumed.
- Observed low RMP in hiPSC-CMs could be influenced by experimental or technical factors rather than intrinsic cellular properties.
- hiPSC-CMs, particularly in EHT formats, show promise for recapitulating native cardiac electrophysiology.
- Further investigation into culture conditions and measurement techniques is warranted to optimize hiPSC-CM models.
Abstract:
Human induced pluripotent stem cell (hiPSC) cardiomyocytes (CMs) show less negative resting membrane potential (RMP), which is attributed to small inward rectifier currents (IK1). Here, IK1 was measured in hiPSC-CMs (proprietary and commercial cell line) cultured as monolayer (ML) or 3D engineered heart tissue (EHT) and, for direct comparison, in CMs from human right atrial (RA) and left ventricular (LV) tissue. RMP was measured in isolated cells and intact tissues. IK1 density in ML- and EHT-CMs from the proprietary line was similar to LV and RA, respectively. IK1 density in EHT-CMs from the commercial line was 2-fold smaller than in the proprietary line. RMP in EHT of both lines was similar to RA and LV. Repolarization fraction and IK,ACh response discriminated best between RA and LV and indicated predominantly ventricular phenotype in hiPSC-CMs/EHT. The data indicate that IK1 is not necessarily low in hiPSC-CMs, and technical issues may underlie low RMP in hiPSC-CMs.
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