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.

Stem Cell Reports
|February 13, 2018
PubMed

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.

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