Low Resting Membrane Potential and Low Inward Rectifier Potassium Currents Are Not Inherent Features of hiPSC-Derived Cardiomyocytes
Author(s) -
András Horváth,
Marc D. Lemoine,
Alexandra Löser,
Ingra Mannhardt,
Frederik Flenner,
Ahmet Umur Uzun,
Christiane Neuber,
Kaja Breckwoldt,
Arne Hansen,
Evaldas Girdauskas,
Hermann Reichenspurner,
Stephan Willems,
Norbert Jost,
Erich Wettwer,
Thomas Eschenhagen,
Torsten Christ
Publication year - 2018
Publication title -
stem cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.207
H-Index - 76
ISSN - 2213-6711
DOI - 10.1016/j.stemcr.2018.01.012
Subject(s) - biology , inward rectifier potassium ion channel , membrane potential , potassium , potassium channel , resting potential , biophysics , microbiology and biotechnology , ion channel , biochemistry , materials science , metallurgy , receptor
Human induced pluripotent stem cell (hiPSC) cardiomyocytes (CMs) show less negative resting membrane potential (RMP), which is attributed to small inward rectifier currents (I K1 ). Here, I K1 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. I K1 density in ML- and EHT-CMs from the proprietary line was similar to LV and RA, respectively. I K1 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 I K,ACh response discriminated best between RA and LV and indicated predominantly ventricular phenotype in hiPSC-CMs/EHT. The data indicate that I K1 is not necessarily low in hiPSC-CMs, and technical issues may underlie low RMP in hiPSC-CMs.
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