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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Here we describe optical acquisition and characterization of action potentials from induced pluripotent stem cell derived cardiomyocytes using a high-speed modular photometry system.

Abstract

Conventional intracellular microelectrode techniques to quantify cardiomyocyte electrophysiology are extremely complex, labor intensive, and typically carried out in low throughput. Rapid and ongoing expansion of induced pluripotent stem cell (iPSC) technology presents a new standard in cardiovascular research and alternate methods are now necessary to increase throughput of electrophysiological data at a single cell level. VF2.1Cl is a recently derived voltage sensitive dye which provides a rapid single channel, high magnitude response to fluctuations in membrane potential. It possesses kinetics superior to those of other existing voltage indicators and makes available functional data equivalent to that of traditional microelectrode techniques. Here, we demonstrate simplified, non-invasive action potential characterization in externally paced human iPSC derived cardiomyocytes using a modular and highly affordable photometry system.

Introduction

Electrophysiological modeling of cardiomyocytes and the construction of efficient platforms for cardiac drug screening is essential for the development of therapeutic strategies for a variety of arrhythmic disorders. Rapid expansion of induced pluripotent stem cell (iPSC) technology has produced promising inroads into human disease modelling and pharmacological investigation using isolated patient derived cardiomyocytes (iPSC-CM). “Gold standard” techniques for electrophysiological characterization of these cells through patch-clamp (current-clamp) can quantify action potential (AP) morphology and duration, however, this method is incredibly complex and sl....

Protocol

1. Cellular preparations

NOTE: Human iPSCs used in this protocol were derived from healthy donors and differentiated in monolayers using fully defined small molecule modulation of WNT signaling and lactate purification techniques as previously described12,13,14. iPSC-CMs were maintained every 2-3 days with a culture medium outlined below.

  1. Prepare a culture medium of basal medium (RPMI 1640.......

Representative Results

figure-representative results-58
Figure 3: Optical action potential (AP) profiles of isolated native cardiomyocytes and human induced pluripotent stem cell derived cardiomyocytes (iPSC-CM). (A) Representative optical AP of a single murine cardiomyocyte (center) with Mean ± SEM of APD50 and APD90 (n = 7, right). (B) Representative optical AP of a singl.......

Discussion

Here we describe a basic protocol to easily acquire detailed AP profiles from isolated iPSC-CMs suitable for electrophysiological modelling and cardiac drug screening. We detect regular, robust APs from our sparsely seeded iPSC-CMs which suggests both indicator functionality and methodological fidelity.

Due to the wide spectrum of commercial methodologies for iPSC reprogramming and lack of standardization for cardiac differentiation protocols, iPSC based models can show immense variability in .......

Acknowledgements

The authors would like to acknowledge Cairn Research Ltd. for their kind financial contribution which covered production costs of this publication. In addition, we thank Ms. Ines Mueller and Ms. Stefanie Kestel for their excellent technical support.

The authors’ research is supported by the German Center for Cardiovascular Research (DZHK), the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation, VO 1568/3-1, IRTG1816 RP12, SFB1002 TPA13 and under Germany’s Excellence Strategy - EXC 2067/1- 390729940) and the Else-Kröner-Fresenius Stiftung (EKFS 2016_A20).

....

Materials

NameCompanyCatalog NumberComments
Reagents
0.25 Trypsin EDTA Gibco 25200056
B27 Supplement Gibco 17504044
CaCl2Carl Roth HN04.2
D(+)-Glucose anhydrous BioChemicaITW ReagentsA1422
Fetal Bovine Serum Gibco 10270-106
FluoVolt Membrane Potential Kit Invitrogen F10488
HEPESCarl Roth HN77.4
KClSigma-Aldrich6781.1
LamaninSigma-Aldrich114956-81-9
Matrigel BD354230
NaCl Sigma-Aldrich9265.2
Nifedipine Sigma-Aldrich21829-25-4
Penicillin/StreptomycinInvitrogen 15140
ROCK Inhibitor Y27632Stemolecule04-0012-10
RPMI 1640 Medium Gibco 61870010
Versene EDTA Gibco 15040033
Equipment
495LP Dichroic Beamsplitter Chroma Technology
Axopatch 200B Amplifier Molecular Devices
Circle Coverslips, Thickness 0Thermo ScientificCB00100RA020MNT0
Digidata 1550BMolecular Devices
Dual OptoLED Power Supply Cairn Research 
ET470/40x Excitation Filter Chroma Technology
ET535/50mChroma Technology
Etched Neubauer HemacytometerHausser Scientific
Filter Cubes Cairn Research 
IX73 Inverted Microscope Olympus 
MonoLEDCairn Research 
Multiport Adaptors Cairn Research 
Myopacer Cell Stimulator IonOptix
Optomask Shutter Cairn Research 
Optoscan System ControllerCairn Research 
PH-1 Temperature Controlled Platform  Warner Instruments 
Photomultiplier Detector Cairn Research 
PMT Amplifier InsertCairn Research 
PMT Supply InsertCairn Research 
RC-26G Open Bath Chamber Warner Instruments 
SA-OLY/2AL Stage Adaptor Olympus 
T565lpxr Dichroic Beamsplitter Chroma Technology
T660lpxr Dichroic BeamsplitterChroma Technology
TC-20 Dual Channel Temperature Controller npi Electronic
UPLFLN 40X ObjectiveOlympus 
USB 3.0 Colour Camera Imaging Source
Software
Clampex 11.1Molecular Devices 
Clampfit 11.1Molecular Devices 
IC Capture 2.4 Imaging Source 
Prism 8Graphpad

References

  1. Miller, E. W. Small molecule fluorescent voltage indicators for studying membrane potential. Current Opinion in Chemical Biology. 33, 74-80 (2016).
  2. Liang, P., et al.

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