Fluorescence-lifetime optical electrophysiology in contracting cardiomyocytes

Precise monitoring of cardiac electrophysiology in vitro is crucial to understanding heart function and cardiac disease. However, high-throughput, contact-free methods for directly measuring excitation-contraction coupling remain limited. Here, we introduce a new paradigm for quantitative electrophysiological imaging that combines fluorescence lifetime and intensity information to capture dynamic cardiac signals with high fidelity. We show that lifetime measurements are intrinsically decoupled from motion artifacts and provide calibrated calcium concentration and membrane potential readouts across wide fields of view. Using a gated single-photon avalanche diode camera, we acquire fluorescence lifetime images at up to 200 frames per second with sufficient signal-to-noise ratio such that each frame contains meaningful lifetime information without temporal averaging. This approach yields spatially resolved maps of absolute voltage and calcium values across contracting cardiomyocyte monolayers, revealing heterogeneous cell behaviors within individual assays and uncovering previously unreported dynamics during late-phase repolarization for real-time analysis of excitation-contraction coupling.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-13
DOI
https://doi.org/10.64898/2026.01.12.699013
Primary Topic
Cardiac electrophysiology and arrhythmias
Type
article
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article

Fluorescence-lifetime optical electrophysiology in contracting cardiomyocytes

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bioRxiv (Cold Spring Harbor Laboratory)
Cardiac electrophysiology and arrhythmias
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Fluorescence-lifetime optical electrophysiology in contracting cardiomyocytes

Jiuxuan Zhao, Eline Huethorst, Edoardo Charbon, Claudio Bruschini, G. Bellingham Smith, Vytautas Žičkus, G. Astrauskaite, Euan Millar, Daniele Faccio, Gregor Gibson Taylor
article en

Abstract

Precise monitoring of cardiac electrophysiology in vitro is crucial to understanding heart function and cardiac disease. However, high-throughput, contact-free methods for directly measuring excitation-contraction coupling remain limited. Here, we introduce a new paradigm for quantitative electrophysiological imaging that combines fluorescence lifetime and intensity information to capture dynamic cardiac signals with high fidelity. We show that lifetime measurements are intrinsically decoupled from motion artifacts and provide calibrated calcium concentration and membrane potential readouts across wide fields of view. Using a gated single-photon avalanche diode camera, we acquire fluorescence lifetime images at up to 200 frames per second with sufficient signal-to-noise ratio such that each frame contains meaningful lifetime information without temporal averaging. This approach yields spatially resolved maps of absolute voltage and calcium values across contracting cardiomyocyte monolayers, revealing heterogeneous cell behaviors within individual assays and uncovering previously unreported dynamics during late-phase repolarization for real-time analysis of excitation-contraction coupling.

bioRxiv (Cold Spring Harbor Laboratory)
Center for Physical Sciences and Technology (LT), École Polytechnique Fédérale de Lausanne (CH), University of Glasgow (GB)
Openalex Percentile: Top 89%
Cardiac electrophysiology and arrhythmias
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