Key result
FLOE enables motion-artifact-free optical mapping of voltage and calcium in contracting cardiomyocytes without uncouplers.
Why the study?
High-throughput, contact-free methods for directly measuring excitation-contraction coupling in vitro remain limited.
p-value: p=0.78
A novel fluorescence-lifetime optical electrophysiology method enables high-fidelity, motion-artifact-free mapping of absolute voltage and calcium in contracting cardiomyocytes.
New in vitro imaging method may advance cardiac electrophysiology research; leaves open clinical translation and validation.
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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Millar et al. (2026) studied Cardiac electrophysiology (in vitro). Fluorescence-lifetime optical electrophysiology (FLOE) vs. Standard fluorescence intensity imaging was evaluated on Action potential duration ratio (APD30/APD90) and motion artifact resilience (p=0.78). Fluorescence-lifetime optical electrophysiology (FLOE) enabled high-speed, motion-artifact-free quantitative mapping of membrane potential and calcium transients in contracting cardiomyocytes without pharmacological uncoupling.
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