ArticlePLoS computational biology2026
Real-time GPU-accelerated coupled cardiac system: Integrating bidirectional interactions between living optogenetic monolayers and computational simulations.
Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
1 citing paper in PubMed.
- Smart Optogenetics for Real-Time Automated Control of Cardiac Electrical Activity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
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Authors and funding
4 authors.
Funding
Abstract
objectiveReentrant arrhythmias are life-threatening cardiac events that are difficult to study due to limited experimental control over the complex circuit dynamics. We present a real-time coupled cardiac system that allows in real-time dynamic manipulation of reentrant pathways in vitro using physiologically relevant simulations.
methodsWe designed a closed-feedback loop system that couples a cultured cardiac monolayer with a two-dimensional computational simulation of cardiac tissue. The simulation, based on GPU-accelerated models (e.g., cellular automata), predicts wave propagation in real-time using the Abubu.js library. Optical mapping captures monolayer activation patterns, and simulation outputs are converted into light-based stimulation via optogenetics, using LEDs and microcontrollers to depolarize cardiac tissue.
resultsOur platform is capable of accurately detecting and responding to electrical waves in real-time, enabling interactive modulation of reentrant circuits. The system replaces traditional fixed-delay stimulation protocols with computationally guided interventions, better mimicking physiological conduction dynamics.
conclusionThis coupled system provides a novel and responsive method to study reentrant arrhythmias. Its integration of optical stimulation, real-time modeling, and tissue feedback enables the construction of user-defined reentry pathways and dynamic interaction with reentrant circuit behavior. SIGNIFICANCE: By merging computational and biological systems, this work introduces a versatile experimental framework for investigating arrhythmias. Built from inexpensive and accessible components, it lowers technical and financial barriers, increasing accessibility across a broad range of researchers and research environments. The platform may inform future control and anti-arrhythmic strategies and pave the way for personalized cardiac electrophysiology studies.
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Registered trials
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