Key result
All-optical closed-loop holographic stimulation controls wavefront dynamics in ~98% of human iPSC-derived cardiomyocytes.
An all-optical closed-loop control strategy using holographic optogenetics successfully modulated wavefront dynamics in human iPSC-derived cardiomyocytes, establishing a foundation for advanced feedback control of arrhythmias.
Heart diseases can trigger life-threatening arrhythmias by disrupting cardiac contraction wavefront propagation. In contrast to conventional treatments like electrical pacemakers, optogenetics offers high spatial and temporal resolution for non-invasive interrogation and modulation of cellular activity. However, combining sensing and actuation into a real-time control loop remains challenging. A major obstacle is the data load associated with dense sensor arrays typically required for spatially resolved wavefront monitoring. To overcome this, we present an all-optical, closed-loop control strategy using adaptive holographic stimulation and sparsely sampled, label-free imaging data, enabling robust classification and quantitative characterization of spatial wavefront properties in real time. We successfully demonstrate spatiotemporal optogenetic closed-loop control of wavefront dynamics in functional syncytia of human induced pluripotent stem cell-derived cardiomyocytes in at least 107 out of 109 evaluated cases across all experiments. This framework establishes a foundation for advanced feedback control strategies aimed at mimicking, detecting and terminating abnormal propagation patterns.
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Wendland et al. (2026) studied Arrhythmias (n=109). All-optical closed-loop control using adaptive holographic stimulation was evaluated on Spatiotemporal optogenetic closed-loop control of wavefront dynamics. All-optical closed-loop control using adaptive holographic stimulation successfully controlled wavefront dynamics in human iPSC-derived cardiomyocytes in at least 107 of 109 evaluated cases (98.2%).
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