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Electrophysiological Characterization of Photoreceptor-like Cells in Retinal Organoids Using Whole-Cell Patch Clamp
Almaqdad Alsalloum1, Daria Kolotova2, Alexey Malyshev2
1Moscow Institute of Physics and Technology, Dolgoprudny, Russia.
Methods in Molecular Biology (Clifton, N.J.)
|April 22, 2026
Summary
The patch clamp technique enables electrophysiological recordings from retinal organoid photoreceptor-like cells. This method characterizes their electrical properties and responses to stimuli, aiding in understanding photoreceptor function.
Area of Science:
- Neuroscience
- Cell Biology
- Electrophysiology
Background:
- Patch clamp electrophysiology is crucial for studying cell membrane electrical properties.
- Retinal organoids offer a model to investigate photoreceptor development and function.
- Understanding photoreceptor electrophysiology is key to comprehending visual processing.
Purpose of the Study:
- To detail the whole-cell patch clamp technique for recording from retinal organoid cells.
- To characterize the electrophysiological properties of photoreceptor-like cells in retinal organoids.
- To demonstrate the response of these cells to electrical stimulation, light, and darkness.
Main Methods:
- Whole-cell patch clamp recordings (voltage clamp and current clamp) were performed.
- Preparation of solutions and fabrication of recording glass electrodes were described.
- Electrophysiological properties and stimulus responses of differentiated cells were measured.
Main Results:
- Patch clamp successfully recorded membrane potential and currents in retinal organoid cells.
- Hyperpolarization and depolarization events were identified in differentiated cells.
- Photoreceptor-like cells exhibited responses to electrical stimuli, light, and darkness.
Conclusions:
- The patch clamp technique is effective for characterizing electrophysiological features of presumptive photoreceptor cells in retinal organoids.
- These findings contribute to understanding the functional development of photoreceptors in vitro.
- The described methods provide a framework for future studies on retinal cell physiology.

