Photostimulation improves maturation of human photoreceptors

Investor logo

Warning

This publication doesn't include Institute of Computer Science. It includes Faculty of Medicine. Official publication website can be found on muni.cz.
Authors

ÇELIKER Canan HRUBÁ Eva KYRIAKOU Konstantina DORGAU Birthe MOLINA GAMBIN Francisco WEISSOVÁ Kamila EDWIN van Oosten PEŠKOVÁ Lucie VAŠKOVICOVÁ Naděžda SAVAGE Michael A HILGEN Gerrit SERNAGOR Evelyne GARANTO Alejandro LAKO Majlinda BÁRTA Tomáš

Year of publication 2026
Type Peer-reviewed scientific article
Magazine / Source Nature communications
MU Faculty or unit

Faculty of Medicine

Citation
web https://www.nature.com/articles/s41467-026-76112-3
Doi https://doi.org/10.1038/s41467-026-76112-3
Keywords RETINAL-PIGMENT EPITHELIUM; VISUAL EXPERIENCE; NEURAL RETINA; CELLS; TRANSPLANTATION; EXPRESSION; TRIGGERS
Description The human retina contains photoreceptor cells that detect light and enable vision. The development of these cells involves a tightly regulated cascade of structural and molecular events, and their dysfunction leads to irreversible blindness in many retinal diseases. Human retinal organoids derived from stem cells have become powerful tools to model retinal development and disease, but they often remain immature and lack key features required for full function. Light is not only the sensory target of photoreceptors but also an important developmental signal in vivo. However, light has rarely been used as a deliberate stimulus during in vitro differentiation. Here we show that exposing retinal organoids to rhythmic light flickering at a specific frequency enhances photoreceptor maturation across multiple levels. This stimulation improves formation of presumptive outer segments, promotes transcriptional shifts from precursor toward more mature photoreceptor states, and is associated with enhanced responsiveness of downstream retinal neurons. These findings identify patterned light as a potent and physiologically relevant signal for driving retinal differentiation in vitro. This approach represents a non-invasive and easily scalable method for improving the quality of retinal organoids, with implications for disease modelling, drug discovery and the preparation of photoreceptors for cell-based therapies.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info