Unified Generation of Regionalized Neural Organoids from Single-Lumen Neuroepithelium

Human brain development begins with the formation of the neural tube, a neuroepithelium organized around a single continuous lumen that is patterned to specify distinct brain regions. Human pluripotent stem cell (hPSC)-derived neural organoids offer powerful models to study this process and its disruption in disease. However, most existing protocols rely on stochastic self-organization of hPSC aggregates, leading to high variability in tissue architecture and cell type composition, which limits reproducibility and fidelity to natural development. This variability has also hindered the broader adoption of brain organoid technology in translational and pharmaceutical research, where robustness and standardization are critical. Here, we present a scalable and reproducible platform that uses uniform, single-lumen neuroepithelium (SLN) as a standardized starting point for generating diverse, regionally specified neural organoids. SLNs form with high efficiency and reproducibility, can be patterned along dorso-ventral and anterior-posterior axes, and mature in suspension culture into organoids representing forebrain, midbrain, hindbrain, and neural retina. This unified and scalable approach provides a reproducible foundation for modeling human brain development, offering broad translational potential for mechanistic studies, disease modeling, and drug discovery.