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Establishing mouse forebrain organoids as models of intrinsic cortical network assembly

March 5, 2026
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Sebastian Hernandez, Hunter E. Schweiger, Isabel Cline, Gregory A. Kaurala, Ash Robbins, Daniel Solis, Samira Vera-Choqqueccota, Jinghui Geng, Tjitse Van Der Molen, Francisco Reyes, Chinweike Norman Asogwa, Kateryna Voitiuk, Mattia Chini, Marco Rolandi, Sofie R. Salama, Bradley M. Colquitt, Tal Sharf, David Haussler, Mircea Teodorescu, Mohammed A. Mostajo-Radji
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Abstract

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The mouse cortex is a canonical model for studying how functional neural networks emerge, yet it remains unclear which topological features arise from intrinsic cellular organization versus sensory input. Mouse forebrain organoids provide a powerful system to investigate these intrinsic mechanisms. We generated dorsal (DF) and ventral (VF) forebrain organoids from mouse pluripotent stem cells and tracked their development using longitudinal electrophysiology. DF organoids showed progressively stronger network-wide correlations, while VF organoids developed more refined activity patterns with enhanced small-world topology and increased modular organization. Both organoid types form small-world networks, but their topological organization differs. These differences emerge without extrinsic inputs and correlate with Pvalb+ interneuron enrichment in VF organoids. Our findings demonstrate how cellular composition influences neural circuit self-organization, establishing mouse forebrain organoids as a tractable platform to study cortical network architecture.