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Abstract
Human brain organoids replicate much of the cellular diversity and developmental anatomy of the human brain. However, the physiology of neuronal circuits within organoids remains under-explored. With high-density CMOS microelectrode arrays and shank electrodes, we captured spontaneous extracellular activity from brain organoids derived from human induced pluripotent stem cells. We inferred functional connectivity from spike timing, revealing a large number of weak connections within a skeleton of significantly fewer strong connections. A benzodiazepine increased the uniformity of firing patterns and decreased the relative fraction of weakly connected edges. Our analysis of the local field potential demonstrate that brain organoids contain neuronal assemblies of sufficient size and functional connectivity to co-activate and generate field potentials from their collective transmembrane currents that phase-lock to spiking activity. These results point to the potential of brain organoids for the study of neuropsychiatric diseases, drug action, and the effects of external stimuli upon neuronal networks.
Brain organoids replicate cellular organization found in the developing human brain. Here, the authors utilize microelectronics to map activity in brain organoids and assemble functional circuits that mirror complexity found in brain networks in vivo.
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1 University of California Santa Barbara, Neuroscience Research Institute, Santa Barbara, USA (GRID:grid.133342.4) (ISNI:0000 0004 1936 9676); University of California Santa Barbara, Department of Molecular, Cellular and Developmental Biology, Santa Barbara, USA (GRID:grid.133342.4) (ISNI:0000 0004 1936 9676); University of California Santa Cruz, Department of Biomolecular Engineering, Santa Cruz, USA (GRID:grid.205975.c) (ISNI:0000 0001 0740 6917)
2 University of California Santa Barbara, Neuroscience Research Institute, Santa Barbara, USA (GRID:grid.133342.4) (ISNI:0000 0004 1936 9676); University of California Santa Barbara, Department of Molecular, Cellular and Developmental Biology, Santa Barbara, USA (GRID:grid.133342.4) (ISNI:0000 0004 1936 9676)
3 ETH Zürich, Department of Biosystems Science and Engineering, Basel, Switzerland (GRID:grid.5801.c) (ISNI:0000 0001 2156 2780)
4 University of California Santa Barbara, Department of Computer Science, Santa Barbara, USA (GRID:grid.133342.4) (ISNI:0000 0004 1936 9676)
5 University of California San Francisco, Memory and Aging Center, Department of Neurology, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811)
6 University of California San Francisco, Department of Radiology and Biomedical Imaging, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811)
7 University of California Santa Barbara, Neuroscience Research Institute, Santa Barbara, USA (GRID:grid.133342.4) (ISNI:0000 0004 1936 9676)
8 University of California Santa Barbara, Neuroscience Research Institute, Santa Barbara, USA (GRID:grid.133342.4) (ISNI:0000 0004 1936 9676); University of California Santa Barbara, Department of Physics, Santa Barbara, USA (GRID:grid.133342.4) (ISNI:0000 0004 1936 9676)