Identification of neural oscillations and epileptiform changes in human brain organoids.
Updated October 31, 2023Brain organoids represent a powerful tool for studying human neurological diseases, particularly those that affect brain growth and structure. However, many diseases manifest with clear evidence of physiological and network abnormality in the absence of anatomical changes, raising the question of whether organoids possess sufficient neural network complexity to model these conditions. Here, we explore the network-level functions of brain organoids using calcium sensor imaging and extracellular recording approaches that together reveal the existence of complex network dynamics reminiscent of intact brain preparations. We demonstrate highly abnormal and epileptiform-like activity in organoids derived from induced pluripotent stem cells from individuals with Rett syndrome, accompanied by transcriptomic differences revealed by single-cell analyses. We also rescue key physiological activities with an unconventional neuroregulatory drug, pifithrin-α. Together, these findings provide an essential foundation for the utilization of brain organoids to study intact and disordered human brain network formation and illustrate their utility in therapeutic discovery.
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Atlas
Analysis Portals
NoneProject Label
Cortex-MGE-fusion-organoidsSpecies
Homo sapiens
Sample Type
organoids
Anatomical Entity
zone of skin
Organ Part
Unspecified
Selected Cell Types
Unspecified
Model Organ
brain
Disease Status (Specimen)
Rett syndrome
Disease Status (Donor)
Rett syndrome
Development Stage
Library Construction Method
10x 3' v3
Nucleic Acid Source
single cell
Paired End
falseAnalysis Protocol
analysis_protocol_1, analysis_protocol_2File Format
Cell Count Estimate
54.9kDonor Count
2