Electrophysiological Properties of Human Cortical Organoids: Current State of the Art and Future Directions.

cortical organoids electrophysiology network activity neurodevelopmental disorders neuronal maturation

Journal

Frontiers in molecular neuroscience
ISSN: 1662-5099
Titre abrégé: Front Mol Neurosci
Pays: Switzerland
ID NLM: 101477914

Informations de publication

Date de publication:
2022
Historique:
received: 19 12 2021
accepted: 24 01 2022
entrez: 7 3 2022
pubmed: 8 3 2022
medline: 8 3 2022
Statut: epublish

Résumé

Human cortical development is an intricate process resulting in the generation of many interacting cell types and long-range connections to and from other brain regions. Human stem cell-derived cortical organoids are now becoming widely used to model human cortical development both in physiological and pathological conditions, as they offer the advantage of recapitulating human-specific aspects of corticogenesis that were previously inaccessible. Understanding the electrophysiological properties and functional maturation of neurons derived from human cortical organoids is key to ensure their physiological and pathological relevance. Here we review existing data on the electrophysiological properties of neurons in human cortical organoids, as well as recent advances in the complexity of cortical organoid modeling that have led to improvements in functional maturation at single neuron and neuronal network levels. Eventually, a more comprehensive and standardized electrophysiological characterization of these models will allow to better understand human neurophysiology, model diseases and test novel treatments.

Identifiants

pubmed: 35250479
doi: 10.3389/fnmol.2022.839366
pmc: PMC8888527
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

839366

Subventions

Organisme : Medical Research Council
ID : MR/L01095X/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S011005/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V034758/1
Pays : United Kingdom

Informations de copyright

Copyright © 2022 Zourray, Kurian, Barral and Lignani.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Clara Zourray (C)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.
Developmental Neurosciences, Zayed Centre for Research Into Rare Disease in Children, GOS-Institute of Child Health, University College London, London, United Kingdom.
Department of Pharmacology, UCL School of Pharmacy, London, United Kingdom.

Manju A Kurian (MA)

Developmental Neurosciences, Zayed Centre for Research Into Rare Disease in Children, GOS-Institute of Child Health, University College London, London, United Kingdom.
Department of Neurology, Great Ormond Street Hospital for Children, London, United Kingdom.

Serena Barral (S)

Developmental Neurosciences, Zayed Centre for Research Into Rare Disease in Children, GOS-Institute of Child Health, University College London, London, United Kingdom.

Gabriele Lignani (G)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.

Classifications MeSH