4.6 Review

Challenges of Organoid Research

Journal

ANNUAL REVIEW OF NEUROSCIENCE
Volume 45, Issue -, Pages 23-39

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-neuro-111020-090812

Keywords

stem cell models; organoids; neural development; neuroscience; human development; modeling human disease

Categories

Funding

  1. National Institutes of Health [U01MH114825, R35NS097305, K99MH125329]
  2. Brain & Behavior Research Foundation Young Investigator Grant

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Organoids derived from human pluripotent stem cells are valuable tools for studying human brain development and neurological diseases. However, their utility is limited by the lack of high-fidelity cell types, limited maturation, atypical physiology, and lack of arealization.
Organoids are 3D cell culture systems derived from human pluripotent stem cells that contain tissue resident cell types and reflect features of early tissue organization. Neural organoids are a particularly innovative scientific advance given the lack of accessibility of developing human brain tissue and intractability of neurological diseases. Neural organoids have become an invaluable approach to model features of human brain development that are not well reflected in animal models. Organoids also hold promise for the study of atypical cellular, molecular, and genetic features that underscore neurological diseases. Additionally, organoids may provide a platform for testing therapeutics in human cells and are a potential source for cell replacement approaches to brain injury or disease. Despite the promising features of organoids, their broad utility is tempered by a variety of limitations yet to be overcome, including lack of high-fidelity cell types, limited maturation, atypical physiology, and lack of arealization, features that may limit their reliability for certain applications.

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