Neural organoids for disease phenotyping, drug screening and developmental biology studies

Brigham J. Hartley, Kristen J. Brennand

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Human induced pluripotent stem cells (hiPSCs) can theoretically yield limitless supplies of cells fated to any cell type that comprise the human organism, making them a new tool by which to potentially overcome caveats in current biomedical research. In vitro derivation of central nervous system (CNS) cell types has the potential to provide material for drug discovery and validation, safety and toxicity assays, cell replacement therapy and the elucidation of previously unknown disease mechanisms. However, current two-dimensional (2D) CNS differentiation protocols do not faithfully recapitulate the spatial organization of heterogeneous tissue, nor the cell-cell interactions, cell-extracellular matrix interactions, or specific physiological functions generated within complex tissue such as the brain. In an effort to overcome 2D protocol limitations, there have been advancements in deriving highly complicated 3D neural organoid structures. Herein we provide a synopsis of the derivation and application of neural organoids and discuss recent advancements and remaining challenges on the full potential of this novel technological platform.

Original languageEnglish
Pages (from-to)85-93
Number of pages9
JournalNeurochemistry International
Volume106
DOIs
StatePublished - Jun 2017

Keywords

  • Cerebral organoids
  • Disease modeling
  • Drug screening
  • Embryonic stem cells
  • Human induced pluripotent stem cells

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