TY - JOUR
T1 - Neural organoids for disease phenotyping, drug screening and developmental biology studies
AU - Hartley, Brigham J.
AU - Brennand, Kristen J.
N1 - Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2017/6
Y1 - 2017/6
N2 - 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.
AB - 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.
KW - Cerebral organoids
KW - Disease modeling
KW - Drug screening
KW - Embryonic stem cells
KW - Human induced pluripotent stem cells
UR - http://www.scopus.com/inward/record.url?scp=85008958159&partnerID=8YFLogxK
U2 - 10.1016/j.neuint.2016.10.004
DO - 10.1016/j.neuint.2016.10.004
M3 - Article
C2 - 27744003
AN - SCOPUS:85008958159
SN - 0197-0186
VL - 106
SP - 85
EP - 93
JO - Neurochemistry International
JF - Neurochemistry International
ER -