Skip to Content
Merck
  • Sliced Human Cortical Organoids for Modeling Distinct Cortical Layer Formation.

Sliced Human Cortical Organoids for Modeling Distinct Cortical Layer Formation.

Cell stem cell (2020-03-07)
Xuyu Qian, Yijing Su, Christopher D Adam, Andre U Deutschmann, Sarshan R Pather, Ethan M Goldberg, Kenong Su, Shiying Li, Lu Lu, Fadi Jacob, Phuong T T Nguyen, Sooyoung Huh, Ahmet Hoke, Sarah E Swinford-Jackson, Zhexing Wen, Xiaosong Gu, R Christopher Pierce, Hao Wu, Lisa A Briand, H Isaac Chen, John A Wolf, Hongjun Song, Guo-Li Ming
ABSTRACT

Human brain organoids provide unique platforms for modeling development and diseases by recapitulating the architecture of the embryonic brain. However, current organoid methods are limited by interior hypoxia and cell death due to insufficient surface diffusion, preventing generation of architecture resembling late developmental stages. Here, we report the sliced neocortical organoid (SNO) system, which bypasses the diffusion limit to prevent cell death over long-term cultures. This method leads to sustained neurogenesis and formation of an expanded cortical plate that establishes distinct upper and deep cortical layers for neurons and astrocytes, resembling the third trimester embryonic human neocortex. Using the SNO system, we further identify a critical role of WNT/β-catenin signaling in regulating human cortical neuron subtype fate specification, which is disrupted by a psychiatric-disorder-associated genetic mutation in patient induced pluripotent stem cell (iPSC)-derived SNOs. These results demonstrate the utility of SNOs for investigating previously inaccessible human-specific, late-stage cortical development and disease-relevant mechanisms.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
IWR-1, ≥98% (HPLC)
Sigma-Aldrich
DL-Dithiothreitol, ≥98% (HPLC), ≥99.0% (titration)
Sigma-Aldrich
Insulin solution from bovine pancreas, 10 mg/mL insulin in 25  mM HEPES, pH 8.2, BioReagent, sterile-filtered, suitable for cell culture