TY - JOUR
T1 - Modeling the marmoset brain using embryonic stem cell-derived cerebral assembloids
AU - Kodera, Tomoki
AU - Takeuchi, Ryosuke F.
AU - Takahashi, Sara
AU - Suzuki, Keiichiro
AU - Kassai, Hidetoshi
AU - Aiba, Atsu
AU - Shiozawa, Seiji
AU - Okano, Hideyuki
AU - Osakada, Fumitaka
N1 - Funding Information:
This study was supported by Grants-in-Aid from the Japan Society for the Promotion of Science (F.O., K.S.), Brain/MINDS from the Japan Agency for Medical Research and Development (F.O., A.A.: JP15dm0207032 ), and CREST from the Japan Science and Technology Agency (F.O.).
Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/5/21
Y1 - 2023/5/21
N2 - Studying the non-human primate (NHP) brain is required for the translation of rodent research to humans, but remains a challenge for molecular, cellular, and circuit-level analyses in the NHP brain due to the lack of in vitro NHP brain system. Here, we report an in vitro NHP cerebral model using marmoset (Callithrix jacchus) embryonic stem cell-derived cerebral assembloids (CAs) that recapitulate inhibitory neuron migration and cortical network activity. Cortical organoids (COs) and ganglionic eminence organoids (GEOs) were induced from cjESCs and fused to generate CAs. GEO cells expressing the inhibitory neuron marker LHX6 migrated toward the cortical side of CAs. COs developed their spontaneous neural activity from a synchronized pattern to an unsynchronized pattern as COs matured. CAs containing excitatory and inhibitory neurons showed mature neural activity with an unsynchronized pattern. The CAs represent a powerful in vitro model for studying excitatory and inhibitory neuron interactions, cortical dynamics, and their dysfunction. The marmoset assembloid system will provide an in vitro platform for the NHP neurobiology and facilitate translation into humans in neuroscience research, regenerative medicine, and drug discovery.
AB - Studying the non-human primate (NHP) brain is required for the translation of rodent research to humans, but remains a challenge for molecular, cellular, and circuit-level analyses in the NHP brain due to the lack of in vitro NHP brain system. Here, we report an in vitro NHP cerebral model using marmoset (Callithrix jacchus) embryonic stem cell-derived cerebral assembloids (CAs) that recapitulate inhibitory neuron migration and cortical network activity. Cortical organoids (COs) and ganglionic eminence organoids (GEOs) were induced from cjESCs and fused to generate CAs. GEO cells expressing the inhibitory neuron marker LHX6 migrated toward the cortical side of CAs. COs developed their spontaneous neural activity from a synchronized pattern to an unsynchronized pattern as COs matured. CAs containing excitatory and inhibitory neurons showed mature neural activity with an unsynchronized pattern. The CAs represent a powerful in vitro model for studying excitatory and inhibitory neuron interactions, cortical dynamics, and their dysfunction. The marmoset assembloid system will provide an in vitro platform for the NHP neurobiology and facilitate translation into humans in neuroscience research, regenerative medicine, and drug discovery.
KW - Cerebral cortex
KW - Inhibitory neurons
KW - Marmoset
KW - Migration
KW - Organoids
KW - Spontaneous neural activity
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U2 - 10.1016/j.bbrc.2023.03.019
DO - 10.1016/j.bbrc.2023.03.019
M3 - Article
C2 - 37002985
AN - SCOPUS:85151472810
SN - 0006-291X
VL - 657
SP - 119
EP - 127
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
ER -