Brainstem organoids from human pluripotent stem cells contain neural crest population
Author:
Eura Nobuyuki, Matsui Takeshi K., Luginbühl Joachim, Matsubayashi Masaya, Nanaura Hitoki, Shiota Tomo, Kinugawa Kaoru, Iguchi Naohiko, Kiriyama TakaoORCID, Zheng Canbin, Kouno Tsukasa, Lan Yan Jun, Kongpracha Pornparn, Wiriyasermkul Pattama, Sakaguchi Yoshihiko M., Nagata Riko, Komeda Tomoya, Morikawa Naritaka, Kitayoshi Fumika, Jong Miyong, Kobashigawa Shinko, Nakanishi Mari, Hasegawa Masatoshi, Saito Yasuhiko, Shiromizu Takashi, Nishimura Yuhei, Kasai Takahiko, Takeda Maiko, Kobayashi Hiroshi, Inagaki Yusuke, Tanaka Yasuhito, Makinodan Manabu, Kishimoto Toshifumi, Kuniyasu Hiroki, Nagamori Shushi, Muotri Alysson R.ORCID, Shin Jay W., Sugie Kazuma, Mori EiichiroORCID
Abstract
SummaryThe brainstem controls heartbeat, blood pressure and respiration, which are life-sustaining functions, therefore, disorders of the brainstem can be lethal. Brain organoids derived from human pluripotent stem cells recapitulate the course of human brain development and are expected to be useful for medical research on central nervous system disorders. However, existing organoid models have limitations, hampering the elucidation of diseases affecting specific components of the brain. Here, we developed a method to generate human brainstem organoids (hBSOs), containing neural crest stem cells as well as midbrain/hindbrain progenitors, noradrenergic and cholinergic neurons, and dopaminergic neurons, demonstrated by specific electrophysiological signatures. Single-cell RNA sequence analysis, together with proteomics and electrophysiology, revealed that the cellular population in these organoids was similar to that of the human brainstem and neural crest, which raises the possibility of making use of hBSOs in grafting for transplantation, efficient drug screenings and modeling the neural crest diseases.
Publisher
Cold Spring Harbor Laboratory
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