TY - JOUR
T1 - Generation of region-specific and high-purity neurons from human feeder-free iPSCs
AU - Sato, Tsukika
AU - Imaizumi, Kent
AU - Watanabe, Hirotaka
AU - Ishikawa, Mitsuru
AU - Okano, Hideyuki
N1 - Funding Information:
We thank Shinya Yamanaka (Kyoto University) for the generous supply of 414C2 iPSCs, Zhi Zhou (Keio University) for providing helpful advice, and all members of the H.O. laboratory for providing encouragement and kind support. This study was supported by funding from the Japan Agency for Medical Research and Development (AMED) (Grant Number JP20bm0804003 ) to H.O. Japan Society for the Promotion of Science (JSPS) (Grant Numbers JP20J21586 to T.S.; JP19K16927 to K.I.), the General Insurance Association of Japan to K.I. and the Program for the Advancement of Research in Core Projects on Longevity of the Keio University Global Research Institute from Keio University to H.O.
Funding Information:
We thank Shinya Yamanaka (Kyoto University) for the generous supply of 414C2 iPSCs, Zhi Zhou (Keio University) for providing helpful advice, and all members of the H.O. laboratory for providing encouragement and kind support. This study was supported by funding from the Japan Agency for Medical Research and Development (AMED) (Grant Number JP20bm0804003) to H.O. Japan Society for the Promotion of Science (JSPS) (Grant Numbers JP20J21586 to T.S.; JP19K16927 to K.I.), the General Insurance Association of Japan to K.I. and the Program for the Advancement of Research in Core Projects on Longevity of the Keio University Global Research Institute from Keio University to H.O.
Publisher Copyright:
© 2021 The Author(s)
PY - 2021/2/16
Y1 - 2021/2/16
N2 - Human induced pluripotent stem cells (iPSCs) have great potential to elucidate the molecular pathogenesis of neurological/psychiatric diseases. In particular, neurological/psychiatric diseases often display brain region-specific symptoms, and the technology for generating region-specific neural cells from iPSCs has been established for detailed modeling of neurological/psychiatric disease phenotypes in vitro. On the other hand, recent advances in culturing human iPSCs without feeder cells have enabled highly efficient and reproducible neural induction. However, conventional regional control technologies have mainly been developed based on on-feeder iPSCs, and these methods are difficult to apply to feeder-free (ff) iPSC cultures. In this study, we established a novel culture system to generate region-specific neural cells from human ff-iPSCs. This system is the best optimized approach for feeder-free iPSC culture and generates specific neuronal subtypes with high purity and functionality, including forebrain cortical neurons, forebrain interneurons, midbrain dopaminergic neurons, and spinal motor neurons. In addition, the temporal patterning of cortical neuron layer specification in the forebrain was reproduced in our culture system, which enables the generation of layer-specific cortical neurons. Neuronal activity was demonstrated in the present culture system by using multiple electrode array and calcium imaging. Collectively, our ff-iPSC-based culture system would provide a desirable platform for modeling various types of neurological/psychiatric disease phenotypes.
AB - Human induced pluripotent stem cells (iPSCs) have great potential to elucidate the molecular pathogenesis of neurological/psychiatric diseases. In particular, neurological/psychiatric diseases often display brain region-specific symptoms, and the technology for generating region-specific neural cells from iPSCs has been established for detailed modeling of neurological/psychiatric disease phenotypes in vitro. On the other hand, recent advances in culturing human iPSCs without feeder cells have enabled highly efficient and reproducible neural induction. However, conventional regional control technologies have mainly been developed based on on-feeder iPSCs, and these methods are difficult to apply to feeder-free (ff) iPSC cultures. In this study, we established a novel culture system to generate region-specific neural cells from human ff-iPSCs. This system is the best optimized approach for feeder-free iPSC culture and generates specific neuronal subtypes with high purity and functionality, including forebrain cortical neurons, forebrain interneurons, midbrain dopaminergic neurons, and spinal motor neurons. In addition, the temporal patterning of cortical neuron layer specification in the forebrain was reproduced in our culture system, which enables the generation of layer-specific cortical neurons. Neuronal activity was demonstrated in the present culture system by using multiple electrode array and calcium imaging. Collectively, our ff-iPSC-based culture system would provide a desirable platform for modeling various types of neurological/psychiatric disease phenotypes.
KW - Feeder-free iPSCs
KW - Neural differentiation
KW - Regional identity control
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UR - http://www.scopus.com/inward/citedby.url?scp=85100427727&partnerID=8YFLogxK
U2 - 10.1016/j.neulet.2021.135676
DO - 10.1016/j.neulet.2021.135676
M3 - Article
C2 - 33516803
AN - SCOPUS:85100427727
SN - 0304-3940
VL - 746
JO - Neuroscience Letters
JF - Neuroscience Letters
M1 - 135676
ER -