TY - JOUR
T1 - Robust production of human neural cells by establishing neuroepithelial-like stem cells from peripheral blood mononuclear cell-derived feeder-free iPSCs under xeno-free conditions
AU - Isoda, Miho
AU - Kohyama, Jun
AU - Iwanami, Akio
AU - Sanosaka, Tsukasa
AU - Sugai, Keiko
AU - Yamaguchi, Ryo
AU - Matsumoto, Takuya
AU - Nakamura, Masaya
AU - Okano, Hideyuki
N1 - Funding Information:
We would like to thank Dr. Yonehiro Kanemura (Osaka National Hospital) for human fetal forebrain tissue-derived neurosphere lines (oh-NSC-3-fb and oh-NSC-7-fb), Dr. Shinya Yamanaka, Keisuke Okita and Masato Nakagawa (Kyoto University) for hiPSC clones (201B7, 1210B2, and 1231A3), and Dr. Austin Smith (University of Cambridge) for AF22 and SAI1. We are also grateful for Dr. Shigeki Ohta for valuable advice regarding this research, Dr. Zhi Zhou for valuable advice in figure preparation, and all the other members of the Okano laboratory for their encouragement and support. This research is supported by the Research Project for Practical Application of Regenerative Medicine from the Japan Agency for Medical Research and Development, AMED (to J.K., A.I. and M.N.). This work was also supported by the Research Center Network for Realization of Regenerative Medicine from the Japan Science and Technology Agency (JST) and the AMED (to H.O. and M.N.).
Publisher Copyright:
© 2016 Elsevier Ireland Ltd and Japan Neuroscience Society
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Neural stem/progenitor cells (NS/PCs) derived from human induced pluripotent stem cells (hiPSCs) are expected to be a valuable cell source for cell therapies that target central nervous system disorders. For clinical applications, NS/PCs should be induced and maintained under clinical grade conditions, which are challenging to achieve. In the present study, we established a procedure to obtain xeno-free long-term self-renewing neuroepithelial-like stem cells (xf-lt-NES cells) from feeder-free hiPSCs using a newly developed xeno-free medium, StemFit®AS200. xf-lt-NES cells were cultured for long periods in StemFit®AS200 while retaining normal karyotypes, NS/PC marker expression and differentiation capacity for neuronal and glial differentiation in vitro and in vivo. Furthermore, the cells were cryopreserved using a defined serum-free freezing reagent, which demonstrated the feasibility of this xeno-free culture system for large-scale lt-NES cell production and cell banking. Taken together, our system represents a promising approach for the manufacture of clinically relevant products for cell therapy using NS/PCs.
AB - Neural stem/progenitor cells (NS/PCs) derived from human induced pluripotent stem cells (hiPSCs) are expected to be a valuable cell source for cell therapies that target central nervous system disorders. For clinical applications, NS/PCs should be induced and maintained under clinical grade conditions, which are challenging to achieve. In the present study, we established a procedure to obtain xeno-free long-term self-renewing neuroepithelial-like stem cells (xf-lt-NES cells) from feeder-free hiPSCs using a newly developed xeno-free medium, StemFit®AS200. xf-lt-NES cells were cultured for long periods in StemFit®AS200 while retaining normal karyotypes, NS/PC marker expression and differentiation capacity for neuronal and glial differentiation in vitro and in vivo. Furthermore, the cells were cryopreserved using a defined serum-free freezing reagent, which demonstrated the feasibility of this xeno-free culture system for large-scale lt-NES cell production and cell banking. Taken together, our system represents a promising approach for the manufacture of clinically relevant products for cell therapy using NS/PCs.
KW - Long-term self-renewing neuroepithelial-like stem cells (lt-NES cells)
KW - Neural induction
KW - Peripheral blood mononuclear cell-derived feeder-free human iPSCs
KW - Regenerative medicine
KW - Xeno-free
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U2 - 10.1016/j.neures.2016.04.003
DO - 10.1016/j.neures.2016.04.003
M3 - Article
C2 - 27083781
AN - SCOPUS:84964627190
SN - 0168-0102
VL - 110
SP - 18
EP - 28
JO - Neuroscience Research
JF - Neuroscience Research
ER -