TY - JOUR
T1 - Naive-like ESRRB+ iPSCs with the Capacity for Rapid Neural Differentiation
AU - Kisa, Fumihiko
AU - Shiozawa, Seiji
AU - Oda, Keisuke
AU - Yoshimatsu, Sho
AU - Nakamura, Mari
AU - Koya, Ikuko
AU - Kawai, Kenji
AU - Suzuki, Sadafumi
AU - Okano, Hideyuki
N1 - Funding Information:
We thank Drs. T. Sanosaka, D. Sipp, F. Renault-Mihara, and S. Morimoto for helpful discussions and technical assistance and all members of the H.O. laboratory for generous support. We also thank Prof. Shinya Yamanaka (Kyoto University) for the human iPSC (201B7). The piggyBac transposase expression vector was kindly provided by Dr. Kosuke Yusa (Wellcome Trust Sanger Institute). Portions of this study were the result of the “Construction of System for Spread of Primate Model Animals,” which was performed under the Strategic Research Program for Brain Sciences of the MEXT and the AMED (to H.O and S.S.), and Scientific Research in Innovative Areas, which is the MEXT Grant-in-Aid Project FY2014-2018: “Brain Protein Aging and Dementia Control” (to H.O.). H.O. is a compensated scientific consultant of San Bio and K-Pharma. F.K. and K.O. are paid by the Ono Pharmaceutical.
Publisher Copyright:
© 2017 The Authors
PY - 2017/12/12
Y1 - 2017/12/12
N2 - Several groups have reported the existence of a form of pluripotency that resembles that of mouse embryonic stem cells (mESCs), i.e., a naive state, in human pluripotent stem cells; however, the characteristics vary between reports. The nuclear receptor ESRRB is expressed in mESCs and plays a significant role in their self-renewal, but its expression has not been observed in most naive-like human induced pluripotent stem cells (hiPSCs). In this study, we modified several methods for converting hiPSCs into a naive state through the transgenic expression of several reprogramming factors. The resulting cells express the components of the core transcriptional network of mESCs, including ESRRB, at high levels, which suggests the existence of naive-state hiPSCs that are similar to mESCs. We also demonstrate that these cells differentiate more readily into neural cells than do conventional hiPSCs. These features may be beneficial for their use in disease modeling and regenerative medicine. Kisa et al. modified several methods for converting human induced pluripotent stem cells (hiPSCs) into a naive state, a form of pluripotency that exists in mouse embryonic stem cells (ESCs). Converted cells express components of the core transcriptional network upregulated in mouse ESCs, including ESRRB. They also show that these cells differentiate more readily into neural cells than do conventional hiPSCs.
AB - Several groups have reported the existence of a form of pluripotency that resembles that of mouse embryonic stem cells (mESCs), i.e., a naive state, in human pluripotent stem cells; however, the characteristics vary between reports. The nuclear receptor ESRRB is expressed in mESCs and plays a significant role in their self-renewal, but its expression has not been observed in most naive-like human induced pluripotent stem cells (hiPSCs). In this study, we modified several methods for converting hiPSCs into a naive state through the transgenic expression of several reprogramming factors. The resulting cells express the components of the core transcriptional network of mESCs, including ESRRB, at high levels, which suggests the existence of naive-state hiPSCs that are similar to mESCs. We also demonstrate that these cells differentiate more readily into neural cells than do conventional hiPSCs. These features may be beneficial for their use in disease modeling and regenerative medicine. Kisa et al. modified several methods for converting human induced pluripotent stem cells (hiPSCs) into a naive state, a form of pluripotency that exists in mouse embryonic stem cells (ESCs). Converted cells express components of the core transcriptional network upregulated in mouse ESCs, including ESRRB. They also show that these cells differentiate more readily into neural cells than do conventional hiPSCs.
KW - human iPSC
KW - naive pluripotency
KW - neural differentiation
KW - reprogramming
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U2 - 10.1016/j.stemcr.2017.10.008
DO - 10.1016/j.stemcr.2017.10.008
M3 - Article
C2 - 29129686
AN - SCOPUS:85033359969
SN - 2213-6711
VL - 9
SP - 1825
EP - 1838
JO - Stem cell reports
JF - Stem cell reports
IS - 6
ER -