2024-03-29T05:14:45Z
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2022-12-14T03:54:11Z
461:848:849
Differentiation of Monkey Embryonic Stem Cells to Hepatocytes by Feeder-Free Dispersion Culture and Expression Analyses of Cytochrome P450 Enzymes Responsible for Drug Metabolism
Maruyama, Junya
Matsunaga, Tamihide
Yamaori, Satoshi
Sakamoto, Sakae
Kamada, Noboru
Nakamura, Katsunori
Kikuchi, Shinji
Ohmori, Shigeru
信州大学博士(医学)・学位論文・平成25年2月13日授与(乙第1155号)・丸山 順也
We reported previously that monkey embryonic stem cells (ESCs) were differentiated into hepatocytes by formation of embryoid bodies (EBs). However, this EB formation method is not always efficient for assays using a large number of samples simultaneously. A dispersion culture system, one of the differentiation methods without EB formation, is able to more efficiently provide a large number of feeder-free undifferentiated cells. A previous study demonstrated the effectiveness of the Rho-associated kinase inhibitor Y-27632 for feeder-free dispersion culture and induction of differentiation of monkey ESCs into neural cells. In the present study, the induction of differentiation of cynomolgus monkey ESCs (cmESCs) into hepatocytes was performed by the dispersion culture method, and the expression and drug inducibility of cytochrome P450 (CYP) enzymes in these hepatocytes were examined. The cmESCs were successfully differentiated into hepatocytes under feeder-free dispersion culture conditions supplemented with Y-27632. The hepatocytes differentiated from cmESCs expressed the mRNAs for three hepatocyte marker genes (alpha-fetoprotein, albumin, CYP7A1) and several CYP enzymes, as measured by real-time polymerase chain reaction. In particular, the basal expression of cmCYP3A4 (3A8) in these hepatocytes was detected at mRNA and enzyme activity (testosterone 6 beta-hydroxylation) levels. Furthermore, the expression and activity of cmCYP3A4 (3A8) were significantly upregulated by rifampicin. These results indicated the effectiveness of Y-27632 supplementation for feeder-free dispersed culture and induction of differentiation into hepatocytes, and the expression of functional CYP enzyme(s) in cmESC-derived hepatic cells.
Article
BIOLOGICAL & PHARMACEUTICAL BULLETIN. 36(2) 292-298 (2013)
journal article
PHARMACEUTICAL SOC JAPAN
2013-02
application/pdf
BIOLOGICAL & PHARMACEUTICAL BULLETIN
2
36
292
298
https://soar-ir.repo.nii.ac.jp/record/7177/files/H24Otsu1155_Maruyama.pdf
eng
10.1248/bpb.b12-00866
https://doi.org/10.1248/bpb.b12-00866
Copyright (c) 2013 The Pharmaceutical Society of Japan