Establishment of human pluripotent stem cell-derived bile ductal disease analysis system using microfluidic device
Project/Area Number |
16K15434
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Gastroenterology
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Research Institution | Tokai University |
Principal Investigator |
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Project Period (FY) |
2016-04-01 – 2018-03-31
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥3,380,000 (Direct Cost: ¥2,600,000、Indirect Cost: ¥780,000)
Fiscal Year 2017: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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Keywords | ヒト多能性幹細胞 / 肝分化 / 胆管細胞 / 肝幹細胞 / 再生医療 / 再生医学 / マイクロ・ナノデバイス |
Outline of Final Research Achievements |
The liver is the central organ of maintenance of the metabolism of the living body, and a method of reconstituting the mini-liver from human pluripotent stem cells in vitro has been developed. On the other hand, it has a disadvantage that it does not have a structure of the functional bile duct network which is important for the function of the liver. In this study, we are developing a culture system that can be applied to the analysis and treatment of human bile duct disease, by constructing a system that induces bile duct like structures from human iPS cell-derived hepatic progenitor cell. We also analyzed about the efficient culture system of mini-liver tissue using fluid devices.
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Report
(3 results)
Research Products
(4 results)
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[Journal Article] Identification of a novel alpha-fetoprotein- expressing cell population induced by Jagged1/Notch2 signal in murine fibrotic liver.2017
Author(s)
Yasuhiro Nakano, Sachie Nakao, Hideaki Sumiyoshi, Kenichiro Mikami, Yuri Tanno, Minako Sueoka, Daigo Kasahara, Hiroshi Kimura, Tadashi Moro, Akihide Kamiya, Katsuto Hozumi, Yutaka Inagaki
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Journal Title
Hepatol Commun
Volume: 印刷中
Issue: 3
Pages: 1-15
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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