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Basic research for development of artificial liver stem cell

Research Project

Project/Area Number 25640055
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Laboratory animal science
Research InstitutionCentral Institute for Experimental Animals

Principal Investigator

SUEMIZU Hiroshi  公益財団法人実験動物中央研究所, その他部局等, 研究員 (40332209)

Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords肝再生 / 肝幹細胞 / ヒト化マウス / FucciTgマウス / Tg-Fucci-S/G2/M-Greenマウス
Outline of Final Research Achievements

The purpose of this study is to identify the genuine liver stem cells that have the ability to reconstitute a liver, and is to create artificial cell with equivalent capabilities to liver stem cells. We established a simple method for inducing direct hyperplasia and compensatory regeneration of hepatocytes by administration of thioacetamide and ganciclovir to HSVtk transgenic mice, respectively. The future challenge is to establish a method for collecting proliferative liver cells, which appeared in both regenerative patterns. We identified 22 genes involved in growth promotion, and 181 genes involved in hepatic maturation by analyzing a cryopreserved human hepatocytes that are well engrafted in injured liver of TK-NOG mice. On the basis of these findings, we will advance in the exploration of “genuine liver stem cells” and the development of “humanized-liver mice model”.

Report

(3 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • Research Products

    (4 results)

All 2014 2013

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 2 results) Presentation (1 results)

  • [Journal Article] A Novel Enhanced Green FluorescentProtein-Expressing NOG Mouse for Analyzingthe Microenvironment of Xenograft Tissues2014

    • Author(s)
      Yuichiro Higuchi, Kenji Kawai, Masafumi Yamamoto, Miyuki Kuronuma, Yasuhiko Ando, Ikumi Katano, Masato Nakamura, Hiroshi Suemizu
    • Journal Title

      Experimental Animals

      Volume: 63 Issue: 1 Pages: 55-62

    • DOI

      10.1538/expanim.63.55

    • NAID

      130003391611

    • ISSN
      0007-5124, 1341-1357, 1881-7122
    • Related Report
      2014 Annual Research Report 2013 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] contributed equally to this work. Hepatocytes buried in the cirrhotic livers of biliary atresia patients proliferate and function in the liver of uPA-NOG mice2014

    • Author(s)
      Suemizu H, Nakamura K, Kawai K, Higuchi Y, Kasahara M, Fujimoto J, Tanoue A, Nakamura M
    • Journal Title

      Liver Transplantation

      Volume: (In press) Issue: 9 Pages: 1127-1137

    • DOI

      10.1002/lt.23916

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] The human hepatic cell line HepaRG as a possible cell source for the generation of humanized liver TK-NOG mice2014

    • Author(s)
      Higuchi Y, Kawai K, Yamazaki H, Nakamura M, Bree F, Guguen-Guillouzo C, Suemizu H
    • Journal Title

      Xenobiotica

      Volume: 44 Pages: 146-153

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Presentation] The human hepatic cell line HepaRG® as a possible cell source for the steady generation of humanized liver TK-NOG mice2013

    • Author(s)
      Hiroshi Suemizu, Yuichiro Higuchi, Kenji Kawai, Hiroshi Yamazaki, Françoise Bree, Christiane Guguen-Guillouzo, and Masato Nakamura
    • Organizer
      4th International Workshop on Humanized Mice
    • Place of Presentation
      韓国、ソウル
    • Related Report
      2013 Research-status Report

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Published: 2014-07-25   Modified: 2019-07-29  

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