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The activation of CBP/beta-catenin signal pathway promotes reprogramming of pluripotency on mice and human cells.

Research Project

Project/Area Number 26861216
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Orthopaedic surgery
Research InstitutionKindai University

Principal Investigator

TAKEHARA Toshiyuki  近畿大学, 医学部, 助教 (60580561)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
KeywordsiPS細胞 / β-catenin / CBP/p300 / リプログラム / 多能性幹細胞 / 転写コアクティベーター / ES細胞 / βcatenin / 再生医療 / beta catenin / リプログラミング / reprogram
Outline of Final Research Achievements

Wnt/beta-catenin signaling pathway is conserved in numerous animal species, and greatly involved in homeostasis mechanism as well as various body developments. We hypothesized the involvement of Wnt/beta catenin, especially CBP/beta catenin signaling pathway is deeply associated with the reprograming of pluripotent stem cell(PSC). In this study, we tried to develop the inducing and culture method of iPS cells independent of characteristics of donor cells. It was promoted reprogramming of fibroblasts to PSC not only in mice but also in human cells by activating the CBP/β-catenin pathway. In addition, it was observed that activation of CBP/β-catenin strongly and positively regulates the maintenance of undifferentiation of mouse PSC as naive state. These results suggest that activation of the CBP/β-catenin pathway is thought to be a highly efficient iPS cell induction and culture method.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (7 results)

All 2017 2015 Other

All Journal Article (1 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 1 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results) Presentation (3 results) (of which Int'l Joint Research: 1 results) Remarks (3 results)

  • [Journal Article] Cdh2 stabilizes FGFR1 and contributes to primed-state pluripotency in mouse epiblast stem cells2015

    • Author(s)
      Toshiyuki Takehara
    • Journal Title

      Scientific Reports

      Volume: 5 Issue: 1 Pages: 14722-14722

    • DOI

      10.1038/srep14722

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Presentation] β-catenin経路に着目した新規iPS細胞誘導技術の開発2017

    • Author(s)
      竹原俊幸、寺村岳士、小野寺勇太、福田寛二
    • Organizer
      第16回日本再生医療学会
    • Place of Presentation
      仙台国際センター 宮城県
    • Year and Date
      2017-03-07
    • Related Report
      2016 Annual Research Report
  • [Presentation] THE ACTIVATION OF CBP/BETA-CATENIN SIGNAL PATHWAY IS INVOLVED IN THE TRANSITION FROM PRIMED- TO NAIVE STATE ON MICE PLURIPOTENT STEM CELLS2015

    • Author(s)
      Toshiyuki Takehara
    • Organizer
      International Society for Stem Cell Research
    • Place of Presentation
      Stockholm, Sweden
    • Year and Date
      2015-06-24 – 2015-06-27
    • Related Report
      2014 Research-status Report
  • [Presentation] The activation of CBP/beta-catenin signal pathway is involved in the transition from primed- to naïve state on mice pluripotent stem cells2015

    • Author(s)
      Toshiyuki Takehara
    • Organizer
      International Society for Stem Cell Research
    • Place of Presentation
      Stockholm, Sweden
    • Year and Date
      2015-06-24
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Remarks] 近畿大学医学部附属病院高度先端総合医療センター 再生医療部

    • URL

      http://www.med.kindai.ac.jp/stemcell/

    • Related Report
      2016 Annual Research Report
  • [Remarks] 近畿大学高度先端総合医療センター再生医療部

    • URL

      http://www.med.kindai.ac.jp/stemcell/

    • Related Report
      2015 Research-status Report
  • [Remarks] 近畿大学医学部附属病院 高度先端総合医療センター 再生医療部

    • URL

      http://www.med.kindai.ac.jp/stemcell/

    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2020-01-20  

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