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The establishment of vascular cell differentiation system from human ES/iPS cells and its application for the clarification of vascular pathology

Research Project

Project/Area Number 26860557
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Cardiovascular medicine
Research InstitutionKyoto University

Principal Investigator

Taura Daisuke  京都大学, 医学(系)研究科(研究院), 助教 (10558612)

Research Collaborator Masakatsu Sone  
Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords血管細胞誘導 / iPS細胞
Outline of Final Research Achievements

Embryonic stem (ES) cells and induced pluripotent stem (iPS) cells have the potential to serve as a tool to investigate human development/differentiation. We modified our vascular differentiation system of human ES/iPS cells and we have induced vascular cells more effectively and stably from various ES/iPS cell clones without any feeder cells.
Using the iPS cells from patients with genetic abnormalities (patient-specific iPS cells) in vessels, we can observe vascular differentiation/development in vitro and identify new susceptibility genes associated with vascular abnormalities. Applying our differentiation system for Moyamoya-iPS, ADPKD-iPS and Takayasu-iPS cells, we have identified several molecules whose expression levels were upregulated or downregulated in vascular cells differentiated from patient-specific-iPSCs as compared to those from normal Japanese iPSCs. These results would contribute to a novel understanding of vascular abnormalities in each disease.

Report

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

    (9 results)

All 2016 2015 2014

All Journal Article (3 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 3 results,  Acknowledgement Compliant: 3 results,  Open Access: 2 results) Presentation (5 results) Book (1 results)

  • [Journal Article] Impaired adipogenic capacity in induced pluripotent stem cells from lipodystrophic patients with BSCL2 mutations2016

    • Author(s)
      1.E. Mori, J. Fujikura, M. Noguchi, K. Nakao, M. Matsubara, M. Sone, D. Taura, T. Kusakabe, K. Ebihara, T. Tanaka, K. Hosoda, K. Takahashi, I. Asaka, N. Inagaki, K. Nakao
    • Journal Title

      Metablism

      Volume: 65 Issue: 4 Pages: 543-556

    • DOI

      10.1016/j.metabol.2015.12.015

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] Biochemical and functional characterization of RNF213(Mysterin) R4810K, a susceptibility mutation of moyamoya disease, in angiogenesis in vitro and in vivo.2015

    • Author(s)
      Kobayashi H, Matsuda Y, Hitomi T, Okuda H, Shioi H, Matsuda T, Imai H, Sone M, Taura D, Harada KH, Habu T, Takagi Y, Mimyamoto S, Koizumi A.
    • Journal Title

      Journal of the American Heart Association

      Volume: Jun 30;4(7)

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Role of endogenous ACTH on circadian aldpsterone rhythm in patients with primary aldosteronism.2014

    • Author(s)
      Sonoyama T, Sone M, Tamura N, Honda K, Taura D,Kojima K,Fukuda Y,Kanamono N, Miura M, Yasoda A, Arai H, Itoh H, Nakao K.
    • Journal Title

      Endocr.Connect.

      Volume: Dec3(4) Pages: 173-179

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Presentation] ヒトES/iPS細胞由来血管構成細胞の内分泌学的評価および疾患特異的iPS細胞を用いた各疾患血管病態機構の解明2016

    • Author(s)
      田浦大輔、曽根正勝、小嶋勝利、錦見俊雄、長船健二、福田賢英、松尾浩司、八十田明宏、中尾一和、稲垣暢也
    • Organizer
      第89回日本内分泌学会学術総会
    • Place of Presentation
      京都
    • Year and Date
      2016-04-21
    • Related Report
      2015 Annual Research Report
  • [Presentation] ヒトES/iPS細胞からの血管細胞誘導技術の心血管ホルモン解析への応用2015

    • Author(s)
      田浦大輔、曽根正勝、小嶋勝利、本田恭子、福田賢英、錦見俊雄、中尾一和、稲垣暢也
    • Organizer
      第88回日本内分学会学術総会
    • Place of Presentation
      東京
    • Year and Date
      2015-04-25
    • Related Report
      2015 Annual Research Report
  • [Presentation] ヒトES/iPS由来血管構成細胞の性質解析および成熟血管細胞との比較2015

    • Author(s)
      田浦大輔、曽根正勝、長船健二、中尾一和、稲垣暢也
    • Organizer
      第14回 日本再生医療学会総会
    • Place of Presentation
      横浜
    • Year and Date
      2015-03-19
    • Related Report
      2014 Research-status Report
  • [Presentation] ヒトiPS細胞由来血管細胞の内分泌学的性質の解析2014

    • Author(s)
      田浦大輔、曽根正勝、錦見俊雄、小嶋勝利、稲垣暢也、中尾一和
    • Organizer
      第87回 日本内分泌学会学術総会
    • Place of Presentation
      福岡
    • Year and Date
      2014-04-25
    • Related Report
      2014 Research-status Report
  • [Presentation] 患者由来疾患特異的iPS細胞を用いた血管障害疾患の病態解明2014

    • Author(s)
      田浦大輔、曽根正勝、長船健二、稲垣暢也、中尾一和
    • Organizer
      第111回日本内科学会総会
    • Place of Presentation
      東京
    • Year and Date
      2014-04-11
    • Related Report
      2014 Research-status Report
  • [Book] 最新肥満症学2014

    • Author(s)
      田浦大輔
    • Total Pages
      7
    • Publisher
      日本臨床
    • Related Report
      2014 Research-status Report

URL: 

Published: 2014-04-04   Modified: 2017-05-10  

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