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Posttranslational modification-dependent FoxO1 target genes in endothelial cells and its medical application

Research Project

Project/Area Number 15K15354
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Endocrinology
Research InstitutionTokyo Medical and Dental University

Principal Investigator

Ogawa Yoshihiro  東京医科歯科大学, 大学院医歯学総合研究科, 教授 (70291424)

Research Collaborator TSUCHIYA Kyoichiro  
SHIBA Kumiko  
Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywordsインスリン抵抗性 / リポカリン2 / 血管内皮細胞 / インスリンシグナル / 培養血管内皮細胞
Outline of Final Research Achievements

Insulin resistance and hyperglycemia activate transcription factor FoxO1 by dephosphorylation and deacetylation, respectively. We aimed to elucidate the pathophysiological roles of FoxO1 in diabetes-associated vascular injury, by identifying target genes of FoxO1 in endothelial cells and examining the regulatory mechanisms by FoxO1. Constitutive active FoxO1 mutant significantly induced Lcn2 (lipocalin-2/NGAL) gene in endothelial cells via Akt/NF-κB-dependent manner. It suggests that FoxO1 promotes type 2 diabetes-associated vascular dysfunction by induction of Lcn2 (lipocalin-2/NGAL) in endothelial cells.

Report

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

    (7 results)

All 2017 2016 2015 Other

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

  • [Journal Article] FoxOs: the biology and pathophysiological roles in diabetes2017

    • Author(s)
      Tsuchiya K, Ogawa Y
    • Journal Title

      J Diabetes Investigation

      Volume: - Issue: 6 Pages: 726-734

    • DOI

      10.1111/jdi.12651

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Roles for cell-cell adhesion and contact in obesity-induced hepatic myeloid cell accumulation and glucose intolerance.2017

    • Author(s)
      Miyachi Y, Tsuchiya K, Komiya C, Shiba K, Shimazu N, Yamaguchi S, Deushi M, Osaka M, Inoue K, Sato Y, Matsumoto S, Kikuta J, Wake K, Yoshida M, Ishii M, Ogawa Y
    • Journal Title

      Cell Rep.

      Volume: 18 Issue: 11 Pages: 2766-2779

    • DOI

      10.1016/j.celrep.2017.02.039

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] FoxOs2015

    • Author(s)
      土屋恭一郎、小川佳宏
    • Journal Title

      Diabetes Frontier

      Volume: 26 Pages: 765-772

    • Related Report
      2015 Research-status Report
  • [Presentation] 血管内皮細胞の代謝シグナルを介した臓器機能調節機構2016

    • Author(s)
      土屋恭一郎、小川佳宏
    • Organizer
      第37回日本肥満学会
    • Place of Presentation
      東京ファッションタウン(東京都・江東区)
    • Year and Date
      2016-10-07
    • Related Report
      2016 Annual Research Report
  • [Presentation] 糖代謝異常における内皮細胞を介した臓器機能調節機構2016

    • Author(s)
      土屋恭一郎、宮地康高、山口 忍、小川佳宏
    • Organizer
      第89回日本内分泌学会学術総会
    • Place of Presentation
      京都 国立京都国際会館
    • Year and Date
      2016-04-21
    • Related Report
      2015 Research-status Report
  • [Remarks] 東京医科歯科大学大学院医歯学総合研究科分子内分泌代謝学分野

    • URL

      http://www.tmd.ac.jp/grad/cme/

    • Related Report
      2016 Annual Research Report
  • [Remarks] 東京医科歯科大学大学院医歯学総合研究科分子内分泌代謝学分野

    • URL

      http://www.tmd.ac.jp/grad/cme/index.html

    • Related Report
      2015 Research-status Report

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Published: 2015-04-16   Modified: 2018-03-22  

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