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Bone-derived factors that act in accordance to bone condition

Research Project

Project/Area Number 26860183
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field General medical chemistry
Research InstitutionHokkaido University (2016)
The University of Tokyo (2014-2015)

Principal Investigator

Sumiya Eriko  北海道大学, 遺伝子病制御研究所, 助教 (50724754)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywords骨分泌因子 / 骨芽細胞 / 臓器間クロストーク
Outline of Final Research Achievements

The aim of this study was to identify bone-derived factor(s) that affect the body and to examine whether the effect was related to the condition of the bone (e.g. sex, age, health condition etc.). First, Igf1 was identified as an osteoblast lineage cell-secreted protein that induces neurite-like structures in cultured cells. Next, to study the physiological effect of Igf1, a genetically-modified mouse that do not produce Igf1 in osteoblasts was generated. Furthermore, a method to estimate bone innervation using mice that express fluorescent proteins in neurons was established. Further studies combining the Igf1 conditional knockout mice and the neuron-labeled mice are required to examine whether the loss of osteoblast-derived Igf1 affects bone innervation.

Report

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

    (5 results)

All 2017 2015 2014

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

  • [Journal Article] Phosphoproteomic analysis of kinase-deficient mice reveals multiple TAK1 targets in osteoclast differentiation.2015

    • Author(s)
      Sumiya E, Negishi-Koga T, Nagai Y, Suematsu A, Suda T, Shinohara M, Sato K, Sanjo H, Akira S, Takayanagi H.
    • Journal Title

      Biochem Biophys Res Commun.

      Volume: 463 Issue: 4 Pages: 1284-90

    • DOI

      10.1016/j.bbrc.2015.06.105

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Diabetic silkworms for evaluation of therapeutically effective drugs against type II diabetes2015

    • Author(s)
      Matsumoto Y, Ishii M, Hayashi Y, Miyazaki S, Sugita T, Sumiya E, Sekimizu K.
    • Journal Title

      Sci Rep

      Volume: 5 Issue: 1 Pages: 10722-10722

    • DOI

      10.1038/srep10722

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] Mesenchymal organizer cell-derived RANKL induces terminal differentiation of LTi cell in the lymph node anlagen2017

    • Author(s)
      Shinichiro Sawa and Eriko Sumiya
    • Organizer
      KTCC 2017
    • Place of Presentation
      京都大学芝蘭会館(京都市)
    • Year and Date
      2017-03-16
    • Related Report
      2016 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 破骨細胞特異的TAK1キナーゼ欠損マウスの解析2015

    • Author(s)
      住谷瑛理子、古賀貴子、篠原正浩、高柳広
    • Organizer
      日本骨代謝学会
    • Place of Presentation
      京王プラザホテル(東京都新宿区)
    • Year and Date
      2015-07-25
    • Related Report
      2015 Research-status Report
  • [Presentation] 神経系の制御に働く骨分泌因子の探索2014

    • Author(s)
      住谷瑛理子、古賀貴子、高柳広
    • Organizer
      第35回日本炎症・再生医学会
    • Place of Presentation
      沖縄、万国津梁館
    • Year and Date
      2014-07-02
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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