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Identification of osteoclast-supporting cells and the investigation of the in vivo functions of the cells using mouse ES cells

Research Project

Project/Area Number 17K11898
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Surgical dentistry
Research InstitutionThe University of Tokyo

Principal Investigator

Okayasu Mari  東京大学, 医学部附属病院, 助教 (10610941)

Co-Investigator(Kenkyū-buntansha) 大庭 伸介  東京大学, 大学院医学系研究科(医学部), 准教授 (20466733)
北條 宏徳  東京大学, 大学院医学系研究科(医学部), 准教授 (80788422)
菅家 康介  東京大学, 医学部附属病院, 登録診療員 (90779810)
Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2019: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords骨代謝 / ES細胞 / 骨芽細胞 / 破骨細胞 / ES細胞
Outline of Final Research Achievements

To better understand molecular mechanisms underlying osteoblast-mediated osteoclast functions, we developed a three dimensional differentiation protocol to direct from mouse ES cells to osteoblasts and osteocytes. We confirmed that bone marrow-derived cells differentiated into osteoclasts under co-culture with the ES cells-directed osteoblasts and osteocytes. We further performed gene expression analysis in stepwise differentiation stages from the ES cells to osteoblasts and osteocytes in order to identify novel cell-populations and factors contributing to osteoclast differentiation. These results provided insights into establishments of in vitro bone remodeling model and candidates of factors regulating osteoclast differentiation.

Academic Significance and Societal Importance of the Research Achievements

本研究で確立したマウスES細胞の三次元分化誘導法は、骨芽細胞だけでなく骨細胞への分化誘導を可能にした。これにより、骨芽細胞・骨細胞と破骨細胞のリモデリングをin vitroで再現できる可能性が示された。さらに本研究で得られた新規破骨細胞制御因子の候補は、将来的に研究が進みその効果が実証された場合は、新たな骨疾患治療薬の候補となる可能性を秘めている。

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (3 results)

All 2020 2018

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

  • [Journal Article] Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers2020

    • Author(s)
      Zujur Denise、Kanke Kosuke、Onodera Shoko、Tani Shoichiro、Lai Jenny、Azuma Toshifumi、Xin Xiaonan、Lichtler Alexander C.、Rowe David W.、Saito Taku、Tanaka Sakae、Masaki Hideki、Nakauchi Hiromitsu、Chung Ung-il、Hojo Hironori、Ohba Shinsuke
    • Journal Title

      Regenerative Therapy

      Volume: 14 Pages: 19-31

    • DOI

      10.1016/j.reth.2019.12.010

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Fabrication of calcium phosphate-loaded carboxymethyl cellulose non-woven sheets for bone regeneration.2018

    • Author(s)
      Qi P, Ohba S, Hara Y, Fuke M, Ogawa T, Ohta S, Ito T
    • Journal Title

      Carbohydr Polym

      Volume: 189 Pages: 322-330

    • DOI

      10.1016/j.carbpol.2018.02.050

    • Related Report
      2018 Research-status Report
    • Peer Reviewed
  • [Presentation] Identification of gene regulatory landscape in skeletal formation and maintenance2018

    • Author(s)
      Ohba S
    • Organizer
      Japan - Latin America Academic Conference 2018
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research / Invited

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Published: 2017-04-28   Modified: 2021-02-19  

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