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Examination of osteonecrosis of the jaw treatment method by autologous iPS cell origin mesenchymal stem cell

Research Project

Project/Area Number 16K11675
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

Nishizawa Satoru  東京大学, 医学部附属病院, 特任助教 (00646200)

Co-Investigator(Kenkyū-buntansha) 浅輪 幸世  東京大学, 医学部附属病院, 特任助教 (10769912)
星 和人  東京大学, 医学部附属病院, 教授 (30344451)
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2018: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords薬剤性顎骨壊死 / iPS細胞 / 細胞治療 / MSC / 顎骨壊死 / 間葉系幹細胞 / 再生医療 / 骨粗鬆症 / 薬剤関連性顎骨壊死 / iPS細胞由来間葉系幹細胞 / iPS / 薬剤関連顎骨壊死
Outline of Final Research Achievements

MSCs used for cell transplantation therapy are harvested from bone marrow or adipose tissue. However, high quality MSCs can not be collected in large quantities. In addition, MSCs are rapidly dedifferentiated by culture and lose cellular properties. Furthermore, MSCs collected from elderly people have reduced proliferative potential. Therefore, treatment for all patients is not possible. We focused on induced pluripotent stem cells (iPSC) as a source of MSCs, and generated MSCs for use in cell therapy from iPSC. At this time, MSCs having different degrees of maturity were produced using the expression level of the Pdgfr gene encoding the platelet-derived growth factor receptor as an index. The MSCs were administered to a jaw bone necrosis disease model mouse to evaluate the therapeutic effect.

Academic Significance and Societal Importance of the Research Achievements

本研究の特色はiPS細胞の分化誘導技術とモデル動物作製技術を組み合わせることで、これまでの骨髄由来MSCを用いた方法では不可能だった大量かつ分化段階の異なるMSCをiPS細胞から誘導し、薬剤性顎骨壊死(ARONJ)モデル動物を用いて細胞移植治療の各種検討をおこなうことでARONJに対する細胞移植治療の有用性を実証することにある。本研究で得られた成果は、口腔外科領域のみならず、脳神経外科、整形外科や形成外科など、骨再建を担う他科においても有意義な知見となるものであり、広く医療に貢献するものと考えている。

Report

(4 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (3 results)

All 2018 2017

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

  • [Journal Article] Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement model2018

    • Author(s)
      Uto Sakura、Nishizawa Satoru、Hikita Atsuhiko、Takato Tsuyoshi、Hoshi Kazuto
    • Journal Title

      Regenerative Therapy

      Volume: 9 Pages: 58-70

    • DOI

      10.1016/j.reth.2018.06.003

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Impairment of the transition from proliferative stage to prehypertrophic stage in chondrogenic differentiation of human induced pluripotent stem cells harboring the causative mutation of achondroplasia in fibroblast growth factor receptor 32017

    • Author(s)
      Naohiro Horie , Atsuhiko Hikita , Satoru Nishizawa , Sakura Uto , Tsuyoshi Takato , Kazuto Hoshi
    • Journal Title

      Regenerative Therapy

      Volume: 6 Pages: 15-20

    • DOI

      10.1016/j.reth.2016.11.002

    • Related Report
      2017 Research-status Report 2016 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Presentation] ゲノム編集による軟骨無形成症特異的ヒトiPS細胞の樹立及び、病態研究2017

    • Author(s)
      堀江尚弘、西澤悟、宇都さくら、髙戸毅、星和人
    • Organizer
      第16回日本再生医療学会総会
    • Place of Presentation
      仙台国際センター 仙台市 宮城
    • Related Report
      2016 Research-status Report

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Published: 2016-04-21   Modified: 2020-03-30  

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