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Development of mouse models of osteoarthritis targeting the Gfd5 gene

Research Project

Project/Area Number 15K06797
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Laboratory animal science
Research InstitutionIwate University

Principal Investigator

Furuichi Tatsuya  岩手大学, 農学部, 教授 (30392103)

Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Keywords変形性関節症 / モデル動物 / GDF5 / コンジェニックマウス / 疾患モデルマウス
Outline of Final Research Achievements

The GDF5 gene is reported to be associated with osteoarthritis (OA) in mice and humans. M451 mouse strain, which possesses the missense mutation (W408R) in Gdf5, develops an early-onset osteoarthritis (OA) of the elbow joint. However, detailed evaluation of M451 strain as OA model animals has not been carried out. We generated congenic mouse strains in which W408R mutation was introduced into the genetic background C57BL/6 or STR/ort. We confirmed the duplicability of an early-onset OA in the C57BL/6 congenic strain. Articular cartilage lesion in the STR/ort congenic strain seemed more severe than that that in STR/ort. These two congenic strains are useful to develop novel OA model animals.

Report

(4 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report
  • Research Products

    (9 results)

All 2018 2017 2016 2015

All Journal Article (4 results) (of which Int'l Joint Research: 3 results,  Peer Reviewed: 4 results,  Open Access: 1 results,  Acknowledgement Compliant: 2 results) Presentation (5 results) (of which Invited: 1 results)

  • [Journal Article] Disruption of the mouse Slc39a14 gene encoding zinc transporter ZIP14 is associated with decreased bone mass, likely caused by enhanced bone resorption.2018

    • Author(s)
      Sasaki S, Tsukamoto M, Saito M, Hojyo S, Fukada T, Takami M, Furuichi T.
    • Journal Title

      FEBS Open Bio

      Volume: 8 Issue: 4 Pages: 655-663

    • DOI

      10.1002/2211-5463.12399

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes2017

    • Author(s)
      Ichimura S, Sasaki S, Murata T, Fukumura R, Gondo Y, Ikegawa S, Furuichi T.
    • Journal Title

      Exp Amin

      Volume: 62 Pages: 138-144

    • NAID

      130005635560

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] Overexpression of BCLXL in Osteoblasts Inhibits Osteoblast Apoptosis and Increases Bone Volume and Strength2016

    • Author(s)
      Moriishi T, Fukuyama R, Miyazaki T, Furuichi T, Ito M, Komori T.
    • Journal Title

      J Bone Miner Res

      Volume: 印刷中 Issue: 7 Pages: 1366-1380

    • DOI

      10.1002/jbmr.2808

    • Related Report
      2016 Research-status Report 2015 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] Endoplasmic reticulum stress-mediated apoptosis contributes to a skeletal dysplasia resembling platyspondylic lethal skeletal dysplasia, Torrance type, in a novel Col2a1 mutant mouse line.2015

    • Author(s)
      Kimura M, Ichimura S, Sasaki K, Masuya H, Suzuki T, Wakana S, Ikegawa S, Furuichi T.
    • Journal Title

      Biochem Biophys Res Commun

      Volume: 468 Issue: 1-2 Pages: 86-91

    • DOI

      10.1016/j.bbrc.2015.10.160

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] 「四肢異常を伴う小眼球症」の新規モデルマウスの樹立と原因遺伝子の同定2016

    • Author(s)
      塚本愛美、佐藤有里子、福村龍太郎、権藤洋一、古市達哉
    • Organizer
      第159回日本獣医学会
    • Place of Presentation
      日本大学生物資源科学部 (神奈川県藤沢市)
    • Year and Date
      2016-09-06
    • Related Report
      2016 Research-status Report
  • [Presentation] 新規Col2a1変異マウスを用いたトーランス型扁平椎異形成症の病態機序の検討2016

    • Author(s)
      木村允、 市村鋭、 桝谷啓志、 鈴木智広、若菜茂晴、 古市達哉
    • Organizer
      第63回日本実験動物学会
    • Place of Presentation
      ミューザ川崎シンフォニーホール (神奈川県川崎市)
    • Year and Date
      2016-05-18
    • Related Report
      2016 Research-status Report
  • [Presentation] 遺伝子改変動物を用いて骨格形成メカニズムに迫る2016

    • Author(s)
      古市達哉
    • Organizer
      第27回東北動物実験研究会
    • Place of Presentation
      秋田温泉プラザ (秋田県秋田市)
    • Related Report
      2016 Research-status Report
    • Invited
  • [Presentation] モデルマウスを用いたトーランス型扁平椎異形成症の病態機序の検討2015

    • Author(s)
      木村允、 市村鋭、 桝谷啓志、 鈴木智広、若菜茂晴、 古市達哉
    • Organizer
      第158回日本獣医学会
    • Place of Presentation
      北里大学(青森県十和田市)
    • Year and Date
      2015-09-09
    • Related Report
      2015 Research-status Report
  • [Presentation] 破骨細胞機能における亜鉛トランスポーターZIP14の役割2015

    • Author(s)
      古市達哉、佐々木俊、北條慎太郎、深田俊幸
    • Organizer
      第62回日本実験動物学会
    • Place of Presentation
      京都テルサ (京都府)
    • Year and Date
      2015-05-28
    • Related Report
      2015 Research-status Report

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Published: 2015-04-16   Modified: 2019-03-29  

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