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Analysis of acid extrusion mechanism through new regulatory protein during bone resorption

Research Project

Project/Area Number 23890241
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Surgical dentistry
Research InstitutionFukuoka Dental College

Principal Investigator

KIMACHI Keiichiro  福岡歯科大学, 歯学部, 助教 (30610977)

Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥3,250,000 (Direct Cost: ¥2,500,000、Indirect Cost: ¥750,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywords骨代謝 / ビスホスホネート / 顎骨壊死 / 破骨細胞 / メバロン酸経路 / ビスフォスフォネート製剤 / ゲラニルゲラニル酸 / ビスフォスフォネート剤 / ファーネシル酸 / 炎症性骨破壊 / ゾレンドロン酸
Research Abstract

The nitrogen-including bisphosphonates(NBP)-related osteonecrosis of the jaws (BRONJ)were suggested to be caused by the decrease in the substrates of prenylation includinggeranylgeranyl acid (GGOH) after treatment of NBPs. Then, in the present study, weexamined the effects of NBP zoledronic acid in presence or absence of the prenylationsubstrate GGOH on mouse osteoclast differentiation. The mouse bone marrowmacrophages was cultivated with or without GGOH in the presence of RANKL (80micro M) and zoledronic acid (7 micro M). To clarify the expression of target moleculesand osteoclast differentiation we performed these methods of TRAP staining, RT- andreal time-PCR and Western blot analysis in the treated cells. The zoledronic acidsuppressed the expression of TRAP the differentiation-related molecule, DC-STAMPand OC-STAMP the cell fusion-related molecules in bone marrow macrophages withRANKL treatment on dose-dependent manner. Furthermore, the zoledronic acidinhibited TRAP-positive multinuclear osteoclast differentiation. However, theincubation of zoledronic acid in the presence of GGOH restored the number ofTRAP-positive osteoclasts together with the recovery of the expression of TRAP,DC-STAMP and OC-STAMP. These results are suggested that NBPs may besuppressed the multi-nucleation in stage of osteoclast fusion. Furthermore, theprenylation substrates partially restored the suppression of osteoclast differentiation,suggesting in the prevention of BRONJ in the patients with treatment of NBPs.

Report

(3 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Annual Research Report
  • Research Products

    (4 results)

All 2013 2012

All Presentation (4 results)

  • [Presentation] 窒素含有ビスホスホネート製剤(NBP)の融合抑制を介した破骨細胞の分化阻害作用2013

    • Author(s)
      長岡良礼、府川晃久、佐々木三奈、永沼香 織、太田信敬、来海慶一郎 、山下善弘、大関悟、池邉哲郎
    • Organizer
      第67回口腔科学会
    • Related Report
      2012 Final Research Report
  • [Presentation] 窒素含有ビスホスホネート製剤(NBP)の融合抑制を介した破骨細胞の分化阻害作用2013

    • Author(s)
      長岡良礼、府川晃久、佐々木三奈、永沼香織、太田信敬、来海慶一郎、山下善弘、大関悟、池邉哲郎
    • Organizer
      第67回口腔科学会
    • Place of Presentation
      栃木県宇都宮市
    • Related Report
      2012 Annual Research Report
  • [Presentation] 窒素含有ビスホスホネート製剤(NBP)による破骨細胞形成阻害とプレニル化促進物質による回復2012

    • Author(s)
      長岡良礼、鍛治屋浩、府川晃久、佐々木三奈、来海慶一郎、山下善弘、大関悟、池邉哲郎、 岡本富士雄、岡部幸司
    • Organizer
      第39回福岡歯科大学学会総会
    • Related Report
      2012 Final Research Report
  • [Presentation] 窒素含有ビスフォスフォネート製剤(NBP)による破骨細胞形成阻害とプレニル化促進物質による回復2012

    • Author(s)
      長岡良礼、鍛治屋浩、府川晃久、佐々木三奈、来海慶一郎、山下善弘、大関悟、池邉哲郎、岡本富士雄、岡部幸司
    • Organizer
      第39回福岡歯科大学学会総会
    • Place of Presentation
      福岡市
    • Related Report
      2012 Annual Research Report

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Published: 2011-09-05   Modified: 2019-07-29  

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