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Investigation of mechanism for anti DKK-1 antibody possessing bone formation

Research Project

Project/Area Number 17K11753
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Prosthodontics/ Dental materials science and
Research InstitutionThe University of Tokushima

Principal Investigator

INOUE Miho  徳島大学, 大学院医歯薬学研究部(歯学域), 助教 (20271059)

Co-Investigator(Kenkyū-buntansha) 井上 正久  徳島文理大学, 薬学部, 教授 (20223274)
宮城 麻友  徳島大学, 大学院医歯薬学研究部(歯学域), 助教 (20625719)
松香 芳三  徳島大学, 大学院医歯薬学研究部(歯学域), 教授 (90243477)
Project Period (FY) 2017-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2020: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2019: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2018: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2017: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords抗DKK-1抗体 / 骨形成 / 骨代謝 / 骨粗しょう症 / TNF-α / 骨形成能 / 骨粗しょう症モデルマウス / 顎骨壊死 / 歯学 / シグナル伝達 / 再生・医学
Outline of Final Research Achievements

In the dental prosthesis, it is necessary the treatment to make up for a bone defect part or the residual ridge. The inhibition of osteoblasts differentiation is reported in Dickkopf1 (DKK-1) produced by a bone cell and osteoblasts. In this study, it was intended that I examined influence on bone differentiation ability to the bone marrow cell of the antiDKK-1 antibody and the osteoplasty ability mechanism in the osteoporosis model mouse.
The influence at the cellular level was not accepted. However, in the osteoporosis model mouse the bone masses increased obviously, a tendency to decrease of the osteoclast was detected. By the antiDKK1 antibody dosage, the possibility that bone masses increased was suggested by bone morphogenetic promotion not inhibition of the bone resorption.

Academic Significance and Societal Importance of the Research Achievements

補綴歯科治療においては、骨欠損部位あるいは吸収した顎堤を補う処置が必要なことが多い。骨細胞や骨芽細胞から産生されるDKK-1は、骨代謝を阻害する因子で、DKK-1による骨芽細胞の分化抑制作用が報告されている。抗DKK-1抗体は全身投与での骨粗しょう症治療薬として期待されており、我々は局所投与においても骨形成促進作用を示すと期待している。

Report

(5 results)
  • 2020 Annual Research Report   Final Research Report ( PDF )
  • 2019 Research-status Report
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (2 results)

All 2019 2018

All Presentation (2 results)

  • [Presentation] 抗Dickkopf1(DKK-1)抗体による骨分化能への影響と骨粗しょう症に対する骨分化能メカニズムの解明2019

    • Author(s)
      井上美穂、Raju Resmi、岩浅匠真、秋山謙太郎、大島正充、窪木拓男、松香芳三
    • Organizer
      公益社団法人日本歯科補綴学会第128回学術大会
    • Related Report
      2019 Research-status Report
  • [Presentation] 抗Dickkopf1(DKK-1)抗体による骨髄細胞の骨分化能への影響2018

    • Author(s)
      Raju R, 井上美穂, 宮城麻友, 秋山謙太郎, 大島正充, 井上正久, 松香芳三.
    • Organizer
      硬組織再生生物学会
    • Related Report
      2018 Research-status Report

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Published: 2017-04-28   Modified: 2022-01-27  

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