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Elucidation of the functional roles of Ca2+-activated potassium channels in osteoclastic bone resorption

Research Project

Project/Area Number 25462907
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Functional basic dentistry
Research InstitutionFukuoka Dental College

Principal Investigator

OKAMOTO FUJIO  福岡歯科大学, 歯学部, 講師 (60153938)

Co-Investigator(Kenkyū-buntansha) KAJIYA Hiroshi  福岡歯科大学, 口腔歯学部, 講師 (80177378)
OKABE Koji  福岡歯科大学, 口腔歯学部, 教授 (80224046)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords骨代謝 / 破骨細胞 / カルシウム活性化カリウムチャネル / TRPチャネル / 骨吸収 / TRPチャネル / アクチンリング / 非選択的陽イオンチャネル
Outline of Final Research Achievements

We investigated the functional role of Ca2+-activated K+ channels (Kca) in osteoclastic bone resorption. Mature osteoclasts derived from mouse bone marrow cells abundantly expressed Kca 3.1. Pharmacological inhibition of Kca 3.1 led to rapid disappearance of ring-like actin conformation (actin-ring) and reduced bone resorption activity. Other Kca blockers had no effect on both the actin-ring conformation and the bone resorption activity. Mature osteoclasts also expressed non-selective cation channels including TRPM7. Inhibition of these cation channels also reduced the bone resorption activity. These results suggest that Kca 3.1 expressed in mature osteoclasts serves as a regulator of Ca2+ influx through the non-selective cation channels, which contribute to the formation of actin-ring, an essential process for the bone resorption.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (5 results)

All 2015 2014

All Presentation (5 results)

  • [Presentation] TRPM7は歯の石灰化に関与する2015

    • Author(s)
      緒方佳代子、福島秀文、圓谷智之、岡 暁子、岡本富士雄、片桐千秋、鍛治屋 浩、松下正之、尾崎正雄、岡部幸司
    • Organizer
      第66回西日本生理学会
    • Place of Presentation
      久留米大学医学部
    • Year and Date
      2015-10-09
    • Related Report
      2015 Annual Research Report
  • [Presentation] Chanzime TRPM7は歯の石灰化に関与する2015

    • Author(s)
      緒方佳代子、福島秀文、岡本富士雄、岡 暁子、永嶌勝之、尾崎正雄、岡部幸司
    • Organizer
      第33回日本骨代謝学会
    • Place of Presentation
      京王プラザホテル(東京)
    • Year and Date
      2015-07-23
    • Related Report
      2015 Annual Research Report
  • [Presentation] TRPM7は象牙芽細胞に高発現する2015

    • Author(s)
      圓谷智之、福島秀文、片桐千秋、岡本富士雄、岡部幸司、松下正之
    • Organizer
      第120回日本解剖学会総会・全国学術集会、第92日本生理学会大会
    • Place of Presentation
      神戸国際会議場
    • Year and Date
      2015-03-21 – 2015-03-23
    • Related Report
      2014 Research-status Report
  • [Presentation] Expression analysis of TRPM7 in the odontoblasts2014

    • Author(s)
      Tomoyuki Tsumuraya, Chiaki Katagiri, Fujio Okamoto, Koji Okabe, Masayuki Matsushita
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2014-11-25 – 2014-11-27
    • Related Report
      2014 Research-status Report
  • [Presentation] 象牙芽細胞におけるTRPM7の発現解析2014

    • Author(s)
      片桐千秋、圓谷智之、岡本富士雄、岡部幸司、松下正之
    • Organizer
      第91回日本生理学会
    • Place of Presentation
      鹿児島大学 郡元キャンパス
    • Related Report
      2013 Research-status Report

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Published: 2014-07-25   Modified: 2019-07-29  

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