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Boron accelerates cultured osteoblastic cell activity through calcium flux

Research Project

Project/Area Number 25670812
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Conservative dentistry
Research InstitutionNagasaki University

Principal Investigator

HAYASHI Yoshihiko  長崎大学, 医歯薬学総合研究科(歯学系), 教授 (20150477)

Co-Investigator(Kenkyū-buntansha) 山田 志津香  長崎大学, 医歯薬学総合研究科(歯学系), 准教授 (00363458)
藤原 守  長崎大学, 医歯薬学総合研究科(歯学系), 客員研究員 (40336178)
井川 一成  長崎大学, 医歯薬学総合研究科(歯学系), 助教 (80584739)
Project Period (FY) 2013-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
KeywordsCaイオンの移動 / 細胞増殖 / 細胞分化 / 骨芽細胞 / Caチャネル / ニフェジピン / Fluo 4-AM / Ca蛍光強度 / ホウ素 / Na+/K+-ATPase / Caイオンチャネル / 細胞膜の活性化 / 石灰化
Outline of Final Research Achievements

The aim of this study was to investigate the effects of 0.1 mM of boron (B) on the membrane function of osteoblastic cells in vitro. The Ca2+ flux was evaluated for the activation of L-type Ca2+ channel for the Ca2+ influx, and that of Na+/K+-ATPase for the Ca2+ efflux. A real-time PCR analysis revealed that the expression of four mineralization-related genes was increased with a B-supplemented medium. Using microarray analyses, five genes involved in cell proliferation and differentiation were up-regulated. Regarding the Ca2+ influx, in the nifedipine-pretreated group, the relative fluorescence intensity for one min after adding B solution did not increase compared with that for one min before addition. Regarding the Ca2+ efflux, in 0.1 mM of B-supplemented medium, the relative fluorescence intensity for 10-min after ouabain treatment revealed a significantly lower slope value. B promotes the proliferation and differentiation of mammalian osteoblastic cells in vitro.

Report

(5 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (4 results)

All 2016 2015 2014

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Acknowledgement Compliant: 1 results) Presentation (3 results)

  • [Journal Article] Boron accelerates cultured osteoblastic cell activity through calcium flux2016

    • Author(s)
      Capati MFL, Namazono A, Igawa K, ookubo K, Yamamoto Y, Yanagiguchi K, Kubo S, Yamada S, Hayashi Y
    • Journal Title

      Biological Trace Element Research

      Volume: 174 Issue: 2 Pages: 300-308

    • DOI

      10.1007/s12011-016-0719-y

    • Related Report
      2016 Annual Research Report 2015 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] 培養骨芽細胞細胞膜Caチャネル活性化への必須微量元素ホウ素の至適添加濃度2015

    • Author(s)
      林 善彦、井川 一成、MLF キャパテイ、山本裕也、山田志津香、大久保賢亮
    • Organizer
      第143回日本歯科保存学会2015年度秋季学術大会
    • Place of Presentation
      文京シビックセンター(東京都・千代田区)
    • Year and Date
      2015-11-12
    • Related Report
      2015 Research-status Report
  • [Presentation] 必須微量元素ホウ素の培養骨芽細胞細胞膜への影響2014

    • Author(s)
      大久保賢亮、井川一成、山本裕也、山田香津香、林 善彦
    • Organizer
      第141回日本歯科保存学会
    • Place of Presentation
      山形テレサ(山形市)
    • Year and Date
      2014-10-31
    • Related Report
      2014 Research-status Report
  • [Presentation] 必須微量元素ホウ素添加によって培養骨芽細胞中で発現が増強する遺伝子2014

    • Author(s)
      林 善彦、山田志津香、井川一成、山本裕也
    • Organizer
      第140回日本歯科保存学会
    • Place of Presentation
      大津市 滋賀県立芸術劇場びわ湖ホール
    • Related Report
      2013 Research-status Report

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

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