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Establishing an advanced cell-base assay to evaluate the safety of resin monomers

Research Project

Project/Area Number 26870678
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Prosthodontics/ Dental materials science and
Functional basic dentistry
Research InstitutionTohoku University

Principal Investigator

Orimoto Ai  東北大学, 大学病院, 医員 (30710967)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
KeywordsARE活性化 / ルシフェラーゼ / レジンモノマー / 歯科材料 / 細胞毒性 / ARE / ルシフェラーゼレポーターアッセイ / 細胞毒性評価 / 歯科生体材料 / ARE活性
Outline of Final Research Achievements

The anti-oxidant responsive element (ARE)-mediated transcription is a key event in cellular detoxification of electrophilic exnobiotics. We previously established a clonal cell line stably transfected with an ARE-destabilized luciferase reporter gene, and showed that 2-hydroxyethyl methacrylate (HEMA), which is more toxic than methyl methacrylate (MMA), highly increased ARE-mediated trancriptional activity at low concentrations than MMA. We here showed the dose-dependent effects of ethyl methacrylate (EMA) on ARE activity and their relation to cytotoxicity. These results showed that the low concentration effects of resin monomers on ARE activity reflect their cytotoxicity probably due to their electroreactivity to intracellular molecules.

Report

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

    (16 results)

All 2017 2016 2015 2014

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 2 results,  Acknowledgement Compliant: 1 results) Presentation (13 results) (of which Int'l Joint Research: 2 results)

  • [Journal Article] F-spondin negatively regulates dental follicle differentiation through the inhibition of TGF-beta activity.2017

    • Author(s)
      Orimoto A, Kurokawa M, Handa K, Ishikawa M, Nishida E, Aino M, Mitani A, Ogawa M, Tsuji T Saito M
    • Journal Title

      Arch Oral Biol

      Volume: 79 Pages: 7-13

    • DOI

      10.1016/j.archoralbio.2017.02.019

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Structure-cytotoxicity relationship of methacrylate-based resin monomers as evaluated by an anti-oxidant responsive element-luciferase reporter assay2016

    • Author(s)
      Egashira M, Suzuki T, Orimoto A, Obata T, Nakamura H, Tanaka M, Kanamori T, Kawai T.
    • Journal Title

      Dental Materials Journal

      Volume: 35 Issue: 6 Pages: 946-951

    • DOI

      10.4012/dmj.2016-207

    • NAID

      130005171599

    • ISSN
      0287-4547, 1881-1361
    • Related Report
      2016 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Isolation and characterization of the human immature osteoblast culture systemf rom the alveolar bones of aged donors for bone regeneration therapy.2014

    • Author(s)
      Aino M, Nishida E, Fujieda Y, Orimoto A, Mitani A, Noguchi T, Makino H,
    • Journal Title

      Expert Opin Biol Ther.

      Volume: 14(12) Issue: 12 Pages: 1731-1744

    • DOI

      10.1517/14712598.2014.960387

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] ADAMTSL6βを介したMarfan症候群の解離性大動脈瘤発症機構の解析2017

    • Author(s)
      折本 愛、二木 正晴、石河 真幸、半田 慶介、齋藤 正寛
    • Organizer
      第146回 日本歯科保存学会2017年度春季学術大会
    • Place of Presentation
      青森、リンクステーションホール青森
    • Year and Date
      2017-06-08
    • Related Report
      2016 Annual Research Report
  • [Presentation] ADAMTSL6β exacerbates tissue destruction of aortic aneurysm and dissection in Marfan syndrome mouse model through promotion of ADAMTS4 activity.2016

    • Author(s)
      Ai Orimoto1, Yousuke Murasawa, Zenzo Isogai, Miyuki Chijiiwa, Satsuki Mochizuki, Kyoko Imanaka- Yoshida, Yasunori Okada, and Masahiro Saito
    • Organizer
      The American Society for Matrix Biology Biennial Meeting 2016
    • Place of Presentation
      Hilton St. Petersburg Bayfront
    • Year and Date
      2016-11-13
    • Related Report
      2016 Annual Research Report
  • [Presentation] ADAMTS superfamilyによるMarfan症候群の解離性大動脈瘤悪化機構の解析2016

    • Author(s)
      折本 愛
    • Organizer
      第4回MatoriCell フォーラム
    • Place of Presentation
      東京、東京理科大学神楽坂キャンパス
    • Year and Date
      2016-09-03
    • Related Report
      2016 Annual Research Report
  • [Presentation] ADAMTS superfamilyによる新規結合組織破壊機構の解析2016

    • Author(s)
      折本 愛、半田 慶介、齋藤 正寛
    • Organizer
      第37回 日本歯内療法学会学術大会
    • Place of Presentation
      名古屋、ウインクあいち
    • Year and Date
      2016-07-23
    • Related Report
      2016 Annual Research Report
  • [Presentation] ADAMTSL6β exacerbates marfan syndrome through the enhancement of ADAMTS4 activity.2016

    • Author(s)
      Ai Orimoto, Masaharu Futagi, Masaki Ishikawa, Keisuke Handa, Masahiro Saito
    • Organizer
      IADR/APR General Session & Exhibition
    • Place of Presentation
      Seoul, Republic of Korea
    • Year and Date
      2016-06-23
    • Related Report
      2016 Annual Research Report
  • [Presentation] The effect of S-PRG filler eluate on periodontitis models.2016

    • Author(s)
      IWAMATSU-KOBAYASHI Yoko, ORIMOTO Ai, VENKATAIAH Venkata Suresh, KANEHIRA Masafumi, HANDA Keisuke and SAITO Masahiro
    • Organizer
      The 6th International symposium for interface oral health science
    • Place of Presentation
      Gonryo Kaikan, Sendai
    • Year and Date
      2016-01-18
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Presentation] Adipose derived stem cell therapy for periodontal tissue regeneration in micro-mini pig model.2016

    • Author(s)
      VENKATAIAH Venkata Suresh, ORIMOTO Ai, FUTAGI Masaharu, ZOU Wei, HANDA Keisuke and SAITO Masahiro
    • Organizer
      The 6th International symposium for interface oral health science
    • Place of Presentation
      Gonryo Kaikan, Sendai
    • Year and Date
      2016-01-18
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Presentation] ADAMTSL6βを介したマルファン症候群モデルにおける組織破壊機構の解析2015

    • Author(s)
      折本 愛、二木 正晴、石河 真幸、半田 慶介、齋藤 正寛
    • Organizer
      第143回日本歯科保存学会秋季学術大会
    • Place of Presentation
      文京シビックホール (東京)
    • Year and Date
      2015-11-12
    • Related Report
      2015 Research-status Report
  • [Presentation] マルファン症候群モデルマウスにおける歯周炎の組織破壊機構に関する研究2015

    • Author(s)
      半田慶介、折本愛、小林洋子、齋藤正寛
    • Organizer
      第142回日本歯科保存学会春季学術大会
    • Place of Presentation
      北九州国際会議場 (北九州)
    • Year and Date
      2015-06-25
    • Related Report
      2015 Research-status Report
  • [Presentation] ADAMTSL6βが誘導する微細線維形成によるマルファン症候群モデルマウスの大動脈瘤悪化機構の解析2015

    • Author(s)
      折本 愛、半田慶介、村澤祐介、磯貝 善蔵、齋藤正寛
    • Organizer
      第47回日本結合組織学会
    • Place of Presentation
      コクヨホール(東京)
    • Year and Date
      2015-05-16
    • Related Report
      2015 Research-status Report
  • [Presentation] ADAMTSL6βは微細線維形成促進を介して大動脈瘤における組織破壊を促進する2015

    • Author(s)
      半田慶介 藤枝宜泰 折本愛 齋藤正寛
    • Organizer
      第14回日本再生医療学会総会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2015-03-19 – 2015-03-21
    • Related Report
      2014 Research-status Report
  • [Presentation] ADAMTSL6βが誘導する微細線維形成異常による大動脈瘤の炎症悪化機構の解析2014

    • Author(s)
      藤枝宜泰 安倍翔太 折本愛 半田慶介 齋藤正寛
    • Organizer
      第 37 回 日本分子生物学会
    • 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] S-PRGフィラー抽出液によるマウス歯周炎モデル予防効果の解析.2014

    • Author(s)
      小林洋子, 安倍翔大, 折本愛, 齋藤正寛
    • Organizer
      第141回日本歯科保存学会春季学術大会
    • Place of Presentation
      山形テルサ
    • Year and Date
      2014-10-30 – 2014-10-31
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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