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Analysis of DNA damage induced by exposure of carbon nanotubes in mesotherial cells

Research Project

Project/Area Number 24590766
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Hygiene
Research InstitutionMeiji Pharmaceutical University

Principal Investigator

OGASAWARA Yuki  明治薬科大学, 薬学部, 教授 (20231219)

Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥3,250,000 (Direct Cost: ¥2,500,000、Indirect Cost: ¥750,000)
Keywords多層カーボンナノチューブ / 中皮種細胞 / DNA損傷 / 脂質過酸化 / 修復酵素 / 暴露指標 / カーボンナノチューブ / 遷移金属 / 酸化ストレスマーカー / 抗酸化酵素 / ナノマテリアル / 胸膜中皮細胞 / 酸化ストレス
Outline of Final Research Achievements

The present study suggests the toxic effects induced by exposure of single- and multi-walled carbon nanotubes (SWCNT and MWCNT) on Met-5A cells, a human lung mesothelial cell as a model system. Met-5A cells were cultured with SWCNT or MWCNT, and various cellular responses were determined to estimate the toxicity of exposure to CNTs. In this study, we have demonstrated that exposure of MeT-5A cells to CNTs led to up-regulation of DNA repair enzymes expression. Using qRT PCR and Western blotting analyses, we have shown that the CNTs-mediated increase in XRCC1, a DNA repair enzymes. Moreover, the decrease in SOD activity suggested the attenuation of protective mechanism against ROS in CNT treated cells. Studies carried out on the effect of CNTs on TBA-RS levels in MeT-5A cells, indicated that aldehyde formation was induced by exposure to CNTs. These results indicated that CNTs might exert genotoxicity via superoxide generation followed by DNA oxidation.

Report

(4 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report
  • Research Products

    (5 results)

All 2015 2014 2013 2012

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Open Access: 1 results) Presentation (3 results)

  • [Journal Article] Irreversible hyperoxidation of peroxiredoxin 2 is caused by tert-butyl hydroperoxide in human red blood cells.2014

    • Author(s)
      Ishida YI, Takikawa M, Suzuki T, Nagahama M, Ogasawara Y
    • Journal Title

      FEBS Open Bio.

      Volume: 4 Issue: 1 Pages: 848-852

    • DOI

      10.1016/j.fob.2014.10.003

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] ヒト胸膜中皮由来細胞に対するカーボンナノチューブ曝露によるDNA損傷作用2012

    • Author(s)
      小笠原裕樹、梅津 石井一行
    • Journal Title

      日本衛生学雑誌

      Volume: 67

    • NAID

      10030212285

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Presentation] ヒト赤血球中還元型および酸化型Peroxiredoxin2の同時分析法の開発2015

    • Author(s)
      瀧川まりあ、船木裕介、小池伸、鈴木俊宏、小笠原裕樹
    • Organizer
      日本薬学会第135年会
    • Place of Presentation
      神戸サンボーホール
    • Year and Date
      2015-03-25 – 2015-03-28
    • Related Report
      2014 Annual Research Report
  • [Presentation] ヒト胸膜中皮由来細胞を用いたカーボンナノチューブの毒性評価2014

    • Author(s)
      松井 勇太,小笠原 裕樹,服部 研之,石井 一行
    • Organizer
      日本薬学会第134年会
    • Place of Presentation
      熊本市総合体育館(熊本)
    • Related Report
      2013 Research-status Report
  • [Presentation] ナノサイズ酸化チタン暴露による酸化的DNA損傷の評価2013

    • Author(s)
      森井 茜、青沼 えり、小笠原 裕樹、野口 拓巳、石井 一行
    • Organizer
      日本薬学会第133年会
    • Place of Presentation
      パシフィコ横浜 (横浜)
    • Related Report
      2012 Research-status Report

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Published: 2013-05-31   Modified: 2019-07-29  

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