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Clarifying the mechanism of MHC class I overexpression on polymyositis muscle fibers with disease specific human iPS cells.

Research Project

Project/Area Number 16H06769
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field General internal medicine(including psychosomatic medicine)
Research InstitutionTokyo Medical and Dental University

Principal Investigator

HASEGAWA Hisanori  東京医科歯科大学, 医学部附属病院, 助教 (00707028)

Project Period (FY) 2016-08-26 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords多発性筋炎 / ヒトiPS細胞 / 筋分化 / MHCクラスI / 多発性筋炎/皮膚筋炎 / サイトカイン
Outline of Final Research Achievements

MHC class I are more expressed on muscle fibers of polymyositis patients (PM Pts) than those of healthy donors (HDs). We considered to evaluate the differences of MHC class I expression and genetic properties between PM Pts and HDs by differentiating myocytes from human iPS cells (hiPSCs). If molecules that induce overexpression of MHC class I on PM muscles are identified, they can be targets for the treatment of PM.
MyoD-hiPSC bulks, which are composed of multiple MyoD-hiPSC clones, were established by transfecting MyoD, a myogenic transcription factor, into PM Pt or HD derived-hiPSC clones. We established also a differential condition for MyoD-hiPS bulks to differentiate into myocytes. Three MyoD-hiPSC bulks from the same donor differentiated similarly into myocytes. However, protein production differed between the three MyoD-hiPSC bulks. We concluded that it is difficult to evaluate the differences of MHC class I expression of PM Pts and HDs with myocytes derived from hiPSCs.

Report

(3 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Annual Research Report
  • Research Products

    (3 results)

All 2017 2016

All Presentation (3 results)

  • [Presentation] MyoDを導入したヒト人工多能性幹細胞の多クローン集団の樹立と筋細胞分化時のサイトカイン産生評価2017

    • Author(s)
      長谷川 久紀、溝口 史高、頼 貞儀、大津 真、上阪 等
    • Organizer
      第3回日本筋学会学術集会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 筋原性転写因子MyoDを導入したヒト人工多能性幹細胞の多クローン集団の樹立と筋細胞分化時のサイトカイン産生評価2017

    • Author(s)
      長谷川 久紀、溝口 史高、頼 貞儀、大津 真、上阪 等
    • Organizer
      第4回日本リウマチ学会ベーシックリサーチカンファレンス
    • Related Report
      2017 Annual Research Report
  • [Presentation] 筋原性転写因子MyoDを導入されたヒト人工多能性幹細胞の多クローン集団の樹立と筋細胞への分化2016

    • Author(s)
      長谷川 久紀、川畑 仁人、頼 貞儀、大津 真、上阪 等
    • Organizer
      第44回日本臨床免疫学会総会
    • Place of Presentation
      東京、京王プラザホテル
    • Year and Date
      2016-09-08
    • Related Report
      2016 Annual Research Report

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Published: 2016-09-02   Modified: 2019-03-29  

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