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Pharmacological study of intracellular signaling pathways involved in hepatic stellate cell reversion for treatment of NASH

Research Project

Project/Area Number 17H07000
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Applied health science
Research InstitutionUniversity of Shizuoka

Principal Investigator

Yamaguchi Momoka  静岡県立大学, 薬学部, 助教 (30804819)

Research Collaborator Morishita Tomoya  
Project Period (FY) 2017-08-25 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords肝星細胞 / 肝線維化 / 脱活性化 / 形質転換 / 非アルコール性脂肪肝炎(NASH) / caffeine
Outline of Final Research Achievements

During liver injury, quiescent hepatic stellate cells (qHSCs) are transdifferentiated into myofibroblast-like activated HSCs (aHSCs), which produce collagen, a major source of liver fibrosis. Therefore, the reversion of aHSC is regarded as a therapeutic target for liver fibrosis. In this study, caffeine (0.1-10 mM) significantly decreased the expression of α-SMA and COL1a1, are markers of aHSC, in a concentration-dependent manner. Further, caffeine significantly increased of the expression of MMP-9 which is a marker of qHSC. CGS-15943, a subtype-nonselective adenosine receptor inhibitor, significantly decreased the expression α-SMA, but had no significant effect on the expression of COL1a1 and MMP-9. These results suggest that caffeine causes the reversion of aHSC and a part of the mechanism of the aHSC reversion is mediated by inhibiting adenosine receptors. We propose that these results lead to effective therapeutic strategies for preventing liver fibrosis.

Academic Significance and Societal Importance of the Research Achievements

肝線維化の責任細胞ということから肝星細胞に関する報告は数多くあるものの、本研究で示したような一度活性化した活性型HSCを静止型HSCに脱活性化させるという報告は少なく、その機構は殆ど分かっていない。すなわち、本研究で示したHSC脱活性化機構の解明は、学術的新規性が高い。さらに、そのシグナル伝達の解明は未だ有効な治療方法が存在しないNASH治療薬の開発に繋がることが期待でき、臨床的な意義も大きい。

Report

(3 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Annual Research Report
  • Research Products

    (11 results)

All 2019 2018 2017

All Presentation (11 results) (of which Int'l Joint Research: 3 results)

  • [Presentation] カフェインは濃度依存的に活性型肝星細胞を復帰変異させる2019

    • Author(s)
      森下智也、山口桃生、齊藤真也、石川智久
    • Organizer
      第92回日本薬理学会年会
    • Related Report
      2018 Annual Research Report
  • [Presentation] Caffeine suppresses the activation of hepatic stellate cells Akt1 is a key molecule for caffeine-induced inhibition of hepatic stellate cell activation2018

    • Author(s)
      Momoka Yamaguchi, Tomoya Morishita, Shin-ya Saito, Tomohisa Ishikawa.
    • Organizer
      18th World Congress of Basic and Clinical Pharmacology (WCP2018)
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Caffeine はアデノシン受容体を阻害し、cAMP や ERK1/2 非依存的にリン酸化 Akt1 の減少を介して肝星細胞の活性化を抑制する2018

    • Author(s)
      山口桃生、森下智也、齊藤真也、石川智久
    • Organizer
      第25回肝細胞研究会
    • Related Report
      2018 Annual Research Report
  • [Presentation] プロスタグランジンE2はカフェイン存在下で肝星細胞の活性化を抑制する2018

    • Author(s)
      山口桃生、齊藤真也、石川智久
    • Organizer
      生体機能と創薬シンポジウム2018
    • Related Report
      2018 Annual Research Report
  • [Presentation] カフェインによる肝星細胞の活性化・脱活性化制御を介した肝線維化改善の可能性2018

    • Author(s)
      山口 桃生、森下 智也、齊藤 真也、石川 智久
    • Organizer
      生理学研究所研究会2018
    • Related Report
      2018 Annual Research Report
  • [Presentation] カフェインはAkt1のリン酸化を介して活性型肝星細胞の復帰変異を引き起こす2018

    • Author(s)
      森下智也、山口桃生、齊藤真也、石川智久
    • Organizer
      日本病院薬剤師会東海ブロック・日本薬学会東海支部合同学術大会 2018
    • Related Report
      2018 Annual Research Report
  • [Presentation] Suppression of hepatic stellate cell activation through antagonism of adenosine receptors with caffeine2018

    • Author(s)
      MOMOKA YAMAGUCHI
    • Organizer
      62nd Annual Meeting - Biophysical Society (BPS18)
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Caffeineはアデノシン受容体を阻害し、cAMPやERK1/2非依存的にリン酸化Akt1の減少を介して肝星細胞の活性化を抑制する2018

    • Author(s)
      山口桃生
    • Organizer
      第25回肝細胞研究会
    • Related Report
      2017 Annual Research Report
  • [Presentation] Akt1 is a key molecule for caffeine-induced inhibition of hepatic stellate cell activation2018

    • Author(s)
      MOMOKA YAMAGUCHI
    • Organizer
      World Perfumery Congress 2018 (WPC2018)
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] アデノシン受容体拮抗作用によりカフェインはリン酸化Akt1の減少を介して肝星細胞の活性化を抑制する2017

    • Author(s)
      山口桃生
    • Organizer
      生体機能と創薬シンポジウム2017
    • Related Report
      2017 Annual Research Report
  • [Presentation] 静止型肝星細胞におけるET-1誘発収縮の発生機序2017

    • Author(s)
      鈴木良輔
    • Organizer
      第27回日本循環薬理学会
    • Related Report
      2017 Annual Research Report

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Published: 2017-08-25   Modified: 2020-03-30  

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