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Therapeutic inhibition of microRNA-34a ameliorates aortic valve calcification via modulation of Notch1-Runx2 signaling

Research Project

Project/Area Number 16K09490
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Cardiovascular medicine
Research InstitutionYamagata University

Principal Investigator

WATANABE Tetsu  山形大学, 医学部, 准教授 (40359568)

Research Collaborator TOSHIMA Taku  
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2018: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords石灰化大動脈弁狭窄症 / micro RNA / Notch1 / Runx2 / ワイヤー傷害 / 大動脈弁狭窄症 / 石灰化 / Micro RNA / microRNA
Outline of Final Research Achievements

Expression of microRNA (miR)-23a, miR-34a, miR-34c, miR-133a, miR-146a, and miR-155 was increased, and expression of miR-27a and miR-204a was decreased in valve tissues from calcific aortic valve stenosis (CAVS) compared with those from aortic regurgitation (AR). Expression of Notch1 was decreased, and expression of Runt-related transcription factor 2 (Runx2) was increased in patients with CAVS compared with those with AR. We selected miR-34a among increased miRs in porcine aortic valve interstitial cells (AVICs) after osteogenic treatment. Inhibition of miR-34a significantly attenuated the calcification signals in AVICs compared with miR-control. In wire injury CAVS mice, locked nucleic acid miR-34a inhibitor suppressed aortic velocity, calcium deposition of aortic valves, and cardiac hypertrophy, which were involved in decreased Runx2 and increased Notch1 expressions.

Academic Significance and Societal Importance of the Research Achievements

ヒト大動脈弁組織、ブタ大動脈弁間質細胞、ワイヤー傷害大動脈弁狭窄症マウスを用い、大動脈弁狭窄症の進展に深く関わるmiRの役割について検討した。先天性二尖弁は三尖に比べ、大動脈弁狭窄症の進行が速いが、これには組織反応障害仮説の関与が示唆される。既に癌治療の分野では、miRNAを用いた臨床試験が始まっている。またmiRsはバイオマーカーとしての応用も行われている。大動脈弁石灰化に密接に関わるmiRNAの同定は、ハイリスク患者の早期発見および治療介入に臨床応用できる可能性が期待できる。

Report

(4 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (3 results)

All 2018 2017

All Presentation (3 results) (of which Int'l Joint Research: 1 results)

  • [Presentation] Therapeutic inhibition of microRNA-34a ameliorates aortic valve calcification via modulation of Notch1-Runx2 signaling in calcific aortic valve stenosis model mice by direct wire injury2018

    • Author(s)
      Taku Toshima, Tetsu Watanabe, Tetsuro Shishido, Takuya Miyamoto, Tetsuya Takahashi Takayuki Sugai, Ken Watanabe, Jun Goto, Isao Kubota and Masafumi Watanabe
    • Organizer
      ESC Congress 2018
    • Related Report
      2018 Annual Research Report
  • [Presentation] Silencing of microRNA-34a ameliorates aortic valve calcification via Notch1-Runx2 signaling in vivo and in vitro experiments2018

    • Author(s)
      Taku Toshima, Tetsu Watanabe, Tetsuro Shishido, Takuya Miyamoto, Takanori Arimoto, Hiroki Takahashi, Mitsuaki Sadahiro, Isao Kubota, and Masafumi Watanabe
    • Organizer
      第2回日本循環器学会基礎研究フォーラム
    • Related Report
      2018 Annual Research Report
  • [Presentation] Inhibition of MicroRNA-34a Attenuates Osteogenic Differentiation via Inhibiting Notch1 Signal in Aortic Valve Interstitial Cells2017

    • Author(s)
      Toshima T, Watanabe T, Shishido T, Watanabe K, Sugai T, Takahashi T, Tamura H, Nishiyama S, Arimoto T, Takahashi H, Kubota I
    • Organizer
      American Heart Association
    • Related Report
      2017 Research-status Report
    • Int'l Joint Research

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Published: 2016-04-21   Modified: 2020-03-30  

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