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Elucidation of fetal wound healing mechanisms in cardiac fibroblasts and its therapeutic implications of myocardial infarction.

Research Project

Project/Area Number 26560399
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Applied health science
Research InstitutionAomori University of Health and Welfare

Principal Investigator

KON ATSUSHI  青森県立保健大学, 健康科学部, 教授 (60271798)

Co-Investigator(Renkei-kenkyūsha) SAWAMURA DAISUKE  弘前大学, 大学院医学研究科, 教授 (60196334)
Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Fiscal Year 2016: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2015: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Keywords胎仔創傷治癒機構 / 心臓線維芽細胞 / 心筋梗塞 / 遺伝子発現 / 発生 / 胎仔創傷治癒
Outline of Final Research Achievements

In this study, we analyzed the specific gene expressed in fetal wound healing (FWH) in mouse cardiac fibroblast cells characterized by without scar formation. By using DNA microarray analysis, anti-fibrosis related genes including Has2, Tm, and Mmp genes, and morphogenesis related genes (Foxo, Hox, and Pax) highly expressed in FWH, whereas the expression of these genes down-regulated in adult wound healing (AWH) with scar formation. Down regulation of Pax gene expression are down regulated by methylation on histone H3 domain, whereas downregulation of other genes were induced by DNA methylation of each promoter region, respectively. Finally, we injected each gene into myocardial infarction tissue of adult mice. As the result, each gene did not induce FWH characterized perfect scarless reaction, suggesting alone administration of each gene was not effective, and cocktail therapy, the combination of multiple genes, are necessary of inducing of FWH.

Report

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

    (2 results)

All 2016

All Presentation (2 results)

  • [Presentation] 胎仔創傷治癒機構におけるヒアルロン酸関連遺伝子の発現について2016

    • Author(s)
      今  淳,田中 翠,柴田歩美,明戸瑞季,佐藤沙紀
    • Organizer
      第89回日本生化学会総会
    • Place of Presentation
      仙台国際センター,仙台市
    • Year and Date
      2016-09-25
    • Related Report
      2016 Annual Research Report
  • [Presentation] ヒアルロン酸合成酵素-2(Has-2)遺伝子の転写制御機構の解析2016

    • Author(s)
      佐藤沙紀,今  淳
    • Organizer
      2016年度青森県保健医療福祉研究発表会、日本ヒューマンケア科学学会第9回学術集会
    • Place of Presentation
      青森県立保健大学,青森市
    • Related Report
      2016 Annual Research Report

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

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