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Identification of novel micro RNA obtained from proangiogenic adipose-derived stem cells

Research Project

Project/Area Number 18K15883
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 53020:Cardiology-related
Research InstitutionKanazawa University

Principal Investigator

Inoue Oto  金沢大学, 附属病院, 医員 (00781147)

Project Period (FY) 2018-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2019: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2018: ¥3,250,000 (Direct Cost: ¥2,500,000、Indirect Cost: ¥750,000)
Keywords血管新生 / 再生医療 / 細胞治療 / 脂肪幹細胞 / 脂肪組織由来間葉系幹細胞 / micro RNA / エクソソーム
Outline of Final Research Achievements

Human SVF cells were obtained subcutaneous adipose tissue. The, CD271+ and CD271- subsets were isolated from SVF by FACS. Both of them were cultivated in normal condition or hypoxic condition. Exosome were isolated using magnet beads. Micro RNAs obtained from exosomes were isolated and analyzed by microarray.

Academic Significance and Societal Importance of the Research Achievements

新規の血管新生因子の探索に関して探索を行うことは、糖尿病などの増加や高齢化社会を迎えるにあたって増加の一途をたどる虚血性疾患の新規治療につながる意義をもつ

Report

(3 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • Research Products

    (2 results)

All 2019 2018

All Presentation (2 results) (of which Int'l Joint Research: 1 results)

  • [Presentation] ヒト脂肪組織由来間質細胞中の血管新生サブセットの同定2019

    • Author(s)
      井上己音
    • Organizer
      日本再生医療学会総会
    • Related Report
      2018 Research-status Report
  • [Presentation] Human CD271-positive Adipose Derived Stem Cells are the Angiogenic Subset with Less-aged and Less-fibrotic gene expression profile2018

    • Author(s)
      Oto Inoue
    • Organizer
      AHA scientific sessions
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research

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Published: 2018-04-23   Modified: 2021-02-19  

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