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Investigation of differentiation induction method of capillary endothelial cells and pericytes by using adipose derived stem cells

Research Project

Project/Area Number 21791739
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Plastic surgery
Research InstitutionThe University of Tokyo

Principal Investigator

HIGASHINO Takuya  The University of Tokyo, 医学部附属病院, 助教 (70433901)

Project Period (FY) 2009 – 2010
Project Status Completed (Fiscal Year 2010)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2010: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2009: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
KeywordsAIC / 増殖因子 / ASC / 血管新生治療 / 血管内皮細胞増殖 / 虚血脂肪組織 / 糖尿病脂肪組織 / 脂肪由来幹細胞 / 血管新生
Research Abstract

Based on the analysis of exudates from injured adipose tissue, we prepared a mixture containing the injury-associated growth factors at the same proportion as the exudates, named adipose injury cocktail (AIC). The purpose of this study is to elucidate the therapeutic potentials of AIC. AIC preferentially activated adipose-derived stem/progenitor/ stromal cells (ASCs) to proliferate, migrate, and form networks compared with vascular endothelialcells. AIC-treated ASCs tended to differentiate into adipocytes or vessel-constituting cells rather than into other cell types. In ischemic adipose tissues of mice, induced by either a surgical intervention or diabetes, AIC administration enhanced proliferation, especially of CD31-/CD34+ ASCs, and mitigated tissue hypoxia by increasing capillary density and reducing fibrogenesis. These results suggest that AIC may have therapeutic potentials for various ischemic/hypoxic conditions by inducing adipose remodeling and neovascularization through activation of ASCs and other cells. Treatment with AIC has many advantages over cell-based therapies regarding morbidity, cost, and physical risks and may be used as an alternative therapy for improving tissue oxygen.

Report

(3 results)
  • 2010 Annual Research Report   Final Research Report ( PDF )
  • 2009 Annual Research Report
  • Research Products

    (4 results)

All 2011 2010 2009

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (3 results)

  • [Journal Article] Adipose Injury-Associated Factors Mitigate Hypoxia in Ischemic Tissues through Activation of Adipose-Derived Stem/Progenitor/Stromal Cells and Induction of Angiogenesis2011

    • Author(s)
      Eto H, Suga H, Inoue K, Aoi N, Kato H, Araki J, Doi K, Higashino T, Yoshimura K
    • Journal Title

      Am J Pathol 178(5)

      Pages: 2322-2332

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Presentation] 急性虚血誘導時の組織内適応変化の解析2010

    • Organizer
      第19回日本形成外科基礎学術集会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2010-06-17
    • Related Report
      2010 Annual Research Report 2010 Final Research Report
  • [Presentation] Injury-associated growth factors improve ischemia through the activation of adipose-derived stem/progenitor cells in obese and non-obese mice2009

    • Author(s)
      江藤ひとみ
    • Organizer
      International Federation for Adipose Therapeutics and Science(IFATS)
    • Place of Presentation
      Hotel Inter-Burgo(Daegu, Korea)
    • Year and Date
      2009-10-16
    • Related Report
      2009 Annual Research Report
  • [Presentation] 創傷治癒因子による脂肪由来幹細胞の活性化を利用した血管新生治療の開発2009

    • Author(s)
      江藤ひとみ
    • Organizer
      第18回日本形成外科学会基礎学術集会
    • Place of Presentation
      都市センターホテル(東京都)
    • Year and Date
      2009-10-01
    • Related Report
      2009 Annual Research Report

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Published: 2009-04-01   Modified: 2016-04-21  

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