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New therapy for Periventricular leucomalacia using mesenchymal stem cell

Research Project

Project/Area Number 24659507
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Embryonic/Neonatal medicine
Research InstitutionTokyo Medical and Dental University

Principal Investigator

TAKI Atsuko  東京医科歯科大学, 医学部附属病院, 助教 (20614481)

Co-Investigator(Renkei-kenkyūsha) KOMAKI Motohiro  東京医科歯科大学, 歯学部付属病院, 准教授 (30401368)
IWASAKI Kengo  東京医科歯科大学, 歯学部付属病院, 講師 (40401351)
Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2014: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords子宮内感染 / 脳室周囲白質軟化症 / 間葉系幹細胞 / 再生治療 / 子宮内感染合併症 / 新生児白質損傷モデル
Outline of Final Research Achievements

In this study we explore the therapeutic effects of MSC or MSC-conditioned medium (MSC-CM) on LPS-induced rat PVL model. Umbilical cord-derived MSC (UCMSC, Lonza) were purchased. Four-day old rats were intraperitoneally challenged with LPS to create PVL model and simultaneously treated by culture medium (control), MSC, or MSC-CM. Immuno-staining of myelin basic protein (MBP) in brain sections was used to evaluate cerebral white matter. Real time-PCR was performed to quantitate proinflammatory cytokine levels in 6-day-old rat brain.Postnatal LPS challenge caused PVL in rats, evaluated by increased inflammatory chytokines on day 6, and loss of MBP on day 12. Both MAS and MSC-CM significantly attenuated the cytokine level whereas only MSC attenuated loss of MBP.Our results showed that therapeutic potential of MSC due to anti-inflammatory effects in rat PVL model. The differences between MSC and MSC-CM suggests direct cellular effects are necessary for preventing MBP loss in PVL.

Report

(4 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report
  • Research Products

    (7 results)

All 2015 2014 Other

All Presentation (7 results)

  • [Presentation] 臍帯由来間葉系幹細胞を用いた脳室周囲白質軟化症の治療効果とその機序の解明2015

    • Author(s)
      森丘千夏子
    • Organizer
      第51回日本周産期新生児学会
    • Place of Presentation
      福岡
    • Year and Date
      2015-07-10 – 2015-07-12
    • Related Report
      2014 Annual Research Report
  • [Presentation] 臍帯由来間葉系幹細胞を用いた脳室周囲白質軟化症の治療法の開発2015

    • Author(s)
      森丘千夏子
    • Organizer
      日本小児科学会
    • Place of Presentation
      大阪
    • Year and Date
      2015-04-16 – 2015-04-19
    • Related Report
      2014 Annual Research Report
  • [Presentation] 実験的子宮内感染症が臍帯由来間葉系幹細胞に及ぼす影響の検討2014

    • Author(s)
      滝敦子
    • Organizer
      第59回日本未熟児新生児学会
    • Place of Presentation
      松山
    • Year and Date
      2014-11-10 – 2014-11-12
    • Related Report
      2014 Annual Research Report
  • [Presentation] 臍帯由来間葉系幹細胞を用いた脳室周囲白質軟化症の治療法の開発2014

    • Author(s)
      森丘千夏子
    • Organizer
      第50回日本周産期新生児学会
    • Place of Presentation
      千葉
    • Year and Date
      2014-07-10 – 2014-07-12
    • Related Report
      2014 Annual Research Report
  • [Presentation] 「ラット子宮内感染モデルを用いた新生児脳室周囲白質軟化症及び慢性肺疾患に対する 臍帯由来間葉系幹細胞を用いた治療の検討」

    • Author(s)
      本多泉、滝敦子、岩崎剣吾、小牧基浩、森田育男
    • Organizer
      第33回日本炎症・再生医学会
    • Place of Presentation
      福岡
    • Related Report
      2012 Research-status Report
  • [Presentation] 「LPS羊水腔内投与によるラット子宮内感染モデルを用いた研究 第1報:胎盤および新生児合併症の解析」

    • Author(s)
      本多泉、滝敦子、森丘千夏子、杉江学、土井庄三郎、水谷修紀、宮坂尚幸
    • Organizer
      第48回周産期・新生児医学会
    • Place of Presentation
      大宮
    • Related Report
      2012 Research-status Report
  • [Presentation] 「LPS羊水腔内投与によるラット子宮内感染モデルと用いた研究:第2報:間葉系幹細胞を用いた治療法の開発」

    • Author(s)
      滝敦子、本多泉、森丘千夏子、杉江学、宮坂尚幸、土井庄三郎、水谷修紀
    • Organizer
      第48回周産期・新生児医学会
    • Place of Presentation
      大宮
    • Related Report
      2012 Research-status Report

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Published: 2013-05-31   Modified: 2019-07-29  

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