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Mechanistic study for the hemophagocytosis-like condition during the induction of hematopoietic cells from human pluripotent stem cells

Research Project

Project/Area Number 22591053
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Hematology
Research InstitutionResearch Institute, International Medical Center of Japan

Principal Investigator

SAEKI Kumiko  独立行政法人国立国際医療研究センター, 疾患制御研究部, 室長 (80322717)

Project Period (FY) 2010 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2010: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
KeywordsヒトiPS細胞 / 血球貪食 / マクロファージ / インターフェロン / ヒトES細胞 / マクロフージ
Research Abstract

By using neutrophil-inducing differentiation culture system of human embryonic stem (ES) cells, we observed macrophage-dominant induction of human induced pluripotent stem (iPS) cells. During the early phase of differentiation of human iPS cells, we observed neutrophil-progenitors and the phagocytosis of these progenitors by macrophage, suggesting that our iPS system represent in vitro model of hemophagocytosis known in human diseases. In the present study, we performed molecular analysis of this in vitro model of hemophagocytosis. We observed expression of IFNα1 、IFNα2 、IFNβ1 during the differentiation of all four iPS cell lines and one of three ES cell lines. However, we observed neutrophil-dominant differentiation of human iPS cells under the low cell density culture condition and macrophage-dominant differentiation of human ES cells in certain ES cell lines. Thus, we were not able to clarify the relationship between ES versus iPS cells and neutrophil versus macrophage induction in our differentiation inducing culture system in this study.

Report

(4 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Annual Research Report
  • 2010 Annual Research Report
  • Research Products

    (8 results)

All 2013 2012 2011

All Journal Article (2 results) (of which Peer Reviewed: 2 results) Presentation (3 results) Patent(Industrial Property Rights) (3 results) (of which Overseas: 2 results)

  • [Journal Article] Production of functional classical brown adipocytes from human pluripotent stem cells using specific hemopoietin cocktail without gene transfer.2012

    • Author(s)
      M Nishio, T Yoneshiro, M Nakahara, S Suzuki, K Saeki, M Hasegawa, Y Kawai, H Akutsu, A
    • Journal Title

      Cell Metabolism

      Volume: 16 Issue: 3 Pages: 394-406

    • DOI

      10.1016/j.cmet.2012.08.001

    • Related Report
      2012 Annual Research Report 2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Early senescence is not an inevitable fate of human induced pluripotent stem-derived cells2011

    • Author(s)
      Gokoh M, Nakamura N, Matsuyama S, Nishio M, Akutsu H, Umezawa A, Yasuda K, Yuo A, Saeki K
    • Journal Title

      Cellular Reprogram

      Volume: 13 Issue: 4 Pages: 361-370

    • DOI

      10.1089/cell.2011.0004

    • Related Report
      2012 Final Research Report 2011 Annual Research Report
    • Peer Reviewed
  • [Presentation] Brown adipocyte differentiation of human pluripotent stem cells without genetic manipulation.2012

    • Author(s)
      Nishio M, Nakahara M, Saeki K, Hasegawa M, Yuo A, Saeki K
    • Organizer
      The 10th Annual Meeting International Society of Stem Cell Research
    • Place of Presentation
      Yokohama, Japan
    • Related Report
      2012 Final Research Report
  • [Presentation] Brown adipocyte differentiation of human pluripotent stem cells without genetic manipulation.2012

    • Author(s)
      Nishio M, et al.
    • Organizer
      The 10th Annual Meeting International Society of Stem Cell Research
    • Place of Presentation
      Yokohama, Japan.
    • Related Report
      2012 Annual Research Report
  • [Presentation] 無フィーダー・無血清環境でのヒトES細胞からの赤血球および造血ストロマ細胞の作製2011

    • Author(s)
      西尾美和子、中村直子、松山さと子、湯尾 明、佐伯久美子
    • Organizer
      第10回日本再生医療学会総会
    • Place of Presentation
      東京
    • Related Report
      2012 Final Research Report 2010 Annual Research Report
  • [Patent(Industrial Property Rights)] 多能性幹細胞由来褐色脂肪細胞、多能性幹細胞由来細胞凝集物と、その製造方法及び細胞療法、内科療法2013

    • Inventor(s)
      佐伯久美子、湯尾 明、西尾美和子、川崎正子、佐伯晃一、長谷川護
    • Industrial Property Rights Holder
      独立行政法人国立国際医療研究センター、ディナベック株式会社
    • Filing Date
      2013-04-26
    • Related Report
      2012 Final Research Report
    • Overseas
  • [Patent(Industrial Property Rights)] 霊長類動物胚性幹細胞の培養及び継代方法、並びにその分化誘導方法2012

    • Inventor(s)
      湯尾 明、佐伯久美子、佐伯晃一、中原正子、中村直子、過足芳子、松山さと子、米田麻子
    • Industrial Property Rights Holder
      独立行政法人国立国際医療研究センター、田辺三菱製薬株式会社
    • Acquisition Date
      2012-08-24
    • Related Report
      2012 Final Research Report
  • [Patent(Industrial Property Rights)] 多能性幹細胞由来褐色脂肪細胞、多能性幹細胞由来細胞凝集物と、その製造方法及び細胞療法、内科療法2012

    • Inventor(s)
      佐伯久美子、他
    • Industrial Property Rights Holder
      独立行政法人国立国際医療研究センター、ディナベック株式会社
    • Filing Date
      2012-04-26
    • Related Report
      2012 Annual Research Report
    • Overseas

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Published: 2010-08-23   Modified: 2019-07-29  

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