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Establishment of a new human reporter cells which can monitor the expression of somatic cell initialization factor and its application for elucidating the molecular mechanism of cell reprogramming

Research Project

Project/Area Number 23659115
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field General physiology
Research InstitutionOsaka City University

Principal Investigator

FUJITA Hisiakazu  大阪市立大学, 医学(系)研究科(研究院), 講師 (30212187)

Project Period (FY) 2011-04-28 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2013: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2012: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords体細胞初期化因子 / 初期化因子
Outline of Final Research Achievements

A homeobox transcription factor, Nanog, is one of the genes which support the self-renewal and pluripotency of embryonic stem (ES) cells. Nanog can reprogram human somatic cells to pluripotent stem cells in combination with OCT4, SOX2, and LIN28. Molecular mechanism(s) of the regulation of Nanog expression is important for understanding of reprogramming process. We sought to establish the reporter cell line, which can monitor the somatic cell initialization factor expression for elucidating the molecular mechanism(s) of cell reprogramming. In addition, stem cell pluripotency and differentiation are regulated by the signal transduction pathways involeved in G protein coupled receptors (GPCRs). Therefore, we investigate ligand binding mode of the representative GPCRs, human formylpeptide receptor (hFPR) and formylpeptide receptor-like 1 (hFPRL1) by three-dimensional homology modeling of receptors and ligand docking simulation.

Report

(5 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (19 results)

All 2014 2013 2012 2011 Other

All Journal Article (5 results) (of which Peer Reviewed: 4 results) Presentation (10 results) Remarks (4 results)

  • [Journal Article] Heterogeneous nuclear ribonucleoprotein Q is a novel substrate of SH2 domain-containing phosphatase-2.2013

    • Author(s)
      Watanabe N, Kato T, Fujita H, Kitagawa S.
    • Journal Title

      J Biochem

      Volume: 154 Issue: 5 Pages: 475-480

    • DOI

      10.1093/jb/mvt078

    • NAID

      40019881450

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Biological Effects of calpain inhibitors on human phagocyte functions.2013

    • Author(s)
      Seiichi Kitagawa, Takayuki Kato, Maki Kitagawa, Megumi Aomatsu, Hisakazu Fujita
    • Journal Title

      Enzymes and Enzyme Activity: Structure, Biology and Clinical Significance

      Volume: 5 Pages: 121-144

    • Related Report
      2012 Research-status Report
  • [Journal Article] Gelsolin Induces Promonocytic Leukemia Differentiation Accompanied by Upregulation of p21CIP12012

    • Author(s)
      Reza Shirkoohi, Hisakazu Fujita, Stephanie Darmanin, Masato Takimoto
    • Journal Title

      Asian Pacific J Cancer Prev.

      Volume: 13(9) Issue: 9 Pages: 4827-4834

    • DOI

      10.7314/apjcp.2012.13.9.4827

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Stimulation of human formyl peptide receptors by calpain inhibitors : Homology modeling of receptors and ligand docking simulation2011

    • Author(s)
      Fujita H, Kato T, Watanabe N, Takahashi T, Kitagawa S
    • Journal Title

      Arch Biochem Biophys

      Volume: 516 Issue: 2 Pages: 121-127

    • DOI

      10.1016/j.abb.2011.09.017

    • Related Report
      2011 Research-status Report
    • Peer Reviewed
  • [Journal Article] Calpain inhibitors stimulate phagocyte functions via activation of human formyl peptide receptors2011

    • Author(s)
      Fujita H, Kato T, Watanabe N, Takahashi T, Kitagawa S
    • Journal Title

      Arch Biochem Biophys

      Volume: 513 Issue: 1 Pages: 51-60

    • DOI

      10.1016/j.abb.2011.06.007

    • Related Report
      2011 Research-status Report
    • Peer Reviewed
  • [Presentation] cAMPによるヒト抗アポトーシスタンパク質Mcl-1の分解抑制の分子機構2014

    • Author(s)
      藤田 寿一, 加藤 隆幸
    • Organizer
      第35回 日本炎症・再生医学会
    • Place of Presentation
      万国津梁館(沖縄県・名護市)
    • Year and Date
      2014-07-01 – 2014-07-04
    • Related Report
      2014 Annual Research Report
  • [Presentation] LPS刺激によって誘導されるヒト好中球からのTNF-α産生のG-CSF/IFN/ATPによる制御機構2013

    • Author(s)
      加藤隆幸,青松恵美,笠原恵美子,藤田寿一,北川誠一
    • Organizer
      第34回 日本炎症・再生医学会
    • Place of Presentation
      京都 国立京都国際会館
    • Related Report
      2013 Research-status Report
  • [Presentation] Regulation of G-CSF/IFN/ATP on TLR agonist-induced TNF-αproduction in human neutrophils2013

    • Author(s)
      加藤隆幸,青松恵美,笠原恵美子,藤田寿一,北川誠一
    • Organizer
      第75回 日本血液学会学術集会
    • Place of Presentation
      札幌 ロイトン札幌・さっぽろ芸文館・札幌市教育文化会館
    • Related Report
      2013 Research-status Report
  • [Presentation] カルパイン阻害剤はヒト・フォルミルペプチド受容体と直接相互作用して活性化する2012

    • Author(s)
      藤田寿一、加藤隆幸、渡邊哲史、高橋達治、北川 誠一
    • Organizer
      第33回 日本炎症・再生医学会
    • Place of Presentation
      ホテル日航福岡 (福岡市)
    • Related Report
      2012 Research-status Report
  • [Presentation] カルパイン阻害剤はヒト・フォルミルペプチド受容体と直接相互作用して細胞機能を活性化する2012

    • Author(s)
      藤田寿一、加藤隆幸、渡邊哲史、高橋達治、北川 誠一
    • Organizer
      第105回 近畿生理学談話会
    • Place of Presentation
      関西医科大学 (守口市)
    • Related Report
      2012 Research-status Report
  • [Presentation] Activation of human formyl peptide receptors by calpain inhibitors2012

    • Author(s)
      藤田寿一、加藤隆幸、渡邊哲史、高橋達治、北川 誠一
    • Organizer
      第74回 日本血液学会学術集会
    • Place of Presentation
      国立京都国際会館 (京都市)
    • Related Report
      2012 Research-status Report
  • [Presentation] Stimulation of Human Formyl Peptide Receptors by Calpain Inhibitors.2012

    • Author(s)
      Hisakazu Fujita
    • Organizer
      Protein and Peptide Conference 2012(招待講演)
    • Place of Presentation
      Beijing, China
    • Related Report
      2011 Research-status Report
  • [Presentation] カルパイン阻害剤はヒトホルミルペプチド受容体を介して食細胞機能を活性化する

    • Author(s)
      藤田寿一、加藤隆幸、渡邊哲史、高橋達治、北川誠一
    • Organizer
      第104回 近畿生理学談話会
    • Place of Presentation
      高槻市・大阪
    • Related Report
      2011 Research-status Report
  • [Presentation] Activation of cell functions by calpain inhibitors via human formyl peptide receptors

    • Author(s)
      藤田寿一、加藤隆幸、福園駿介、渡邊哲史、高橋達治、北川誠一
    • Organizer
      第73回 日本血液学会学術集会
    • Place of Presentation
      名古屋市・愛知
    • Related Report
      2011 Research-status Report
  • [Presentation] カルパイン阻害剤はヒトホルミルペプチド受容体を介して細胞機能を活性化する

    • Author(s)
      藤田寿一、加藤隆幸、福園駿介、渡邊哲史、高橋達治、北川誠一
    • Organizer
      第32回 日本炎症再生 医学会
    • Place of Presentation
      京都市・京都
    • Related Report
      2011 Research-status Report
  • [Remarks] 大阪市立大学大学院医学研究科・細胞情報学

    • URL

      http://www.med.osaka-cu.ac.jp/physiology2/

    • Related Report
      2014 Annual Research Report
  • [Remarks] 大阪市立大学大学院医学研究科・細胞情報学

    • URL

      http://www.med.osaka-cu.ac.jp/physiology2/

    • Related Report
      2013 Research-status Report
  • [Remarks] 大阪市立大学大学院医学研究科細胞情報学

    • URL

      http://www.med.osaka-cu.ac.jp/physiology2/

    • Related Report
      2012 Research-status Report
  • [Remarks]

    • URL

      http://www.med.osaka-cu.ac.jp/physiology2/

    • Related Report
      2011 Research-status Report

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Published: 2011-08-05   Modified: 2019-07-29  

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