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Analysis of the regulation of asymmetric cell division by using the artificially induced polarization of HeLa cells.

Research Project

Project/Area Number 24657088
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field Functional biochemistry
Research InstitutionNagoya University

Principal Investigator

HANAFUSA Hiroshi  名古屋大学, 理学(系)研究科(研究院), 講師 (00345844)

Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords細胞極性 / LRRK1 / スピンドル配向 / 非対称分裂 / Spindle orientation / NuMA / Dynein
Research Abstract

Asymmetric cell division is an important mechanism that regulates growth or differentiation of stem cells. In this project, we tried to reveal the role of important factors in asymmetric cell division by using the artificially induced polarization of HeLa cells, in which expressed the chimera molecules between Echinoid, an cell-cell adhesion molecule, and a factor, which activates the polarization signal pathway. We found that ROCO family kinase LRRK1 plays an important role in the control of the axis of cell division by regulating the mitotic spindle.

Report

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

    (15 results)

All 2013 2012 Other

All Journal Article (1 results) Presentation (13 results) Remarks (1 results)

  • [Journal Article] EGFR-dependent phosphorylation of leucine-rich repeat kinase LRRK1 is important for proper endosomal trafficking of EGFR2012

    • Author(s)
      Ishikawa, K., Nara, A., Matsumoto K., and Hanafusa, H.
    • Journal Title

      Mol. Biol. Cell

      Volume: 23 Pages: 1294-1306

    • Related Report
      2013 Final Research Report 2012 Research-status Report
  • [Presentation] The regulation of the intracellular trafficking of EGFR by ROCO family kinase LRRK12013

    • Author(s)
      花房洋、慶田城迅、渡辺崇、貝淵弘三、松本邦弘
    • Organizer
      第65回日本細胞生物学会年会
    • Place of Presentation
      ウインク愛知
    • Related Report
      2013 Final Research Report
  • [Presentation] LRRK1 regulates the maturation of autolysosome by phosphorylating Rab72013

    • Author(s)
      Haruka Ikeda, Hiroshi Hanafusa, Tomoki Nishioka, Kozo Kaibuchi, Kunihiro Matsumoto, Kyoko Shirakabe
    • Organizer
      第36回日本分子生物学会年会
    • Place of Presentation
      神戸ポートアイランド
    • Related Report
      2013 Final Research Report
  • [Presentation] LRRK1 regulates EGFR intracellular trafficking by phosphorylating CLIP-1702013

    • Author(s)
      Shin Kedashiro, Hiroshi Hanafusa, Takashi Watanabe, Kozo Kaibuchi, Kunihiro Matsumoto
    • Organizer
      第36回日本分子生物学会年会
    • Place of Presentation
      神戸ポートアイランド
    • Related Report
      2013 Final Research Report
  • [Presentation] ROCOファミリーキナーゼLRRK1によるEGFR細胞内トラフィック制御2013

    • Author(s)
      花房洋 慶田城迅 渡辺崇 貝淵弘三 松本邦弘
    • Organizer
      日本細胞生物学会
    • Place of Presentation
      ウインクあいち
    • Related Report
      2013 Annual Research Report
  • [Presentation] LRRK1はM期中心体のintegrity維持に必要である2012

    • Author(s)
      小松日菜子、花房洋、松本邦弘
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡国際会議場
    • Related Report
      2013 Final Research Report
  • [Presentation] PP5はLRRK1キナーゼ活性を負に制御することで紡錘体の多極化を防いでいる2012

    • Author(s)
      佐井和人、花房洋、松本邦弘
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡国際会議場
    • Related Report
      2013 Final Research Report
  • [Presentation] LRRK1はキネトコアとスピンドル微小管との接着を安定化する2012

    • Author(s)
      伊藤裕志、花房洋、松本邦弘
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡国際会議場
    • Related Report
      2013 Final Research Report
  • [Presentation] LRRK1はCLIP170をリン酸化することによりEGFRの微小管上の輸送を制御する2012

    • Author(s)
      慶田城迅、花房洋、高島成二、松本邦弘
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡国際会議場
    • Related Report
      2013 Final Research Report
  • [Presentation] PLK1-LRRK1経路によるM期紡錘体配向の制御機構2012

    • Author(s)
      花房洋、手塚基弘、豊島文子、松本邦弘
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Related Report
      2013 Final Research Report
  • [Presentation] EGFR依存的なLRRK1のリン酸化は適切なEGFR細胞内トラフィックに重要である2012

    • Author(s)
      石川光紀、花房洋、奈良篤樹、松本邦弘
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Related Report
      2013 Final Research Report
  • [Presentation] LRRK1はPrefoldin複合体と相互作用することで星状体微小管の形成に機能している2012

    • Author(s)
      宇佐美学史、花房洋、松本邦弘
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Related Report
      2013 Final Research Report
  • [Presentation] セリンスレオニンフォスファターゼPP5によるLRRK1キナーゼ活性の制御機構2012

    • Author(s)
      佐井和人、花房洋、松本邦弘
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Related Report
      2013 Final Research Report
  • [Presentation] LRRK1はaggregatesの輸送を介してaggresome形成を制御する2012

    • Author(s)
      崔恵蘭、花房洋、松本邦弘
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Related Report
      2013 Final Research Report
  • [Remarks]

    • URL

      http://bunshi3.bio.nagoy-u.ac.jp/~bunshi6/matsumoto_japanese/

    • Related Report
      2013 Final Research Report

URL: 

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

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