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Regulation of directional movement during leukocyte chemotaxis by cell polarity proteins

Research Project

Project/Area Number 24590385
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Pathological medical chemistry
Research InstitutionKyushu University

Principal Investigator

KAMAKURA Sachiko  九州大学, 医学(系)研究科(研究院), 助教 (80398081)

Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywordsケモタキシス / 好中球 / 細胞極性 / 白血球
Outline of Final Research Achievements

Cell movement directed by a gradient of a diffusible chemoattractant is known as chemotaxis, which plays a vital role in developmental morphogenesis and immune responses. Neutrophilic leukocytes, crucial for host defense, move toward the source of chemoattractants, which are derived from invading microbes and/or produced by infected hosts, thereby arriving correctly at sites of infection for pathogen killing. Although neutrophil chemotaxis requires not only increased motility but also directional movement, molecular mechanisms for directionality control have remained largely unknown. We have shown that Inscuteable protein regulates directionality of chemotaxing neutrophils by tethering chemoattractant-elicited trimeric-Gi-protein signaling to an evolutionarily-conserved Par-polarity-protein complex.

Report

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

    (10 results)

All 2015 2014 2013 2012

All Journal Article (7 results) (of which Peer Reviewed: 7 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results) Presentation (3 results) (of which Invited: 2 results)

  • [Journal Article] Structural basis of cofactor-mediated stabilization and substrate recognition of the α-tubulin acetyltransferase αTAT12015

    • Author(s)
      Yuzawa S, Kamakura S, Hayase J, Sumimoto H
    • Journal Title

      Biochem J.

      Volume: 467 Issue: 2 Pages: 103-113

    • DOI

      10.1107/s2053230x14028143

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] The cell polarity protein mInsc regulates neutrophil chemotaxis via a noncanonical G protein signaling pathway2013

    • Author(s)
      Kamakura S., Nomura M., Hayase J., Iwakiri Y., Nishikimi A., Fukui Y., Takayanagi R., Sumimoto H.
    • Journal Title

      Dev Cell

      Volume: 26 Issue: 3 Pages: 292-302

    • DOI

      10.1016/j.devcel.2013.06.008

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] The WD40 protein Morg1 facilitates Par6-aPKC binding to Crb3 for apical identity in epithelial cells2013

    • Author(s)
      Hayase J, Kamakura S, Iwakiri Y, Yamaguchi Y, Izaki T, Ito T, Sumimoto H
    • Journal Title

      J. Cell Biol

      Volume: 200 Issue: 5 Pages: 635-650

    • DOI

      10.1083/jcb.201208150

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Interaction of NuMA protein with the kinesin Eg5: its possible role in bipolar spindle assembly and chromosome alignment2013

    • Author(s)
      Iwakiri Y, Kamakura S, Hayase J, Sumimoto H
    • Journal Title

      Biochem. J

      Volume: 451 Issue: 2 Pages: 195-204

    • DOI

      10.1042/bj20121447

    • Related Report
      2013 Research-status Report 2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Ubiquitination of the heterotrimeric G protein α subunits Gαi2 and Gαq is prevented by the guanine nucleotide exchange factor Ric-8A2013

    • Author(s)
      Chishiki, K., Kamakura, S., Yuzawa, S., Hayase, J., Sumimoto, H.
    • Journal Title

      Biochem Biophys Res Commun

      Volume: 435 Issue: 3 Pages: 414-419

    • DOI

      10.1016/j.bbrc.2013.04.103

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] The WD40 protein Morg1 facilitates Par6-aPKC binding to Crb3 for apical identity in epithelial cells.2013

    • Author(s)
      Hayase J, Kamakura S, Iwakiri Y, Yamaguchi Y, Izaki T, Ito T, Sumimoto H.
    • Journal Title

      J. Cell Biol.

      Volume: 200 Pages: 635-650

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Rab27 effector Slp2-a transports the apical signaling molecule podocalyxin to the apical surface of MDCK II cells and regulates claudin-2 expression.2012

    • Author(s)
      Yasuda T, et al.
    • Journal Title

      Molecular Biology of the Cell

      Volume: 23 Issue: 16 Pages: 3229-3239

    • DOI

      10.1091/mbc.e12-02-0104

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Presentation] 好中球ケモタキシスにおける遊走方向制御の分子機構2014

    • Author(s)
      鎌倉 幸子、住本 英樹
    • Organizer
      平成26年度 日本生化学会九州支部会例会 シンポジウム
    • Place of Presentation
      福岡
    • Year and Date
      2014-05-17
    • Related Report
      2014 Annual Research Report
    • Invited
  • [Presentation] GPCRからの新しいシグナリング経路:白血球の遊走制御機構2014

    • Author(s)
      鎌倉 幸子、野村 政壽、早瀬 純也、岩切 優子、錦見 昭彦、高柳 涼一、福井 宣規、住本 英樹
    • Organizer
      第87回日本内分泌学会学術総会 シンポジウム
    • Place of Presentation
      福岡
    • Year and Date
      2014-04-24 – 2014-04-26
    • Related Report
      2014 Annual Research Report
    • Invited
  • [Presentation] 細胞極性制御因子mInscは 非典型的な3量体Gタンパク質経路を介して好中球のケモタキシスを制御する2013

    • Author(s)
      鎌倉 幸子、野村 政壽、早瀬 純也、岩切 優子、錦見 昭彦、高柳 涼一、福井 宣規、住本 英樹
    • 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 Research-status Report

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

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