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Elucidation of pathology caused by heterolysis and development of its visualization method using MRI

Research Project

Project/Area Number 16K15231
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Pathological medical chemistry
Research InstitutionKanazawa University

Principal Investigator

HANAYAMA Rikinari  金沢大学, 医学系, 教授 (40403191)

Research Collaborator MIYATAKE Yuji  大阪大学, 医学系, 大学院生
Project Period (FY) 2016-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2017: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords他者融解 / リソソーム / MRI / 可視化 / リソソーム酵素
Outline of Final Research Achievements

Secretion of lysosomal enzymes from macrophages or neutrophils is called heterolysis, but what kind of physiological phenomena or pathological condition can be induced by heterolysis remains elusive. We recently identified a candidate molecule that regulates this process and confirmed that this molecule actually promotes heterolysis. When cardiovascular inflammation was induced in mice deficient in this molecule, the onset of cardiovascular inflammation was reduced as compared with the wild type mice. Furthermore, in order to clarify what type of lysosomal enzyme is actually released to cause organ and tissue damage in vivo by using MRI, we developed a new smart probe using 19F nanoparticles and a gadolinium complex.

Report

(3 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • Research Products

    (7 results)

All 2018 2017 2016

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Open Access: 1 results) Presentation (5 results) (of which Int'l Joint Research: 1 results,  Invited: 5 results)

  • [Journal Article] Induction of live cell phagocytosis by a specific combination of inflammatory stimuli.2017

    • Author(s)
      Ishidome T, Yoshida T, Hanayama R.
    • Journal Title

      EBioMedicine.

      Volume: 22 Pages: 89-99

    • DOI

      10.1016/j.ebiom.2017.07.011

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Mechanisms of lysosomal exocytosis by immune cells.2016

    • Author(s)
      Song J and Hanayama R
    • Journal Title

      Chronic Inflammation

      Volume: - Pages: 369-375

    • DOI

      10.1007/978-4-431-56068-5_29

    • ISBN
      9784431560661, 9784431560685
    • Related Report
      2016 Research-status Report
    • Peer Reviewed
  • [Presentation] Mechanisms of hemophagocytosis and heterolysis by phagocytes.2018

    • Author(s)
      華山力成
    • Organizer
      金沢大学-ゲント大学 研究交流国際シンポジウム(ベルギー)
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] 自己炎症疾患の発症機序とエクソソームの役割2017

    • Author(s)
      華山力成
    • Organizer
      第52回 インスリン研究会
    • Place of Presentation
      東京
    • Year and Date
      2017-02-04
    • Related Report
      2016 Research-status Report
    • Invited
  • [Presentation] 自己炎症疾患の発症機序とエクソソームの役割2017

    • Author(s)
      華山力成
    • Organizer
      第49回 日本小児感染症学会総会(金沢)
    • Related Report
      2017 Annual Research Report
    • Invited
  • [Presentation] 自己炎症疾患の発症機序とエクソソームの役割2017

    • Author(s)
      華山力成
    • Organizer
      第52回 インスリン研究会(東京)
    • Related Report
      2017 Annual Research Report
    • Invited
  • [Presentation] Mechanisms of hemophagocytosis and heterolysis by phagocytes.2016

    • Author(s)
      Rikinari Hanayama
    • Organizer
      第45回 日本免疫学会大会
    • Place of Presentation
      沖縄
    • Year and Date
      2016-12-07
    • Related Report
      2016 Research-status Report
    • Invited

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Published: 2016-04-21   Modified: 2023-03-16  

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