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Analysis of tissue macrophage development and its function in vivo

Research Project

Project/Area Number 23890095
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Immunology
Research InstitutionOsaka University

Principal Investigator

ISE Masako (KOHYAMA Masako)  大阪大学, 微生物病研究所, 特任研究員(常勤) (70311339)

Project Period (FY) 2011
Project Status Completed (Fiscal Year 2011)
Budget Amount *help
¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2011: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywordsリンパ球 / 自然免疫 / 免疫監視
Research Abstract

Red pulp macrophage(RPM) is a tissue macrophage which localized in spleen. Spi-C is a transcriptional factor that control RPM development. We made Spi-C IRES-GFP knock-in mouse and Spi-C conditional knockout mice. We identified cells that had a potential to differentiate into RPMs. And also, we found the factor, one of the metabolite of red blood cell, which could induce Spi-C expression

Report

(2 results)
  • 2011 Annual Research Report   Final Research Report ( PDF )
  • Research Products

    (3 results)

All 2011 Other

All Presentation (1 results) Remarks (2 results)

  • [Presentation] Red pulp macrophageの脾臓に存在する前駆細胞の同定2011

    • Author(s)
      香山雅子
    • Organizer
      第40回日本免疫学会学術集会
    • Place of Presentation
      幕張メッセ(千葉県)
    • Year and Date
      2011-11-27
    • Related Report
      2011 Annual Research Report 2011 Final Research Report
  • [Remarks]

    • URL

      http://immchem.biken.osaka-u.ac.jp/

    • Related Report
      2011 Final Research Report
  • [Remarks]

    • URL

      http://immchem.biken.osaka-u.ac.jp/

    • Related Report
      2011 Annual Research Report

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Published: 2011-09-05   Modified: 2020-03-17  

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