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Basic studies of protective immunity and immune response on catechins.

Research Project

Project/Area Number 20680035
Research Category

Grant-in-Aid for Young Scientists (A)

Allocation TypeSingle-year Grants
Research Field Eating habits, studies on eating habits
Research InstitutionHokkaido University

Principal Investigator

HAYAKAWA Sumio  Hokkaido University, 遺伝子病制御研究所, 助教 (00368292)

Project Period (FY) 2008 – 2009
Project Status Completed (Fiscal Year 2009)
Budget Amount *help
¥10,660,000 (Direct Cost: ¥8,200,000、Indirect Cost: ¥2,460,000)
Fiscal Year 2009: ¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2008: ¥6,110,000 (Direct Cost: ¥4,700,000、Indirect Cost: ¥1,410,000)
Keywords自然免疫 / 感染症 / 生理活性 / 栄養学
Research Abstract

Green tea, one of the most popular beverage consumed in japan, contains a series of polyphenols known as catechins. The catechins have been reported to posses various biological and pharmacological effects, such as anticancer and antibacterial activities, and lowering of plasma lipids and glucose level. The present study was designed to examine the effect of catechins on the innate immune response. Virus infection elicits potent cellular responses that contain virus spread before the adaptive immune system can intervene, and production of type I interferons (IFN α/β) is central to this process. The sensor involved in coupling recognition of virus infection with the induction of IFN α/β have recently been discovered. These sensors include RIG-I and MDA5, RNA-binding DExD/H box helicases. Recent study indicated that cytosolic DNA-dependent RNA polymerase III converts pathogen dsDNA into dsRNA that has a 5' triphosphate (3pRNA). This RNA species is then sensed by the RNA sensor RIG-I, leading to INF-β production and activation of innate immunity. In this experiments, we found that new function molecule "SCI-2" enhanced the innate immune responses by 3pRNA. These results suggest that SCI-2 is important in recognition of nucleic acids derived from virus. Furthermore, to reveal the underlying mechanisms of action at a molecular level correlation between catechins and SCI-2, we will examine the effect of tea catechin on the virus infection in transgenic mouse.

Report

(3 results)
  • 2009 Annual Research Report   Final Research Report ( PDF )
  • 2008 Annual Research Report
  • Research Products

    (14 results)

All 2009 2008 Other

All Journal Article (4 results) (of which Peer Reviewed: 4 results) Presentation (8 results) Remarks (2 results)

  • [Journal Article] Cytokine-rich autologous serum system for cartilaginous tissue engineering.2008

    • Author(s)
      Isogai, N., et al.
    • Journal Title

      Ann. Plast. Surg. 60巻

      Pages: 703-709

    • Related Report
      2009 Final Research Report
    • Peer Reviewed
  • [Journal Article] Subcellular localization of human heparanase and its alternative splice variant in COS-7 cells.2008

    • Author(s)
      Sato, M,., et al.
    • Journal Title

      Cell. Biochem. Funct. 26巻

      Pages: 676-683

    • Related Report
      2009 Final Research Report
    • Peer Reviewed
  • [Journal Article] Subcellular localization of human heparanase and its alternative splice variant in COS-7 cells2008

    • Author(s)
      Sato, M,. et.al.
    • Journal Title

      Cell Biochem Funct 26

      Pages: 676-683

    • Related Report
      2008 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Cytokine-rich autologous serum system for cartilaginous tissue engineering2008

    • Author(s)
      Isogai, N., et.al.
    • Journal Title

      Ann Plast Surg 60

      Pages: 703-709

    • Related Report
      2008 Annual Research Report
    • Peer Reviewed
  • [Presentation] 自然免疫におけるI FN応答の新たな制御メカニズム2009

    • Author(s)
      高岡晃教, 早川清雄
    • Organizer
      第32回日本分子生物学会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2009-12-10
    • Related Report
      2009 Final Research Report
  • [Presentation] 自然免疫におけるIFN応答の新たな制御メカニズム2009

    • Author(s)
      早川清雄
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2009-12-10
    • Related Report
      2009 Annual Research Report
  • [Presentation] 核酸を介する自然免疫活性化機構の解析2009

    • Author(s)
      早川清雄, 高岡晃教
    • Organizer
      第39回日本免疫学会総会・学術集会
    • Place of Presentation
      大阪国際会議場
    • Year and Date
      2009-12-03
    • Related Report
      2009 Final Research Report
  • [Presentation] 核酸を介する自然免疫活性化機構の解析2009

    • Author(s)
      早川清雄
    • Organizer
      第39回日本免疫学会総会・学術集会
    • Place of Presentation
      大阪国際会議場(大阪)
    • Year and Date
      2009-12-03
    • Related Report
      2009 Annual Research Report
  • [Presentation] SCI2を介する自然免疫シグナル制御2009

    • Author(s)
      高岡晃教, 早川清雄
    • Organizer
      第82回日本生化学会大会
    • Place of Presentation
      神戸ポートアイランド
    • Year and Date
      2009-10-29
    • Related Report
      2009 Final Research Report
  • [Presentation] SCI2を介した自然免疫応答制御2009

    • Author(s)
      高岡晃教
    • Organizer
      第82回日本生化学会大会
    • Place of Presentation
      神戸ポートアイランド(神戸)
    • Year and Date
      2009-10-24
    • Related Report
      2009 Annual Research Report
  • [Presentation] Novel function of DNA triggered innate immune responses2008

    • Author(s)
      早川清雄, 高岡晃教
    • Organizer
      T he 8th Awaji International Forum on Inf ection and Immunity
    • Place of Presentation
      淡路夢舞台国際会議場
    • Year and Date
      2008-09-09
    • Related Report
      2009 Final Research Report
  • [Presentation] Novel function of DNA triggered innate immune responses2008

    • Author(s)
      早川清雄
    • Organizer
      The 8th Awaji International Forum on Infection and Immunity
    • Place of Presentation
      淡路夢舞台国際会議場
    • Year and Date
      2008-09-07
    • Related Report
      2008 Annual Research Report
  • [Remarks]

    • URL

      http://www.igm.hokudai.ac.jp/sci/

    • Related Report
      2009 Annual Research Report
  • [Remarks]

    • URL

      http://www.igm.hokudai.ac.jp/sci/

    • Related Report
      2008 Annual Research Report

URL: 

Published: 2008-04-01   Modified: 2016-04-21  

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