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Regulatory mechanisms of gene expression in anti-inflammatory M2 macrophages

Research Project

Project/Area Number 21592371
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Functional basic dentistry
Research InstitutionMeikai University

Principal Investigator

OHMORI Yoshihiro  明海大学, 歯学部, 教授 (50194311)

Co-Investigator(Kenkyū-buntansha) HIROI Miki  明海大学, 歯学部, 助教 (30419717)
Co-Investigator(Renkei-kenkyūsha) SEKINE Keisuke  横浜市立大学, 医学部, 助教 (00323569)
Project Period (FY) 2009 – 2011
Project Status Completed (Fiscal Year 2011)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2011: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2010: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2009: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywordsシグナル伝達 / M2マクロファージ / 腫瘍 / Il-4 / マクロファージ / STAT6 / IL-4 / 免疫組織 / CD163 / 口腔扁平上皮癌 / 遺伝子発現 / 抗炎症 / IL-13 / 低酸素
Research Abstract

Macrophages(Mφ) polarized with Th1 cytokines are called M1 Mφ, and are important for the clearance of pathogens and tumor cells. Mφactivated by Th2 cytokines IL4/IL-13 are classified as M2 Mφ, and are important in tissue repair and angiogenesis. We initially evaluated infiltrated Mφabout their phenotype by immunostainning in oral cancer tissue. We found that the infiltrated Mφhave an M2 phenotype. To further elucidate the mechanisms responsible for the M2-polarization of Mφin cancer, we examined the mechanisms of expression of the Arg-1 gene. Hypoxia further enhanced the IL-4/IL-13 induced Arg-1 mRNA expression. Although IL-4/IL-13-induced the Arg-1 expression has been shown to be dependent on STAT6 activation, hypoxia has no stimulatory effect on the STAT6-mediated transcriptional activation. These results suggest that hypoxia-mediated upregulation of the Arg-1 gene expression may result from cooperative interaction with different type of transcription factors and coactivators.

Report

(4 results)
  • 2011 Annual Research Report   Final Research Report ( PDF )
  • 2010 Annual Research Report
  • 2009 Annual Research Report
  • Research Products

    (5 results)

All 2011 2010 2009

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (4 results)

  • [Journal Article] Infiltration of M2 tumor-associated macrophages in oral squamous cell carcinoma correlates with tumor malignancy2011

    • Author(s)
      K. Mori, M. Hiroi, J. Shimada and Y. Ohmori
    • Journal Title

      Cancers

      Volume: 3 Issue: 4 Pages: 3726-3739

    • DOI

      10.3390/cancers3043726

    • Related Report
      2011 Annual Research Report 2011 Final Research Report
    • Peer Reviewed
  • [Presentation] 抗炎症性M2マクロファージにおけるArg-1遺伝子発現制御機構2011

    • Author(s)
      廣井美紀, 大森喜弘
    • Organizer
      歯科基礎医学会
    • Place of Presentation
      岐阜
    • Year and Date
      2011-10-02
    • Related Report
      2011 Final Research Report
  • [Presentation] 抗炎症性M2マクロファージにおけるArg-1遺伝子発現制御機構2011

    • Author(s)
      廣井美紀、大森喜弘
    • Organizer
      第53回日本歯科基礎医学会総会
    • Place of Presentation
      岐阜、長良川国際会議場
    • Year and Date
      2011-10-02
    • Related Report
      2011 Annual Research Report
  • [Presentation] 口腔扁平上皮癌における腫瘍関連M2マクロファージの局在2010

    • Author(s)
      森一将
    • Organizer
      第52回歯科基礎医学会総会
    • Place of Presentation
      タワーホール船堀(東京)
    • Year and Date
      2010-09-22
    • Related Report
      2010 Annual Research Report
  • [Presentation] 低酸素による抗炎症性M2マクロファージの遺伝子発現制御2009

    • Author(s)
      廣井美紀
    • Organizer
      第51回歯科基礎医学会
    • Place of Presentation
      朱鷺メッセ 新潟コンベンションセンター(新潟)
    • Year and Date
      2009-09-11
    • Related Report
      2009 Annual Research Report

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Published: 2009-04-01   Modified: 2016-04-21  

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