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The inhibition of fibronectin ED-A suppresses the development of proliferative vutreoretinopathy

Research Project

Project/Area Number 25462722
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Ophthalmology
Research InstitutionOita University

Principal Investigator

KIMOTO KENICHI  大分大学, 医学部, 准教授 (50315339)

Co-Investigator(Kenkyū-buntansha) 久保田 敏昭  大分大学, 医学部, 教授 (30205140)
山田 喜三郎  大分大学, 医学部, 講師 (50452909)
Research Collaborator YOKOYAMA Katsuhiko  
Project Period (FY) 2013-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2013: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywords増殖硝子体網膜症 / TGF-β2 / 網膜色素上皮細胞 / 細胞外マトリックス / fibronectin ED-A / 網膜色素上皮 / TGF-β / Fibronectin ED-A / 増殖性硝子体網膜症 / Smad / p38MAPK / Rho-kinase / PI3K
Outline of Final Research Achievements

TGF-β2 induces epithelial mesenchymal transition (EMT) in retinal pigment epithelium (RPE). Therefore, it has been implicated as the key mediator of proliferative vitreoretinopathy. Type I collagen and fibronectin ED-A production were activated by TGF-β2 in RPE. Anti-fibronectin ED-A antibody inhibited TGF-β2-induced type I collagen mRNA expression and type I collagen synthesis. Fibronectin ED-A may be a new therapeutic target for treating proliferative vitreoretinopathy.

Report

(5 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (3 results)

All 2017 2016

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 3 results)

  • [Journal Article] Foveal hypoplasia in patients with stickler syndrome.2017

    • Author(s)
      Matsushita I, Nagata T, Hayashi T, Kimoto K, Kubota T, Ohji M, Kusaka S, Kondo H.
    • Journal Title

      Ophthalmology

      Volume: 印刷中

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] A Japanese family with autosomal dominant oculocutaneous albinism type4.2017

    • Author(s)
      Oki R, Yamada K, Nakano S, Kimoto K, Yamamoto K, Kondo H, Kubota T.
    • Journal Title

      Invest Ophthalmol Vis Sci.

      Volume: 58 Issue: 2 Pages: 1008-1016

    • DOI

      10.1167/iovs.16-20612

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Three cases of pigmented cosmetic dermatitis-like eruptions associated with primary Sjogren syndrome or anti-SSA antibody.2016

    • Author(s)
      Takeo N, Sakai T, Saito-Shono T, Ishikawa K, Hatano Y, Katagiri K, Takahashi Y, Kawano K, Kimoto K, Kubota T, Eshima N, Kojima H, Fujiwara S.
    • Journal Title

      J Dermatol.

      Volume: 43 Issue: 8 Pages: 947-50

    • DOI

      10.1111/1346-8138.13300

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access

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Published: 2014-07-25   Modified: 2019-07-29  

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