The inhibition of fibronectin ED-A suppresses the development of proliferative vutreoretinopathy
Project/Area Number |
25462722
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Ophthalmology
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Research Institution | Oita University |
Principal Investigator |
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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)
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Research Collaborator |
YOKOYAMA Katsuhiko
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Project Period (FY) |
2013-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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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.
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Report
(5 results)
Research Products
(3 results)
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[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.
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Journal Title
J Dermatol.
Volume: 43
Issue: 8
Pages: 947-50
DOI
Related Report
Peer Reviewed / Open Access