2011 Fiscal Year Final Research Report
Study of vitreous body : Analysis of microenvironmental control and development of novel treatment.
Project/Area Number |
20390450
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Ophthalmology
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Research Institution | Kagoshima University |
Principal Investigator |
SAKAMOTO Taiji 鹿児島大学, 医歯学総合研究科, 教授 (10235179)
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Co-Investigator(Kenkyū-buntansha) |
SONODA Koh-hei 山口大学, 医学系・研究科, 教授 (10294943)
MARUYAMA Ikuro 鹿児島大学, 医歯学総合研究科, 特任教授 (20082282)
TAKAO Sonshin 鹿児島大学, 医用ミニブタ・先端医療開発研究センター, 教授 (80171411)
KOSAI Ken-ichiro 鹿児島大学, 医歯学総合研究科, 教授 (90258418)
SUDA Yasuo 鹿児島大学, 理工学部・研究科, 教授 (70179282)
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Project Period (FY) |
2008 – 2011
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Keywords | 硝子体細胞 / SDF-1 / 硝子体免疫 / 薬物治療 / 超音波 |
Research Abstract |
We performed the study of vitreoretinal diseases from the points of its pathogenesis, molecular mechanism, and treatment. First, the relationship between intravitreous damage-associated molecular pattern and retinal damage was analyzed. As a result, retinal pathology was strongly affected not only by bioactive molecules such as cytokines, but rather by damaged cells and its related proteins. The experimental treatment using KO animals was very effective. The present findings are quite beneficial for developing a new treatment with minimal tissue damage.
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Research Products
(45 results)
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[Journal Article] Intraocular expression and release of high-mobility group box 1 protein in retinal detachment2009
Author(s)
Arimura N, Ki-i Y, Hashiguchi T, Kawahara K, Biswas KK, Nakamura M, Sonoda Y, Yamakiri K, Okubo A, Sakamoto T, Maruyama I.
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Journal Title
Lab Invest
Volume: 89(3)
Pages: 278-289
DOI
Peer Reviewed
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[Presentation] NSAIDs点眼による脈絡膜血管新生抑制2011
Author(s)
吉永就正, 有村昇, 大塚寛樹, 竹之内和則, 貞村ゆかり, 野間聖, 川原幸一, 園田祥三, 橋口照人, 丸山征郎, 坂本泰二
Organizer
第65回日本臨床眼科学会
Place of Presentation
東京国際フォーラム(東京都)
Year and Date
2011-10-08
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