2006 Fiscal Year Final Research Report Summary
The role of transcriptional factor in neovascularization of proliferative diabetic retinopathy
Project/Area Number |
17591846
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Ophthalmology
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Research Institution | Chiba University (2006) Sapporo Medical University (2005) |
Principal Investigator |
MITAMURA Yoshinori Chiba University, Graduate School of Medicine, Associate Professor, 大学院医学研究院, 助教授 (30287536)
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Co-Investigator(Kenkyū-buntansha) |
OHGURO Hiroshi Sapporo Medical University, Professor, 医学部, 教授 (30203748)
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Project Period (FY) |
2005 – 2006
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Keywords | Diabetic retinopathy / Neovascularization / Transcriptional factor |
Research Abstract |
To assess the potential role of transcriptional factor in nevascularization of proliferative diabetic retinopathy (PDR), we examined the expression of activator protein-1 (AP-1) and nuclear factor kappa B (NFkB) in epiretinal membrane (ERM) of PDR and performed in vitro studies. Expression of AP-1 and NFkB in PDR ERMs 1) AP-1 mRNA was detected in all (100%) of the 19 eyes with PDR, but in only 7 (44%) of the 16 eyes with idiopathic ERM (P<0.05). NFkB mRNA was detected in 14 (74%) of the 19 eyes with PDR, but in only 6 (38%) of the 16 eyes with idiopathic ERM (P<0.05). 2) AP-1 protein was detected in PDR ERMs and was coexpressed with the glial-specific marker vimentin. Also, NFkB protein was detected in PDR ERMs and was coexpressed with vimentin and MCP-1. in vitro study 1) Glycated albumin stimulation significantly increased AP-1 phosphorylation in glial cells. Also, glycated albumin stimulation induced NFkB activationation and translocation to nuclei in glial cells.
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Research Products
(6 results)