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The effect of angiogenesis of the product of RPE specific pp344 gene

Research Project

Project/Area Number 15591863
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Ophthalmology
Research InstitutionSaga University (2004)
佐賀医科大学 (2003)

Principal Investigator

OKINAMI Satoshi  Saga University, Faculty of Medicine, Ophthalmology, Professor, 医学部, 教授 (70089100)

Co-Investigator(Kenkyū-buntansha) KOBAYASHI Hiroshi  Saga University, Faculty of Medicine, Ophthalmology, Associate Professor, 助教授 (00215360)
KOBAYASHI Kaori  Saga University, Faculty of Medicine, Ophthalmology, Assistant Professor, 講師 (60325595)
Project Period (FY) 2003 – 2004
Project Status Completed (Fiscal Year 2004)
Budget Amount *help
¥2,900,000 (Direct Cost: ¥2,900,000)
Fiscal Year 2004: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2003: ¥1,700,000 (Direct Cost: ¥1,700,000)
Keywordsretinal pigment epithelium / angiogenesis / 血管内皮管腔形成 / セリンプロテアーゼインヒビター / in situハイブリダイゼーション / 免疫組織化学 / RT-PCR
Research Abstract

The pP344 gene was identified as a marker of chick retinal pigment epithelium(RPE). The predicted pP344 protein has high homology to a protein which represents a novel class of inhibitory TGF-beta binding protein. The member of TGF-beta superfamily has the various effects of angiogenesis. This study was undertaken to determine the expression and distribution of pP344 protein in the monkey retina, and investigate the effects of the pP344 protein on tubule formation in in vitro angiogenesis assay. The expression of mRNA corresponding to pP344 gene was examined by RT-PCR. The distribution of PP344 protein in monkey eye was investigated by immunohistochemical study. The effects of purified pP344 protein on tubule formation were studied in human umbilical vein endothelial cells, which were co-cultured with human fibroblasts in a 24-well plate over a period of 11 days. Endothelial tubulogenesis was visualized by immunostaining for CD31 on day 11. Endothelial cell-derived tubules were quantified by computer image analysis. RT-PCR analysis demonstrated the expression of pP344 gene in monkey RPE. By immunohistochemical analysis, the distribution of the PP344 protein was shown in the monkey RPE and choroid. The pP344 protein was also widely distributed in the monkey retina. With the addition of pP344 fusion protein, the length of endothelial cell derived tubules was increased in a concentration-dependent manner. The pP344 fusion protein promotes tubule formation in in vitro angiogenesis assay. These results indicated pPP344 protein may have a significant role in ocular neovascularization.

Report

(3 results)
  • 2004 Annual Research Report   Final Research Report Summary
  • 2003 Annual Research Report

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Published: 2003-03-31   Modified: 2016-04-21  

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