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ARVO Poster 2005

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Please use this identifier to cite or link to this item: http://hdl.handle.net/1928/3523

ARVO Poster 2005

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dc.contributor.author McGuire, Paul
dc.date.accessioned 2007-12-03T16:08:53Z
dc.date.available 2007-12-03T16:08:53Z
dc.date.issued 2007-12-03T16:08:53Z
dc.identifier.uri http://hdl.handle.net/1928/3523
dc.description.abstract Purpose: Hepatocyte growth factor (HGF), acting through its receptor, c-met, is a cytokine whose role in promoting cell migration has been extensively documented. HGF and c-met have been implicated in the progression of angiogenesis in many cancer models and in the mouse model of retinal neovascularization. However, HGF mediation of protease expression and of an endothelial cell migratory phenotype in the retina has not been explored. We determined if HGF and/or hypoxia effects cell migration and protease levels in retinal microvascular endothelial cells and in a mouse model of retinal neovascularization. Methods: Bovine retinal microvascular endothelial cells (BRMVEC) were grown to near confluence and then stimulated with HGF (10ng/ml and 30 ng/ml) under normoxic and/or hypoxic conditions. At varying time points, conditioned media and cell extracts were collected and analyzed by zymography or by reverse-transcription PCR. Stable hypoxic conditions were achieved by adding 100M CoCl2 to the cell media. Migration assays were performed by growing BRMVEC’s to confluence with or without HGF and wounding the monolayer. After 24 hours, the amount of cellular migration into the wound was analyzed. Retinal neovascularization was induced in newborn mice by exposure to 75% oxygen followed by room air. Eyes were collected at day 17 following removal from high oxygen, fixed in 10% formalin and embedded in paraffin. Sections were cut, and immunohistochemistry was performed to localize retinal c-met expression. Results: After 24 hours of HGF stimulation there is a hypoxia-dependent, and dose-dependent increase in the 54 kDa form of urokinase in endothelial cells. This expression pattern correlated with the PCR analysis of uPA and uPAR mRNA. There is also a hypoxia-dependent and dose dependent increase in the active form of MMP 2. The wound assay demonstrated that HGF significantly increased BRMVEC cell migration compared to control samples. Immunohistochemical staining showed localized c-Met expression in the retina, which was increased in experimental animals compared to control. Conclusion: HGF, acting through its receptor c-met, may play an important role in the initial stages of retinal angiogenesis by stimulating a migratory phenotype and endothelial cell protease production. en_US
dc.format.extent 5216768 bytes
dc.format.mimetype application/vnd.ms-powerpoint
dc.language.iso en en_US
dc.subject HGF en_US
dc.subject Angiogenesis en_US
dc.title ARVO Poster 2005 en_US
dc.type Presentation en_US


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