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Publication : Platelet-derived growth factor receptor alpha is associated with oxidative stress-induced retinal cell death.

First Author  Kanamoto T Year  2011
Journal  Curr Eye Res Volume  36
Issue  4 Pages  336-40
PubMed ID  21405954 Mgi Jnum  J:179792
Mgi Id  MGI:5303053 Doi  10.3109/02713683.2011.556301
Citation  Kanamoto T, et al. (2011) Platelet-derived growth factor receptor alpha is associated with oxidative stress-induced retinal cell death. Curr Eye Res 36(4):336-40
abstractText  PURPOSE: The purpose of this study was to investigate the role played by platelet-derived growth factor-alpha (PDGFRalpha) in oxidative stress-induced retinal cell death. A previous proteomic study from our laboratory showed that expression of PDGFRalpha is elevated considerably in the retinas of an animal model of glaucoma-the excitatory amino acid carrier (EAAC) 1-deficient (EAAC1-/-) mouse. METHODS: Retinal sites and expression patterns of PDGFRalpha were determined by immunohistochemistry in the retinas of EAAC1-/- and control CRL:CD1(ICR) mice. A retinal cell line was exposed to hydrogen peroxide, and expression PDGFRalpha determined by Western blot analysis. Effects of PDGF-AA and PDGFRalpha-siRNA on hydrogen peroxide-induced retinal cell death were examined. RESULTS: PDGFRalpha was detected in the retinal ganglion cell layer (RGL) of both EAAC1-/- and ICR mice, and was also localized in the internal nuclear layer (INL) of EAAC1-/- mice. While treatment with excess PDGF-AA had no additional effect on retinal cell death, expression of PDGFRalpha increased with exposure to hydrogen peroxide. Hydrogen peroxide-induced retinal cell death was inhibited by exposure to PDGF-AA via phosphatidylinositol 3 kinase (PI3K); cell death was promoted by PDGFRalpha-siRNA. CONCLUSIONS: PDGFRalpha is expressed in mouse retina, where it is essential for retinal cell survival under conditions of oxidative stress.
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