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Kan Ding, Marzia Scortegagna, Robyn Seaman, David G. Birch, Joseph A. Garcia; Retinal Disease in Mice Lacking Hypoxia-Inducible Transcription Factor-2α. Invest. Ophthalmol. Vis. Sci. 2005;46(3):1010-1016. doi: 10.1167/iovs.04-0788.
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purpose. To characterize ocular disease in HIF-2α-null mice.
methods. Histologic, electroretinographic (ERG), and molecular studies were performed on samples obtained from age- and gender-matched HIF-2α-null (HIF-2α-KO), HIF-2α-heterozygous (HIF-2α-HET), and wild-type (WT) littermate mice.
results. HIF-2α-KO mice exhibited marked thinning of the retina and abnormal retinal vasculature. The pathologic changes in HIF-2α-KO mice were associated with a virtual absence of postreceptor function. The expression of a surrogate marker for HIF-2α mRNA localized to vascular endothelial, amacrine, and retinal pigment epithelial (RPE) cells. Several HIF-2α target genes involved in angiogenesis, retinal protection, and stress responses have altered expression patterns in HIF-2α-KO retinas.
conclusions. HIF-2α-KO mice exhibit marked retinopathy consistent with complete loss of vision by 1 month of age. Impaired HIF-2α signaling in HIF-2α-KO mice likely produces functional deficits in cell types in which HIF-2α normally is expressed, ultimately resulting in retinopathy. Future studies will address whether the molecular abnormalities described in this study are directly responsible for the retinal disease in HIF-2α-KO mice.
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