Suppression of Retinal Neovascularization by shRNA Targeting HIF-1α

Abstract

Purpose: To investigate whether vector-based HIF-1α -targeted shRNA expression system (pSUPERsiHIF-1α) can inhibit HIF-1α and VEGF expression in vitro and suppress retinal neovascularization in the murine model of oxygen-induced retinopathy. Methods: pSUPERsiHIF − 1α from which siRNA targeting HIF-1α could be generated was constructed and transfected to human umbilical vein endothelial cell lines (HUVECs). Then the expression levels of HIF-1α and VEGF in the cultured cells were measured by RT-PCR, immunoblot, and ELISA assays. Subsequently, pSUPERsiHIF − 1αwas intravitreally injected into the murine model of oxygen-induced retinopathy (OIR). Retinal neovascularization was evaluated by angiography using fluorescein-labeled dextran and quantitated histologically. Moreover, RT-PCR and immunoblot analysis were used to determine whether local administration of pSUPERsiHIF-1αcould affect the expression levels of HIF-1α and VEGF in murine retinas. Results: HIF-1α and hypoxia-induced vascular endothelial growth factor (VEGF) increase in cultured cells were greatly abolished by pSUPERsiHIF-1α. Meanwhile, retinal neovascularization in the eye with pSUPERsiHIF-1αinjection was significantly reduced compared with that of the contralateral control eye. Histological analysis indicates that neovascular nuclei protruding into the vitreous cavity were decreased by nearly 65%. Furthermore, HIF-1α and VEGF expression levels were down-regulated in the murine retinas treated with pSUPERsiHIF-1α. Conclusions: RNAi targeting HIF-1α could inhibit the retinal neovascularization by approximately 65% through down-regulating the expression of HIF-1α and VEGF in the murine retinas, which may provide a powerful and novel therapeutic tool for ischemic-induced retinal diseases.