Suppression of retinal neovascularization by shRNA targeting HIF-1alpha

Curr Eye Res. 2008 Oct;33(10):892-902. doi: 10.1080/02713680802416670.

Abstract

Purpose: To investigate whether vector-based HIF-1alpha -targeted shRNA expression system (pSUPER(siHIF-1alpha)) can inhibit HIF-1alpha and VEGF expression in vitro and suppress retinal neovascularization in the murine model of oxygen-induced retinopathy.

Methods: pSUPER(siHIF-1alpha) from which siRNA targeting HIF-1alpha could be generated was constructed and transfected to human umbilical vein endothelial cell lines (HUVECs). Then the expression levels of HIF-1alpha and VEGF in the cultured cells were measured by RT-PCR, immunoblot, and ELISA assays. Subsequently, pSUPER(siHIF-1alpha)was 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 pSUPER(siHIF-1alpha)could affect the expression levels of HIF-1alpha and VEGF in murine retinas.

Results: HIF-1alpha and hypoxia-induced vascular endothelial growth factor (VEGF) increase in cultured cells were greatly abolished by pSUPER(siHIF-1alpha). Meanwhile, retinal neovascularization in the eye with pSUPER(siHIF-1alpha)injection 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-1alpha and VEGF expression levels were down-regulated in the murine retinas treated with pSUPER(siHIF-1alpha).

Conclusions: RNAi targeting HIF-1alpha could inhibit the retinal neovascularization by approximately 65% through down-regulating the expression of HIF-1alpha and VEGF in the murine retinas, which may provide a powerful and novel therapeutic tool for ischemic-induced retinal diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Blotting, Western
  • Cell Culture Techniques
  • Disease Models, Animal
  • Endothelium, Vascular / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Fluorescein Angiography
  • Gene Expression Regulation / physiology
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Infant, Newborn
  • Mice
  • Mice, Inbred C57BL
  • Oxygen / toxicity
  • RNA Interference*
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / pharmacology*
  • Retinal Neovascularization / genetics
  • Retinal Neovascularization / pathology
  • Retinal Neovascularization / prevention & control*
  • Retinopathy of Prematurity / genetics
  • Retinopathy of Prematurity / pathology
  • Retinopathy of Prematurity / prevention & control*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transfection
  • Umbilical Veins / cytology
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • RNA, Messenger
  • RNA, Small Interfering
  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, mouse
  • Oxygen