Reduction of experimental diabetic vascular leakage by delivery of angiostatin with a recombinant adeno-associated virus vector
Journal
Molecular Vision
Journal Volume
13
Pages
133-141
Date Issued
2007
Author(s)
Abstract
Purpose: To evaluate the efficacy of recombinant adeno-associated virus (rAAV) vector expressing mouse angiostatin (Kringle domains 1 to 4) in reducing retinal vascular leakage in an experimental diabetic rat model. Methods: rAAV-angiostatin was delivered by intravitreal injection to the right eyes of Sprague-Dawley rats. As a control, the contralateral eye received an intravitreal injection of rAAV-lacZ. Gene delivery was confirmed by reverse-transcriptase polymerase chain reaction (RT-PCR). Diabetes was induced by intravenous injection of streptozotocin (STZ). Vascular permeability changes were evaluated by extravascular albumin accumulation and leakage of intravenous-injected fluorescein isothiocynate-bovine serum albumin (FITC-BSA). Effects of rAAV-angiostatin on expression of vascular endothelial growth factor (VEGF), pigment epithelium-derived factor (PEDF), occludin, and phospho-p42/p44 MAP kinase in retina tissue were analyzed by western blotting. Results: The rAAV-angiostatin injections led to sustained angiostatin gene expression in retina as confirmed by RT-PCR, and reduced extravascular albumin accumulation in STZ-induced diabetic retina. Further, rAAV-angiostatin significantly decreased intravascularly injected FITC-BSA leakage at 5 days (p=0.001), 10 days (p<0.001), and 15 days (p=0.001) after STZ-induced diabetes, as compared to the control eyes receiving rAAV-lacZ. Expression of VEGF and phosphorylation of p42/p44 MAP kinase in retina was reduced by rAAV-angiostatin at day 1 (p=0.043 for both VEGF and phospho-p42/ p44 MAP kinase) after STZ-induced diabetes compared with rAAV-lacZ eyes. rAAV-angiostatin reduced retinal occludin loss at 10 days after STZ-induced diabetes (n=5, p=0.041). There was no significant difference in retinal PEDF expression between eyes injected with rAAV-angiostatin and rAAV-lacZ. Conclusions: Intravitreal delivery of rAAV-angiostatin reduces vascular leakage in an STZ-induced diabetic model. This effect is associated with a reduction in the retinal occludin loss induced by diabetes and downregulation of retinal VEGF and phosphor-p42/p44 MAP kinase expression. This gene transfer approach may reduce diabetic macular edema, providing protection in diabetic patients at risk for macular edema. ? 2007 Molecular Vision.
SDGs
Other Subjects
adenovirus vector; angiostatin; beta galactosidase; bovine serum albumin; complementary DNA; fluorescein isothiocyanate; mitogen activated protein kinase 1; occludin; pigment epithelium derived factor; vasculotropin; animal experiment; animal model; animal tissue; article; blood retina barrier; blood vessel permeability; controlled study; diabetes mellitus; diabetic retinopathy; down regulation; drug efficacy; drug mechanism; enzyme phosphorylation; eye protection; gene expression; human; human cell; male; nonhuman; priority journal; protein analysis; protein depletion; protein expression; protein function; rat; retina macula edema; retina vascular leakage; reverse transcription polymerase chain reaction; Sprague Dawley rat; streptozocin diabetes; viral gene delivery system; viral gene therapy; virus recombinant; Western blotting; Angiostatins; Animals; Blood-Retinal Barrier; Capillary Permeability; Dependovirus; Diabetes Mellitus, Experimental; Diabetic Retinopathy; Down-Regulation; Eye Proteins; Gene Transfer Techniques; Male; Membrane Proteins; Mice; Mitogen-Activated Protein Kinase 1; Mitogen-Activated Protein Kinase 3; Nerve Growth Factors; Phosphorylation; Rats; Rats, Sprague-Dawley; Recombination, Genetic; Retina; Retinal Vessels; Serpins; Vascular Endothelial Growth Factor A; Vitreous Body
Type
journal article