1. Increased expression and activity of 12-lipoxygenase in oxygen-induced ischemic retinopathy and proliferative diabetic retinopathy: implications in retinal neovascularization.
- Author
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Al-Shabrawey M, Mussell R, Kahook K, Tawfik A, Eladl M, Sarthy V, Nussbaum J, El-Marakby A, Park SY, Gurel Z, Sheibani N, and Maddipati KR
- Subjects
- Analysis of Variance, Animals, Blotting, Western, Diabetic Retinopathy genetics, Enzyme Inhibitors pharmacology, Enzyme-Linked Immunosorbent Assay, Eye Proteins genetics, Eye Proteins metabolism, Flavanones pharmacology, Humans, Hydroxyeicosatetraenoic Acids metabolism, Immunohistochemistry, Mass Spectrometry, Mice, Nerve Growth Factors genetics, Nerve Growth Factors metabolism, Retinal Neovascularization genetics, Retinal Vessels drug effects, Reverse Transcriptase Polymerase Chain Reaction, Serpins genetics, Serpins metabolism, Vascular Endothelial Growth Factor A genetics, Vascular Endothelial Growth Factor A metabolism, Vitreous Body metabolism, Arachidonate 12-Lipoxygenase metabolism, Diabetic Retinopathy metabolism, Ischemia metabolism, Retinal Neovascularization metabolism, Retinal Vessels metabolism
- Abstract
Objective: Arachidonic acid is metabolized by 12-lipoxygenase (12-LOX) to 12-hydroxyeicosatetraenoic acid (12-HETE) and has an important role in the regulation of angiogenesis and endothelial cell proliferation and migration. The goal of this study was to investigate whether 12-LOX plays a role in retinal neovascularization (NV)., Research Design and Methods: Experiments were performed using retinas from a murine model of oxygen-induced ischemic retinopathy (OIR) that was treated with and without the LOX pathway inhibitor, baicalein, or lacking 12-LOX. We also analyzed vitreous samples from patients with and without proliferative diabetic retinopathy (PDR). Western blotting and RT-PCR were used to assess the expression of 12-LOX, vascular endothelial growth factor (VEGF), and pigment epithelium-derived factor (PEDF). Liquid chromatography-mass spectrometry was used to assess the amounts of HETEs in the murine retina and human vitreous samples. The effects of 12-HETE on VEGF and PEDF expression were evaluated in Müller cells (rMCs), primary mouse retinal pigment epithelial cells, and astrocytes., Results: Retinal NV during OIR was associated with increased 12-LOX expression and 12-, 15-, and 5-HETE production. The amounts of HETEs also were significantly higher in the vitreous of diabetic patients with PDR. Retinal NV was markedly abrogated in mice treated with baicalein or mice lacking 12-LOX. This was associated with decreased VEGF expression and restoration of PEDF levels. PEDF expression was reduced in 12-HETE-treated rMCs, astrocytes, and the retinal pigment epithelium. Only rMCs and astrocytes showed increased VEGF expression by 12-HETE., Conclusions: 12-LOX and its product HETE are important regulators of retinal NV through modulation of VEGF and PEDF expression and could provide a new therapeutic target to prevent and treat ischemic retinopathy.
- Published
- 2011
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