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From the Vascular Biology Center* and the Departments of Pharmacology and Toxicology, Cellular Biology and Anatomy, and Ophthalmology, Medical College of Georgia, Augusta, Georgia
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Abstract |
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-nitro-L-arginine methyl ester, 50 mg/kg/day) or peroxynitrite scavenger (uric acid, 160 mg/kg/day) blocked the breakdown in the BRB and prevented the increases in formation of lipid peroxides and tyrosine nitration as well as the increases in expression of VEGF and uPAR. Taken together, these data indicate that early diabetes causes breakdown of the BRB by a mechanism involving the action of reactive nitrogen species in promoting expression of VEGF and uPAR.
Multiple interrelated biochemical mechanisms have been postulated to explain the adverse effects of diabetes and hyperglycemia on vascular cells including increased flux of glucose through the polyol pathway, enhanced nonenzymatic glycation and activation of protein kinase C and increased formation of reactive oxygen species (ROS), including nitric oxide (NO), superoxide (O2.-) and their product peroxynitrite (ONOO-).7-11 Increased formation of ROS and lipid peroxides occurs early in diabetic retinopathy.12,13 Analyses done with endothelial cells in vitro have shown that high glucose increases the expression of eNOS.14 High glucose also greatly increases endothelial cell formation of O2.- leading to reduced bioavailability of NO.15-17 Research demonstrating the presence of nitrotyrosine residues in placental vessels10 and plasma11 of diabetic patients supports a role for ONOO- in the development of diabetic complications. Peroxynitrite can contribute to vascular injury by causing lipid peroxidation and nitration of tyrosine residues, inactivating key metabolic enzymes, and reducing cellular antioxidant defenses by oxidation of thiol pools.18,19 Peroxynitrite may also cause NOS-uncoupled production of O2.- because of oxidation of the NOS co-factor tetrahydrobiopterin (BH4),20 the L-arginine transporter CAT-121 or eNOS itself.22
Our analyses in vitro support the role of eNOS uncoupling and ONOO- formation in high glucose-induced endothelial dysfunction. We found that retinal endothelial cells maintained in high glucose have significant increases in eNOS expression and activity as well as in formation of O2.- and nitrotyrosine.23 Each of these alterations was blocked by the NOS inhibitor, L-NAME, or the peroxynitrite scavenger, uric acid, lending further support to the role of eNOS uncoupling and ONOO- formation in high glucose-induced vascular injury. We have also shown that VEGF increases permeability of bovine retinal endothelial cells by activating urokinase plasminogen activator (uPA) and inducing the expression of its receptor urokinase plasminogen activator (uPAR).24 uPA cleaves tissue plasminogen into the active enzyme plasmin, which in turn activates matrix metalloproteinases.25 uPAR localizes these events at the cell membrane where cell-cell and cell-substrate attachments are altered. Therefore, we postulated that diabetes causes BRB dysfunction by causing ROS-mediated increases in expression of VEGF and uPAR. The goals of this study are 1) to define the role of NOS activity and formation of reactive nitrogen species in breakdown of the BRB; 2) to determine the correlation between diabetes-induced ROS formation and the expression of VEGF and its down stream target uPAR; and 3) to directly test whether or not reducing NOS activity or peroxynitrite formation protects diabetic rat retinas from diabetes-induced increase in VEGF expression and BRB breakdown.
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Materials and Methods |
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All procedures with animals were done in accordance with the Public Health Service Guide for the Care and Use of Laboratory Animals (DHEW Publication, NIH 80-23). Sprague-Dawley rats were made diabetic by a single intravenous injection of STZ (65 mg/kg) dissolved in 0.1 mol/L of fresh citrate buffer, pH 4.5. Three sets of animals were prepared for a total of 102 rats. In experiment 1, six rats were made diabetic and six rats were controls and in experiment 2, nine rats were made diabetic and nine rats were controls. In experiment 3, to study the effects of inhibitors, 36 rats were made diabetic and 36 rats were control. One group of diabetic animals (12 rats) and one control group (12 rats) received NOS inhibitor N--nitro-L-arginine methyl ester (L-NAME) in their drinking water (50 mg/kg/day). Another group of diabetic animals (12 rats) and controls (12 rats) received uric acid (peroxynitrite scavenger) in their drinking water (160 mg/kg/day). Others were untreated control (n = 12) and untreated diabetic (n = 12) rats. After 2 weeks, the animals were sacrificed by decapitation, blood was collected and their retinas were removed, frozen in liquid nitrogen, and stored at -80°C until further analysis. Both retinas were collected from each rat and analyzed separately in independent experiments. Measurement of nitrite/nitrate, lipid peroxidation, nitrotyrosine, maximum NOS activity, and NOS expression were repeated in three independent experiments. The results are expressed as mean ± SEM. Differences among experimental groups were evaluated by analysis of variance and the significance of differences between groups was assessed by Fisher’s post-hoc least significant difference test when indicated. Significance was defined as P < 0.05.
Measurement of BRB Function
Integerity of the BRB was measured as described by others previously.1 Rats received tail vein injections of 100 mg/kg of bovine serum albumin (BSA)-Alexa-Fluor 488 conjugate (Molecular Probes, Eugene, OR). After 30 minutes, the animals were sacrificed and the eyes were enucleated, embedded in OCT medium, and snap-frozen in liquid nitrogen. Plasma was assayed for Alexa-Fluor 488 concentration using a Cyto Fluor 4000 spectrofluorometer (Foster City, CA). Frozen retinal sections (10 µm) collected at 60-µm intervals were viewed with a fluorescence microscope fitted with a spot camera. Images were collected from 10 retinal areas (200 µm2) in each section. The average retinal fluorescence intensity was calculated and normalized to a noninjected control retina and to plasma fluorescence intensity for each animal. Through serial sectioning of each eye, this technique allowed quantification of barrier function in each retina.
Measurement of NO Formation in Rat Retinas
NO production was determined by measuring the levels of nitrite and nitrate, the oxidized products of NO, in the supernatant of phosphate-buffered saline (PBS) homogenate of the control or diabetic rat retinas by modified Greiss Reagent assay. Briefly, 210 µl of homogenate were incubated with nitrate reductase enzyme (10 mU) and NADPH (12.5 mmol/L) for 30 minutes at 37°C. Then the total nitrite in each sample was determined by addition of 200 mU of L-glutamate dehydrogenase, 100 mmol/L NH4Cl, and freshly prepared 4 mmol/L of 
-ketogluterate. Enzymatic reduction of nitrate to nitrite was monitored by including an NO3- standard. The mixture was incubated at 37°C for 10 minutes followed by addition of 250 µl of Greiss Reagent and incubation for another 5 minutes at 37°C. The absorbance at 543 nm was recorded and concentrations of NO2 were calculated from a standard curve constructed using NaNO2 standards. Protein levels were measured by the Bradford method (Bio-Rad, Hercules, CA) and nitrite/nitrate level was expressed as mmol/mg protein.
Measurement of Retinal NOS Protein Expression
Retinal protein was extracted in RIPA lysis buffer (20 mmol/L Tris, pH 7.4, 2.5 mmol/L EDTA, pH 8, 1% Triton X-100, 1% deoxycholate, 1% sodium dodecyl sulfate, 50 mmol/L sodium fluoride, and 10 mmol/L sodium pyrophosphate) containing 1 mmol/L of phenylmethyl sulfonyl fluoride. Samples equated for protein content were separated on 10% sodium dodecyl sulfate gel and transferred to nitrocellulose membranes. Levels of eNOS, nNOS, and iNOS proteins were analyzed using corresponding monoclonal antibodies (Transduction Laboratories, Lexington, KY) and electrochemiluminescence (ECL; Amersham, Buckinghamshire, UK). The bands were scanned by densitometry and normalized to ß-actin as an internal standard.
Determination of Retinal NOS Activity
Maximal NOS activity was quantified using an assay for the conversion of [3H]-L-arginine to [3H]-L-citrulline.26 Retinas were homogenized on ice in a 250 µl buffer composed of 50 mmol/L Tris-HCl, 0.1 mmol/L EDTA, 0.1 mmol/L EGTA (pH 7.4), 1 µmol/L pepstatin, 2 µmol/L leupeptin, 1 µmol/L bestatin, and 1 mmol/L phenylmethyl sulfonyl fluoride. The homogenate was centrifuged at 8000 x g for 10 minutes and the supernatant was collected and 100 µl was incubated in the previously described buffer containing 100 nmol/L calmodulin, 1 mmol/L NADPH, 3 µmol/L tetrahydrobiopterin, and 10 µmol/L L-arginine combined with 0.6 µCi L-[2,3-3H]-arginine. The incubation mixture also contained 1 mmol/L L-citrulline to minimize conversion of the formed [3H]-L-citrulline to [3H]-L-arginine. Ice-cold buffer, 1 ml (20 mmol/L Tris-HCl, 0.2 mmol/L EDTA, 0.2 mmol/L EGTA, pH 5.5) was used to stop the reaction. Reaction mixtures were applied to Dowex 50W-8 (Na form) columns and the eluted [3H]-L-citrulline activity was determined by scintillation counting spectroscopy. NOS activity was expressed as pmol/L/30 minutes/mg protein.
Measurement of Retinal Lipid Peroxidation
Lipid peroxide concentration was determined by a method that measures the amount of thiobarbituric acid reactivity by the amount of malondialdehyde formed during acid hydrolysis of the lipid peroxide compound.27 Retinas were washed with 0.9% NaCl and tissue homogenate was prepared at a ratio of 1 g wet tissue to 9 ml of 1.15% KCl. The reaction mixture contained 0.2 ml of sample, 0.2 ml of 8.1% sodium dodecyl sulfate, 1.5 ml of 20% acetic acid solution (buffered to pH 3.5), and 1.5 ml of 0.8% thiobarbituric acid. The mixture was then incubated at 95°C for 1 hour. After cooling, 1 ml of distilled water and 5 ml of a mixture of n-butanol and pyridine (15:1, v/v) were added and the final mixture was shaken vigorously. After centrifugation at 1500 x g for 10 minutes absorbance of the solvent layer was measured at 532 nm. Tetraethoxypropane was used to establish the standard curve. Lipid peroxide level was expressed in terms of nmol/L malondialdehyde per mg protein.
Measurement of Retinal Nitrotyrosine
Nitrotyrosine immunoreactivity was measured as an indicator for ONOO- formation by slot blot and immunostaining.28,29 For slot blot analysis of total nitrotyrosine levels, retinas were homogenized in RIPA lysis buffer. Duplicate protein samples were immobilized onto a polyvinylidene difluoride membrane using a slot blot microfiltration unit. After blocking with 5% nonfat milk, the polyvinylidene difluoride membrane was reacted with a monoclonal anti-nitrotyrosine antibody (Cayman Chemical Co., Ann Arbor, MI) followed by peroxidase-labeled goat anti-mouse IgG and enhanced chemiluminescence. Relative levels of nitrotyrosine immunoreactivity were determined by densitometry and comparison with a standard curve generated from ONOO--modified BSA.
The distribution of nitrotyrosine in retinal sections was analyzed using immunolocalization techniques. Retinal sections were fixed with 4% paraformaldehyde then reacted with a polyclonal rabbit anti-nitrotyrosine antibody (Upstate Biotechnology, Lake Placid, NY) followed by Oregon green-conjugated goat anti-rabbit antibody (Molecular Probes). Data were analyzed using fluorescence microscopy and Ultra View morphometric software to quantify intensity of immunostaining.
Control experiments to demonstrate specificity of the nitrotyrosine antibody were done by processing the sections in the absence of primary antibody and by neutralizing the primary antibody.30 Briefly, the antibody was neutralized by incubation with 10 mmol/L of 3-nitrotyrosine in PBS solution (Cayman Chemical Co.). The specificity of measurement of nitrotyrosine as indicator for peroxynitrite and the efficacy of uric acid as a scavenger of peroxynitrite were confirmed by in vitro techniques. Cultured bovine retinal endothelial cells were treated with 100 µmol/L of peroxynitrite (Upstate Biotechnology) in the presence or absence of 1 mmol/L of uric acid (Sigma Chemical Co., St. Louis, MO) for 1 hour and analyzed for nitrotyrosine formation as described above.
Real-Time Quantitative Polymerase Chain Reaction (PCR) Analysis of VEGF and uPAR RNA
SYBR Green provides a convenient way to detect and quantify reverse transcriptase (RT)-PCR product. The quantification is based on the amounts of SYBR Green-bound DNA measured at the end of each cycle of PCR. In brief, reverse transcription of the retinal RNA was performed by conventional methods using AMV RT and random primers. The use of random primers allowed the simultaneous amplification of the 18-S rRNA as reference or internal marker for each sample. A pair of rat-specific uPAR primers was synthesized based on the cDNA sequence31 accession no. x71899 and was used to amplify a 200-bp DNA fragment (corresponding to nucleotides 764 to 963) by conventional PCR. For VEGF analysis, primers designed for bovine VEGF based on the cDNA sequence32 accession no. M32976 were used to amplify a 200-bp amplicon (corresponding to nucleotides 853 to 1053). The uPAR and VEGF amplicons prepared by conventional PCR were used as standard templates in the subsequent analysis. Quantitative PCR was performed using a Light Cycler apparatus (Roche Diagnostics Ltd., Lewes, UK) using a kit provided by the same vendor. The specificity of the assay was determined at the completion of cycling by plotting the melting profile of each PCR product. In our experiments, this melting profile always overlapped with the melting profile of the standard samples in which pure template was used. Two RT reactions were performed and two light cycler reactions were performed for both uPAR and VEGF for each RNA sample. For internal controls, the RT samples were diluted 50- to 100-fold and were primed with 18S rRNA primers (Universal 18S Primer Pair; Ambion, Austin, TX).
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Results |
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The body weights of the diabetic rats decreased significantly (19%) whereas those of the controls increased (18%, Table 1
). Blood glucose levels were significantly increased (fourfold) in the STZ-induced diabetic rats compared with the controls. Administration of L-NAME and uric acid did not affect body weight or blood glucose levels of either control or diabetic animals.
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Assessment of BRB function using BSA-Alexa-Fluor 488 showed significant permeability increases within the diabetic retina. Microscopic images showed prominent accumulation of the tracer within retinal layers containing blood vessels—the nerve fiber layer and the inner and outer plexiform layers (Figure 1A)
. Quantitative analysis showed a twofold increase (P < 0.01) in the fluorescence intensity in the diabetic retinas (Figure 1B)
. Treatment with the NOS inhibitor, L-NAME (50 mg/kg/day) or the ONOO- scavenger, uric acid (160 mg/kg/day), completely blocked the permeability breakdown in the diabetic rats. The control rat retinas were not affected by either treatment.
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Our results showed that diabetes increased the formation of reactive nitrogen species as indicated by nitrite/nitrate, nitrotyrosine, maximum NOS activity, and NOS expression and increased oxidative stress as indicated by lipid peroxidation. Biochemical measures of oxidative stress and reactive nitrogen species formation were repeated and confirmed in three independent experiments. The data shown represent results from experiments 2 and 3.
Diabetes Increases Retinal Nitrite/Nitrate Levels
Direct measurement of NO formation in vivo is difficult because of its short half-life. Therefore, the evaluation of the stable NO end products, nitrite and nitrate, has been widely used to estimate NO production. As shown in Figure 2
, the formation of nitrate/nitrite in diabetic retinas was approximately twofold higher than in the controls (P < 0.01). Administration of either L-NAME (50 mg/kg/day) or uric acid (160 mg/kg/day) blocked this increase, but did not alter basal values in controls.
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The neural retina has a high content of polyunsaturated fatty acids and hence, is extremely susceptible to oxidative insult by ROS. Levels of lipid peroxides were measured by the thiobarbituric acid test and expressed as nmol/L of malondialdehyde. Malondialdehyde levels were increased 
2.5-fold in the diabetic retinas in comparison with the controls (Figure 3)
. Administration of either L-NAME (50 mg/kg/day) or uric acid (160 mg/kg/day) completely blocked the increased formation of lipid peroxides in diabetic retina. Neither agent altered lipid peroxidation in the control retina.
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ONOO- is a short-lived molecule at physiological pH, but it has been shown to nitrate protein tyrosine residues. Therefore, determination of nitrotyrosine can be used as an indicator of ONOO- formation.29
The specificity of the nitrotyrosine antibody was confirmed by complete blocking of the signal in the absence of the primary antibody or when the primary antibody was neutralized using 3-nitrotyrosine (Figure 4A)
. The specificity of detecting nitrotyrosine as indicator of peroxynitrite was further confirmed by our in vitro studies in bovine endothelial cells exposed to 100 µm of ONOO-. These experiments showed significant increases in tyrosine nitration in ONOO--treated cells. Further, this effect was totally blocked by uric acid (1 mmol/L) demonstrating the efficiency of this agent as a scavenger for ONOO- (Figure 4B)
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). Treatment of the diabetic rats with either L-NAME or uric acid completely blocked this effect, whereas control levels were unchanged. Parallel studies also examined nitrotyrosine immunolocalization in retinal sections. In the control animals, nitrotyrosine residues were distributed within the inner segment, outer plexiform, inner plexiform, and nerve fiber/ganglion cell layers of the retina. In the diabetic retina, the intensity of the immunoreactivity of nitrotyrosine residues increased significantly in these layers, particularly within the areas where blood vessels are found—the nerve fiber/ganglion cell layer and the inner and outer plexiform layers (Figure 4D)
. Treatment of diabetic animals with L-NAME or uric acid inhibited the increase in nitrotyrosine immunostaining. Diabetes Increases Constitutive NOS Expression
Maximal NOS activity was determined in retinal tissue homogenates using an assay for conversion of [3H]-L-arginine to [3H]-L-citrulline. This assay serves to indicate changes in total levels of NOS protein because the enzyme is fully activated when tissue homogenate is reacted with both substrate and co-factors. NOS activity was increased 1.5-fold in the diabetic retina in comparison to the control retina (P < 0.01, Figure 5A
). Treatment of diabetic rats with L-NAME or uric acid blocked the effect of diabetes increasing maximum NOS activity, but did not alter the NOS activity in the control retinas. Addition of L-NAME to the tissue homogenates almost totally blocked formation of [3H]-L-citrulline (95% inhibition), demonstrating specificity of the reaction.
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. Treatment with L-NAME or uric acid inhibited the increases in eNOS and nNOS expression in diabetic retina, but did not alter NOS expression in the control rat retinas. No difference in iNOS expression was found between diabetic and normal retinas (data not shown). Diabetes Induces Increased Expression of VEGF and uPAR
Quantitative analysis of VEGF mRNA expression using real-time PCR showed a significant increase (P < 0.01) in the diabetic retina as compared to the control retina (Figure 6)
. This was positively correlated with the increases in ROS formation and the BRB breakdown shown by the above results. Treatment with L-NAME or uric acid prevented the increase in VEGF expression in diabetic animals.
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. The increase in uPAR mRNA expression was associated with a significant increase in uPAR protein expression levels in diabetic retina compared to control retinas (Figure 7B)
. Treatment with L-NAME or uric acid inhibited the increases in uPAR in diabetic retinas.
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Discussion |
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The source of the increase in ROS in the diabetic retina is likely to include NOS. Our data showed a significant increase in nitrate/nitrite levels in the diabetic retinas indicating an increase in NO formation. Measurement of maximal NOS activity confirmed significant increases in levels of NOS protein within the diabetic retina. Significant increases in eNOS and nNOS protein were also observed in the diabetic retina, whereas iNOS expression was unchanged from the control levels. A previous study observed similar increases in constitutive NOS protein expression in diabetic rats.5 However, another group attributed increases in NOS activity to iNOS, based on their findings in diabetic and control retinas comparing a selective iNOS inhibitor, aminoguanidine, with a selective constitutive NOS inhibitor, L-NAME.33 Because our Western blotting analyses failed to show an increase in iNOS expression, we determined diabetes’ effects on the expression of iNOS mRNA. Our RT-PCR analyses also showed no difference in iNOS expression between the diabetic and control retinas (data not shown). Because the increases we observed in eNOS and nNOS protein expression (2- and 1.8-fold, respectively) were similar in magnitude to the increases in maximum NOS activity and nitrite formation (1.5- and 2-fold, respectively), we conclude that the increase in nitrite formation reflects an overall increase in expression of the constitutive NOS isoforms.
Increases in the formation of NO and O2.- have been described previously in early diabetic retinopathy and in bovine aortic endothelial cells cultured in high glucose conditions.14-17 However, our study is the first we know of to show that diabetic retinas also have significant increases in formation of reactive nitrogen species as indicated by increases in protein tyrosine nitration. Although several pathways of tyrosine nitration have been suggested in addition to peroxynitrite formation, nitrotyrosine is considered to be a likely indicator for peroxynitrite, particularly under conditions of simultaneous production of NO and superoxide.34-36
In diabetic rat retinas, the increases in formation of NO, lipid peroxidation, and tyrosine nitration were correlated with the BRB breakdown. This observation is in agreement with previous studies showing that S-nitroso-N-acetylpenicillamine (SNAP) and 3-morpholinosydnonimine (SIN-1) can cause increases in permeability of epithelial cells in vitro37 and of rat brain endothelial cells in vivo.38 SIN-1 releases O2.- and NO simultaneously, whereas SNAP releases only NO. However, SNAP appears to induce intracellular production of O2.- under some conditions.37,38 These effects of SNAP and SIN-1 on increasing permeability were blocked by scavengers of ONOO- or O2.-, suggesting that the permeability enhancing actions involve increased ONOO- formation.
Further support for the role of ONOO- in causing the BRB breakdown comes from our finding that the diabetes-induced increases in ROS formation and the BRB breakdown could be blocked by inhibiting NOS and by scavenging ONOO-. Uric acid is a naturally occurring product of purine metabolism that has a selective effect in inhibiting tyrosine nitration. It’s action as a peroxynitrite scavenger has been demonstrated by its capacity to bind peroxynitrite but not nitric oxide39
and by its ability to inhibit the action of peroxynitrite in causing tyrosine nitration40
(see Figure 4B
). Interestingly, the diabetic rats in our study had significantly lower levels of uric acid compared to the control rats. In support of this observation, patients with type I diabetes also show significantly lower serum uric acid levels in comparison to healthy controls or to type II diabetics.41
It is important to note that treatments that inhibit NOS can reduce ONOO- formation by blocking the action of eNOS in forming O2.- as well as preventing the formation of NO.42 Our tissue culture analyses in retinal endothelial cells maintained in high glucose conditions indicate that eNOS becomes uncoupled and generates O2.- as well as NO, leading to ONOO- formation.23 These data support a relationship between ONOO- and diabetes-induced vascular dysfunction. Observation of increased nitrotyrosine formation in the ganglion cell layer suggest that ONOO- may also contribute to neuronal injury that has been described previously in diabetic rats and humans.43
Diabetic retinopathy is clinically divided into an early stage of nonproliferative retinopathy and a late stage of proliferative neovascular disease. Breakdown of the BRB and progressive vascular occlusion are hallmarks of early diabetic retinopathy that continue with progression of the disease.44,45 Under diabetic conditions, BRB breakdown is thought to occur because of diabetes-induced increases in the formation of vasoactive factors such as VEGF/vascular permeability factor.1-5 Although diabetes-induced vascular dysfunction in the rodent model does not progress to proliferative retinopathy, increases in retinal vascular permeability are well established. Our data confirmed a breakdown of the BRB at 2 weeks after the onset of diabetes, which is accompanied by a substantial increase in VEGF expression.
Our finding that retinal VEGF mRNA expression is increased in the early stages of diabetes is consistent with previous data showing that ischemia, hyperglycemia, and oxidative stress can increase growth factor expression.46-50 Induction of VEGF expression by hypoxia provides a pathogenic link between ischemic retinal diseases and the accompanying neovascularization.51 Experiments in animal models of hypoxia-induced ocular neovascularization have shown that VEGF is up-regulated several fold before the onset of neovascularization.50,52-54
Another potential inducer of VEGF gene expression in diabetic tissue is the increased generation of ROS.55
Our data showing a significant increase of lipid peroxidation in diabetic retinas are in agreement with several reports correlating formation of lipid peroxides with oxidative stress in early experimental diabetes.12,13
The mechanism by which ROS increase VEGF gene expression has been suggested to involve an increase in VEGF mRNA stability.54
It has also been demonstrated that ROS activate intracellular signaling events leading to the stabilization of HIF-155
and the subsequent VEGF mRNA expression during hypoxia.56,57
The effects of VEGF in increasing vascular permeability are well established, yet the mechanisms of this action remain poorly understood. Our studies in cultured retinal endothelial cells have shown that VEGF-induced permeability increases are mediated by activation of urokinase plasminogen activator (uPA) and expression of its receptor (uPAR).24 uPA is involved in numerous biological processes requiring cell movement and tissue remodeling. It has been suggested that uPAR enhances uPA function by localizing plasmin formation at the cell membrane. Hence, increases in uPAR expression may be involved in the breakdown of cell junctions and permeability barrier function. This concept was supported by our analyses of uPAR mRNA showing significant increases in both uPAR mRNA and protein expression in the diabetic retina. The fact that the increase in uPAR expression was inhibited in by L-NAME or uric acid strongly supports the role of ROS-induced VEGF expression in the diabetic retina. This is also consistent with the above findings showing that treatment with the NOS inhibitor or peroxynitrite scavenger could prevent the diabetes-induced increases in VEGF expression and maintain the integrity of the BRB. These observations also indicate a critical role of uPA and uPAR in the diabetes-induced permeability breakdown. Taken together, these data strongly indicate that ONOO- plays an important role in the pathogenesis of early diabetic vascular dysfunction as indicated by the BRB breakdown and that this process could be mediated by VEGF-induced increases in expression of uPAR. Although the influence of ROS on increasing VEGF expression54,55 and the involvement of VEGF in diabetes-induced BRB breakdown has been reported,3,50-52 the increased formation of reactive nitrogen species and potential involvement of uPAR in BRB breakdown have not been shown previously. Further investigation is required to define the role of uPAR in the diabetes-induced breakdown in retinal endothelial cell permeability barrier function and to elucidate the relationship between uPA/uPAR activation and previously identified mediators of the BRB breakdown during early diabetes, such as increased expression of intercellular adhesion molecule (ICAM-1) and leukeostasis.6,58
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Footnotes |
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Supported by grants from the National Institutes of Health (EY04618 and EY11766), postdoctoral fellowships from Association for Research in Vision and Ophthalmology/Ciba Vision Inc., and the American Heart Association.
Accepted for publication March 5, 2003.
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References |
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protein by the oxidative stressor arsenite. J Biol Chem 2001, 276:48066-48076This article has been cited by other articles:
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A. B. El-Remessy, I. E. Khalil, S. Matragoon, G. Abou-Mohamed, N.-J. Tsai, P. Roon, R. B. Caldwell, R. W. Caldwell, K. Green, and G. I. Liou Neuroprotective Effect of(-){Delta}9-Tetrahydrocannabinol and Cannabidiol in N-Methyl-D-Aspartate-Induced Retinal Neurotoxicity: Involvement of Peroxynitrite Am. J. Pathol., November 1, 2003; 163(5): 1997 - 2008. [Abstract] [Full Text] [PDF]
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