Vision 2008; 14:1965-1973
Received 02 August 2007 | Accepted 22 March 2008 | Published 30 October 2008
Xiao-bo Xia, Si-qi Xiong, Wei-tao Song, Jie Luo, Yu-ke Wang, Rong-rong Zhou
Department of Ophthalmology, Xiangya Hospital, Central South University, Changsha, China
Correspondence to: Dr. Xiao-bo Xia, Department of Ophthalmology, Xiangya Hospital, Central South University, Changsha, 410008, China; Phone: 0086-731-4328960; FAX: 0086-731-4328960; email: email@example.com
Purpose: To investigate whether vector-based vascular endothelial growth factor 165 (VEGF)165 targeted siRNA expression system (pSilencersiVEGF) could inhibit VEGF165 expression in vitro and suppresses retinal neovascularization in the murine model of oxygen-induced retinopathy.
Methods: pSilencersiVEGF, from which siRNA targeting VEGF165 could be generated, was constructed and transfected to human umbilical vein endothelial cells. Then the level of VEGF isoforms in cultured cells was measured by RT–PCR and ELISA. Intravitreal injection of pSilencersiVEGF was performed in mice with ischemic retinopathy. Retinal neovascularization was evaluated by angiography using fluorescein-labeled dextran and quantitated histologically. The levels of VEGF164, which is equivalent to human VEGF165 in murine retinas were determined by RT–PCR and western immunoblotting.
Results: Expression of VEGF165 in cultured cells was greatly curtailed by pSilencersiVEGF under both normoxia and hypoxia conditions. However, the other isoforms, VEGF189 and VEGF121, were expressed to a similar degree regardless of whether pSilencersiVEGF was administered. Based on angiography and histological analysis, retinal neovascularization in the eyes treated with pSilencersiVEGF were significantly reduced compared to the control eyes. Furthermore, the VEGF164 levels in the murine retinas were suppressed by pSilencersiVEGF.
Conclusions: Retinal neovascularization in the murine model was significantly attenuated by pSilencersiVEGF through decreasing VEGF164 levels in the retinas. pSilencersiVEGF seems to be a potential therapeutic tool for ischemic-induced retinal diseases.
Retinal neovascularization, abnormal formation of new vessels from preexisting capillaries in the retina, is a common complication of many ocular diseases, such as advanced diabetic retinopathy, and retinopathy of prematurity. Neovascularization can lead to fibrosis and disruption of delicate tissues required for vision. Laser photocoagulation as conventional treatment is effective in halting the progression of angiogenesis in the short-term. However, it is also destructive to the retinal tissue, leads to immediate and sometimes significant loss of vision, and does not address the underlying angiogenic mechanisms of the disease. Therefore, therapy targeting molecular mechanisms underlying retinal neovascularization may provide better treatment result and fewer detrimental side effect.
Angiogenesis is a complex process, involving multiple gene products expressed by different cell types, all contributing to an integrated sequence of events. However, laboratory studies have demonstrated that vascular endothelial growth factor (VEGF) plays a central role in several retinal vascular diseases. Clinical trials have confirmed the importance of VEGF in disease pathogenesis [1,2]. Consequently, VEGF becomes an optimal target for inhibition of retinal neovascularization. Accumulated data indicate that attenuation of VEGF activity could effectively suppress retinal neovascularization. Recent treatments based on antibody technology have been proven to be efficacious. Lucentis, a anti-VEGF antibody fragment, has been approved as an antiangiogenic drug for the treatment of ocular neovascularization . Although antibodies are effective, they are not efficient. Large amounts of antibodies are needed to suppress the targeted protein, and the inhibitory effects of antibodies are transient unless these high doses are administered repeatedly.
RNA interference (RNAi) is a recently developed technique to silence proteins in a sequence-specific manner by inhibiting mRNA and consequently reducing protein expression. The high efficiency and specificity of RNAi has made it a powerful and widely used tool for gene therapy. The functional mediator of RNAi is a short double strand RNA (dsRNA) oligonucleotide called small interfering RNA (siRNA) . A growing number of investigations are examining the use of siRNA as a candidate therapeutic agent, Currently, there are two siRNA-based molecules: Cand5, which is a siRNA against all isoforms of VEGF, and siRNA-027, a kind of siRNA targeting VEGF receptor 1 . Acuity Pharmaceuticals (Philadelphia, PA) has begun a Phase II clinical trial for Cand5, and Sirna Therapeutics (San Francisco, CA) is on a Phase 1 clinical trial for siRNA-027. However, due to differential pre-mRNA splicing, a single VEGF gene gives rise to many different VEGF isoforms. To date, five isoforms of human VEGF have been identified: VEGF121, VEGF145, VEGF165, VEGF189, and VEGF206 . Although VEGF is highly conserved throughout evolution, the murine homologs contain one fewer amino acid. The murine designation for the human VEGF165 is VEGF164. Of the various isoforms, VEGF165 (VEGF164) appears to be the major pathological VEGF isoform in the eye . Because VEGF165 is a major disease-causing isoform in models of neovascular eye disease, we expected to identify whether retinal angiogenesis could be attenuated by siRNA targeting VEGF165.
In this report, we used a vector-based siRNA expression system, which overcomes the limitations of transience and high cost in synthetic siRNAs, to specifically inhibit VEGF165 expression in the murine model of proliferative retinopathy. Our data confirm the potential VEGF165 inhibitors for the treatment of ocular angiogenesis.
The cDNA oligonucleotides targeting VEGF165 mRNA were designed and examined by Guan et al. . A pair of 63 nucleotide oligos containing endonuclease restriction sites at both ends was synthesized by the Sangong Company (Shanghai, China). The sequences used were: First strand-5′–GAT CCG ATA GAG CAA GAC AAG AAA TTC AAG AGA TTT CTT GTC TTG CTC TAT CTT TTT TGG AAA–3′; Second strand-5′–AGC TTT TCC AAA AAA GAT AGA GCA AGA CAA GAA ATC TTT GAA TTT CTT GTC TTG CTC TAT CG–3′ (complementary sequence is indicated in red). The annealed dsDNA oligonucleotides were ligated between the BamHI and HindIII sites on the pSilencer2.1-U6 hygro vector. The targeted VEGF165 sequences were GAT AGA GCA AGA CAA GAA A. All inserted sequences were confirmed by DNA sequencing.
Human umbilical vein endothelial cell lines (HUVECs) were purchased from the American Type Culture Collection (Manassas, VA). HUVECs were grown in F12K medium, containing 0.1 mg/ml heparin, 20% fetal bovine serum, 0.03 mg/ml endothelial cell growth supplement (BD Biosciences, San Jose, CA), and antibiotic mixtures of 100 U/ml penicillin G and 100 μg/ml streptomycin sulfate. Cells were cultured in an incubator at 37 °C in an atmosphere of 95% air and 5% CO2. In the vitro studies, an oxygen concentration of 20% was considered normoxic. Hypoxia was 1% oxygen. In the vivo studies, normoxic mice were raised in room-air-raised. For hyperoxia, mice were kept in 75±2% oxygen. Transfection reagent lipofectamine2000 was used to transfer the pSilencersiVEGF to the HUVECs according to the manufacturer’s protocol (Invitrogen, Carlsbad, CA). In brief, 2×105 HUVECs cells were seeded into six-well plates. A 2.5:1 ratio of lipofectamine–pSilencersiVEGF (Invitrogen) complexes were prepared and added to the HUVECs.
Whole RNA of cultured cells or murine retinas were isolated with TRIzol® reagent (Invitrogen). Total RNA was isolated using Trizol reagents (Gibco-BRL Life Technologies, Gibco, Carlsbad, CA), followed by treatment for 45 min with RNase-free DNase at 37 °C (Message Clean; GeneHunter Corp., Nashville, TN), phenol:chloroform (ratio 1:1) extraction, ethanol precipitation, and stabilizing in DEPC-treated water. RNA concentration was determined by spectrophotometric readings at 260 and 280 nm. Each 2 mg of RNA extract was reverse-transcribed into cDNA with RevertAidTM First Strand cDNA Synthesis Kit (MBI, Burlington, MD). PCR was performed in 50 µl of a solution containing Taq DNA polymerase, dNTP, VEGF primer, or β-actin primer and RT products. The primer pair, 5′-CGA AGT GGT GAA GTT CAT GGA TG-3′ (sense) and 5′-TTC TGT ATC AGT CTT TCC TGG TGA G-3′ (antisense), was used to amplify human VEGF isoforms in cultured cells. The primer pair, 5′-CCT CCG AAA CCA TGA ACT TTC TGC TC-3′ (sense) and 5′-CAG CCT GGC TCA CCG CCT TGG CTT-3′ (antisense), was designed to yield the PCR products of murine VEGF isoforms. The primer pair, 5′ CGT TGA CAT CCG TAA AGA C 3′ (sense) and 5′ TGG AAG GTG GAC AGT GAG 3′ (antisense), was used to obtain the PCR product of β-actin. After a preincubation for 5 min at 94 °C, 30 cycles of amplification (94 °C for 45 s, 60 °C for 45 s, and 72 °C for 45 s) were performed, and β-actin was used as an internal control. Amplified products were run in a 1.5% ethidium bromide agarose gel, band intensities were captured with a ChemiDoc system and LabWorks software (UVP, Upland, CA), and values were transferred to an Excel spreadsheet for calculation of means and standard errors.
The medium from normoxia and hypoxia cultured cells was collected, centrifuged at 750×g for 5 min, and stored at −70 °C. Concurrently, cells were trypsinized and counted. The concentration of the secreted VEGF165 isoform in the media was determined with an ELISA kit (R&D Systems, Minneapolis, MN) according to the manufacturer’s instructions and was expressed as pg VEGF/105 cells.
The study protocol conformed to the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research. The reproducible murine model of oxygen-induced retinopathy (OIR) has been described previously . C57BL/6J mice were bought from Experimental Animal Center of Central South University, Changsha, Hunan province, China. The mice were exposed to less than 300 lx of 12 h cyclical broad spectrum light. The oxygen-treated mice were housed in an incubator. Oxygen concentration was monitored with a Beckman oxygen analyzer (Model D2; Beckman,. Irvine, CA). The cage temperature was maintained at 23 °C±2 °C. The mice were placed in the oxygen chamber with enough food and water to sustain them for 5 days. Postnatal day 7 (P7) C57BL/6J mice and their nursing mothers were exposed to 75%±2% oxygen for five days. On P12, the mice were removed from the chamber and maintained in room air until P17. Mice of the same strain and of the same age were kept in room air and used as control subjects. Intravitreal injections of liposome–pSilencersiVEGF complexes were performed at P12 as described in the next section. At P17, the mice were sacrificed by cardiac perfusion of 4% paraformaldehyde in phosphate-buffered saline (PBS) catalog number of PBS is 20012043 (Gibco), and their eyes were enucleated for RT–PCR and immunohistologic analysis. Alternatively, some mice underwent retinal fluorescein angiography, as described in the next section.
At P12, mouse pups were deeply anesthetized with a 30 mg/kg intraperitoneal injection of sodium pentobarbital. The lid fissure was opened with a no. 11 scalpel blade, and the eye was proptosed. Intravitreal injections were performed by first entering the eye with an Ethicon TG140–8 suture needle at the posterior limbus. A 32-gauge Hamilton needle and syringe were used to deliver 1 µl liposome-pSilencersiVEGF complex (0.5 µl liposome and 1–1000 ng of pSilencersiVEGF) or 1 µl control complex (0.5 µl liposome and 0.5 µl of 2 mg/ml pSilencer null vector) into the vitreous cavity.
At P17, mice were anesthetized with a 30 mg/kg intraperitoneal injection of sodium pentobarbital sodium, and cardiac perfusion was performed with 1 ml PBS containing 50 mg/ml fluorescein-labeled dextran (2×106 average molecular weight; Sigma, St Louis, MO), clarified by centrifugation for 5 min at 10,600 xg. Subsequently, the mice were sacrificed, and their eyes were enucleated. The retinas were dissected and flatmounted on microscope slides with glycerol gelatin.
The eyes of sacrificed P17 mice were enucleated, fixed overnight with 4% paraformaldehyde in PBS, and embedded in paraffin. Half of the group of mice were used for angiography with high-molecular-weight fluorescein-dextran, and the other half were used for histological analysis of neovascularization. Paraffin-embedded axial serial sections of the retina, 6 µm thick, were obtained starting at the optic nerve head. After staining with periodic acid-Schiff reagent and hematoxylin, we evaluated 10 intact sections of equal length, each 30 µm apart, for a span of 300 µm. All retinal vascular cell nuclei anterior to the internal limiting membrane were counted in each section according to a masked protocol. The mean of all ten counted sections yielded average neovascular cell nuclei per 6μm section per eye.
The murine retinas were collected and lysed in lysis buffer composed of 150 mmol/l NaCl, 50 mmol/l Tris-HCl, pH 7.4, 2 mmol/l EDTA, and 1% NP-40 that also contained protease inhibitors (Boehringer Mannheim, Mannheim, Germany). Total protein (30 μg per lane) was loaded on SDS-polyacrylamide gel and transferred onto a nitrocellulose membrane and incubated with a 1:500 dilution rat monoclonal anti-VEGF antibody Santa Cruz (Santa Cruz, CA, catalog number sc-80436) and a 1:10,000 dilution mouse monoclonal anti-β-actin antibody (Sigma, St. Louis, MO), followed by incubation with corresponding secondary antibodies (peroxidase conjugated). The enhanced chemiluminescence (ECL) chemiluminescence reagent was added to the membrane according to the manufacturer’s directions. The membrane was exposed to an X-ray film for 1 min before it was developed and fixed. Images of blots were entered into a computer using a scanner (Epson, Nagano, Japan) and analyzed using LabWorks Software (UVP). Then, values were transferred to an Excel spreadsheet for calculation of means and standard errors.
The results were expressed as mean±standard error of mean (SEM). One-way ANOVA followed by the least significant difference (LSD)-t-test were used to evaluate significant differences. A p value <0.05 was considered statistically significant.
To determine whether vector-based VEGF165 targeted siRNA expression system (pSilencersiVEGF) could suppress the expression of VEGF165, we transfected pSilencersiVEGF plasmid to HUVECs. Then the transfected cells were further cultured under normoxia (20% O2) and hypoxia (1% O2) conditions for 24 h, together with null vector transfected and non-transfected HUVECs (as control). All these cells were later used for RT–PCR and ELISA analysis. As shown in Figure 1A,B, VEGF165 mRNA levels in pSilencersiVEGF transfected cells were dramatically decreased under both normoxic and hypoxic conditions compared to the control cells (p<0.05), while VEGF121 and VEGF189 were expressed to a similar degree regardless of whether pSilencersiVEGF was applied. Correspondingly, the amount of VEGF165 protein secreted into the medium of cultured cells was greatly inhibited after pSilencersiVEGF transfection (Figure 1C), indicating that pSilencersiVEGF could specifically decrease VEGF165 expression in cultured cells without alteration of other VEGF isoforms expression under both normoxia and hypoxia conditions.
Injection of liposome –pSilencersiVEGF complexes was performed at P12. Injection of fluorescein-labeled dextran into left ventricle was done at P17, followed by retina flatmount. The retinas of room air-raised mice revealed a normal capillary network without nonperfusion area and neovascular tufts. However, retinas from hyperoxia-exposed mice with pSilencer null vector injection or without any injection contained multiple neovascular tufts and central nonperfusion areas. In contrast, fewer neovascular complexes could be found in retinas of mouse eyes injected with pSilencersiVEGF (Figure 2).
Neovascularization was assessed histologically by counting the endothelial cell nuclei anterior to the inner limiting membrane. Retinas from hyperoxia-exposed mice with injection of 1000 ng pSilencer null vector or without any injection (OIR model) were found to contain multiple neovascular tufts extending into the vitreous. In contrast, fewer neovascular complexes were observed in pSilencersiVEGF-injected retinas (Figure 3). Administration of 1–1000 ng doses of pSilencersiVEGF resulted in a dose-dependent decrease in endothelial cell nuclei numbers anterior to the inner limiting membrane (i.e., inhibition of retinal neovascularization), with a maximum inhibitory effect of 50% at the 1000 ng dose (Figure 4).
To determine whether intravitreal injection of pSilencersiVEGF could decrease VEGF164 expression in the murine retinas, we extracted retinas and assessed them by RT–PCR and immunohistochemical analysis. Some retinas were used for RNA extraction and RT–PCR analysis, the others were embedded in paraffin and examined by immunohistochemistry. Figure 5A,B show the PCR products of VEGF isoforms in the murine retinas. Compared to the control eyes, the level of VEGF164 mRNA was significantly downregulated in the retinas of hypoxic animals treated with pSilencersiVEGF, whereas VEGF120 and VEGF188 levels in the murine retinas remained unchanged after local administration of pSilencersiVEGF. To confirm the effect of pSilencersiVEGF on the expression level of VEGF164 at the protein level, we performed immunohistochemical studies to investigate VEGF164 expression patterns in the retinas of the murine model of OIR. We performed western immunoblotting to assess the VEGF164 protein level in the retinas of the murine model of OIR. As shown in Figure 5C,D, local administration of pSilencersiVEGF significantly decreased expression of VEGF protein in the murine retinas.
Vascular homeostasis is regulated by two counter-balancing systems: angiogenic stimulators and angiogenic inhibitors [9,10]. Under pathological conditions, such as diabetic retinopathy and retinopathy of prematurity, the retina increases the production of angiogenic stimulators and reduces the production of angiogenic inhibitors, which would disrupt the balance between the positive and negative regulators of angiogenesis . VEGF as major angiogenic stimulator is upregulated in ocular neovascular diseases . However, due to alternative splicing of mRNA, VEGF has multiple isoforms. VEGF165 (VEGF164 in mice) is the major disease-causing isoform in models of neovascular eye disease. VEGF165 was found to be more potent than other VEGF isoforms in inducing vascular leakage and breakdown of blood–retinal barrier . Hence, VEGF165 was selected for this study as a target for suppressing retinal neovascularization. We hoped that therapy targeting VEGF165 in the retina could increase specificity and efficacy of the treatment.
To decrease pathological VEGF165 upregulation, we constructed a vector-based VEGF165 targeted siRNA expression system (pSilencersiVEGF) for our studies. pSilencersiVEGF has been shown to specifically inhibit VEGF165 expression in normoxia-cultured tumor cells . It has been hypothesized that sustained overproduction of VEGF by hypoxia retinal cells promotes retinal neovascularization in several neovascular eye diseases . Consequently, close attention was paid to whether pSilencersiVEGF could work properly under hypoxia conditions. VEGF165 was found to be decreased dramatically not only in the hypoxia cultured cells but also in the hypoxia retinal cells in the murine animal models, suggesting that hypoxia-induced VEGF could be abrogated by pSilencersiVEGF under hypoxia conditions. We surmise that overproduction of VEGF by hypoxia retinal cells may also be blocked by pSilencersiVEGF in human neovascular eye diseases such as diabetic retinopathy.
In the current study, retinal neovascularization in the murine model was greatly inhibited by 1000 ng of pSilencersiVEGF. This dramatic decrease in retinal neovascularization could be attributed to the following reasons. First, the localization of plasmids mediated by cationic liposome is close to the site of hypoxia-induced VEGF generation. VEGF164 level in the retinas of the murine model was found to increase in the inner nuclear layer and ganglion cell layer in this study, which was consistent with a previous study . However, cationic liposome has been confirmed as an effective reagent for retinal gene transfer, which could carry plasmids into retinal ganglion cells and retinal pigment epithelial cells through the injection of plasmids and liposome complex into the vitreous . Accordingly, intravitreal injections of pSilencersiVEGF could be successfully carried into retinal cells, which are in charge of producing hypoxia-induced VEGF by liposome. Second, the catalytic nature of RNAi entered the retinal cells. Small hairpin RNA (shRNA) targeting VEGF165 could be generated and processed into siRNA in these cells. The siRNA targeting VEGF165 binds to the RNA induced silencing complex (RISC), which in turn becomes activated. The activated RISC complex seeks out the VEGF165 mRNA and then splices the mRNA at the site of the homologous sequence . Furthermore, in multiple turnover kinetic fashion, the activated RISC can seek another VEGF165 mRNA to bind and destroy. One activated RISC complex can bind and destroy hundreds of VEGF165 mRNA. Finally, the high efficiency of pSilencersiVEGF is attributed to the divisional rate of the retinal cells. The division rate of cells that have taken in siRNA is an important factor when determining durability of silencing in cells , which leads to dilution of the activated RISC as it is divided between daughter cells. Because the division rate of retinal cells is slow, the silencing effect in the cells could last until upregulation of VEGF in ischemic retina disappears.
In summary, we found that siRNA targeting VEGF165 expressed from pSilencersiVEGF could decrease VEGF165 expression in vitro and reduce retinal neovascularization in a murine model of OIR. However, further experiments are necessary to determine whether detrimental side effects will appear after local administration of pSilencersiVEGF.
This research was supported by National Natural Science Foundation of China.