- Open Access
Silver nanoparticles inhibit VEGF-and IL-1β-induced vascular permeability via Src dependent pathway in porcine retinal endothelial cells
- Sardarpasha Sheikpranbabu†1,
- Kalimuthu Kalishwaralal†1,
- Deepak Venkataraman1,
- Soo Hyun Eom2,
- Jongsun Park3 and
- Sangiliyandi Gurunathan1, 4Email author
© Sheikpranbabu et al; licensee BioMed Central Ltd. 2009
- Received: 26 June 2009
- Accepted: 30 October 2009
- Published: 30 October 2009
The aim of this study is to determine the effects of silver nanoparticles (Ag-NP) on vascular endothelial growth factor (VEGF)-and interleukin-1 beta (IL-1β)-induced vascular permeability, and to detect the underlying signaling mechanisms involved in endothelial cells. Porcine retinal endothelial cells (PRECs) were exposed to VEGF, IL-1β and Ag-NP at different combinations and endothelial cell permeability was analyzed by measuring the flux of RITC-dextran across the PRECs monolayer. We found that VEGF and IL-1β increase flux of dextran across a PRECs monolayer, and Ag-NP block solute flux induced by both VEGF and IL-1β. To explore the signalling pathway involved VEGF- and IL-1β-induced endothelial alteration, PRECs were treated with Src inhibitor PP2 prior to VEGF and IL-1β treatment, and the effects were recorded. Further, to clarify the possible involvement of the Src pathways in endothelial cell permeability, plasmid encoding dominant negative(DN) and constitutively active(CA) form of Src kinases were transfected into PRECs, 24 h prior to VEGF and IL-1β exposure and the effects were recorded. Overexpression of DN Src blocked both VEGF-and IL-1β-induced permeability, while overexpression of CA Src rescues the inhibitory action of Ag-NP in the presence or absence of VEGF and IL-1β. Further, an in vitro kinase assay was performed to identify the presence of the Src phosphorylation at Y419. We report that VEGF and IL-1β-stimulate endothelial permeability via Src dependent pathway by increasing the Src phosphorylation and Ag-NP block the VEGF-and IL-1β-induced Src phosphorylation at Y419. These results demonstrate that Ag-NP may inhibit the VEGF-and IL-1β-induced permeability through inactivation of Src kinase pathway and this pathway may represent a potential therapeutic target to inhibit the ocular diseases such as diabetic retinopathy.
- Vascular Endothelial Growth Factor
- Silver Nanoparticles
- Vascular Permeability
- Interstitial Cystitis
- Endothelial Cell Monolayer
Vascular endothelial barrier dysfunction occurs in a large number of disease processes including diabetic retinopathy, stroke, pulmonary edema, myocardial infarction, inflammatory bowel disease, nephropathies, rheumatoid arthritis, and tumours. In these diseases, increased vascular permeability is associated with elevated levels of either one or more growth factors or cytokines . Vascular endothelial growth factor (VEGF) has received considerable attention as a tumour-secreted vascular permeability factor [2, 3]. VEGF is determined to posses 50,000 times more potency than histamine in inducing vasopermeability in the dermal vasculature. Previous reports indicate the correlation between the increases in permeability in ischemic retinopathies and possibly also in exudative macular degeneration and uveitis and the increased VEGF levels [4–7]. In fact, VEGF antagonists have been successfully used to reduce retinal/macular edema in neovascular eye diseases such as age-related macular degeneration with stabilization or even improvement of visual acuity in a subset of affected patients . Although VEGF is thought to play a major role in stimulating vascular permeability, this process undoubtedly involves multiple other factors as well, including inflammatory cytokines such as interleukin-1beta (IL-1β) . Previously IL-1β was shown to induce the permeability through the vasculature of the blood retinal barrier in rats .
Now a great deal of research is focused on the development of inhibitors for vascular permeability. In fields like drug delivery, imaging and diagnosis & treatment of cancer various nanoparticles are proposed to function as a tool [11, 12]. Furthermore, currently efforts are being made to investigate the use of nanomaterials in various therapeutic applications, where the nanoparticles could be the active component or could just be the physical support for the functional moieties. In addition, the importance of augmenting the performance of conventional drugs by incorporating the nanoparticles cannot be overstated as the synergistic effect may offer valuable alternatives with minimization of harmful consequences. Therefore, the development of novel therapeutic strategies that specifically target diabetic retinopathy is desired for patients with diabetes. As the size of the smallest capillary is in the order of 5-6 μm, nanomaterials are highly advantageous in this regard as their size allows exceptional access to targets at various parts of human body. Studies have shown that the properties of the nanoparticles vary according to the cell types. Ultrafine particles (1-10 nm) are found to cause inflammatory responses, where as relatively larger particles (50 nm) are internalized readily through the endothelial cells without much toxicity [13–15]. A recent study reported that intravesical administration of nanocrystalline silver (1%) has decreased the levels of urine histamine, bladder tumour necrosis factor-alpha and mast cell activation without any toxic effect. This action might be useful for interstitial cystitis . In addition, it has been suggested that the effect of NPI 32101 on suppression of inflammatory cytokines and MMP-9 may be responsible for its anti-inflammatory activity .
Endothelial cells play a central role in angiogenesis, carcinogenesis, atherosclerosis, myocardial infarction, limb and cardiac ischemia, and tumour growth [18, 19]. Endothelium is an important target for various drug and gene therapy. The vascular endothelial monolayer forms a semi-selective permeability barrier between blood and the interstitial space to control the movement of blood fluid, proteins, and macromolecules across the vessel wall. Alteration of permeability barrier integrity plays a major role in drug-based therapies, as well as the pathogenesis of cardiovascular diseases, inflammation, acute lung injury syndromes, and carcinogenesis [20, 21].
Solute flux assay has been successfully employed to study the effects of VEGF  and corticosteroids on retinal endothelial cell permeability. In the present study, we have investigated the molecular mechanism of silver nanoparticles on VEGF-and IL-1β- induced retinal endothelial cell permeability. We show that both VEGF and IL-1β increase endothelial cell permeability via Src dependent pathway. Silver nanoparticles were found to block VEGF-and IL-1β-induced permeability in retinal endothelial cells from porcine retina and this inhibitory effect was dependent on the modulation via Src phosphorylation at Y419. The results obtained in this study may provide some insights into the translocation pathways of nanoparticles in general.
Biosynthesis of silver nanoparticles
In a typical experiment, 2 g of wet Bacillus licheniformis biomass was taken in an erlenmeyer's flask. 1 mM AgNO3 solution was prepared using deionized water and 100 ml of the solution mixture was added to the biomass. Then the conical flask was kept in a shaker at 37°C (200 rpm) for 24 h for the synthesis of nanoparticles [23, 24].
Characterization of silver nanoparticles
Silver nanoparticles were synthesized using B. licheniformis. The synthesized nanoparticles were primarily characterized by UV-Visible spectroscopy followed by XRD and Transmission electron microscopic analysis. Finally, the size distribution of the nanoparticles was evaluated using DLS measurements, which were conducted with a Malvern Zetasizer ZS compact scattering spectrometer (Malvern Instruments Ltd., Malvern, UK).
Purification of nanoparticles
Bacteria were grown in a 1000 ml Erlenmeyer flask that contained 200 ml of nitrate medium. The flasks were incubated for 24 h in an environmental shaker set at 120 rpm and 37°C. After the incubation period, the culture was centrifuged at 4,000 × g and the supernatant used for the synthesis of silver nanoparticles. 1 mM of AgNO3 was mixed with 200 ml of cell filtrate in a 1000 ml Erlenmeyer flask. Bio-reduction was monitored by recording the UV-Vis absorption spectra as a function of time of the reaction mixture. The particles were washed five times by centrifugation and re-dispersed in water to remove excess of silver. They were then transferred to a dialysis tube with a 12,000 molecular weight cut off. Nanoparticles were resuspended in 1 ml of HEPES buffer (20 mM, pH 7.4) supplemented with sucrose to reach a density of 2.5 g/ml and gradient was made according to method described earlier [25–27]. The solution was placed at the bottom of a centrifuge tube (13 ml). Twelve millilitres of a linear gradient of sucrose (0.25-1 M) density was layered on the nanoparticle suspension and submitted to ultracentrifugation (200,000 g at 4°C for 16 h) by using an SW41 rotor (Beckman Instruments, Fullerton, CA, USA). Fractions (1 ml) were collected and purified sample was further characterized by UV-Vis and TEM. The purified Ag-NP was utilized for further experiments.
Porcine retinal endothelial cells (PRECs) were isolated and cultured as described previously . Briefly, freshly isolated retinas from porcine eye were washed and cut into 3 mm segments and transferred to a tube containing 4 ml of an enzyme cocktail (1 ml/retina) which consisted of 500 μg/ml collagenase type-IV (Sigma), 200 μg/ml DNase (Sigma) and 200 μg/ml pronase (Sigma) in 10 mM phosphate buffered saline containing 0.5% bovine serum albumin (BSA) at 37°C for 30 min. The resultant enzyme digests were passed through 53 μm steel mesh (W.S Tyler, UK). The trapped blood vessels were washed three times with minimal essential medium (MEM: Sigma St Louis, MO) by centrifugation at 400 × g for 5 min. The pellet containing microvessel fragments were finally suspended in Iscove's Modified Dulbecco's Medium (IMDM: Sigma St Louis, MO) with growth supplements on 35 × 10 mm culture dish coated with 1.5% gelatin type-A and incubated at 37°C with 5% CO2.
Cell viability assay
The 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide dye reduction assay using 96-well microtiter plates was performed according to the manufacturer's instructions (Roche Diagnostics, Mannheim, Germany). The assay relies on the reduction of MTT by the mitochondrial dehydrogenases of viable cells to yield a blue formazan product, which can be measured using a scanning multiwell spectrophotometer (Biorad, Model 680, Japan). PRECs were seeded at a density of 2 × 103 cells per well into 96-well culture plates and starved in IMDM with 0.5% serum for 5 h. To examine the effect of Ag-NP, VEGF-165B (Abcam, Cambridge, UK) and IL-1β (Abcam, Cambridge, UK) on cell viability, PRECs were treated with various concentrations of Ag-NP (from 0.1-1000 nM), VEGF and IL-1β and incubated for 24 h. After 24 h of incubation (37°C, 5% CO2 in a humid atmosphere), 10 μl of MTT (5 mg/ml in PBS) was added to each well, and the plate was incubated for a further 4 h (at 37°C). The produced formazan was dissolved in 100 μl of the dissolving buffer (provided as part of the kit) and absorbance of the solution was read at 595 nm. All measurements were carried out in triplicate.
Pharmacological inhibitor assay
To assess the Src activity, the pharmacological inhibitor PP2 (Calbiochem, Germany) was used. Briefly, PRECs were seeded at a density of 2 × 103 cells per well into 96-well culture plates and starved in IMDM with 0.5% serum for 5 h. Cells were incubated with 10 μM of PP2 for 30 min before treatment with VEGF-and IL-1β. The assays were conducted over a 24 h incubation period at 37°C in a 5% CO2 incubator, and cell permeability was assessed.
Plasmid constructs and transient transfection assay
The mutants at Lys295 (Kinase-deficient HA-Src KD K295 M) and Tyr527 (constitutive-active HA-Src-CA Y527F) were kindly provided by our collaborators and the constructs were employed as reported earlier . PRECs were transiently transfected using nucleofection technique (Amaxa Biosystems, Koeln, Germany) and cultured to 80% confluence in IMDM medium. Briefly, cells were harvested by trypsinization and centrifuged at 1,500 × g for 10 min. The pellet was resuspended in the nucleofector solution (Basic nucleofector kit, Amaxa Inc, Germany) to a final concentration of 4-5 × 105 cells/100 μl. At the time of transfection, 1-3 μg of DNA encoding green fluorescent protein (pmaxGFP), constitutively active Src or dominant negative Src was added along with nucleofector solution and then subjected to electroporation using a nucleofector device-II (Amaxa Biosystems, Koeln, Germany: Program M-003) according to manufacturer's instructions. After electroporation, transfected cells were resuspended in 35 × 15 mm gelatin coated dishes containing 1 ml of prewarmed IMDM media and incubated in 5% CO2 at 37°C. The transfection efficiency was about 80-90% determined using pmaxGFP plasmid (Amaxa Biosystems) and cell viability determined by trypan blue exclusion was about 90%.
Transwell monolayer permeability assay
To measure solute flux across endothelial cells, retinal endothelial cells were seeded onto 12-mm diameter Transwell filter inserts with a 0.4 μm pore size (Corning Inc); the inserts were placed into 12-well tissue culture plates. In some experiments, cells were first transfected with mutant Src constructs and then transferred to chambers. Chambers were examined microscopically for confluence, integrity, and uniformity of endothelial cell monolayers. 10 μM of rhodamine isothiocyanate (RITC)-dextran (70-kDa) (Sigma St Louis, MO) were applied to the apical chamber of the transwell inserts with a confluent endothelial cell monolayer. Growth factors were added for the designated times. Where applicable, Ag-NP was added 30 minutes prior to VEGF and IL-1β treatments. In some experiments, Src inhibitors were added to endothelial cell cultures 30 min prior to growth factor addition. The media volumes used equalized fluid heights in the apical and basolateral chambers, so that only diffusive forces were involved in solute permeability. At the indicated times after cytokine treatment, 100 μl samples were taken from the basolateral chamber and placed in a 96-well plate. A sample was taken from the apical chamber at the last time point; the amount of fluorescence in this chamber did not change significantly over the course of the experiment. Aliquots were quantified using a fluorescence multiwell plate reader (Biotek, Vermount, USA)
Quantification of phospho-Src Y419 in cell lysate
Concentrations of phospho-Src were quantified by using a human phosphor-Src (Y419) ELISA kit based upon peptide competitive analysis(R & D systems, Minneapolis, MN) as per manufacturer's instructions. Briefly, 1 × 107cells were seeded in a 60 mm tissue-culture dish and grown for 24 h. After the cells had attached and grown to confluence, the monolayer was starved for 6 h in IMDM with 0.5% FBS. After various treatments, cells were washed with 1× PBS (centrifuged at 2,000 × g, 10 min) and lysed using lysis buffer containing 1 mM EDTA, 0.05% Triton X-100, 5 mM NaF, 6 M Urea, 5 mM PMSF, 1 mM Na3VO4, 2.5 mM sodium pyrophosphate and a protease inhibitors (Sigma St. Louis, MO). After centrifugation at 2,000 × g for 10 min at 4°C, the supernatant containing proteins was removed and 6- fold dilution was made with buffer containing 1 mM EDTA, 0.5% Triton X-100, 1 M urea in 1× PBS. 100 μl of samples was added to each well of 96-well microplate coated with phospho-Src (Y419) capture antibody and incubated for 2 h at room temperature. After incubation, the plate were washed twice with PBS and incubated in blocking solution for 30 min. Following another wash with PBS, cells were incubated with the phospho-Src (Y419) detection antibody for 2 h at room temperature. After washing, 100 μl of streptavidin-HRP was added into each well and incubated for 20 min and then, 100 μl tetramethylbenzidine/H2O2 was added to the plates followed by the addition of 50 μl of stop solution. Colour formation was measured at an absorbance of 450 nm using a plate reader, which is directly proportional to the concentration of phospho-Src in the samples. The concentration of phospho-Src was determined using a calibration curve by generating a four parameter logistic curve fit.
Transmission electron microscopy (TEM) analysis
TEM sample preparation involving cells, however, was performed by treating cells with silver nanoparticles for 6 h with under serum-free conditions. After the incubation, PRECs were centrifuged initially at 2,500 × g for 10 min. The resultant cell pellets were then washed thrice with PBS, and fixed in Trump's fixative (1% glutaraldehyde and 4% formaldehyde in 0.1 M phosphate buffer, pH 7.2). Thin section (90 nm) of samples for transmission electron microscopy (TEM) analysis were prepared on carbon-coated copper TEM grids and stained with lead citrate. TEM measurements were performed on a JEOL model 1200EX instrument operated at an accelerating voltage of 120 kV.
All results were expressed as the mean ± standard error of the mean (SEM) values. Statistical significance difference was evaluated using ANOVA followed by paired two-tailed Student's t-test to compare with control group. A significance level of P < 0.05 was considered to be statistically significant.
Characterization of silver NPs
Cytotoxic effects of silver nanoparticle on PRECs
VEGF and IL-1β increase permeability of retinal endothelial cells in a dose-dependent manner
Silver nanoparticles inhibit VEGF-and IL-1β-induced cell viability in PRECs
Silver nanoparticles blocks VEGF-and IL-1β-induced permeability
Src mediates VEGF- and IL-1β induction of endothelial cell permeability
Over-expression of constitutively active Src rescues Ag-NP- induced permeability
Ag-NP blocks the VEGF-and IL-1β-induced Src phosphorylation (Y419) in PRECs
Src modulates the blocking effect Ag-NP on VEGF -and IL-1β-induced Src phosphorylation (Y419)
Vascular endothelial barrier dysfunction characterizes a diverse array of disease processes and plays an important pathophysiological role in many diseases including diabetic retinopathy . The development of new therapeutic strategies aimed at reducing excessive vasopermeability could therefore have serious clinical implications. In particular, the characterization of new molecules with anti-permeability properties and elucidation of their mechanisms of action could facilitate efficient treatments.
Neovascularization occurs when there is an increase in the level of angiogenic factors like VEGF. Blood vessel formation is a complex phenomenon which involves a multi-step process that includes activation by angiogenic molecules, release of degradative enzyme production, migration and proliferation. To characterise potential anti-angiogenic activity of silver nanoparticles, their effects on the different steps involved in angiogenesis must be investigated. As endothelium is the target for many therapies, in the recent work we have demonstrated the effect of biologically-synthesized silver nanoparticles on VEGF-induced cell proliferation and migration in bovine retinal endothelial cells (BRECs) . Silver nanoparticles of near-uniform size (40-50 nm), synthesized by the bacterium, Bacillus licheniformis were, found to block the proliferation and migration in BRECs  and to induce apoptosis . In the current study we investigated the effect of silver nanoparticles on retinal endothelial cell permeability.
As induction of permeability is one of the major problems in angiogenic related diseases, many molecules are under consideration for therapy. Angiopoietin 1, for instance, has been found to have an impressive effect in blocking blood vessel leakage in animal models [33, 34]. Pigment epithelium-derived factor (PEDF) has recently emerged as a molecule that can regulate vascular permeability. PEDF is known to have strong anti-angiogenic effects in vivo  and to regulate endothelial cell actions such as migration, proliferation, and survival in vitro [36–38]. In vivo studies have demonstrated that PEDF blocks VEGF-induced vascular permeability in the retina . But, one of the disadvantages of all these molecules is the cost of the final product.
Our findings indicate that Ag-NP may have therapeutic benefits in addition to its anti-angiogenic properties . The ability of Ag-NP to block both angiogenesis and permeability may render it uniquely beneficial as an agent of therapeutic choice for diverse complications. The production of VEGF by tumour cells may enhance metastasis by tumour cell extravasation from the bloodstream via endothelial barrier [45, 46]. Disruption of Src signalling by pharmacologic blockade or by genetic approaches abrogated this VEGF effect. Therefore silver nanoparticles may have therapeutic potential in the treatment of cancer.
Our findings indicate that Ag-NP may have potential therapeutic benefits in addition to their anti-angiogenic properties. Disruption of Src signalling by pharmacologic blockade or by Ag-NP approaches abrogated these VEGF and IL-1β effect. Our results indicate that Ag-NP have a therapeutic benefit in vascular permeability. Therefore Ag-NP may potentially provide attractive and cheap therapeutic alternative for treating various conditions characterized by excessive vasopermeability.
The opinions expressed in this article are those of the authors and do not necessarily represent any agency determination or policy.
Prof. G. Sangiliyandi was supported by grant from Council of Scientific and Industrial Research (CSIR), New Delhi (Project No. 37/0347). Prof. Soo Hyun Eom was supported by grants from the Cell Dynamics Research Center, GIST (R11-2007-007-03001-0), the National Research Foundation of Korea (NRF), Ministry of Education, Science and Technology (MEST) (20090065566), the "Systems biology infrastructure establishment grant" provided by GIST in 2009, Republic of South Korea. Prof. Jongsun Park was supported by grant from the Korean government (Ministry of Science and Technology: Engineering Research Center Program (2009-0062916)). The authors gratefully acknowledge the support of Dr. Pushpa Viswanathan, Professor, Cancer Institute (WIA), Chennai, who helped us with TEM analysis.
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