- Research article
- Open Access
Anti-proliferative activity of silver nanoparticles
© AshaRani et al; licensee BioMed Central Ltd. 2009
- Received: 2 June 2009
- Accepted: 17 September 2009
- Published: 17 September 2009
Nanoparticles possess exceptional physical and chemical properties which led to rapid commercialisation. Silver nanoparticles (Ag-np) are among the most commercialised nanoparticles due to their antimicrobial potential. Ag-np based cosmetics, therapeutic agents and household products are in wide use, which raised a public concern regarding their safety associated with human and environmental use. No safety regulations are in practice for the use of these nanomaterials. The interactions of nanomaterials with cells, uptake mechanisms, distribution, excretion, toxicological endpoints and mechanism of action remain unanswered.
Normal human lung fibroblasts (IMR-90) and human glioblastoma cells (U251) were exposed to different doses of Ag-nps in vitro. Uptake of Ag-nps occurred mainly through endocytosis (clathrin mediated process and macropinocytosis), accompanied by a time dependent increase in exocytosis rate. The electron micrographs revealed a uniform intracellular distribution of Ag-np both in cytoplasm and nucleus. Ag-np treated cells exhibited chromosome instability and mitotic arrest in human cells. There was efficient recovery from arrest in normal human fibroblasts whereas the cancer cells ceased to proliferate. Toxicity of Ag-np is mediated through intracellular calcium (Ca2+) transients along with significant alterations in cell morphology and spreading and surface ruffling. Down regulation of major actin binding protein, filamin was observed after Ag-np exposure. Ag-np induced stress resulted in the up regulation of metallothionein and heme oxygenase -1 genes.
Here, we demonstrate that uptake of Ag-np occurs mainly through clathrin mediated endocytosis and macropinocytosis. Our results suggest that cancer cells are susceptible to damage with lack of recovery from Ag-np-induced stress. Ag-np is found to be acting through intracellular calcium transients and chromosomal aberrations, either directly or through activation of catabolic enzymes. The signalling cascades are believed to play key roles in cytoskeleton deformations and ultimately to inhibit cell proliferation.
- Silver Nanoparticles
- U251 Cell
- Dicentric Chromosome
- Clathrin Dependent Endocytosis
- Normal Human Lung Fibroblast
The convergence of nanotechnology with nanomedicine has added new hope in the therapeutic and pharmaceutical field. The unique nature of nanoparticles is being exploited by scientists, in hope of developing novel diagnostic and antimicrobial agents . Silver nanoparticles (Ag-np) are widely used in medicine, physics, material sciences and chemistry . However, the rapid progress in nanotechnology was accompanied by insufficient data on biohazard identification. Exposure to nanomaterials occurs through inhalation, ingestion, injection for therapeutic purposes and through physical contact at cuts or abraded skin. From the site of deposition, the nanoparticles are translocated to different parts of the body through the circulatory or lymphatic system. In vivo studies showed that exposure to nanoparticles could result in inflammation, oxidative stress, myocardial infarction and thrombosis . In addition, a few of the nanoparticles can alter the permeability of blood brain barrier . Although these concepts are applicable to nanomaterials in general, a detailed study is necessary for each nanoparticle in use.
Ag-nps are classified as antimicrobial agents [5, 6] and are widely used in treating wounds, burns and catheter related infections . Even though silver complexes were used for decorating sweets, as components of dental alloys  and antimicrobial agents in ancient times, lack of information regarding the toxicity remained an important issue. A few reports demonstrated the toxicity of silver nitrate on human dermal fibroblasts  and on aquatic species . We had identified in vivo targets of silver nanoparticle in zebrafish embryos . Silver nanoparticles were found to be deposited in various organs in zebrafish embryos giving rise to distinct developmental defects. Recent reports on Ag-np toxicity have identified the mitochondria  as primary targets of silver nanoparticles in rat liver cells. Moreover, Ag-nps were reported to act via reactive oxygen species (ROS) production and glutathione depletion in rat liver cells . The recent work by Skebo and colleagues  claimed that Ag-nps coated with polysaccharide exhibited less cytotoxicity compared to other Ag-nps employed for the study.
Ag-nps are believed to alter the membrane structure by attaching to the sulphur containing proteins of the cell membrane thereby damaging the cell membrane of the bacteria [14, 15]. Recent reports emphasised on the size and shape dependent interactions of Ag-nps with bacterial cells, which played a crucial role in their bactericidal properties . The occupational hazard associated with the nanoparticle exposure and the molecular mechanisms underlying Ag-np toxicity are still unknown. Here, we set to investigate the mechanism of Ag-np toxicity by employing various techniques like fluorescence in situ hybridisation (FISH) to detect the chromosomal abnormalities and real-time reverse transcriptase polymerase chain reaction (RT-PCR) for monitoring change in gene expression patterns occurred due to nanoparticle treatment. The uptake and exocytosis rates of nanoparticles were estimated. Also, the Ca2+ transients in the nanoparticle treated cells were monitored and the propagation of Ag-np signals was identified. A model is proposed based on the data which might explain the mechanism of Ag-np toxicity.
Cellular uptake and exocytosis of nanoparticles
Recovery and colony formation
Up regulation of stress response genes
Intracellular distribution of Ag-np
Chromosomal aberrations in Ag-np treated cells
Summary of chromosomal aberrations observed in cancer cells and normal cells with or without Ag-np treatment
Aberrant cells (%)
(Mean ± s.e.)
(Mean ± s.e.)
46 ± 0
46 ± 0
0.094 ± 0.042
Aberrant cells (%)
(Mean ± s.e.)
(Mean ± s.e.)
93 ± 2.25
0.18 ± 0.062
96 ± 2.46
0.32 ± 0.097
Calcium fluctuations in Ag-np treatment
Morphological changes in cells
Mechanism of uptake of Ag-nps is an unidentified area, which could shed light to the mechanisms of toxicity as well as potential therapeutic application of nanoparticles. In the present study, we have observed that Ag-np uptake occurs mainly through endocytosis where clathrin mediated process and macropinocytosis were involved. This observation corroborates with the electron micrographs which showed uncoated endosomes of size ~ 150 nm. The survival of cells from nanoparticle mediated damage depends on their ability to expel the nanoparticles. Previous reports have emphasised the role of exocytosis process in expelling gold nanoparticles from the cells to avoid critical loss of function . Hence, exocytosis rates of Ag-nps were monitored for a better understanding of the cellular retention and expulsion of nanoparticles. Such approaches might have implications on long term deposition of nanoparticles in cells and chronic toxicity. Exclusion of Ag-np followed a slow and time dependant pattern. Though the cells were able to remove nanoparticles efficiently, the nanoparticle concentrations in cells were well within detectable limits of Ag concentration even after 48 hours of recovery, which suggests active nanoparticle retention and chances of a continuous and prolonged Ag-np mediated stress.
Metallothioneins are considered as essential biomarkers in metal-induced toxicity  facilitating metal detoxification and protection from free radicals . Recent reports on heavy metal toxicity in Javanese medaka had shown that MT upregulation occurs in silver mediated toxicity . HO-1 is an ROS sensor and a cryoprotective agent possessing antioxidant and anti-inflammatory properties. HO-1 break down heme to antioxidant biliverdin, carbon monoxide and iron under stress conditions [23, 24]. Rahman et al. studied upregulation of oxidative stress response genes (superoxide dismutase 2, glutathione reductase 1 etc) in mouse brain following Ag-np exposure . Our results substantiate existing animal studies data where upregulation of HO-1 mRNA signifies oxidative stress. Due to the antioxidant and metal detoxifying properties of HO-1 and MT, upregulation of the genes might defend the cells against the stress induced by Ag-np.
Electron micrographs have indicated endocytosis of Ag-np in to the cells and its presence in the nucleus. The exact outcome due to the nuclear deposition of Ag-np is unknown; however, it is expected to have lethal effects in DNA synthesis, DNA damage, chromosomal morphology and segregation. The deposition of metal particles inside the nucleus could affect the DNA and cell division. Genotoxic studies of titanium dioxide (TiO2) nanoparticles revealed dose dependant DNA damage, chromosomal aberrations and errors in chromosome segregation  and formation of sister chromatic exchanges . Treatment with Ag-np induced the production of micronuclei (MN) , a marker of chromosome damage. Mroz et al.  speculated that nanoparticles and reactive oxidative species induce DNA damage, activating p53 and proteins related to DNA repair, mimicking irradiation related carcinogenesis. The observed genotoxic response, in our study, could be a consequence of oxidative damage to DNA .
Our experiments on Ag-np treated cells demonstrate the occurrence of calcium transients. There are substantial evidences linking oxidative stress to Ca2+ transients  which can increase Ca2+ by permeability changes of mitochondria. Ca2+ ions are indispensable for cellular functions viz. cellular transport through actin dynamics and mitosis. Although Ca2+ signalling occurs rapidly, a time dependant study was adopted based on the fact that nanoparticle diffusion and subsequent binding to specific receptors on cellular organelles could result in direct Ca2+ transients or activation through other pathways, which will take time to initialize. Even though the binding of Ag-np to plasma membrane receptors is rapid, the rates of diffusion or endocytosis and subsequent binding with intracellular targets are relatively slow. The possibilities of continuous diffusion of nanoparticles and sustained activation of Ca2+ channels are high throughout the incubation period. Moutin et al  provided evidence that Ag+ ions act on the same site as Ca2+ ions, regulating the release of Ca2+ from sarcoplasmic reticulum. Also, higher concentration of Ag+ ion inhibited Ca2+ release from the intracellular stores in a similar way as higher concentrations of Ca2+ ions, giving a bell shaped curve . Ag-np could release Ag+ ions through surface oxidation , which could trigger Ca2+ fluctuations in a similar way.
Disruption of calcium homeostasis plays a major role in pathological and toxicological conditions and is an early sign of cell injury. Calcium ions have the potential to activate catabolic enzymes like phospholipase, proteases and endonuclease that further augment the toxicity . Repeated calcium influx and efflux in mitochondria could result in mitochondrial membrane damage, resulting in ROS production and inhibition of ATP synthesis . This report links the oxidative stress, Ca2+ and ATP depletion occurred in Ag-np treated cells. Moreover, Ca2+ overload in mitochondria could release apoptogenic factors such as cytochrome C, endonuclease G and other apoptosis inducing factors to the cytosol to initiate apoptosis . It was observed that the rise in concentration of Ca2+ ions occurred within 48 hours. Hence, it is possible that the mitochondria mediated Ca2+ ions homeostasis occurred during the later stages of incubation period resulting in a delayed induction of apoptosis. It is known that an early sign of Ca2+ homeostasis disruption is indicated by blebbing of plasma membrane which is a consequence of cytoskeletal injury . SEM investigations to study the cytoskeletal injury revealed altered spreading patterns which may be linked to Ca2+ fluctuations. Yet, the difference in response between cancer cells and normal cells towards Ca2+ response and cell recovery adds on to the complexity of the mechanism.
This work concludes that Ag-nps have multiple cellular targets that vary among cell types. We have identified that the major route of nanoparticle uptake is through clathrin dependent endocytosis and macropinocytosis. Also, exocytosis occurs in a time dependant manner in cancer cells. Exposure of Ag-nps resulted in chromosomal abnormalities, inhibition of proliferation, observed as failure to form colonies, and absence of recovery selectively in cancer cells, which add new hopes for preventing cancer cell metastasis. A uniform intracellular distribution of Ag-np was observed in the treated cells. Moreover, the upregulation of cryoprotective genes like HO-1 and MT-1F showed that the cellular defense mechanisms are still active in normal cells.
Synthesis of silver nanoparticles
Silver nanoparticles were synthesized and characterized as described in our previous publication . Briefly, 1 mM silver nitrate was reduced by 0.03 gm of sodium borohydride, followed by stabilisation with soluble potato starch (0.28 gm) at 70°C. Electron micrographs showed the nanoparticle size (6-20 nm).
Normal human lung fibroblasts (IMR-90) (Coriell Cell Repositories, USA) were cultured in Dulbecco's modified Eagles medium (DMEM, Sigma-Aldrich, USA) supplemented with 15% foetal bovine serum (Hyclone, USA), 2% essential amino acids and 1% each of non-essential amino acid, vitamins and penicillin-streptomycin (GIBCO, Invitrogen, USA). The cells (passage 18 ± 2) were maintained at 37°C in presence of 5% CO2 at log phase. Human glioblastoma cells (U251 cells) (from Dr. Masao Suzuki, National Institute of Radiological Sciences, Chiba, Japan) were maintained in DMEM supplemented with 10% foetal bovine serum (FBS, GIBCO) and 1% penicillin-streptomycin. IMR-90 cells served as a representative for normal primary cells as well as a cell type of lung origin, which is a common route of nanoparticles exposure. Ag-nps are known to localise in brain , thus glioblastoma cells provide a suitable model for studying interactions of nanoparticles in brain cells. Also, use of a cancer cell and normal cell allows comparison of responses between normal and cancer cells.
Quantitation of cellular uptake of Ag-np
The nanoparticle uptake by the cells was quantitated using inductively coupled plasma-optical emission spectroscopy (ICP-OES, Perkin Elmer Optima 5300 DV). Cells were seeded at a density of 1.5 × 105 cells in T-75 flask and treated with Ag-np to achieve a final concentration of 100, 200 and 400 μg/mL of Ag-np. Higher concentrations were employed to show the stability of the nanoparticles in cell culture medium. To study the uptake mechanism of Ag-np, U251 cells were incubated with 100, 200 and 400 μg/mL of Ag-np under three different conditions. The initial step was to calculate the rate of uptake of nanoparticles when the cells were incubated for 2 hours at normal culture conditions (37°C). Endocytosis was considered as a possible mechanism of uptake based on our electron micrographs which showed endosomes with nanoparticles. Hence cells were treated with 0, 100, 200 and 400 μg/mL of Ag-np at 4°C for 2 hours to inhibit endocytosis. Low temperature treatments inhibit endocytosis in cells . The transmission electron micrographs (TEM) did not show the presence of coated endosomes. This raised a suspicion that nanoparticles could be taken up by a method apart from clathrin coated pits. Hence, cells were pretreated with K+ depleted medium for 30 minutes prior to nanoparticle treatment for 2 hours. This treatment blocked formation of clathrin but facilitated formation of uncoated pits (caveoli) . Involvement of other uptake pathways such as macropinocytosis and caveoli dependant endocytosis were investigated by selective inhibition of the pathways in presence of specific inhibitors wortmannin  and nystatin , respectively. Analyses for macropinocytosis and caveoli mediated processes were carried out as per previous reports [36, 37]. Following incubation period, medium was removed and flasks were washed 5 times with 1× phosphate buffered saline (PBS, 1st Base, Singapore). Cells were harvested using trypsin - EDTA (ethylene diamine tetra acetic acid, GIBCO, Invitrogen, Grand Island, NY, USA), washed 3-4 times in PBS and resuspended in 10 mL PBS. The cell number in all tubes was adjusted to 2 million and one millilitre of the lysate was analysed after homogenization. Concentration of silver estimated from cells treated under normal conditions for 2 hours were compared with results from low temperature incubation (endocytosis blocking), K+ depleted treatment (clathrin inhibition), wortmannin (macropinocytosis inhibition) and Nystatin (caveoli inhibition).
Rate of exocytosis was studied by treating U251 cells using similar concentrations of Ag-np as described above. Following 3 hours of incubation, nanoparticles were completely washed away with buffer and further incubated for 2, 6, 24 and 48 hours in fresh medium. At the end of individual incubation period, medium and cells were collected separately, homogenised and assayed.
Transmission electron microscopy of cells treated with Ag-np
Cells were treated with 25 μg/mL of Ag-np washed well to remove unbound Ag-np. Cells were fixed in 2.5% gluteraldehyde for 2 hours and washed in phosphate buffer. Post fixation was done in 1% osmium tetroxide for 1 hour. Cells were washed further in phosphate buffer and dehydrated in alcohol for 15 minutes each (50%, 70%, 80%, 95% and 100%). Cells were further treated with propylene oxide (30 min), propylene oxide-resin mixture (overnight) and pure resin (48 hours). Embedding was done in BEEM capsules using pure Spurr's low viscosity resin at 80°C for 48 hours. Ultrathin sections were taken using Reichert Jung Ultratome and negatively stained.
Chromosomal Analysis by Fluorescence in situ hybridisation (FISH)
Cells were plated in T-75 flasks at a density of 8 × 105 and incubated with 0, 25, 50 and 100 μg/mL of Ag-np for 48 hours and metaphase spreads were prepared as explained earlier . Briefly, treated cells were allowed to grow in fresh medium for 24 hours. Cells were then arrested at metaphase with 10 μL/mL karyomax colcemid solution (Gibco) before being subjected to hypotonic swelling in warm 0.075 M KCl and fixation with Carnoy's fixative (3:1 Methanol: Acetic Acid solution). FISH was performed on metaphase spreads using telomere and centromere specific peptide nucleic acid (PNA) probes (Applied Biosystems) labelled with Cy-3 and FITC respectively as explained earlier [38, 39]. Fifty spreads were captured per sample, using Zeiss Axioplan-2 imaging (Carl Zeiss, Germany). The data were analysed using the in situ imaging software (Metasystems, Germany). Chromosomal analysis was done to detect abnormalities like chromosome breaks, fusions and abnormal segregation.
Gene expression profile using real time-reverse transcriptase- polymerase chain reaction (RT-PCR)
Light cycler RNA amplification kit SYBR green 1 (Roche, Switzerland) was used for RT-PCR analyses as per manufacturer's instructions. Cells were treated with 200 μg/mL of Ag-nps and total RNA was isolated using RNA isolation kit (Qiagen, Germany). The concentration and integrity of RNA was measured using nanodrop spectrophotometer prior to the experiment. Primers were designed using cybrgene primer design utility. The primer (1st Base, Singapore) sequence for metallothionein - 1F were 5'CCA CTG CTT CTT CGC TTC TC 3' and 5'AGG AGC AGC AGC TCT TCT TG 3' (Annealing temperature (TA) - 61°C) for forward and reverse primer, respectively. HO-1 gene was amplified using 5' GAG ACG GCT TCA AGC TGG TGA TGG 3' and 5' CCA CGG GGA AAG TGG TCA TGG 3' (TA - 61°C) as forward and reverses primers, respectively. The house keeping gene was 18s ribosomal RNA. Filamin was amplified using 5' AAGTGACCGCCAATAACGAC 3' and 5' AAGTGACCGCCAATAACGAC 3' (TA- 58°C) as forward and reverse primer. Amplification of the 18S rRNA was performed using 5' GTA ACC CGT TGA ACC CCA TT-3'and 5' CCA TCC AAT CGG TAG TAG CG 3' (TA-61°C) as forward and reverse primers, respectively.
Intracellular calcium measurement
The Ca2+ measurements were done using Fluo-2NW calcium assay kit, (Invitrogen, USA). The assay was designed to measure Ca2+ transients occurring in target cells. The assay was performed as per the supplier's instructions. Ag-nps were added to the wells and incubated for different time intervals starting from 0s, 4 hours, 24 hours and 48 hours. Kinetic study was performed by prior loading of the cells with Ca2+ sensors at 37°C for 30 minutes followed by incubation at room temperature for 30 minutes. Different concentrations of Ag-nps (25, 50, 100, 200 and 400 μg/mL) were added to the wells containing the dye and readings were taken immediately. End point measurements (4 hours, 24 hours and 48 hours) were taken after treatment with Ag-nps and subsequent loading with the dye. Fluorescence measurements were taken using TECAN Genios plus and BioTek Flx 800 spectrofluorometer.
Qualitative analysis of cell morphology by SEM
Cells grown on sterile coverslips were treated with Ag-np (400 μg/mL) for 48 hours and fixed in 2.5% gluteraldehyde for 30 minutes. The coverslips were washed 5 times in Sorensen buffer and post fixed in 1% osmium tetroxide for 1 hour. Dehydration of the cells was done in ethanol series (50%, 70%, 90% and 100%). Critical point drying and platinum coatings were done as per standard SEM procedures. The slides were analysed using JEOL JSM 6701F with an accelerating voltage of 5 KV.
Colony formation assay
This assay identifies the cell populations that are destined to die or survive following a cytotoxic drug treatment. Cells were seeded at a density of 2.5 × 104 cells in T-25 flasks and treated with 0, 25, 100, 200 and 400 μg/mL of Ag-np and incubated for 48 hours. At the end of the incubation period, medium containing Ag-np was replaced with fresh medium and formation of colony and recovery period were recorded. Two experiments were conducted for fibroblasts to ensure complete recovery from Ag-np induced stress. In the first batch of experiments fibroblasts recovered were subjected to cell cycle analysis . Second set of recovered cells were assayed for the concentration of silver inside the cells.
We thank Mr. Aik Kia Khaw for his help with the graphics and Ms. Grace Low for her valuable suggestion about this manuscript. This study was supported by grants from the Agency for Science, Technology and Research (ASTAR), Singapore and NUSNNI to PVA and SV and from the Academic Research Fund, Ministry of Education, Singapore (T206B3108; WBS: 185-000-153-112) to MPH.
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