Non-chemotoxic induction of cancer cell death using magnetic nanowires
Authors Contreras M, Sougrat R, Zaher A, Ravasi T, Kosel J
Received 5 November 2014
Accepted for publication 10 January 2015
Published 17 March 2015 Volume 2015:10(1) Pages 2141—2153
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Prof. Dr. Thomas J. Webster
Maria F Contreras,1 Rachid Sougrat,2 Amir Zaher,3 Timothy Ravasi,1,3 Jürgen Kosel3
1Division of Biological and Environmental Sciences and Engineering, 2Advanced Nanofabrication Imaging and Characterization, 3Division of Computer, Electrical and Mathematical Sciences and Engineering, King Abdullah University of Science and Technology, Thuwal, Kingdom of Saudi Arabia
Abstract: In this paper, we show that magnetic nanowires with weak magnetic fields and low frequencies can induce cell death via a mechanism that does not involve heat production. We incubated colon cancer cells with two concentrations (2.4 and 12 µg/mL) of nickel nanowires that were 35 nm in diameter and exposed the cells and nanowires to an alternating magnetic field (0.5 mT and 1 Hz or 1 kHz) for 10 or 30 minutes. This low-power field exerted a force on the magnetic nanowires, causing a mechanical disturbance to the cells. Transmission electron microscopy images showed that the nanostructures were internalized into the cells within 1 hour of incubation. Cell viability studies showed that the magnetic field and the nanowires separately had minor deleterious effects on the cells; however, when combined, the magnetic field and nanowires caused the cell viability values to drop by up to 39%, depending on the strength of the magnetic field and the concentration of the nanowires. Cell membrane leakage experiments indicated membrane leakage of 20%, suggesting that cell death mechanisms induced by the nanowires and magnetic field involve some cell membrane rupture. Results suggest that magnetic nanowires can kill cancer cells. The proposed process requires simple and low-cost equipment with exposure to only very weak magnetic fields for short time periods.
Keywords: cell death induction, low frequency alternating magnetic field, nanomedicine, nanowire internalization, nickel nanowires
Micro- and nanostructured materials have become relevant to the life sciences mainly because manufacturing advances now permit their sizes to be tailored in a controlled fashion such that they match the sizes of biological entities, which can range from tens of nanometers (average size of a virus) to tens of micrometers (average size of a mammalian cell).1 Given the high surface area to volume ratio of such materials, the chances of a bond to be created or a payload to be delivered are dramatically increased with the use of nanostructured materials. Surface areas are commonly decorated with coatings that are intended for two purposes: to enhance the biocompatibility of the nanoparticle and to gain bioactivity, ie, to become an active player in the biological niche of interest. This bioactivity has been exploited for cell targeting,2,3 cargo payload (drug and gene delivery),4–6 contrast agents,7 or a combination of these, giving multifunctionality to a nanostructure.8–10
Magnetic nanoparticles (MNPs) can be remotely manipulated by magnetic fields. Using direct current fields, MNPs can be trapped, concentrated,11–14 or used in cell separation.15–17 Under alternating fields, MNPs can be heated18 or rotated,19,20 and, in cases of elongated structures, they can transmit forces or torques to whatever they are in contact with.
Investigation of magnetic nanostructures for biomedical applications has increased recently. Most previous studies utilized magnetic nanobeads, but recent studies have reported diverse bioapplications of magnetic nanowires (NWs) as well. NWs offer advantages over nanobeads, such as larger magnetic moments per unit of volume and larger surface area to volume ratios, which allow them to bind more efficiently to cells, producing purer populations during cell separation.21,22
The two magnetic materials usually used as NWs in biomedical applications are Fe and Ni. Out of these two, Fe NWs tend to aggregate more, since they have a higher remanence magnetization value,23 making Ni a better material in that regard. Furthermore, Ni NWs have proven to be efficient in cell separation, manipulation, and purification16,17,21,22,24–26 as well as in delivering cargoes of various macro-particles including biological entities.27 Recent studies have investigated their use as therapeutic agents for hyperthermia28 and cell inflammation induction29 in cultures of human embryonic cells. They have also been shown to work as apoptotic agents for pancreatic cancer cells.30
The large number of studies that use Ni NWs in comparison to Fe might suggest that Ni is a better candidate material despite its reported genotoxicity and cytotoxicity in Ni-containing dust particles.31 Even though no work has been done that directly compares the cytotoxicity of Fe and Ni NWs under the same experimental conditions (cell line, incubation times, concentrations), a cross-comparison among studies32,33 reveals that Fe NWs are considerably less toxic at a given concentration than are Ni NWs. However, as mentioned above, the stronger aggregation of Fe NWs limits the use of pristine NWs, requiring passivation to overcome this limitation.
In addition to work on biological and biomedical applications, fundamental studies involving internalization into different cell lines,34 the dependence of cytotoxicity on incubation time and NW concentration,33,34 and length-dependent cytotoxicity35 have been reported. Moreover, cellular processes such as increased levels of reactive oxygen species,27 cell viability reduction,27,36 and cell membrane leakage36 have been shown to be activated solely by the incubation of cells with Ni NWs.
Alterations in cellular features due to magnetomechanical effects from alternating magnetic fields (AMFs) have been studied before. The first study applied a low-frequency (1–10 Hz), high-gradient magnetic field and mechanical vibration to mesenchymal stem cells and showed that both mechanisms play an important role in F-actin remodeling and regulation of adipogenic differentiation.37 The next two studies38,39 incubated magnetic particles (iron oxide nanoparticles and permalloy microdisks, respectively) with cells in culture and applied AMFs. In the first one,38 a hyperthermia-like field was employed (16 mT, 260 kHz), while in the second one,39 a low-frequency field was used (9 mT, 20 Hz). Both studies induced cell death in coincubated cells and particles after AMF exposure. Common changes in the cells included cell membrane leakage and cell shrinkage. The permalloy particles were functionalized with antibodies directed towards overexpressed cancer cell membrane receptors.
There have also been a few studies in which Ni NWs in combination with magnetic fields were used. Two studies have been conducted that used low-frequency magnetic fields to exploit the rotational response of Ni NWs.29,40 In the first one, Choi et al29 measured interleukin-6 (IL-6) expression (a common proinflammatory cytokine) after a 13 hour coincubation of cells with Ni NWs and application of a field (field strength not mentioned) for 5 minutes. The IL-6 expression fold-changes (compared to cells incubated with NWs only, no applied field) were: 5, 4.5, and 1.5 for 1.7 Hz, 8.3 Hz, and 11.6 Hz, respectively. The second study consisted of the addition of Ni NWs to mouse fibroblasts in culture and the subsequent application of a very strong field (240 mT, 1 Hz) for 20 minutes. Fung et al showed an 89% cell viability reduction.40 Moreover, the NWs by themselves did not induce elevated expression of IL-6 when cocultured with mouse fibroblasts for 12 hours, despite the moderate cytotoxicity reported for Ni41 and the strong hypersensitivity of human skin.42
The studies mentioned here used NWs with diameters ranging from 150 to 280 nm. For assessing cell damage, optical microscopy and quantitative real-time polymerase chain reaction (PCR) were used. Only Fung et al40 used a colorimetric method to compare viability of a given cell population before and after application of the low-frequency AMF.
In the present study, we applied a low-frequency, small-amplitude AMF to cells that had been incubated with Ni NWs. Compared with previous studies, the applied magnetic field was much weaker in our experimental setup and the NWs were about one order of magnitude thinner than those used in previous work. The motivation behind this experimental setup is the exploitation of a non-chemotoxic way of inducing cancer cell death.
Here, we consider NW–cell interactions by using transmission electron microscopy (TEM) images that reveal the NW internalization process and the location of the magnetic NWs inside cancer cells. We also consider AMF–cell interactions when the magnetic field is applied for short periods of time (10 or 30 minutes) to cells in culture. Finally, we discuss NW–AMF interactions and estimate the forces exerted by a single NW, along with the combined effects of NW–cell interaction in the presence of an AMF, which we call AMF treatment. We report on cell population assays that measured viability and membrane leakage.
Materials and methods
Fabrication of magnetic NWs
The NWs were fabricated by electrodeposition into alumina membranes. Full details of the aluminum anodization43 and pulsed electrodeposition processes can be found elsewhere.44,45 Briefly, a highly pure aluminum substrate (99.999%; Goodfellow, London, UK) was cleaned and electropolished. A two-step anodization of the polished aluminum under specific conditions (0.3 M oxalic acid, 4°C, 40V) resulted in the growth of a porous anodic alumina template with hexagonally arranged nanopores with diameters from 30 to 40 nm, which was used as the template for NW fabrication. Pulsed electrodeposition was employed to deposit Ni with current pulses limited to 30 mA. The NW length was controlled by the deposition time, and 4 μm long Ni NWs (4.1±1.4 μm) were fabricated.
Afterwards, the template containing the NWs was dissolved with 1 M NaOH. The NWs were collected with a magnetic rack (DynaMag™-2; Life Technologies, Carlsbad, CA, USA), rinsed thoroughly with ethanol with 5-second sonication steps in between the cleaning steps, and resuspended in cell culture medium. The cell culture medium was changed three times to remove any remaining ethanol.
Characterization of magnetic NWs
The NW morphology and geometrical features were investigated with scanning electron microscopy (SEM) and TEM (SEM: Quanta 3D; FEI Company, Hillsboro, OR, USA; and TEM: Tecnai BioTWIN; FEI Company). The length and diameter distributions were obtained directly from SEM images using ImageJ software. The NW composition was measured using energy-dispersive X-ray spectroscopy (scanning TEM Tecnai BioTWIN; FEI Company). All electron microscopic images were taken of NWs freshly released from the template after rinsing several times with ethanol. Once released, the NWs were sonicated for 10 minutes to achieve a better dispersion.
The NWs were quantified via an indirect method. After electrodeposition, the samples were briefly immersed in a chromium-based solution to partly reveal the NWs. After washing with ethanol, they were imaged with SEM, and the pore filling was found to be above 95%. The number of pores of a certain area, quantified from an SEM image, was extrapolated from the total deposition area determined by the experimental setup. Due to the high pore filling, the total number of NWs was considered to be equal to the total number of pores.
Magnetization loops of NWs inside the alumina membrane were measured at room temperature with a vibrating sample magnetometer (VSM model MicroMag™ 3900; Princeton Measurement Corporation, Westerville, OH, USA) (maximum field used: 1 T; sensitivity: 0.5 μemu; standard deviation at 1 second per measured point).
The surface charge of Ni NWs was measured by dynamic light scattering (Zetasizer Nano ZS, He–Ne laser 633 nm; Malvern Instruments, Malvern, UK). A concentrated solution of NWs was resuspended in complete culture medium, put into a capillary cell, and measured.
HCT116 (ATCC© CCL-247™) colorectal carcinoma cells were cultured following vendor recommendations in McCoy’s 5A medium supplemented with 10% fetal bovine serum and 1% penicillin/streptomycin (final concentration). The doubling time of the cells in culture was found to be 17 hours.
Cells were seeded in 96-well plates (5×104 cells/well). After a 24-hour growth period and a confluence of about 80%, NWs were added at concentrations of 2.4 μg/mL or 12 μg/mL. The NWs were incubated with the cells for 1 hour before the magnetic field was applied for 10 or 30 minutes. Each experiment included negative controls (no NWs added and no field applied), a field-only control, and a NW-only control. Each experiment was carried out on three independent biological replicas. The AMF was produced using an in-house-made four-layer coil with six turns per layer of Litz wire in combination with a bipolar amplifier (AL-200-HF-A; Amp-Line Corporation, West Nyack, NY, USA) and a signal generator (33250A; Agilent Technologies, Santa Clara, CA, USA). The field amplitude was 0.5 mT and the frequencies tested were 1 Hz and 1 kHz. The power required to generate this magnetic field corresponded to about 50 mW.
The effects of the different experiments on the cell viability were evaluated using two methods based on cell toxicity: a colorimetric assay that measures the reduction of the yellow compound, 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyl tetrazolium bromide (MTT), to purple formazan by mitochondrial enzymes in active cells;46 and a fluorescent cell membrane integrity assay that measures the amount of lactate dehydrogenase (LDH), normally present inside cells, in the cell culture medium. The experimental details for each of the assays used are described below.
Immediately after AMF treatment, the cells were incubated with 100 μL of 10% (v/v) MTT solution (0.5 mg/mL in phosphate-buffered saline) in cell culture medium for 2 hours. The MTT solution was carefully removed and the cells were lysed by adding 100 μL of lysis solution (20% [wt/v] sodium dodecyl sulfate +0.6% [v/v] 37% HCl in dimethyl sulfoxide).47 The MTT formazan crystals were dissolved by gently tapping the plate, and their optical density (OD) was measured by a microplate reader (xMark™ microplate-absorbance-spectrophotometer; Bio-Rad Laboratories Inc., Hercules, CA, USA) at a test wavelength of 570 nm and a reference wavelength of 630 nm. The cell viability was calculated as the percentage of optical density of the treated cells compared with the negative control (NC), ie, the untreated cells:
For the membrane integrity assay, HCT 116 cells were seeded in medium supplemented with 5% fetal bovine serum, as the 10% concentration led to a higher background (BKGD) fluorescence. Additional controls were seeded for each experiment: BKGD wells (only 5% cell culture medium), positive control (PC; lysed untreated cells to get a maximum cell membrane leakage value), and apoptotic cells (untreated cells exposed for 1 hour to ultraviolet light). After AMF treatment, 96-well plates were equilibrated to room temperature for 30 minutes. After this, 2 μL of lysis solution (9% [w/v] Triton® X-100 in water) were added to the PC wells. Then, 120 μL of Cytotox-ONE™ reagent was added to each well to initiate the reaction that would lead to the production of the fluorescent product (resorufin) proportional to the amount of LDH in the medium. After 10 minutes at room temperature, the reaction was stopped by addition of 50 μL of stop solution. The fluorescence signal was collected with the GloMax Multi Detection System (Promega Corporation, Fitchburg, WI, USA), using a green fluorescent filter (excitation 525 nm, emission 580–640 nm). The percentage of LDH leakage was calculated as the average fluorescence values of the treated cells minus the average BKGD fluorescence signal normalized to the PC, ie, the maximum membrane leakage less the average BKGD fluorescence signal:
Internalization of magnetic NWs
Colon cancer cells were seeded in six-well plates until reaching a confluency of 80%. Ni NWs were added in independent wells at a NW concentration of 2.4 μg/mL for 1 hour. Then, the medium was gently aspirated and the cells were fixed with 2 mL of 2.5% (v/v) glutaraldehyde in cacodylate buffer (0.1 M, pH 7.4) for a minimum of 48 hours. The cells were kept at 4°C until further processing. Fixed cells were treated with reduced osmium (1:1 mixture of 2% aqueous potassium ferrocyanide) as described previously,48 dehydrated in ethanol and embedded in epoxy resin. One hundred to 150 nm thick sections were collected on copper grids and stained with lead citrate.
Imaging was performed using a transmission electron microscope operating at 300 kV (Titan Cryo Twin; FEI Company). The images were recorded by a 4k ×4k CCD camera (Gatan Inc., Pleasanton, CA, USA).
The data are expressed as means ± standard deviation. The statistical comparisons of means were performed using one-way analysis of variance. The differences were considered to be significant for P-values of less than 0.05.
Results and discussion
Characterization of magnetic NWs
Figures 1A and B show SEM and TEM images of Ni NWs, respectively. In both cases, dendrites, a feature resulting from the fabrication process, are distinguishable at one end of the NWs. The inset in Figure 1B shows in detail a NW section in which an outer layer of 6.0±1.2 nm thickness can be observed. Its composition was corroborated using single point energy-dispersive X-ray spectroscopy. Spectra of Figures 1C and D show the composition of the core and outer shell, respectively. The same materials are found in both cases but in different proportions; the core is predominantly composed of Ni as expected whereas the outer later contains mainly oxygen and carbon (the latter most likely comes from the ethanol in which NWs are stored). This oxide layer forms during the exposure of the NWs to air, NaOH (for the dissolution of the alumina), and ethanol cleaning steps.
Figure 2 shows the magnetization loops of an array of NWs embedded in the alumina oxide template. Array values of saturation magnetization (MS) and coercive field (HC) for the field that was applied parallel to the NWs are 46.7 Am2/kg and 79 mT, respectively. The MS value is smaller than the MS values reported for bulk Ni in the literature (54.3 Am2/kg).49 We attributed this to the surface oxidation of the NWs.
It is important to note that the magnetization loop of a single NW deviates considerably from the one of an array, in which NWs interact magnetostatically with each other. Single Ni NWs show single domain properties. Therefore, they are permanently magnetized with the MR value being equivalent to the one of MS measured in the parallel direction.50
Magnetic NWs–cells interaction
Once the NWs are in close proximity to the cellular membrane, an uptake mechanism is triggered that in turn determines the intracellular fate of the nanostructures. Endocytosis has been accepted as the most common passive mechanism for MNP uptake by different cellular types (HeLa, fibroblast, and dendritic cells).38 Also, uptake and intracellular location of nanostructures have been shown to depend on several factors such as the NW aspect ratio, cell line, NW surface charge, etc.51
The zeta potential measured for the Ni NWs was found to be −15.1 mV. Such a value is considered low,52 yielding only a small electrostatic repelling force. The NWs tend to aggregate, which is in agreement with the observations made for released NWs.
Negatively charged particles bind less efficiently to cell surfaces compared with neutral or positively charged particles.53 The efficacy of internalization is improved in positively charges particles.54 In the case of Ni NWs, the surface charge (almost neutral) is favorable to internalization efficacy, which under the conditions tested here was rather high, given that some NWs were found to be fully internalized after only 1 hour of incubation. Similar results were previously reported for thick Ni NWs (200 nm diameter) that were observed to cross the cell membrane after 40 minutes of incubation with rat neuroblastoma cells17 and for thin magnetic NWs (50 nm diameter) that were fully internalized after 2 hours of incubation with HeLa cells.32
To analyze the uptake and intracellular fate of Ni NWs, colon cancer cells incubated with Ni NWs were fixed, carefully sliced, and imaged by TEM. Two cell samples were prepared and imaged in replicate: a control sample (no NWs added) and a sample of cells incubated with Ni NWs.
Figure 3A shows four cells to which no NWs were added. Typical cell compartments and organelles are clearly identified, such as the nucleus, mitochondria, Golgi apparatus (GA), and the plasma membrane. Moreover, additional features include dark-colored vesicles that correspond to lipid droplets. Lipid droplets and bilayer membranes (nuclear, cellular, and from organelles like mitochondria and GA) can be easily distinguished, as they are darker. This is because the osmium stain used in the sample preparation tints glycoproteins and lipids. A final feature is the polarity observed in the cells. Colon cancer cells are epithelial cells with a polarity that is characterized by cilia-like formations in their apical membrane (bottom-right corner of Figure 3A).
Figure 3B shows NWs attached to the cell surface, particularly to the cilia-like structures from the apical membrane. Figures C and D show the cell membrane invagination process that starts from contact areas between the cell and NWs. The inset in Figure 3C shows in detail the formation process of a vesicle. Red arrows in both insets of Figure 3D show the cell membrane surrounding two NWs, indicating the invagination or engulfment process. Finally, Figures 3E and F show fully internalized NWs. Figure 3E shows a group of NWs completely contained inside a vesicle and Figure 3F shows a large aggregation of NWs again completely internalized. Some organelle reorganization is seen and is highlighted with the red arrow pointing at the GA that changed shape.
The images in Figure 3 show that within 1 hour of incubation time, all internalization steps (binding, invagination, and full internalization) were completed. It is very likely that the aggregates observed in some cases were already formed before being internalized by the cell. However, considering the micron-scale sizes of these aggregates (Figure 3F), the internalization of such structures was considerably fast. This is not entirely a surprise, since it has been shown that cells in culture can uptake micron-sized structures, the largest being a 3 μm diameter sphere made of a cobalt–copper alloy55 and the longest a 20 μm-long Ni NW.
Figure 4 shows the dependence of cell viability on the NW concentration using the MTT assay. A concentration of 2.4 μg/mL did not significantly affect cell viability, whereas a significant difference (P<0.01) was measured for 12 μg/mL, which caused a slightly less than 90% drop in viability. The results suggest that NWs at the given concentrations do not induce major cytotoxic effects on cells. However, our experiments were carried out for an incubation time of only 1 hour. The cytotoxic effects might increase with longer incubation times, as has been shown before.33,36 This would have to be taken into account in in vivo applications. For instance, it has been shown that iron oxide nanoparticles remain in an organism for several days56 or even up to 6 months.57
Figure 5 shows MTT results when an AMF was applied to colon cancer cells using the MTT assay. When the AMF was applied for 10 minutes, the viability did not change with both field frequencies. When the AMF was applied for 30 minutes, the viability was lower but significantly different (P<0.05) only for the 1 kHz frequency, for which the viability dropped to 95%.
The influence of similar AMFs on living organisms has been reported to be detrimental to bacteria,58–60 favorable to cancer cells,55 and neutral to mammalian cells.61,62 Exposing bacteria (Escherichia coli and Staphylococcus aureus) to fields about ten-times higher in strength than in our experiments (50 Hz, 10 mT) for 10 minutes slightly negatively affected the colony forming unit density.58 Another study on three mammalian cell lines found that cell proliferation increased by 30% for all cell lines after applying an AMF (1 mT and 50 Hz) for 72 hours accompanied by DNA damage.62 Even though the field parameters in these earlier studies were close to the ones used in our experiments, the reason for different results (without considering variations inherent to the experimental setup and specific cell-line responses) might come from the long times the cells were exposed to fields (24, 48, and 72 hours)62 compared with 10 or 30 minutes in this study.
The behavior of a magnetic NW in the presence of an AMF is governed by its magnetization. In the case of NWs made of Ni, the orientation of the magnetization is determined by the strong shape anisotropy, which dominates the weak magnetocrystalline anisotropy, and the magnetic easy axis, which lies along the NW axis.23 Therefore, when the NWs are exposed to an AMF, they will experience torque while trying to align the magnetic moment with the field.
The continuous realignment with the AMF was experimentally visualized with an inverted microscope (Nikon Eclipse Ti) of an agglomeration of released Ni NWs resuspended in cell culture medium with an AMF of 0.5 mT and various frequencies (0.1, 1, and 10 Hz; Video S1, S2, and S3, respectively).
The magnetic torque, τm, exerted by the field on a single NW is given by:
where m is the magnetic moment, B the magnetic field, μ0 the permeability of free space, H the magnetic field strength, and θ the angle between m and H. Considering m = MV (M is the magnetization and V the volume), V = πr2l (with r the NW radius and l its length), and H = H0sin(ωt), equation 3 can be rewritten as:
In equation 4, the value of MR replaces M, which for a single NW can be calculated from the value of MS measured for the array. This value is obtained from Figure 2, and together with the estimation of the total number of NWs in the measured piece (determined as described in the Materials and methods section), MR of a single NW is 47.4 Am2/kg. The maximum value of τm is obtained for θ=90° and it corresponds to 0.81×10−18 N·m. From this value, the force a NW exerts on a cell in the presence of an AMF can be calculated using the simple model illustrated in Figure 6.
If we assume that the NW rotates about its midpoint, the magnitude of the force acting on each of its ends is 0.2 pN. This value is well below the force required to disrupt the membrane, which is on the order of 100 pN.63 However, there are other mechanisms affecting the cells that rely on much weaker forces.64 Forces of a few pN can cause changes in protein conformation65 and clustering of membrane-associated molecules66 that could lead to the activation of various signaling pathways influencing cellular behavior and fitness. Such processes might be activated when the AMF treatment is applied and can be partly responsible for the measured reduction in cell viability. AMF treatment significantly reduces the cell viability (Figure 7), which drops to about 78% in the case of a concentration of 2.4 μg/mL, and to between 60% and 70% in the case of 12 μg/mL. For the 2.4 μg/mL concentration, the frequency does not influence the cell viability values, whereas at 12 μg/mL, the viability is slightly more affected at higher frequencies, yielding a drop of 38%.
During the AMF treatment, the temperature was monitored and a maximum difference of 1.9°C was measured with respect to the control cells. Such small temperature changes have been shown to slightly affect cell numbers with incubation times of 1 hour.67 Since the cells in our experiments were exposed to the temperature change for only 10 minutes, we attribute the reduction in cell viability to the magnetic actuation of the NWs. This is in agreement with the observed independence of frequency from viability, since the force exerted by the NWs on the cells was independent of the frequency (as long as the dynamic responses of the NWs could follow the field). Even though there was a five-fold difference in NW concentrations between the two concentrations tested, the drop in cell viability did not increase by a factor of more than two. A possible explanation for this was NW aggregation, which led to a nonuniform distribution of the NWs, when added to cells, and which became more evident when the NW concentration was increased.
Figure 8 shows the cell membrane leakage when the cells with the two NW concentrations underwent AMF treatment. The cells exhibited LDH leakage between 32% and 36%, which turns out to be significantly different from the leakage from negative control cells and cells in which apoptosis was induced. While the calculations above indicated that the force exerted by a NW on the cell membrane was not large enough to result in a rupture of the cell membrane, the AMF treatment did affect the integrity of the cell membrane. We attribute this to two effects. The first is that the effect of the combined forces of several single NWs acting on a membrane can be considerably larger than the effect of force of a single NW. For such an effect to occur is highly likely considering that the NW concentrations were equivalent to 100 NWs/cell and 500 NWs/cell (Table S1). The second effect is from NW agglomerations, which we frequently observed during the experiments, from which the generated forces can be many times higher than the force of a single NW. Membrane leakage was also evaluated for cells incubated with only NWs and cells in which only AMF was applied for 10 minutes (Figure S1). The NWs and the AMFs turned out to influence membrane integrity to the same degree (leakage values were between 18% and 23%).
The interactions between cultured cancer cells, magnetic NWs, and AMFs were studied. The results showed that Ni NWs are quickly internalized (within less than 1 hour) by cultured colon cancer cells and do not cause extensive cytotoxicity at a concentration of 2.4 μg/mL and an incubation time of 1 hour, which confirms previous results obtained for incubation times up to 72 hours.33 The highest and significant viability drop of 11% was found for a higher NW concentration (12 μg/mL) and 1 hour incubation.
Exposing the cells to AMFs of 1 kHz for 30 minutes led to small drops (maximum 5%) in cell viability. Under the other AMF conditions tested, the cell viability values decreased slightly.
However, when an AMF is applied to cells that have internalized NWs, the cytotoxicity is strongly modulated, depending on the AMF frequency and NW concentration. The most efficient combination was observed at a NW concentration of 12 μg/mL, where the cell viability dropped by 38% in case of a 1 kHz field. For the 2.4 μg/mL concentration, the cell viability reduction was around 24% at both frequencies. Moreover, there was no relevant difference when applying the treatment for 10 minutes or 30 minutes. This evidence suggests that cell death induction mechanisms affect cells quickly, and treatment over an extended period of time does not add any benefits. Cell viability reduction was accompanied by cell membrane leakage, which is not a desirable process if the intended cell death pathway is apoptosis. Theoretically, leakage should not be caused by a single NW, because the force it exerts on the cell membrane is too small to rupture it. Rather, it seems to be the result of the forces generated by several NWs or agglomerated NWs.
While many underlying details of the mechanisms induced by magnetic NWs on cells under AMFs have yet to be elucidated, this study shows a possible approach to developing a non-chemotoxic or radiotoxic method to treat cancer cells. Figure 9 shows a schematic of the possible cell features accompanying cell death induction. An intriguing aspect of the method is the low power of the applied magnetic field. Not only does this low-power magnetic field have less chance of developing negative side effects, but treatment with a low-power magnetic field can be realized with compact and inexpensive equipment.
Figure 9 Schematic of the possible mechanism of cell death due to interaction of cancer cells with NWs and the subsequent application of a low-frequency, low-amplitude magnetic field.
To take full advantage of this promising method, more fundamental studies as well as enhancements are required. For instance, cancer-cell specificity studies (using peptides or antibodies) and dispersion improvement studies to ensure homogeneous NW distribution within a cell population are needed. Regarding the latter, an issue observed throughout the experiments that could have a strong influence on the results is aggregation of NWs. Currently, protocols are being adapted to coat the NWs with polymers20 to improve their dispersion. Fundamental studies characterizing the particular type of cell death and its distinctive features as well as analyzing the molecular-biology mechanisms that can be triggered by the treatment, such as Ca2+ signaling and overexpression of proinflammatory cytokines, would be very useful.
Research reported in this publication was supported by the King Abdullah University of Science and Technology (KAUST).
The authors report no conflicts of interest in this work.
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Table S1 Ni NW concentrations expressed in equivalent units
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