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International Journal of Nanomedicine logoLink to International Journal of Nanomedicine
. 2018 May 31;13:3235–3250. doi: 10.2147/IJN.S165289

Chitosan gold nanoparticles induce cell death in HeLa and MCF-7 cells through reactive oxygen species production

Ana Carolina Martínez-Torres 1,✉, Diana G Zarate-Triviño 1, Helen Yarimet Lorenzo-Anota 1, Andrea Ávila-Ávila 1, Carolina Rodríguez-Abrego 1, Cristina Rodríguez-Padilla 1
PMCID: PMC5987788  PMID: 29910612

Abstract

Background

Nanotechnology has gained important interest, especially in the development of new therapies; the application of gold nanoparticles (AuNPs) in the treatment and detection of diseases is a growing trend in this field. As cancer represents a serious health problem around the world, AuNPs are studied as potential drugs or drug carriers for anticancer agents. Recent studies show that AuNPs stabilized with chitosan (CH) possess interesting biological activities, including potential antitumor effects that could be selective to cancer cells.

Materials and methods

In this study, we synthesized sodium citrate-AuNPs and CH-capped AuNPs of 3–10 nm, and analyzed their cytotoxicity in cervical (HeLa) and breast (MCF-7) cancer cells, and in peripheral blood mononuclear cells (PBMCs). Then, we evaluated the clonogenic potential, cell cycle, nuclear alterations, caspase dependence, and reactive oxygen species (ROS) production in HeLa and MCF-7 cells after chitosan gold nanoparticles (CH-AuNPs) exposure.

Results

Our data showed that CH-AuNPs are cytotoxic in a dose-dependent manner in the cancer cell lines tested, while they induce low cytotoxicity in PBMCs. Sodium citrate gold nanoparticles did not show cytotoxic effects. In both HeLa and MCF-7 cell lines, CH-AuNPs inhibit clonogenic potential without inducing cell cycle arrest or nuclear alterations. The cell death mechanism is specific for the type of cancer cell line tested, as it depends on caspase activation in HeLa cells, whereas it is caspase independent in MCF-7 cells. In all cases, ROS production is mandatory for cell death induction by CH-AuNPs, as ROS inhibition with N-acetyl cysteine inhibits cell death.

Conclusion

Our results show that CH-AuNPs are selective for HeLa and MCF-7 cancer cells, rather than normal PBMCs, and that ROS production seems to be a conserved feature of the cell death mechanism induced by CH-AuNPs. These results improve the knowledge of CH-AuNPs and open the way to the design of new pharmacological strategies using these agents against cancer.

Keywords: AuNPs, cancer, PBMC, nuclear alterations, cell cycle, ROS

Introduction

Nanotechnology research has increased in many different areas in the last years, including biomedicine, where nanoparticles have been assessed by their potential to be used against different diseases like cancer. Nanoparticles have been shown to be interesting options in cancer diagnostics and therapeutics,1–3 as an alternative to nonviral delivery systems.4 Among the different types of nanoparticles, gold nanoparticles (AuNPs) have been demonstrated to inhibit proliferation and induce cell death on different types of cancer cell lines;1–3,5–7 moreover, they have been shown to be safe in several biological models, and interesting agents for drug delivery and photothermal therapy against cancer.8

Cervical cancer and breast cancer are among the leading causes of mortality in women around the world.9 These cancers have several mutations that make cells proliferate continuously and evade regulated cell death (RCD), a mechanism by which the cell activates its own machinery to self-destruct.10 The first-line therapies for breast and cervical cancers consist of surgery, immunotherapy, polyamine synthesis inhibitors, individual micronutrient supplementation, hormonal therapy, chemotherapy, and radiotherapy; however, these treatments also cause many side effects. Moreover, it is known that mutations or deletions in proteins related to apoptosis induce resistance to conventional treatments.11 These are the reasons why nanotechnology shows great promise for the improvement of traditional cancer treatments.

It has been observed that the efficacy and effect of nanoparticles on cancer and healthy cells are determined by several conditions of synthesis such as size, shape, and, especially, the reducing agent used.12,13 We propose the use of AuNPs stabilized with chitosan (chitosan gold nanoparticles [CH-AuNPs]), a polycationic natural polymer shown to be biocompatible, biodegradable, and cytotoxic to cancer cells.14,15 The synthesis of AuNPs coated with chitosan is an interesting approach, as it confers a positive charge to AuNPs, thus increasing their affinity with the negative charge of the cell membrane.16,17 This is the reason why the use of chitosan in the design of agents for drug delivery has increased over the last years, and its association with nanostructures is of great importance.15 Many investigations have determined that the cytotoxicity of nanoparticles depends on their physicochemical properties.18–20 These properties give a variety of effects that depend on the kind of cancer and healthy cells analyzed.20 For this reason, it is essential to study the particular characteristics of the nanoparticles and to evaluate them in different types of cells. Few reports have described the biological effects of CH-AuNPs in cancer cells,5,17 and there is no description of their effect in primary healthy cells. Additionally, their mechanism of action in cancer cells is poorly understood.

Thus, the purpose of this study was to analyze the cytotoxicity of AuNPs in cervical (HeLa) and breast (MCF-7) cancer cell lines, and in peripheral blood mononuclear cells (PBMCs) using chitosan (CH) and sodium citrate (SC, our control) as reducing agents. We further characterized the mechanism of cytotoxicity of CH-AuNPs in cancer cells, as we assessed the clonogenic potential, cell cycle, DNA alterations, caspase dependence, and reactive oxygen species (ROS) production after treatment with CH-AuNPs.

Materials and methods

Nanoparticle synthesis

CH-AuNPs and sodium citrate gold nanoparticles (SC-AuNPs) were synthesized using the Turkevich method, with adaptations of the protocol described by Arvizo et al.18 In brief, an acid solution of chitosan (2% w/w in acetic acid 0.4 M) was obtained by dissolving chitosan (medium molecular weight, 300,000 g/mol, with 75%–85% of deacetylation) in 2 mM hydrochloroauric acid solution (HAuCl4), and it was homogenized at room temperature for 15 minutes on a magnetic plate at 80–90 rpm. The resulting solution was heated (100°C±5°C in glycerol bath for 15 minutes on a magnetic plate at 80–90 rpm) until it changed color to wine red. SC-AuNPs were obtained by heating HAuCl4 (2 mM) at 140°C (±5°C) in a glycerol bath for 5 minutes on a magnetic plate at 80–90 rpm, and then 1% sodium citrate solution (Milliporesigma, St Louis, MO, USA) was added by slow drip until it changed color to wine red.

Nanoparticle characterization

Mean particle diameter and Z potential were measured by dynamic light scattering (DLS) using Nanosizer NS90 (Siemens, Malvern, PA, USA). The sample was dispersed in distilled water (1:1,000). The surface plasmon resonance was detected by Ultra visible spectroscopy using a Nanodrop spectrophotometer 2000c (Thermo Fisher Scientific, Bartlesville, OK, USA). The morphology of the particles was observed with field emission scanning electron microscopy (SEM, Nova NanoSEM200; FEI, Hillsboro, OR, USA).

Cell culture

Human cervix adenocarcinoma cells, HeLa, were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). Human breast adenocarcinoma cell line, MCF-7, was a gift from Dr J Gutierrez-Uribe (Nutriomics group, ITESM) who obtained the cell line from ATCC; this was approved by the Institutional Ethics Committee at the Universidad Autónoma de Nuevo León, College of Biological Sciences.

Peripheral blood was collected from six volunteers not showing an apparent disease (men and women, with age ranging 18–30 years) after obtaining written informed consent. This study was approved by the Institutional Ethics Committee at the Universidad Autónoma de Nuevo León, College of Biological Sciences. PBMCs were obtained through density centrifugation with Ficoll-Hypaque-1119 (Milliporesigma). HeLa and MCF-7 cells were cultured in DMEM-F12 while PBMCs were cultured in Roswell Park Memorial Institute (RPMI) 1640 (Gibco, Grand Island, NY, USA). Both the culture media were supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin–streptomycin (Gibco) and were maintained in a humidified incubator containing 5% CO2 at 37°C. Cells were routinely grown in plastic tissue-culture dishes (Corning, NY, USA).

Cell viability assessment

Cell growth inhibition was determined by MTT dye absorbance by living cells; this assay consists in measurement and quantified spectrophotometric means of reduction of yellow tetrazo-lium (3-(4, 5-dimethylthiazilyl-1) -2, 5-diphenyl tetrazolium bromide) (Milliporesigma) by metabolically active cells in intracellular purple formazan. In brief, 5×103 cells per well were seeded in 96-well microtiter plates (Corning) for MTT assays. After exposure to CH-AuNPs, SC-AuNPs, chitosan, and HACl4 at different concentrations (25, 50, 75, 100, and 150 µM) for 24 hours, 20 µL of MTT solution (2 mg/mL in phosphate-buffered saline [PBS]) was added to each well. The concentrations of CH-AuNPs and SC-AuNPs (µM) were determined based on the µM concentration of the precursor salt (HACl4) used for the synthesis of AuNPs. The plates were incubated for three additional hours at 37°C, after which the MTT solution in the medium was aspirated and 200 µL of dimethyl sulfoxide (DMSO) (Milliporesigma) was added to each well to solubilize the formazan crystals formed in the viable cells. The optical density was measured at 570 nm using a microplate reader (Synergy2, Biotek, Winooski, VT, USA).

Cell death analysis

Cell death was determined by staining cells with Annexin V-allophycocyanin (APC) (AnnV, 0.1 µg/mL; BD Biosciences Pharmingen, San Jose, CA, USA) and propidium iodide (PI; 0.5 µg/mL; Milliporesigma). 4×104 cells were seeded in 24-well plates (Corning) and were incubated at different concentrations of CH-AuNPs (50, 75, and 100 µM) for 24 hours to find the median cytotoxic concentration of CH-AuNPs required to reduce cell viability by 50% (CC50). After 24 hours, the cells were detached and washed twice with PBS and then resuspended in 200 µL of binding buffer (10 mM HEPES/NaOH pH 7.4, 140 mM NaCl, 2.5 mM CaCl2) containing AnnV (0.1 µg/mL) and PI (0.5 µg/mL). Cells were then assessed with flow cytometer (BDAccury6; Becton Dickinson, San Jose, CA, USA) and analyzed using FlowJo Software (Tree Star Inc., Ashland, OR, USA).

Cell death induction and inhibition

Etoposide (Enzo, Farmingdale, NY, USA), and QVD (BioVision, Milpitas, CA, USA) were dissolved in DMSO. N-acetyl-l-cysteine (NAC; Sigma, Shanghai, China) was dissolved in MilliQ water. For cell death inhibition, we used QVD, a caspase inhibitor. To determine ROS-dependent cell death, we used NAC as an ROS inhibitor. QVD and NAC were added 30 minutes before treatment with CH-AuNPs. All stock solutions were wrapped in foil and stored at −20°C.

Clonogenic assay

Cell proliferation and clonogenicity were assessed using the clonogenic assay technique. In brief, 100 or 500 cells were plated in 6-well plates for control (only cell culture media) or CH-AuNPs treatment, respectively, and were incubated overnight. Once attached, cells were exposed to either treatment or control for 24 hours. Afterward, the medium was changed and cells were allowed to grow until colony formation (10 days). Then, the colonies were fixed with methanol (100%) and glacial acetic acid (3:1), stained with 0.5% Gentian Violet. Colonies with >50 cells were counted manually. Finally, cell survival was determined by equating the number of colonies in treated wells over those in control, both normalized with the percentage of cell colonies counted over the number of cells seeded.

Cell cycle analysis

Cell cycle distributions were determined by PI staining. In brief, 5×105 cells in 6-well dishes were incubated with concentration required to reduce cell viability by 25% (CC25), CC50, and concentration required to reduce cell viability by 75% (CC75) of CH-AuNPs for 24 hours. Cells were then washed with PBS and fixed in 70% ethanol. Cells were washed again with PBS, then incubated with PI (10 µg/mL) with simultaneous RNase treatment at 37°C for 30 minutes. Cell DNA contents were measured using a flow cytometer (Becton Dickinson) and analyzed using FlowJo Software. For DNA degradation, we analyzed the SubG1 population obtained from cell cycle analysis using a flow cytometer (BDAccury6; Becton Dickinson) and FlowJo Software (Tree Star Inc.).

Nuclear assessment

For chromatin condensation after CH-AuNPs treatment we did Hoechst staining (Enzo). In brief, 10×105 cells were incubated in 6-well plates, then treated with CH-AuNPs CC50, and then washed in PBS and fixed with paraformaldehyde 4%. We stained the cells for 5 minutes using 5 µg/mL Hoechst 33342. Cells were then washed with PBS, observed using a fluorescence microscope (OLYMPUS IX70), and analyzed with Image-J software.

Caspase analysis

Caspase activity was measured using Caspase 3 (active) FITC staining kit (ABCAM, Eugene, OR, USA). In brief, 5×105 cells in 6-well dishes (Corning) were incubated with CH-AuNPs CC50. Cells were then recovered and stained following the manufacturer’s instructions. Caspase activity was measured using a flow cytometer (BDAccury6; Becton Dickinson) and analyzed using FlowJo Software (Tree Star Inc.).

ROS production assay

ROS generation was measured using 2.5 µM of dichlorodihydrofluorescein diacetate (DCFDA; Invitrogen, St Louis, MO, USA). In brief, 5×105 cells were incubated in 6-well dishes (Corning) with the indicated concentration of CH-AuNPs. Cells were then recovered, washed with PBS, stained, incubated at 37°C for 30 minutes, and measured using a flow cytometer (Becton Dickinson, BDAccury6), and analyzed using FlowJo Software (Tree Star Inc.).

Statistical analysis

The results given in this study represent the mean of at least three independent experiments done in triplicate (mean±SD). The data were analyzed using GraphPad Prism (GraphPad Software, San Diego, CA, USA). Statistical analysis was done using paired Student’s t-test. The statistical significance was defined as p<0.05.

Results

Nanoparticles

CH-AuNPs have a Z potential of +27 mV upon synthesis, while control SC-AuNPs showed a Z potential of −5 mV (Table 1). Both types of AuNPs have a size range of 3–10 nm (Table 1; Figure 1A). The polydispersity of SC-AuNPs and CH-AuNPs was 0.3 (Table 1), and they show a typical surface plasmon resonance of AuNPs22 at 520 nm (Table 1; Figure 1B). We confirmed the size and shape of the CH-AuNPs by SEM (Figure 1C). Table 1 shows the comparative physicochemical properties of CH-AuNPs and SC-AuNPs.

Table 1.

Overview of the gold nanoparticles used in this study

Sample Surface coating Zeta potential (mV) ±SD Range size (nm) Mean size ±SD (nm) Polydispersity Solvent Surface plasmon resonance (nm)
SC-AuNPs Sodium citrate 0.1% −5±0.1 3–10 3±0.5 0.3 Water 520
CH-AuNPs Chitosan 0.2% +27±0.1 3–10 4±0.6 0.3 Water 520
SC-AuNPs Sodium citrate 0.1% −7±0.2 3–10 3±0.6 0.2 PBS 522
CH-AuNPs Chitosan 0.2% +22±0.2 3–10 4±0.5 0.2 PBS 522
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Notes: Size, Z potential, and surface plasmon resonance of AuNPs were measured as stated in the “Materials and methods” section. AuNPs were diluted in water or PBS before the assessment of their physicochemical properties.

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; PBS, phosphate buffered saline; SC-AuNPs, sodium citrate gold nanoparticles.

Figure 1.

Figure 1

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Size, surface plasmon resonance, and shape of CH-AuNPs.

Note: Representative (A) size distribution obtained from DLS analysis, (B) UV–Vis absorption spectrum, and (C) SEM images of CH-AuNPs.

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; DLS, dynamic light scattering; SEM, scanning electronic microscopy; CIMAV, Centro de Investigación en Materiales Avanzados S.C.; SE, secondary electron; LEI, lower detector; WD, working distance.

CH-AuNPs but not SC-AuNPs diminish cell viability in cancer cells

CH-AuNPs have been shown to suppress cell viability in lung adenocarcinoma cell lines (A549, NCI-H460, and A431) and acute monocytic leukemia cell line (THP-1).5,17,23 However, there are no reports regarding its cytotoxic effect on cervical cancer and breast cancer cells, and on primary PBMC. Thus, we determined the effect of SC-AuNPs, CH-AuNPs, and the vehicles used to synthesize CH-AuNPs (chitosan and HAuCl4) on HeLa and MCF-7 cancer cell lines, and PBMC. CH-AuNPs induced a concentration-dependent cell viability diminution in cancer cells, whereas SC-AuNPs did not induce an important cell viability loss (Figure 2A and B). The CC50 of CH-AuNPs for HeLa and MCF-7 cells after 24 hours of treatment was 75 µM, which increased with the concentration, reaching 85% and 100% of cell viability loss, respectively, at 150 µM (Figure 2A and B). We observed a clear selectivity for cancer cells, because cell viability diminution in PBMCs was observed when the concentration reached 75 µM, attaining 40% of cell viability loss when using the highest concentration tested (150 µM, Figure 2C). Additionally, although CH-AuNPs showed more cytotoxicity in HeLa and MCF-7 cell lines after 48 hours of treatment, PBMC showed the same sensitivity for CH-AuNPs (Figure S1). Furthermore, neither chitosan nor HAuCl4 alone induces high cytotoxicity in any of the cell type assessed (Figure 2D–F).

Figure 2.

Figure 2

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Effect of AuNPs, AuHCl4, and chitosan on HeLa, MCF-7, and PBMC cell viability.

Notes: HeLa (A), MCF-7 (B), and PBMC (C) were treated with various concentrations of CH-AuNPs and SC-AuNPs (25, 50, 75, 100, and 150 µM). HeLa (D), MCF-7 (E), and PBMC (F) were treated with vehicles (chitosan and HAuCl4) at same concentrations as in (A–C) for 24 hours. Cell viability was measured by MTT assay. The percentages refer to relative cell viability represented as percentage of control (nontreated cell viability=100%).

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; PBMC, peripheral blood mononuclear cell; SC-AuNPs, sodium citrate gold nanoparticles.

Chitosan-capped gold nanoparticles induce cell death in cancer cells

Because SC-AuNPs were not effective against cancer cells at the same doses as CH-AuNPs, we continued to evaluate whether cell death was induced by CH-AuNPs in HeLa, MCF-7, and PBMC. We evaluated cell death by assessing phosphatidylserine (PS) exposure (AnnV) and membrane permeability (PI) after 24 hours of treatment with different concentrations of CH-AuNPs (Figure 3). PS exposure on the outer leaflet of the plasma membrane is an “eat-me” signal of dying cells.24 In HeLa and MCF-7 cells, CH-AuNPs induced a small population of AnnV and PI-positive cells at a concentration of 50 µM; at 75 µM this percentage increased, and at 100 µM most of the cells were double positive to AnnV and PI staining (Figure 3A). On the other hand, at the three concentrations tested, they induced only a slight population of AnnV and PI-positive PBMC (Figure 3A). Contrary to the results obtained with the use of etoposide, where we observed resistance to cell death in MCF-7 cells and no selectivity for PBMCs (Figure S2), with CH-AuNPs we observed <15% of cell death in PBMC at the CC50 of MCF-7 and HeLa cells, and <20% at their CC75 (Figure 3B). As expected from the MTT results, CH-AuNPs induced cell death in a concentration-dependent manner, and cell death in cancer cells was detected at the same doses observed in MTT (Figure 3).

Figure 3.

Figure 3

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Phosphatidylserine exposure and membrane permeability of HeLa and MCF-7 cells after CH-AuNPs treatment.

Notes: (A) Cell death was measured by flow cytometry through AnnV and PI staining in HeLa and MCF-7 cells treated with different concentrations (50, 75, and 100 µM) of CH-AuNPs for 24 hours. (B) The percentages of cell death refer to AnnV-positive and/or PI-positive staining.

Abbreviations: AnnV, Annexin-V; CH-AuNPs, chitosan gold nanoparticles; PBMC, peripheral blood mononuclear cells; PI, propidium iodide.

CH-AuNPs inhibit long-term proliferation of cancer cells

Once we assessed that PBMCs were only slightly affected by CH-AuNPs, we focused on deciphering the cytotoxic mechanism of CH-AuNPs in cancer cells. First, we assessed if MCF-7 and HeLa cells could recover after 24 hours of treatment with CH-AuNPs. The cells were treated for 24 hours with the CC25 and CC50 of CH-AuNPs for each cancer cell line tested, then treatment was stopped and washed, and cells were cultured until colony formation. Clonogenic assay showed that CH-AuNPs have antiproliferative activity, as they reached complete inhibition of colony formation at the CC25 of CH-AuNPs; this result was confirmed with the CC50 in HeLa (Figure 4A) and MCF-7 cells (Figure 4B). Thus, even if the CC25 and CC50 of CH-AuNPs were not able to kill all of the cells, these concentrations were able to inhibit long-term cell growth, after a 24 hour exposure.

Figure 4.

Figure 4

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Clonogenic assay shows the long-term effects of CH-AuNPs treatment of HeLa and MCF-7 cells.

Notes: HeLa (A) and MCF-7 (B) cells were treated with CC25 and CC50 of CH-AuNPs for 24 hours, the number of colonies formed on the culture plate 10 days after treatment was expressed as surviving fractions. Data are reported as percentage of colonies compared with untreated control (left). Photograph of petri-dish of a representative experiment is shown (right).

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; CC25, concentration required to reduce cell viability by 25%; CC50, concentration required to reduce cell viability by 50%.

CH-AuNPs do not modify the cell cycle of cancer cells

It has been shown that AuNPs can induce cell cycle arrest in different cancer cells25 and that chitosan induces cell cycle arrest in G1 and S phases in oral cancer cells;26 thus, we further assessed cell cycle after CH-AuNPs treatment. Even though AuNPs and chitosan separately induce cell cycle arrest in several cancer cell lines, treatment with CC25, CC50, or CC75 of CH-AuNPs for 24 hours does not induce changes in the cell cycle of HeLa (Figure 5A) or MCF-7 (Figure 5B) cell lines. This indicates that cell viability diminution is due to cell death induction.

Figure 5.

Figure 5

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Cell cycle changes after CH-AuNPs treatment of HeLa and MCF-7 cells.

Notes: Representative cell cycle distribution of HeLa (A) and MCF-7 (B) cells treated with CC25, CC50, and CC75 of CH-AuNPs for 24 hours. The results were analyzed using FlowJo software and graphed.

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; PI, propidium iodide; CC25, concentration required to reduce cell viability by 25%; CC50, concentration required to reduce cell viability by 50%; CC75, concentration required to reduce cell viability by 75%; NS, not significant.

CH-AuNPs do not induce nuclear alterations in HeLa and MCF-7 cells

Endonucleases can cause DNA fragmentation and nuclear condensation during different types of cell death.27 Because some types of AuNPs have been shown to induce DNA fragmentation in diverse cell types, depending on the reducing agent that was used,17,25,28 we decided to asses if CH-AuNPs were able to cause DNA fragmentation. To assess DNA degradation, we quantified sub-G1 population of cells treated with CC25, CC50, or CC75 of CH-AuNPs. DNA degradation was not detected in HeLa (Figure 6A) or MCF-7 (Figure 6B) cells at the tested concentrations. To further discard nuclear alterations, we stained HeLa and MCF-7 cells with Hoechst, and nuclear morphology was assessed using a fluorescence microscope. HeLa (Figure 6C) and MCF-7 (Figure 6D) cells treated with CH-AuNPs do not show nuclear condensation after 24 hours of treatment with CC50 (Figure 6).

Figure 6.

Figure 6

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Nuclear alterations induced by CH-AuNPs in HeLa and MCF-7 cells.

Notes: Degradation of DNA in HeLa (A) and MCF-7 (B) cells treated with CC25, CC50, and CC75 of CH-AuNPs. Nuclear morphology of HeLa (C) and MCF-7 (D) cells treated with CC50 of CH-AuNPs for 24 hours, stained with Hoechst 33342, and visualized using fluorescence microscopy (OLYMPUS IX70) (40×) (left). The percentages refer to nuclear size measured using Image-J software, and is represented as a % control (nontreated nuclear size=100%) (right).

Abbreviation: CH-AuNPs, chitosan gold nanoparticles; CC25, concentration required to reduce cell viability by 25%; CC50, concentration required to reduce cell viability by 50%; CC75, concentration required to reduce cell viability by 75%; NS, not significant.

CH-AuNPs induce caspase-dependent cell death in HeLa cells and caspase-independent cell death in MCF-7 cells

We continued to verify if caspases were the main molecular regulators of this type of cell death. We assessed caspase activity and, as shown in Figure 7A, CH-AuNPs induce caspase-3 activation in HeLa cells, whereas MCF-7 cells do not show caspase-3 activity because they are deficient for this caspase29 (Figure 7B).

Figure 7.

Figure 7

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Caspase-3 activity and effects of pan-caspase inhibition on CH-AuNPs-treated HeLa and MCF-7 cells.

Notes: Caspase-3 activation was measured by flow cytometry in HeLa (A) and MCF-7 (B) cells after treatment with CH-AuNPs for 24 hours (left). Data were then analyzed and graphed (right). Cell viability was determined by flow cytometry in HeLa (C) and MCF-7 (D) cells that were left alone or pretreated with QVD and then treated with CC50 of CH-AuNPs for 24 hours (left). The percentages of the graph bars (right) refer to AnnV-positive and/or PI-positive staining.

Abbreviations: AnnV, Annexin-V; CH-AuNPs, chitosan gold nanoparticles; PI, propidium iodide; QVD, quinoline-val-asp-difluorophenoxymethyl ketone.

Caspase activity can be detected even if these enzymes are not necessary to induce cell death. To determine if this type of cell death was dependent on caspase activity, we used the pan-caspase inhibitor QVD30 and found that while HeLa cell death was partially inhibited by QVD (Figure 7C), MCF-7 cell death was independent of caspase activation (Figure 7D). In fact, the use of this pan-caspase inhibitor significantly increased the cell death induced by CH-AuNPs in MCF-7 cells (Figure 7D right). These results show that RCD induced by CH-AuNPs relies differently on caspase activation and that this depends on the cell type.

CH-AuNPs induce ROS production and ROS-dependent cell death in HeLa and MCF-7 cells

AuNPs induced ROS production in several cell types. Because we observed that caspases were not a major feature of cell death induced by CH-AuNPs, we assessed whether CH-AuNPs were able to induce ROS production in MCF-7 and HeLa cells. As seen in Figure 8, CH-AuNPs treatment induced ROS production in HeLa (Figure 8A) and MCF-7 cells (Figure 8B) as detected by DCFDA staining.

Figure 8.

Figure 8

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ROS production in HeLa and MCF-7 cells upon treatment with CH-AuNPs.

Notes: ROS levels were measured by flow cytometry through DCFDA staining in HeLa (A) and MCF-7 (B) cells left alone or treated with CC50 of CH-AuNPs for 24 hours (left). Data were then analyzed and graphed (right).

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; DCFDA, dichlorodihydrofluorescein diacetate; ROS, reactive oxygen species.

We further analyzed if ROS production was playing a role in cell death. Generation of ROS has been associated with caspase-dependent and caspase-independent cell death.24,31 Moreover, different types of nanoparticles induce ROS production,32–34 including CH-AuNPs in lung-derived cell lines.35 However, the role of ROS production by CH-AuNPs has not been reported. To investigate the role of ROS in CH-AuNPs-RCD, we used the ROS inhibitor NAC, an antioxidant that increases intracellular glutathione levels and possesses thiol-disulfide exchange activity,36 and assessed cell death. As shown in Figure 9, NAC was able to inhibit cell death, as observed by the complete reduction of AnnV staining in both HeLa (Figure 9A) and MCF-7 (Figure 9B) cell lines. These results indicate that ROS production is a major and conserved feature of CH-AuNPs; however, CH-AuNPs did not induce ROS production in PBMCs, even at 100 µM (Figure S3).

Figure 9.

Figure 9

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Effect of ROS inhibition upon CH-AuNPs treatment of HeLa and MCF-7 cells.

Notes: Cell death of HeLa (A) and MCF-7 (B) cells left alone or pretreated with NAC and then treated with CC50 of CH-AuNPs for 24 hours was analyzed by flow cytometry through AnnV staining (left). The results were analyzed and graphed (right).

Abbreviations: AnnV, Annexin-V; CH-AuNPs, chitosan gold nanoparticles; NAC, N-acetyl-L-cysteine; ROS, reactive oxygen species; CC50, concentration required to reduce cell viability by 50%.

Discussion

The cytotoxicity of AuNPs in cancer cells depends on their size, dose, shape, surface chemical radicals, and charge.6 We synthesized AuNPs using chitosan and SC and obtained particles of 3–10 nm of diameter with a surface plasmon resonance at 520 nm, which is a characteristic of AuNPs.22 Our results showed that CH-AuNPs induced cell viability loss in HeLa and MCF-7 cancer cells, while they slightly affected PMBC. SC-AuNPs were not cytotoxic in any of the cell types tested, even though both types of nanoparticles had the same size. Previous studies have shown that the physicochemical properties of nanoparticles are determinant to biological impact;18–20 such is the case of their size37 and shape.38 Small-sized AuNPs (synthesized using different reducing agents) induce low cytotoxicity in dendritic cells39 and dermal fibroblasts,40 while they are cytotoxic to HeLa41 and A54928,42 cancer cells. However, the effect of AuNPs also depends on surface charge. It has been demonstrated that positively charged AuNPs are more cytotoxic than negatively charged AuNPs, even when both are of the same size and used in the same cell lines, at the same concentration.13 This effect is related to the affinity of the positive charges of the nanoparticles with the negative charge of the cell membrane.16,17 Additionally, previous studies have reported that the formation of protein corona, a structure of proteins formed between nanoparticles and biological medium, is not dependent on the positive or negative character of the nanoparticle, but that the charge of the nanostructure is responsible for the interactions with specific cellular receptors and therefore the outcome in the target cell.5,43

Our results showed that nanoparticles effectively induce cell death in HeLa and MCF-7 cell lines. The induction of cell death is one of the main targets in the development of new therapies against cancer. Furthermore, it is known that deregulation of the molecules involved in apoptosis can lead to resistance to first-line chemotherapies.11 We also showed that CH-AuNPs have selectivity to cancer cells compared to PBMC, at the same concentrations and times. While CH-AuNPs show a dose- and time-dependent cytotoxicity in cancer cells, in PBMCs we observed a dose-dependent effect only, which was maintained after 24 and 48 hours of treatment. Cell-dependent cytotoxicity is a common feature in AuNPs, as it has previously been described in HT29,8 MCF-7,28 HeLa,32 and A45925,42 cells. Another example is the one described by Patra et al who found that AuNPs of the same size (13 nm) and the same reducing agent (Citrate) are not toxic in Hep2G human liver carcinoma cells and in noncancerous hamster cells, BHK21, but are cytotoxic in A549 human lung carcinoma cells.16

Reduction in cell viability can be due to the induction of cell cycle arrest and/or cell death. Here we showed that CH-AuNPs induce cell death without affecting cell cycle in the two cancer cell lines tested. This result contrasts with another study where CH-AuNPs were used to treat different lung cancer cell lines, and cell cycle alterations were observed.21 Our result resembles another study that used AuNPs with triphenylphosphine monosulfonate and found no alterations in the cell cycle of HeLa cells.32 These differences and similarities can be due to the different molecular mechanisms induced by AuNPs, depending on the cell type and the reducing agent used.

Additionally, we observed that a single exposure to CH-AuNPs for 24 hours inhibits the clonogenic potential of the cells, even though there was no cell cycle arrest, and only 25% of cells were dead after a 24-hour treatment. Clono-genic analyses have also been used to predict the metastatic potential of cancer cells.44 Thus, our results not only indicate that CH-AuNPs compromise HeLa and MCF-7 cells to clonogenic death, but also that CH-AuNPs could potentially be antimetastatic. However, more studies should be done, as it has also been reported that clonogenic analyses in some cases are not related to the metastatic potential of the cells.45,46

Two unexpected aspects of the cell death mechanism induced by CH-AuNPs were the absence of DNA alterations and the selectivity for caspase dependence. The absence of DNA damage in cancer cells exposed to CH-AuNPs contrasts with other studies where DNA fragmentation was observed after treatment with AuNPs.32,47,48 However, this was never assessed using chitosan as a reducing agent; thus, these differences can be due to the physicochemical differences of the AuNPs including chitosan. Even though many studies have found that AuNPs and chitosan themselves rely on caspases to induce cell death,13,28,49 certain types of AuNPs can induce caspase-independent cell death,48 even in HeLa cells,32 which contrasts with our results that show caspase-dependent cell death in HeLa cells. This difference may be due to the different agents used to synthesize AuNPs: we used chitosan, whereas Pan et al used triphenylphosphine mono-sulfonat.41 Additionally, in our study, we found that even when using the same AuNPs, these differences can be due to the characteristics of each cell line, such as the absence of caspase-3 in MCF-7 cells.29

Despite caspase dependence not being a common feature of CH-AuNP-induced cell death, we found that ROS production was. ROS production has been a recurrent feature in different types of nanoparticle-induced responses,38 such as cell death.32,49 Previous studies with other types of AuNPs have also demonstrated that ROS production is indispensable for cell death induction.32,41,49 Additionally, a previous report stated that CH-AuNPs induced ROS production in lung adenocarcinoma cells.5 The importance of ROS production for CH-AuNPs-RCD, however, has not been assessed. The fact that caspase dependence is not conserved in both cell lines and ROS production indicates that ROS could be an upstream event in cell death. It has previously been described that ROS production by nanoparticles can cause mitochondrial alterations leading to other types of RCD, such as the activation of caspases or regulated necrosis.42 This finding supports the role of ROS production as a shared feature of CH-AuNPs cytotoxicity, and may be one of the first steps of their RCD pathway, particularly since ROS production was not observed in PBMCs, even at the concentration of 100 µM. Thus, further analysis should be performed to better understand the mechanism by which CH-AuNPs exert their cytotoxicity.

Conclusion

Our findings confirm that CH-AuNPs have a more potent cytotoxic effect than SC-AuNPs. Additionally, this study improves the understanding of the cytotoxicity of CH-AuNPs, as it demonstrates for the first time that they are barely cytotoxic to healthy PBMC, while they induce a concentration-dependent cell death in cancer cells and inhibit their clonogenic potential without inducing DNA damage or cell cycle arrest. We also demonstrated that they induce different cell death modalities in HeLa and MCF-7 cells, but that CH-AuNPs-induced RCD relies on ROS production. This work opens the way to further characterize this type of cell death that might work in parallel with apoptosis-inducing chemotherapies in functionalized models.

Data availability

All datasets generated during the current study are available from the corresponding author on reasonable request.

Supplementary materials

Figure S1

Effect of CH-AuNPs on HeLa, MCF-7, and PBMC cell viability after 48 hours of treatment.

Notes: HeLa, MCF-7, and PBMC were treated with various concentrations of CH-AuNPs (25, 50, 75, 100, and 150 µM) for 48 hours. Cell viability was measured by MTT assay. The percentages refer to relative cell viability represented as percentage of control (nontreated cell viability was normalized to 100%).

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; PBMC, peripheral blood mononuclear cell.

ijn-13-3235s1.tif (206KB, tif)
Figure S2

Cell death induced by etoposide in HeLa, MCF-7, and PBMC after 24 hours of treatment.

Notes: Cell death was measured by flow cytometry through AnnV and PI staining in HeLa, MCF-7, and PBMC treated with etoposide for 24 hours. Data were then analyzed and graphed.

Abbreviations: AnnV, Annexin-V; PBMC, peripheral blood mononuclear cell; PI, propidium iodide.

ijn-13-3235s2.tif (80.4KB, tif)
Figure S3

ROS production in PBMC upon treatment with CH-AuNPs.

Notes: ROS levels were measured by flow cytometry through DCFDA staining in PBMC left alone or treated with the indicated concentrations of CH-AuNPs for 24 hours. Representative histograms of ROS production assessed in PBMCs (n=3 donors assessed in triplicate).

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; DCFDA, dichlorodihydrofluorescein diacetate; PBMC, peripheral blood mononuclear cell; ROS, reactive oxygen species.

ijn-13-3235s3.tif (147.5KB, tif)

Acknowledgments

We thank Zugeeissy Samantha de Leon-Chavez for the preliminary data, Martin Gerardo García-Juarez for article revision and overall help, Sergio Galindo (Departamento de Química de la Facultad de Ciencias Biológicas, UANL) for technical help, and Alejandra Arreola for article revision. HYLA thanks CONACyT for scholarship 745665. We thank PAICYT and CONACYT for funding, and the Laboratorio de Inmunología y Virología for the funding and the facilities provided to perform this work.

This work was supported by a research grant from the Consejo Nacional de Ciencia y Tecnología, Ciencia Básica (CB 252017) to C Rodriguez-Padilla, the Proyecto de Apoyo a la Investigación Científica y Tecnológica (PAICYT SA092-15) to AC Martinez-Torres and by the Laboratorio de Inmunología y Virología.

Footnotes

Author contributions

ACMT, DGZT, HYLA, AAA, CRA, and CRP analyzed and interpreted data. ACMT, DGZT, HYLA, AAA, and CRA performed statistical analysis. DGZT, HYLA, AAA, and CRA synthesized AuNPs. HYLA, AAA, and CRA carried out cell viability, cell cycle and cell death analysis, caspase, microscopy, and ROS assessment. DGZT conceived and supervised the synthesis and characterization of nanoparticles. DGZT, HYLA, and CRP helped to draft the manuscript. AAA and CRA revised the manuscript. ACMT conceived and designed the experiments, supervised work, and wrote the manuscript. All authors approved the final manuscript.

Disclosure

The authors report no conflicts of interest in this work.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Figure S1

Effect of CH-AuNPs on HeLa, MCF-7, and PBMC cell viability after 48 hours of treatment.

Notes: HeLa, MCF-7, and PBMC were treated with various concentrations of CH-AuNPs (25, 50, 75, 100, and 150 µM) for 48 hours. Cell viability was measured by MTT assay. The percentages refer to relative cell viability represented as percentage of control (nontreated cell viability was normalized to 100%).

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; PBMC, peripheral blood mononuclear cell.

ijn-13-3235s1.tif (206KB, tif)
Figure S2

Cell death induced by etoposide in HeLa, MCF-7, and PBMC after 24 hours of treatment.

Notes: Cell death was measured by flow cytometry through AnnV and PI staining in HeLa, MCF-7, and PBMC treated with etoposide for 24 hours. Data were then analyzed and graphed.

Abbreviations: AnnV, Annexin-V; PBMC, peripheral blood mononuclear cell; PI, propidium iodide.

ijn-13-3235s2.tif (80.4KB, tif)
Figure S3

ROS production in PBMC upon treatment with CH-AuNPs.

Notes: ROS levels were measured by flow cytometry through DCFDA staining in PBMC left alone or treated with the indicated concentrations of CH-AuNPs for 24 hours. Representative histograms of ROS production assessed in PBMCs (n=3 donors assessed in triplicate).

Abbreviations: CH-AuNPs, chitosan gold nanoparticles; DCFDA, dichlorodihydrofluorescein diacetate; PBMC, peripheral blood mononuclear cell; ROS, reactive oxygen species.

ijn-13-3235s3.tif (147.5KB, tif)

Data Availability Statement

All datasets generated during the current study are available from the corresponding author on reasonable request.

Articles from International Journal of Nanomedicine are provided here courtesy of Dove Press

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