Quantum dots (QDs) are unique semi-conductor fluorescent nanoparticles with potential uses in a variety of biomedical applications. However, concerns exist regarding their potential toxicity, specifically their capacity to induce oxidative stress and inflammation. In this study we synthesized CdSe/ZnS core/shell QDs with a tri-n-octylphosphine oxide, poly(maleic anhydride-alt-1-tetradecene) (TOPO-PMAT) coating and assessed their effects on lung inflammation in mice. Previously published in vitro data demonstrated these TOPO-PMAT QDs cause oxidative stress resulting in increased expression of antioxidant proteins, including heme oxygenase, and the glutathione (GSH) synthesis enzyme glutamate cysteine ligase (GCL). We therefore investigated the effects of these QDs in vivo in mice deficient in GSH synthesis (Gclm +/− and Gclm −/− mice). When mice were exposed via nasal instillation to a TOPO-PMAT QD dose of 6 µg cadmium (Cd) equivalents/kg body weight, neutrophil counts in bronchoalveolar lavage fluid (BALF) increased in both Gclm wild-type (+/+) and Gclm heterozygous (+/−) mice, whereas Gclm null (−/−) mice exhibited no such increase. Levels of the pro-inflammatory cytokines KC and TNFα increased in BALF from Gclm +/+ and +/− mice, but not from Gclm −/− mice. Analysis of lung Cd levels suggested that QDs were cleared more readily from the lungs of Gclm −/− mice. There was no change in matrix metalloproteinase (MMP) activity in any of the mice. However, there was a decrease in whole lung myeloperoxidase (MPO) content in Gclm −/− mice, regardless of treatment, relative to untreated Gclm +/+ mice. We conclude that in mice TOPO-PMAT QDs have in vivo pro-inflammatory properties, and the inflammatory response is dependent on GSH synthesis status. Because there is a common polymorphism in humans that influences GCLM expression, these findings imply that humans with reduced GSH synthesis capabilities may be more susceptible to the pro-inflammatory effects of QDs.
Citation: McConnachie LA, Botta D, White CC, Weldy CS, Wilkerson H-W, et al. (2013) The Glutathione Synthesis Gene Gclm Modulates Amphiphilic Polymer-Coated CdSe/ZnS Quantum Dot–Induced Lung Inflammation in Mice. PLoS ONE 8(5): e64165. doi:10.1371/journal.pone.0064165
Editor: Lynette Kay Rogers, The Ohio State Unversity, United States of America
Received: December 18, 2012; Accepted: April 10, 2013; Published: May 27, 2013
Copyright: © 2013 McConnachie et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by National Institutes of Health grants R01ES016189, U19ES019545, P01HL098067, P30ES007033 and T32ES007032 (www.NIH.gov), and by a grant from the Parker B. Francis Foundation (www.francisfellowships.org). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Engineering efforts over the last several years have resulted in stunning advances in the production of nanomaterials that can be utilized for a wide variety of applications. These advances, leading to a broad array of novel nanomaterials, have occurred at such a rapid pace that efforts to understand and characterize the impact of nanomaterial exposure on human health are lagging. One such class, semi-conductor quantum dots (QDs) hold great promise as biological imaging agents, but concerns have been expressed related to their core components which typically consist of potentially toxic heavy metals such as cadmium, selenium, lead and tellurium. Pelley et al  and Botrill and Green  present excellent reviews of recent QD toxicity studies. In these reviews, the authors cite several examples whereby QDs elicit toxicity in a variety of in vitro systems, particularly via the generation of reactive oxygen intermediates . Furthermore, previous in vitro work in our lab indicated that heme oxygenase-1 is a highly robust and reproducible biomarker of QD exposure indicating activation of oxidative stress signaling across a variety of cell types of either human or murine origin .
While in vitro studies of QD exposure have indicated the ability to evoke toxicity in a variety of cell culture systems, in vivo studies utilizing rodent models may be more informative when attempting to predict potential deleterious human health effects. The potential for QDs to elicit toxicity in the lung is important when considering occupational exposure scenarios, especially during the manufacturing process . Moreover, recent studies indicate that QDs evoke pulmonary inflammation in rodents when delivered via intratracheal instillation or inhalation , . QDs are of concern when considering pulmonary exposure not only because of their ability to incite inflammation but also of their aforementioned heavy metal core constituents. While chemical modifications to the surface are known to play a large role in QD toxicity, it is also important to consider possible effects associated with metal release upon QD degradation. Cadmium, a potent oxidant, exhibits a long half-life in human kidney and liver tissue, and is a well-characterized renal toxicant . The toxicity of Cd is modulated, in part, by glutathione (GSH) due to the propensity of free Cd to deplete thiols such as GSH through reactive oxygen species generation and/or direct binding and sequestration . Furthermore, GSH is known to modulate inflammatory responses and is generally protective against inflammatory pathologies , . To this end, recent work in our laboratory has indicated that GSH status plays a pivotal role in determining the degree of inflammatory response in the lung following exposure to diesel exhaust particulate . In that report, transgenic mice with partially compromised capacity for GSH synthesis exhibited a significantly higher degree of neutrophil influx into the lung following diesel particulate exposure relative to mice with normal GSH synthesis capacity.
Although the amphiphilic polymer coated tri-n-octylphosphine oxide, poly(maleic anhydride-alt-1-tetradecene) (TOPO-PMAT) QDs employed in the present study are designed to be stable , , there is nevertheless the possibility they will degrade and release free Cd+2 causing downstream toxicity via the generation of reactive oxygen species and GSH depletion. Therefore, the goal of the present study was to examine the role of GSH in modulating TOPO-PMAT QD pro-inflammatory properties in mice when dosed via nasal instillation. This particular route of administration is a useful screening paradigm to identify materials that have the potential to cause toxicity and inflammation in the lung following inhalation exposure.
The first and rate-limiting step in GSH biosynthesis is the ligation of glutamate and cysteine to form γ-glutamylcysteine (γ-GC). This reaction is catalyzed by glutamate-cysteine ligase (GCL), a heterodimer composed of catalytic and modifier subunits. Mice lacking the modifier subunit of GCL (Gclm −/−), have a dramatically compromised ability to synthesize GSH in all tissues relative to their wild-type counterparts (Gclm +/+). Mice heterozygous for Gclm (+/−) have slightly lower levels of GSH than wild type Gclm +/+ mice, but can be sensitive to certain toxic exposures, presumabely because they are less able to rapidly re-synthesize GSH following challenge , .
To investigate the role of GSH in modulating QD induced inflammation and toxicity, we exposed mice of all three Gclm genotypes (+/+, +/−, and −/−) to TOPO-PMAT QDs and examined markers of pulmonary inflammation and toxicity at various time-points up to 24-hours following exposure. Overall, we found that the degree of inflammation, as measured by neutrophil influx and pro-inflammatory cytokines, was highly dependent on Gclm genotype, and hence GSH levels. Collectively, these results indicate that GSH status plays a potential role in determining the toxicity and disposition of TOPO-PMAT QDs. Because there are relatively common functional genetic polymorphisms in the human GCLM gene that can limit the expression of GCLM and thus re-synthesis of GSH under conditions of oxidative challenge, these findings also suggest caution is warranted when considering potential human exposures to such nanomaterials.
Materials and Methods
Quantum Dot Synthesis and Characterization
We utilized TOPO-PMAT coated CdSe/ZnS core/shell QDs for all studies. The characteristics of these QDs have been described previously . In brief, CdSe/ZnS core/shell quantum dots coated with tri-n-octylphosphine oxide (TOPO) were supplied by Ocean Nanosciences (Springdale, AR). They were further coated with poly(maleic anhydride-alt-tetradecene) (PMAT) (Sigma Aldrich, St. Louis MO). Figure 1 describes the structure and composition of the TOPO-PMAT QDs. Immediately prior to dosing, the QDs were vortexed and diluted in sterile injection grade 0.9% sodium chloride to a final concentration of 5 nM. The QDs were tested for endotoxin using a Kinetic-QCL™ LAL Assay (Lonza, Inc., Walkersville, MD).
Figure 1. Schematic representation of a TOPO-PMAT quantum dot.
The central sphere represents the CdSe/ZnS core/cap structure, surrounded next by tri-n-octylphosphine oxide (TOPO), and then the poly(maleic anhydride-alt-1-tetradecene (PMAT) polymer coating. (Modified from ).doi:10.1371/journal.pone.0064165.g001
All animal experiments were conducted in accordance with the National Institutes of Health Guide for the Use and Care of Laboratory Animals and were approved by the University of Washington Institutional Animal Care and Use Committee (protocol #2384-08). All efforts were taken to minimize suffering. Male Gclm +/+, +/−, and −/− mice, previously backcrossed onto a C57BL/6 background , were used for all studies. Mice were housed in a modified specific pathogen free vivarium on a 12-hour light/dark cycle and allowed access to chow and water ad libitum.
Quantum Dot Treatments
Eight to 24 week old mice (median age 9 weeks) of all three Gclm genotypes were randomly assigned to receive either saline or TOPO-PMAT QD (1.53 µL/gm body weight of a 5 nM solution; 6 µg Cd equivalents/kg BW) via nasal instillation. Nasal instillation was performed following induction of light anesthesia (intraperitoneal injection of 0.01 mL/g body weight of a 0.44 mg/mL Xylazine, 6.5 mg/mL Ketamine solution in sterile saline) and by slowly depositing half the dose of TOPO-PMAT QD solution (or saline vehicle) into each nostril. Mice were held in an upright position following dosing (for one minute) to ensure complete inspiration of saline or TOPO-PMAT QDs. At specified time-points (30 min, 1, 3, 8 or 24 hours following nasal instillation) mice were sacrificed by CO2 narcosis followed by cervical dislocation. After collecting bronchoalveolar lavage fluid (described below) the lungs were inflated with 1 mL of Tissue-Tek* CRYO-OCT cutting compound (Fischer Scientific, Pittsburgh, PA), and the left lobe was resected and snap frozen in liquid nitrogen. The right lung lobes were embedded in OCT for cyrosectioning. Portions of the left lobe were then processed for Cd analysis at all of the above listed time points, and the remaining assays described below were performed on samples collected at the 8-hour time point.
Bronchoalveolar lavage (BAL) was performed as previously described . In brief, after lavage, collected cells were pelleted by centrifugation and prepared for flow cytometry analysis to quantitate the percentage of neutrophils present. The supernatant was reserved for cytokine analyses.
We utilized a Beckman-Coulter Altra fluorescence activated cell sorter (Beckman-Coulter, Miami, FL) to quantitatively assess the percentage of neutrophils in BAL by flow cytometry. Cells obtained from BAL were stained with anti-F4/80 conjugated to Alexafluor 488 (eBioscience, San Diego, CA), and biotinylated anti-mouse Ly6G/Ly6C (Gr1) (BioLegend, San Diego, CA) followed by streptavidin Alexafluor 350 (Invitrogen, Carlsbad, CA). Neutrophils were identified as cells having low F4/80 and high Gr1 staining as indicated on green versus blue fluorescence intensity bivariate dot-plots.
Total Lung Glutathione Determination
Total lung glutathione (GSH) was determined as previously described . In brief, clarified lung homogenates from mice (8 hours post-exposure) were prepared from snap frozen lung tissue. GSH was derivatized with napthelene-2,3-dicarboxaldehyde and the relative fluorescence intensity of derivatized products was determined. GSH levels were determined by interpolation on a GSH standard curve prepared identically to test samples. All determinations were carried out in triplicate.
Fluorogenic 5′ Nuclease-based Assay and Quantitative RT-PCR
The Functional Genomics Laboratory at the University of Washington developed fluorogenic 5′ nuclease-based assays to quantitate the mRNA levels of specific genes. Briefly, reverse transcription was performed according to the manufacturer’s established protocol using 1 ug of total RNA and the SuperScript® III First-Strand Synthesis System (Invitrogen, Carlsbad, CA). For gene expression measurements, 2 µL of cDNA were included in a PCR reaction (12 µL final volume) that also consisted of the appropriate forward (FP) and reverse (RP) primers, probes and TaqMan Gene Expression Master Mix (Applied Biosystems Inc., Foster City, CA). The PCR primers and the dual-labeled probes for the genes were designed using ABI Primer Express v.1.5 software (Applied Biosystems). Several genes were analyzed using the ABI inventoried TaqMan® Gene Expression Assays mix according to the manufacturer’s protocol (Applied Biosystems). All oligonucleotide sequences are listed in Table S1.
Amplification and detection of PCR amplicons were performed with the ABI PRISM 7900 system (Applied Biosystems) with the following PCR reaction profile: 1 cycle of 95°C for 10 min., followed by 40 cycles of 95°C for 30 sec, and 62°C for 1 min. GAPDH amplification plots derived from serial dilutions of an established reference sample were used to create a linear regression formula in order to calculate expression levels, and GAPDH gene expression levels were utilized as an internal control to normalize the data.
To determine Cd content, lung tissue was initially subjected to microwave digestion in concentrated nitric acid. Because the lungs were instilled with OCT fixative, we were unable to obtain an accurate mass of the tissue for normalization purposes. Therefore, it was necessary to normalize cadmium content to another metal that was invariant with respect to genotype or treatment. Following a survey of metals present in multiple lung samples from mice of all Gclm genotypes and treatments, we determined that molybdenum was invariant (data not shown). Thus we used tissue molybdenum levels for normalization. Cadmium and molybdenum content analyses were performed using an inductively coupled plasma mass spectrometer (ICP-MS) following EPA Method 6020A with an Agilent 7500ce ICP-MS.
Myeloperoxidase (MPO) content in lung homogenates was assessed by ELISA for the 8-hour time point and performed as previously described . Briefly, lungs were homogenized in tissue lysis buffer (Sigma- Aldrich) with proteinase inhibitor (Roche Applied Science, Indianapolis, IN, USA), aliquoted, and snap frozen in liquid nitrogen. A 96-well microtiter plate was loaded with capture antibody overnight at room temperature and after blocking with 5% BSA in PBS for 1 hour, incubated with sample or standard (0.4 to 250 ng/mL) overnight at 4°C. After washing, wells were incubated with biotinylated detection antibody. After 2 hours, wells were washed and then incubated with Streptavidin conjugated to horseradish peroxidase for 20 minutes. Wells were washed again, and TMB Substrate (Sigma-Aldrich) was added to each well and incubated for 5–20 minutes. One hundred µL of 0.5 M H2SO4 were used to stop the reaction, and plates were read at 450 nm using a spectrophotometric plate reader (Synergy 4 Multi-Mode, BioTek, Winooski, VT).
Matrix Metalloproteinase Activity
Matrix metalloproteinase (MMP) activity in lung homogenates from the 8-hour time point was measured as previously described . Total MMP activity was determined with the OmniMMP fluorogenic substrate (P-126, Biomol International, Plymouth Meeting PA).
Multiplex Bead-based Cytokine Assays for CXCL1 (KC), TNFα, MIP2 and MCP-1
Mouse lavage fluid samples were analyzed in the Center for Ecogenetics and Environmental Health Functional Genomics Laboratory at the University of Washington using the MILLIPLEX MAP Mouse bead-based multiplex cytokine assays (Millipore, Billerica, MA) according to the manufacturer’s instructions. Briefly, 25 µL of each standard from a series of 4-fold dilutions and samples were incubated with the target capturing beads on a 96-well plate for 16 hours at 4°C, followed by one hour of incubation with specific biotinylated detection antibodies at room temperature. Next, Streptavidin-Phycoerythrin was added to each well and incubated for 30 minutes at room temperature. Filtration and washing were incorporated after each incubation step with wash buffer using a vacuum manifold. Samples were resuspended in sheath fluid prior to reading them on a Luminex 100™ (Austin, TX) suspension array reader. Each sample was analyzed in duplicate.
Cd contents were normalized to tissue molybdenum content (Mo). The average concentration of Cd in the lung tissue from PMAT-TOPO QD treated mice (N = 5–7) at each time-point for the toxicokinetic parameter calculations at 0, 0.5,1, 3, 8, and 24 h. The calculation of the compartmental toxicokinetic model was conducted with PKSolver . One compartment toxicokinetic models were found to be the best-fit for simulating lung Cd content.
Data were analyzed using two-way analysis of variance (ANOVA) for genotypes, treatments, and interactions. Quantal- quantal plots were used to check that residuals from the 2-way ANOVA were approximately normally distributed. Post-hoc comparisons were corrected for multiple testing by using a multivariate t-distribution to compute corrected p-values based upon the variance-covariance matrix for the set of contrasts describing the post-hoc comparisons . The post hoc tests were to detect significant increases in neutrophils, gene expression, protein, activity, or content after treatment with QDs for each Gclm genotype.
TOPO-PMAT Quantum Dot Characterization
When measured by dynamic light scattering, the TOPO-PMAT QDs used in this study had a hydrodynamic diameter of 12.7±0.5 nm and a core diameter of 6.8±0.5 nm. Endotoxin contamination of these preparations was found to be negligible (0.013 EU/ml for the instilled QD solution). More in-depth information regarding the physical and chemical characteristics of these particular QDs is presented in McConnachie et al .
Neutrophil Influx into the Lungs as Assessed by Bronchoalveolar Lavage
To investigate the potential pro-inflammatory properties of TOPO-PMAT QDs when dosed via nasal instillation, we determined the percentage of neutrophils present in bronchoalveolar lavage fluid (BALF) 8 hours after QD administration. Mice instilled with an equal volume of saline served as vehicle controls. QD instillation elicited a strong and statistically significant neutrophil influx in both Gclm +/+ and Gclm +/− mice at 8 hours (p<0.05 relative to saline treated controls of the same genotype). Importantly, TOPO-PMAT QD treatment failed to elicit any such neutrophil response in the Gclm −/− mice (Figure 2). The resistance to neutrophil influx in Gclm −/− mice may indicate that they are unable to mount an inflammatory response to QD exposure or that there are differences in QD disposition in the lungs of these mice.
Figure 2. % Neutrophil influx into the bronchoalveolar lavage fluid.
Data represent the mean ± S.E.M. for % neutrophils (cells exhibiting low F4/80 and high Gr1 staining) present in the bronchoalveolar lavage fluid as measured by flow cytometry 8 hours following saline or TOPO-PMAT QD administration. * = p<0.05 relative to saline treated mice. The number of replicates is indicated in each bar.doi:10.1371/journal.pone.0064165.g002
Lung Glutathione Content
Cadmium is a core constituent of the TOPO-PMAT QDs and may be released upon their degradation. Furthermore, cadmium toxicity is modulated in part by GSH levels , . Additionally, oxidative stress and subsequent GSH depletion may be an integral component of the pro-inflammatory potential of heavy metal containing nanoparticles , . For these reasons, we were interested in the effect of TOPO-PMAT QD exposure on lung GSH levels. We determined the lung GSH content 8 hours following nasal instillation of either saline or TOPO-PMAT QDs (Figure 3). TOPO-PMAT QD treatment had no effect on lung GSH levels, relative to saline treatment, regardless of genotype. As expected, the levels of GSH present in the lungs of saline-treated Gclm −/− and Gclm +/− mice were approximately 17% and 77%, respectively, of that in saline-treated Gclm +/+ mice. These data are in agreement with previously reported values for these mice , .
Figure 3. Lung glutathione content.
Total glutathione was measured in clarified lung homogenates 8 hours following saline or TOPO-PMAT QD administration. Data represent the mean ± S.E.M., ** = p<0.01 and *** = p<0.001 relative to treatment-matched Gclm +/+ mice as determined by Students t-test. The number of replicates is indicated in each bar.doi:10.1371/journal.pone.0064165.g003
Real Time PCR Assessment of Stress Response and Inflammatory Cytokine mRNA Expression
We analyzed the mRNA expression level of genes involved in both oxidative stress signaling and inflammatory pathways (Figure 4). Genes in the former group were glutamate cysteine ligase catalytic subunit (Gclc), glutamate cysteine ligase modifier subunit (Gclm), heme oxygenase-1 (Hmox1) and metallothionein-1/2 (Mt1/2). While there was a trend towards increasing Gclc expression with QD exposure in +/+ and +/− mice, this did not achieve statistical significance. There was no difference in Gclc expression after QD treatment in −/− mice relative to saline-treated controls. Conversely, QD-treatment resulted in marked increases in Gclm expression in +/− mice (p<0.05) and a suggestion of an increase in Gclm +/+ mice, relative to the saline-treated control groups. As expected, Gclm −/− mice had no detectable levels of Gclm mRNA in either the saline- or QD-treated groups. This pattern of induction in Gclm +/+ and +/− mice with QD treatment was also observed for Hmox1 mRNA (although not statistically significant). Gclm −/− mice, on the other hand, did not exhibit any perturbation in Hmox1 expression following QD treatment. In addition, there were treatment related changes noted in Mt1 expression by 2-way ANOVA analysis. It should also be noted that there appeared to be an inverse trend for Mt1 expression relative to Gclm copy number. Mt2 expression changes were minimal and did not achieve statistical significance, although there was a trend towards increasing expression with TOPO-PMAT QD treatment. Taken together, the data from the stress-response gene expression analyses indicate mild to moderate up-regulation of these pathways associated with TOPO-PMAT QD exposure in the Gclm +/+ and +/− mice but no effects in the Gclm −/− mice.
Figure 4. mRNA expression of stress-response genes as measured by qRT-PCR.
The effects of saline and TOPO-PMAT QD administration on A) Gclc, B) Gclm, C) Hmox1, D) Mt1 and E) Mt2 mRNA expression are shown. Data represent the mean ± S.E.M., * = p<0.05 relative to saline treated Gclm +/− mice. The number of replicates is indicated in each bar.doi:10.1371/journal.pone.0064165.g004
We analyzed mRNA expression for the following genes involved in inflammation: interleukin-1β (Il1β), monocyte chemotactic protein-1 (Mcp1), tumor necrosis factor-α (Tnfα), granulocyte-macrophage colony stimulating factor (Gmcsf), and keratinocyte derived cytokine (KC, Cxcl1) (Figure 5). Although there was a suggestion of an increase in several of these mRNAs relative to saline-treated controls in Gclm +/+ and Gclm +/− mice, especially with respect to KC levels, these did not achieve statistical significance. Furthermore, as observed with the % neutrophil data and stress response gene analyses, Gclm−/− mice were non-responsive to QD exposure.
Figure 5. mRNA expression of inflammatory cytokine genes as measured by qRT-PCR.
The effects of saline or TOPO-PMAT QD administration on A) Il1β, B) Mcp1, C) Tnfα, D) Gmcsf and E) KC mRNA expression are shown. Data represent the mean ± S.E.M. of the indicated number of replicates in each bar.doi:10.1371/journal.pone.0064165.g005
Assessment of KC and TNFα Protein Concentrations in Bronchoalveolar Lavage Fluid
In order to further clarify the potential pro-inflammatory properties of the TOPO-PMAT QD, we also analyzed the level of inflammatory cytokines keratinocyte-derived cytokine (KC) and TNFα protein present in the BAL fluid 8 hours after either saline or TOPO-PMAT QD instillation (Figure 6). QD treatment resulted in an increase in KC levels in Gclm +/+ mice relative to treatment with saline alone (p<0.05). A similar trend was observed for TNFα levels, although this did not achieve statistical significance. In contrast, Gclm −/− mice exhibited a more muted KC and TNFα response to QD treatment. There were no significant differences in these cytokines across Gclm genotypes for the saline-treated mice, indicating a similar low-level response to saline regardless of GSH status. In general, the findings of this analysis are consistent with the neutrophil data presented in Figure 2.
Figure 6. Inflammatory cytokine protein expression in lung tissue.
The effect of saline or TOPO-PMAT QD administration on A) KC and B) TNFα protein levels as assessed in a cytokine array panel. Data represent the mean ± S.E.M. of the indicated number of replicates in each bar. * = p<0.05 relative to saline treated mice.doi:10.1371/journal.pone.0064165.g006
Matrix Metalloproteinase Activity and Myeloperoxidase Content
Matrix metalloproteinase (MMP) activity serves to promote neutrophil influx via shedding of extracellular matrix proteins, facilitating neutrophil chemotaxis into the lung. Thus, an increase in MMP activity may facilitate neutrophil recruitment into the lung following QD treatment. Additionally, neutrophils express high levels of myeloperoxidase (MPO), which can be considered a biomarker of neutrophil presence in the lung. Analysis of lung MMP activity and MPO levels revealed few significant effects of TOPO-PMAT QD instillation in lung tissue (Figure 7). A notable exception is observed for Gclm +/+ mice where we observed that QD exposure led to a significant increase in MPO content. This finding is consistent with the % neutrophil data presented in Figure 2. Interestingly, the level of MPO was lower in Gclm −/− mice, relative to Gclm +/+ mice, regardless of treatment, which is consistent with the lower levels of neutrophils in the BAL fluid from these mice.
Figure 7. Lung matrix metalloproteinase activity and myeloperoxidase content.
The effect of TOPO-PMAT QD administration on A) matrix metalloproteinase (MMP) activity and B) myeloperoxidase (MPO) content. Data represent the mean ± S.E.M. of 4 replicates ** = p<0.01 relative to saline treated mice.doi:10.1371/journal.pone.0064165.g007
Toxicokinetic Modeling of Cadmium Disposition in Lung Tissue
The parameters in Table 1 are for a one compartment model for the lung concentration of Cd. The parameters A and alpha are the uptake concentration and uptake rate for Cd entering the lung, and the parameter beta is the rate at which it leaves the lung:
where t is the time post exposure in hours. The results of applying these rates in a one compartment lung model are shown in Figure 8 and provided an excellent fit for lung Cd data; the r2 values between the observed and predicted Cd content are 0.99, 0.99 and 0.95, for Gclm +/+, +/− and −/− mice, respectively. The kinetic rate constants derived from the modeling reveal again several striking differences between genotypes suggesting Gclm status plays an integral role in the disposition of TOPO-PMAT QDs. There was rapid deposition of Cd for all three genotypes and we could not distinguish between the delivery rates, alpha, which had an deposition half time of 12.6 minutes. The deposited concentration of Cd, A, appeared to be lower for the Gclm −/− mice with a value of 0.62 ng Cd/mg Mo compared to 0.95 and 0.93 ng Cd/mg Mo for the Gclm +/+ and +/− mice. The rate of clearance of Cd from the lung, beta, was much more rapid for the Gclm −/− mice with a half life of 4.6 hours compared to the Gclm +/+ and +/− genotypes with half lives of 46 hours and over 400 hours respectively.
Figure 8. Toxicokinetic modeling of TOPO-PMAT QD disposition.
Lung cadmium content was determined by inductively coupled plasma-mass spectrometry (ICP-MS) analysis, and TOPO-PMAT QD disposition was modeled using PKSolver as described in Methods. A one-compartment model resulted in the best fit of simulated QD disposition curves relative to measured Cd content.doi:10.1371/journal.pone.0064165.g008
To investigate the role of GSH in TOPO-PMAT QD induced pulmonary toxicity, we utilized mice with partially or severely diminished GSH synthesis capacities (Gclm +/− and Gclm −/−, respectively). In these studies we employed nasal instillation to model inhalation exposure, an important route of exposure when considering exposures in occupational settings. Several interesting findings arose from these studies, namely that (1) Gclm status is a major determinant of the degree of pulmonary inflammation following TOPO-PMAT QD exposure via nasal instillation and (2) despite all mice receiving equivalent doses of TOPO-PMAT QDs, there are large differences in lung Cd disposition kinetics which were also dependent on GSH status.
The degree of neutrophil influx into the airways of Gclm −/− mice was much lower than mice with relatively normal GSH levels 8 hours following TOPO-PMAT QD exposure. This finding may seem counter-intuitive, in that Gclm −/− mice would be expected to be more, rather than less sensitive to the potential oxidative properties of the TOPO-PMAT QDs. It has been shown that GSH status is an important determinant of both innate and acquired immunity in the lung , , . Interestingly, Villa and colleagues , have shown that pharmacological depletion of GSH in mice was associated with a decreased influx of neutrophils into the peritoneal space in a sepsis model (cecal ligation and puncture), while simultaneously increasing the numbers of neutrophils present in the lung. Alternatively, administering GSH-ethyl ester to counteract LPS-induced GSH depletion resulted in protection from LPS-induced lung injury . These effects are likely attributable to differences in local conditions in these organs that govern neutrophil trafficking and may be related to the expression of molecules that are critical for extravasation of neutrophils (e.g. intercellular adhesion molecule-1 and its cognate receptor on neutrophils, CD18) and/or gradients of chemokines/cytokines known to attract neutrophils to the sites of inflammation (e.g. KC, TNFα, IL1β, GMCSF, MIP2 and MCP1). In turn, the expression of these factors is to a large extent governed by the activation of transcription factors such as NFκB and AP-1. Interestingly, while moderate oxidation can increase NFκB signaling , which may be dependent on S-glutathionylation of IKKβ  or IκB , further oxidation can diminish the binding of NFκB to DNA . This inactivation of NFκB under strongly oxidizing conditions has been demonstrated whereby severely depleted GSH can suppress NFκB signaling because of oxidation of a cysteine group that is critical for DNA binding , . Moreover, we  and Johansson and colleagues  have shown that Gclm −/− mice are not necessarily more sensitive to the pulmonary toxicants diesel exhaust particulate (DEP) or ozone, respectively. This is presumably because of compensatory up-regulation of alternative antioxidant and anti-inflammatory pathways , . Interestingly, Gclm +/− mice appear to have increased susceptibility to inflammation when exposed to diesel exhaust particles (DEP) . As common single nucleotide polymorphisms (SNPs) in the 5′-promoter regions of both GCLM and GCLC have been associated with various clinical conditions in human populations , including lung diseases , it is important to understand the role of GSH synthesis in mediating deleterious effects following exposure to environmental toxicants. Humans who have certain common GCLM and GCLC genetic polymorphisms have relatively normal GSH levels, but appear to be unable to rapidly synthesize de novo GSH in response to oxidative challenge, apparently because of compromised induction of GCLM and GCLC mRNAs that normally occurs under conditions of oxidative stress. This phenotype is similar to what we observe in Gclm +/− mice, in that they demonstrate relatively normal levels of GSH, but seem to be unable to adequately synthesize de novo GSH following oxidative challenge. Due to these observations, we believe that our data supports the contention that humans with SNPs within GCLM and GCLC may demonstrate heightened sensitivity to environmental toxicants that cause oxidative stress.
Although the Gclm +/− mouse represents a model that is more clinically relevant to the human condition of GCLM SNPs, the Gclm −/− mouse provides a unique model to investigate the effect of severely compromised de novo GSH synthesis on mounting an inflammatory response following QD challenge. Our results suggest that Gclm −/− mice, despite severely reduced GSH levels, do not mount an inflammatory response to intranasal QD treatment whereas this response does occur in Gclm +/+ and Gclm +/− mice.
In order to examine the possibility that the lack of neutrophils in the BALF in Gclm −/− mice may be due to interference with cytokine/chemokine signaling, we determined the mRNA levels of a number of such factors using qRT-PCR. These data suggest that the innate immune response in these mice may in fact be compromised. Specifically, the mRNA expression of GMCSF, MCP1 and IL1β appears to be muted in Gclm −/− mice following TOPO-PMAT QD exposure, relative to Gclm +/− and Gclm +/+ mice (Figure 5). In addition, the protein levels of KC and TNFα were also unaffected by TOPO-PMAT QD exposure in Gclm −/− mice (Figure 6). Diminished expression of these acute-phase early-response proteins may prevent the downstream events necessary for neutrophil recruitment and infiltration. In this regard, we have shown that MMP-dependent shedding of KC bound to the extracellular matrix protein syndecan-1 is a crucial signal for neutrophil migration into the alveolar spaces , . Similarly, TNFα is known to be shed by TNFα converting enzyme (TACE; also know as ADAM17) following activation of pro-inflammatory signaling pathways , . Consistent with these observations and the presently reported neutrophil influx data, both KC and TNFα were elevated in the Gclm +/− and −/− mice. However, MMP activity was not significantly altered with QD exposure, regardless of genotype. Interestingly, the lower levels of neutrophils in the BAL fluid of Gclm −/− mice were in agreement with MPO activity in the lung tissue of these mice as it was also diminished relative to both Gclm +/+ and +/− mice. Had the levels not been lowered, we may have concluded the neutrophils were recruited to the lungs in Gclm −/− mice but had not migrated to the alveolar space.
An alternate mechanistic explanation for the lack of neutrophil influx into the BALF of Gclm −/− mice is that these mice clear the TOPO-PMAT QD more rapidly from their lungs such that a threshold necessary for pro-inflammatory signaling is not achieved. Data from the kinetic modeling analysis would indicate that, indeed, a more rapid clearance of QDs (as indicated by Cd levels in the lung tissue) is evidenced in Gclm −/− mice. The mechanism for enhanced clearance is unknown but may be related to more rapid transit of the QDs out of the lung and into either the pulmonary circulation or the draining lymphatic circulation. QDs are known to accumulate in the lymph system  and while speculative, it may be that the Gclm −/− mice have more motile QD-laden macrophages or more rapid interstitial fluid transport of QD to the thoracic lymph nodes. Regarding direct transport of QD into the circulation, we were unable to find evidence of QD deposition in organs of the reticulo-endothelial system known to sequester QDs such as the liver, spleen, and kidney at any time points examined (data not shown). More rapid mucociliary clearance of the QD from the lungs of Gclm −/− mice may also contribute to enhanced clearance out of the lung and bronchial tree. Indeed, GSH is known to play a pivotal role in gap junctional intercellular communication , , a process important for coordinating ciliary function in respiratory epithelium . Mice lacking GSH may have compensated for the loss of anti-oxidant capacity by up-regulating alternate pathways resulting in more rapid ciliary beat frequency. It is therefore possible that the Gclm −/− mice simply clear QDs via mucociliary transport more rapidly than Gclm +/+ and Gclm +/− mice.
In conclusion, mice with normal or slightly diminished capacity for GSH synthesis are susceptible to the pro-inflammatory potential of TOPO-PMAT exposure via nasal instillation. Because there are relatively common functional genetic polymorphisms in the human GCLM gene that have been associated with partially compromised GSH synthesis capacity, caution is warranted when considering human exposure scenarios to such nanomaterials. Conversely, the attenuated GSH synthesis capacity in Gclm −/− mice is associated with a diminished ability to mount an inflammatory response and/or a more rapid clearance of QDs from the lung. These findings suggest that people with severely compromised GSH status may also fail to respond to such exposures especially if there is up-regulation of compensatory factors similar to those occurring in this mouse model. The mechanisms responsible for this unexpected result are currently under investigation as well as the long term consequences associated with exposure to QDs.
Primers and probes for fluorescent 5′nuclease quantitative PCR assays are provided online in the Supporting Information file.
Conceived and designed the experiments: LAM DB EMF WCP FF XG DLE TJK. Performed the experiments: LAM DB CCW CSW HWW JY RD SEG XH TJK. Analyzed the data: LAM DB WCG SEG EMF TJK. Contributed reagents/materials/analysis tools: XH XG XY WCG. Wrote the paper: LAM CSW HWW WCG SEG DLE TJK.
- 1. Pelley JL, Daar AS, Saner MA (2009) State of Academic Knowledge on Toxicity and Biological Fate of Quantum Dots. Toxicol Sci 112: 276–296. doi: 10.1093/toxsci/kfp188
- 2. Bottrill M, Green M (2011) Some aspects of quantum dot toxicity. Chem Commun (Camb) 47: 7039–7050. doi: 10.1039/c1cc10692a
- 3. Lu HY, Shiao NH, Chan WH (2006) CdSe Quantum Dots Induce Apoptosis via Activation of JNK and PAK2 in a Human Osteoblast Cell Line. J Med Biol Eng 26: 89–96.
- 4. McConnachie LA, White CC, Botta D, Zadworny ME, Cox DP, et al.. (2012) Heme oxygenase expression as a biomarker of exposure to amphiphilic polymer-coated CdSe/ZnS quantum dots. Nanotoxicology.
- 5. Madl AK, Pinkerton KE (2009) Health effects of inhaled engineered and incidental nanoparticles. Crit Rev Toxicol 39: 629–658. doi: 10.1080/10408440903133788
- 6. Ma-Hock L, Brill S, Wohlleben W, Farias PM, Chaves CR, et al. (2012) Short term inhalation toxicity of a liquid aerosol of CdS/Cd(OH)(2) core shell quantum dots in male Wistar rats. Toxicol Lett 208: 115–124. doi: 10.1016/j.toxlet.2011.10.011
- 7. Ho CC, Chang H, Tsai HT, Tsai MH, Yang CS, et al.. (2011) Quantum dot 705, a cadmium-based nanoparticle, induces persistent inflammation and granuloma formation in the mouse lung. Nanotoxicology.
- 8. Prozialeck WC, Edwards JR (2012) Mechanisms of Cadmium-Induced Proximal Tubule Injury: New Insights with Implications for Biomonitoring and Therapeutic Interventions. J Pharmacol Exp Ther.
- 9. Rikans LE, Yamano T (2000) Mechanisms of cadmium-mediated acute hepatotoxicity. J Biochem Mol Toxicol 14: 110–117. doi: 10.1002/(SICI)1099-0461(2000)14:2<110::AID-JBT7>3.0.CO;2-J
- 10. Ghezzi P (2011) Role of glutathione in immunity and inflammation in the lung. Int J Gen Med 4: 105–113. doi: 10.2147/IJGM.S15618
- 11. Coppo L, Ghezzi P (2011) Thiol regulation of pro-inflammatory cytokines and innate immunity: protein S-thiolation as a novel molecular mechanism. Biochem Soc Trans 39: 1268–1272. doi: 10.1042/BST0391268
- 12. Weldy CS, White CC, Wilkerson HW, Larson TV, Stewart JA, et al. (2011) Heterozygosity in the glutathione synthesis gene Gclm increases sensitivity to diesel exhaust particulate induced lung inflammation in mice. Inhal Toxicol 23: 724–735. doi: 10.3109/08958378.2011.608095
- 13. Pellegrino T, Manna L, Kudera S, Liedl T, Koktysh D, et al. (2004) Hydrophobic nanocrystals coated with an amphiphilic polymer shell a general route to water soluble nanocrystals. Nano Lett 4: 703–707. doi: 10.1021/nl035172j
- 14. Bagalkot V, Gao X (2011) siRNA-aptamer chimeras on nanoparticles: preserving targeting functionality for effective gene silencing. ACS Nano 5: 8131–8139. doi: 10.1021/nn202772p
- 15. McConnachie LA, Mohar I, Hudson FN, Ware CB, Ladiges WC, et al. (2007) Glutamate cysteine ligase modifier subunit deficiency and gender as determinants of acetaminophen-induced hepatotoxicity in mice. Toxicol Sci 99: 628–636. doi: 10.1093/toxsci/kfm165
- 16. Gill SE, Huizar I, Bench EM, Sussman SW, Wang Y, et al. (2010) Tissue inhibitor of metalloproteinases 3 regulates resolution of inflammation following acute lung injury. Am J Pathol 176: 64–73. doi: 10.2353/ajpath.2010.090158
- 17. Zhang Y, Huo M, Zhou J, Xie S (2010) PKSolver: An add-in program for pharmacokinetic and pharmacodynamic data analysis in Microsoft Excel. Comput Methods Programs Biomed 99 306–314.
- 18. Bretz F, Hothorn T, Westfall P (2010) Multiple Comparisons Using R. Boca Raton: Chapman and Hall/CRC. 205.
- 19. MacKinnon Y, Kapron CM (2010) Reduction in cadmium-induced toxicity and c-Jun N-terminal kinase activation by glutathione in cultured mouse embryonic cells. Birth Defects Res A Clin Mol Teratol 88: 707–714. doi: 10.1002/bdra.20703
- 20. Wimmer U, Wang Y, Georgiev O, Schaffner W (2005) Two major branches of anti-cadmium defense in the mouse: MTF-1/metallothioneins and glutathione. Nucleic Acids Res 33: 5715–5727. doi: 10.1093/nar/gki881
- 21. Nel A, Xia T, Mädler L, Li N (2006) Toxic Potential of Materials at the Nanolevel. Science 311: 622–627. doi: 10.1126/science.1114397
- 22. Biswas SK, Rahman I (2009) Environmental toxicity, redox signaling and lung inflammation: the role of glutathione. Mol Aspects Med 30: 60–76. doi: 10.1016/j.mam.2008.07.001
- 23. Rahman I, Biswas SK, Jimenez LA, Torres M, Forman HJ (2005) Glutathione, stress responses, and redox signaling in lung inflammation. Antioxid Redox Signal 7: 42–59. doi: 10.1089/ars.2005.7.42
- 24. Villa P, Saccani A, Sica A, Ghezzi P (2002) Glutathione protects mice from lethal sepsis by limiting inflammation and potentiating host defense. J Infect Dis 185: 1115–1120. doi: 10.1086/340042
- 25. Aggarwal S, Dimitropoulou C, Lu Q, Black SM, Sharma S (2012) Glutathione supplementation attenuates lipopolysaccharide-induced mitochondrial dysfunction and apoptosis in a mouse model of acute lung injury. Front Physiol 3: 161. doi: 10.3389/fphys.2012.00161
- 26. Park HS, Jung HY, Park EY, Kim J, Lee WJ, et al. (2004) Cutting edge: direct interaction of TLR4 with NAD(P)H oxidase 4 isozyme is essential for lipopolysaccharide-induced production of reactive oxygen species and activation of NF-kappa B. J Immunol. 173: 3589–3593.
- 27. Finn NA, Kemp LM (2012) Pro-oxidant and antioxidant effects of N-acetylcysteine regulate doxorubicin-induced NF-kappa B activity in leukemic cells. Mol Biosyst 8: 650–662. doi: 10.1039/c1mb05315a
- 28. Kil IS, Kim SY, Park JW (2008) Glutathionylation regulates IkappaB. Biochem Biophys Res Commun 373: 169–173. doi: 10.1016/j.bbrc.2008.06.007
- 29. Hansen JM, Moriarty-Craige S, Jones DP (2007) Nuclear and cytoplasmic peroxiredoxin-1 differentially regulate NF-kappaB activities. Free Radic Biol Med 43: 282–288. doi: 10.1016/j.freeradbiomed.2007.04.029
- 30. Toledano MB, Leonard WJ (1991) Modulation of transcription factor NF-kappa B binding activity by oxidation-reduction in vitro. Proc Natl Acad Sci U S A 88: 4328–4332. doi: 10.1073/pnas.88.10.4328
- 31. Matthews JR, Kaszubska W, Turcatti G, Wells TN, Hay RT (1993) Role of cysteine62 in DNA recognition by the P50 subunit of NF-kappa B. Nucleic Acids Res. 21: 1727–1734. doi: 10.1093/nar/21.8.1727
- 32. Johansson E, Wesselkamper SC, Shertzer HG, Leikauf GD, Dalton TP, et al. (2010) Glutathione deficient C57BL/6J mice are not sensitized to ozone-induced lung injury. Biochem Biophys Res Commun 396: 407–412. doi: 10.1016/j.bbrc.2010.04.105
- 33. Franklin CC, Backos DS, Mohar I, White CC, Forman HJ, et al. (2009) Structure, function, and post-translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase. Mol Aspects Med 30: 86–98. doi: 10.1016/j.mam.2008.08.009
- 34. Siedlinski M, Postma DS, van Diemen CC, Blokstra A, Smit HA, et al. (2008) Lung function loss, smoking, vitamin C intake, and polymorphisms of the glutamate-cysteine ligase genes. Am J Respir Crit Care Med 178: 13–19. doi: 10.1164/rccm.200711-1749OC
- 35. Li Q, Park PW, Wilson CL, Parks WC (2002) Matrilysin shedding of syndecan-1 regulates chemokine mobilization and transepithelial efflux of neutrophils in acute lung injury. Cell 111: 635–646. doi: 10.1016/S0092-8674(02)01079-6
- 36. Gopee NV, Roberts DW, Webb P, Cozart CR, Siitonen PH, et al. (2007) Migration of intradermally injected quantum dots to sentinel organs in mice. Toxicol Sci 98: 249–257. doi: 10.1093/toxsci/kfm074
- 37. Black RA, White JM (1998) ADAMs: focus on the protease domain. Curr Opin Cell Biol 10: 654–659. doi: 10.1016/S0955-0674(98)80042-2
- 38. Horiuchi K, Kimura T, Miyamoto T, Takaishi H, Okada Y, et al. (2007) Cutting edge: TNF-alpha-converting enzyme (TACE/ADAM17) inactivation in mouse myeloid cells prevents lethality from endotoxin shock. J Immunol 179: 2686–2689.
- 39. Upham BL, Kang KS, Cho HY, Trosko JE (1997) Hydrogen peroxide inhibits gap junctional intercellular communication in glutathione sufficient but not glutathione deficient cells. Carcinogenesis 18: 37–42. doi: 10.1093/carcin/18.1.37
- 40. Hu J, Cotgreave IA (1995) Glutathione depletion potentiates 12-O-tetradecanoyl phorbol-13-acetate(TPA)-induced inhibition of gap junctional intercellular communication in WB-F344 rat liver epithelial cells: relationship to intracellular oxidative stress. Chem Biol Interact 95: 291–307. doi: 10.1016/0009-2797(94)03568-S
- 41. Sanderson MJ, Chow I, Dirksen ER (1988) Intercellular communication between ciliated cells in culture. Am J Physiol 254: C63–74.
- 42. Smith WE, Brownell J, White CC, Afsharinejad Z, Tsai J, et al. (2012) In Vitro Toxicity Assessment of Amphiphillic Polymer-Coated CdSe/ZnS Quantum Dots in Two Human Liver Cell Models. ACS Nano 6: 9475–9484. doi: 10.1021/nn302288r