Pulmonary exposure to carbon black nanoparticles and vascular effects
© Vesterdal et al; licensee BioMed Central Ltd. 2010
Received: 28 May 2010
Accepted: 5 November 2010
Published: 5 November 2010
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© Vesterdal et al; licensee BioMed Central Ltd. 2010
Received: 28 May 2010
Accepted: 5 November 2010
Published: 5 November 2010
Exposure to small size particulates is regarded as a risk factor for cardiovascular diseases.
We exposed young and aged apolipoprotein E knockout mice (apoE -/- ) to carbon black (Printex 90, 14 nm) by intratracheal instillation, with different dosing and timing, and measured vasomotor function, progression of atherosclerotic plaques, and VCAM-1, ICAM-1, and 3-nitrotyrosine in blood vessels. The mRNA expression of VCAM-1, ICAM-1, HO-1, and MCP-1 was examined in lung tissue.
Young apoE -/- mice exposed to two consecutive 0.5 mg/kg doses of carbon black exhibited lower acetylcholine-induced vasorelaxation in aorta segments mounted in myographs, whereas single doses of 0.05-2.7 mg/kg produced no such effects. The phenylephrine-dependent vasocontraction response was shifted toward a lower responsiveness in the mice exposed once to a low dose for 24 hours. No effects were seen on the progression of atherosclerotic plaques in the aged apoE -/- mice or on the expression of VCAM-1 and ICAM-1 and the presence of 3-nitrotyrosine in the vascular tissue of either young or aged apoE -/- mice. The expression of MCP-1 mRNA was increased in the lungs of young apoE -/- mice exposed to 0.9-2.7 mg/kg carbon black for 24 hours and of aged apoE -/- mice exposed to two consecutive 0.5 mg/kg doses of carbon black seven and five weeks prior to sacrifice.
Exposure to nano-sized carbon black particles is associated with modest vasomotor impairment, which is associated neither with nitrosative stress nor with any obvious increases in the expression of cell adhesion proteins on endothelial cells or in plaque progression. Evidence of pulmonary inflammation was observed, but only in animals exposed to higher doses.
The development of nanotechnology has increased attention to the possible toxicological effects of nanoparticles. Among the many possible effects, cardiovascular outcomes are considered important, because exposure to ambient particulate matter elevates the risk of cardiovascular disease and mortality in epidemiological studies [1–4]. Even though nanoparticles only account for a small volume of the total mass of particles , it is believed that their large surface area and number concentration make them an important contributor to these health effects [5, 6]. Particulate matter in the small size range have previously been shown to induce altered activity of the fibrinolytic system, a procoagulant state, and endothelial dysfunction and cardiac effects [6–8]. Hallmarks of initial events in atherogenesis include the expression of cell adhesion molecules on the surface of the endothelium, inflammation, and endothelial dysfunction [9, 10]. Endothelial dysfunction is an early sign of atherosclerosis  and it is believed to be an event that leads to atherosclerosis as well as being a marker of the severity of it . The endothelium plays an important role in maintaining the vascular homeostasis by producing vasoactive factors, that regulate the tone of the vascular system in response to cell surface receptor stimulation or mechanical stress . Moreover, the endothelium is an important factor in the regulation of vascular inflammation and thrombosis . In experimental settings, the vasomotor function can be assessed as endothelial dependent (acetylcholine) or independent (sodium nitroprusside) vasorelaxation or as receptor dependent vasocontraction (phenylephrine). In apolipoprotein E knockout mice (apoE -/- ), which are deficient in apolipoprotein E and represent a model for atherosclerosis in humans, vasomotor function is inversely correlated with plaque-size, whereas it is not affected by hypercholesterolemia . It has been shown that in apoE-/- mice, the acetylcholine-induced vasorelaxation was decreased and the phenylephrine-induced maximal vasocontraction was enhanced after 5 months inhalation exposure to concentrated air pollution particles [14, 15]. A number of studies have shown acute effects of particle exposure on vasomotor function. For instance, ultrafine TiO2 particles were more potent in inducing systemic microvascular dysfunction in rats than fine TiO2 particles after inhalation of doses with minimal pulmonary effects . Furthermore, we have shown that systemic exposure to diesel exhaust particles or C60 fullerenes by intraperitoneal injection reduced acetylcholine-elicited vasorelaxation in apoE-/- mice with a mild degree of atherosclerosis, whereas opposite effects were seen in wild type mice [17, 18]. Research concerning the effects of nanosized carbon black (CB) particles on vasomotor function is, however, still very sparse. Nanosized CB is widely used as a component in rubber and as a pigment in paints and inks  and it is therefore considered likely that people employed in the manufacture of these product are exposed to nanosized CB. Most CB particles including Printex 90 consist of pure carbon and do not contain adhered polycyclic aromatic hydrocarbons as for instance DEP [20, 21]. A number of studies show that airway exposure to concentrated ambient particles and single wall carbon nanotubes promotes the progression of atherosclerosis in apoE-/- mice [22–24]. Similarly, pulmonary exposure to nano-sized CB is associated with accelerated plaque area development in the aorta of low-density lipoprotein receptor knockout mice which are also predisposed to develop atherosclerosis . In addition, studies investigating the effects of exposure to particulate matter in the form of air pollution or diesel exhaust particles have shown an increased area of atherosclerotic plaques in the aorta of Watanabe heritable hyperlipidemic rabbits [26, 27].
The purpose of the present study was to investigate the concentration-response and timing of effects of single and repeated intratracheal (i.t.) instillations with CB nanoparticles at different time points after exposure of apoE-/- mice, which exhibited either a mild or a more severe degree of atherosclerosis. We chose Printex 90 CB which is very well characterised, widely studied for other endpoints than vascular function and may serve as benchmark for carbon based nanoparticles with environmental and occupational health relevance. The effects on vasomotor function were assessed in young apoE -/- mice (11-13 weeks) as we have previously shown that the vasomotor function was severely impaired in aged apoE-/- mice . The effects on progression of atherosclerosis were assessed in aged apoE -/- mice (48-49 weeks) in which a substantial amount of plaques had developed. We assessed the expression of vascular adhesion molecule (VCAM-1) and intercellular adhesion molecule (ICAM-1) on the endothelium as well as the presence of 3-nitrotyrosine in the vascular tissue. VCAM-1 and ICAM-1 are markers of the immune cell recruitment which is an early event in atherosclerotic plaque formation [28, 29] and 3-nitrotyrosine is a biomarker of peroxynitrite . Moreover, the gene expression of VCAM-1 and ICAM-1 as well as macrophage/monocyte chemoattractant protein 1 (MCP-1) and heme oxygenase 1 (HO-1) was assessed in lung tissue. MCP-1 and HO-1 were assessed as markers of inflammation and oxidative stress, respectively.
EC50 and Emax values of concentration-response curves
Exposure to carbon black
24 + 2 hours
2 × 0.0 mg/kg
2 × 0.5 mg/kg
We found no significant correlation between the relative precontraction tension and the maximal acetylcholine-induced vasorelaxation (Spearman, r = -0.21, P = 0.11). This indicates that the observed decrease in acetylcholine-induced vasorelaxation in the CB exposed mice cannot be attributed to differences in relative precontraction tension.
The results obtained in the present study show an effect on vasomotor function in aorta of apoE-/- mice after i.t. instillation with CB. This alteration occurred without overt differences in expression of vascular endothelial cell adhesion proteins and nitrosative stress in the endothelium, but to a certain extent with increases in pulmonary inflammation.
The altered response to acetylcholine-induced vasorelaxation in the particle-exposed group, with unaltered sodium nitroprusside-induced response, suggests that endothelial NO availability, rather than the smooth muscle sensitivity to or extracellular consumption of NO, is affected by the pulmonary exposure to CB. The same type of effect has been observed for TiO2 particles [16, 31]. This effect could come about by either decreased NO production or quenching of NO by excessive production of reactive oxygen species in the endothelium. In addition, acetylcholine also induces vasorelaxation through other mechanisms (e.g. cyclooxygenase) and future studies are needed to determine these differences. The mechanisms could be pursued in future studies with focus on the NO system and oxidative stress, including animal pretreatment with e.g. eNOS cofactors, anti-inflammatory or antioxidant compounds and addition of similar compounds to vessel segments. Studies of vasomotor function in the aorta of apoE -/- mice have shown that the mechanisms of endothelial dysfunction involved depletion of NO by reaction with superoxide anion radicals as well as decay of tetrahydrobiopterin by peroxynitrite [32, 33]. The uncoupling of eNOS is characterized by a biochemical vicious circle in which eNOS begins to generate peroxynitrite and then gradually shifts towards only generating superoxide anion radicals . Evidence of eNOS uncoupling has been observed in cardiac tissue of mice exposed to CB by inhalation . There is also evidence that exposures to diesel exhaust and concentrated air pollution particles are associated with eNOS uncoupling in endothelial cells and vasomotor dysfunction [36, 37]. Excessive production of peroxynitrite can be assessed as increased production of 3-nitrotyrosine residues on proteins . In the present study no dose-dependent increase in intensity of 3-nitrotyrosine staining in aorta and BCA vessels was observed. It is possible that the duration of the exposure may have been too short to allow sufficient accumulation of 3-nitrotyrosine residues on proteins. In contrast, clear evidence of 3-nitrotyrosine staining as well as accelerated plaque progression was observed in a study of 6 months exposure to concentrated air pollution particles .
The decreased endothelium-dependent acetylcholine response was only observed in the apoE -/- mice exposed to two successive i.t. instillations of CB, whereas the response was unaffected both 2 hours and 24 hours after a single instillation. This indicates that repeated exposures of small doses of CB are more important than a single large dose in the generation of endothelial impairment in apoE -/- mice. Whether this effect might be attributed to a translocation of CB nanoparticles from the lungs to the vascular system is unknown. Translocation of ultrafine particles to the systemic circulation after i.t. instillation has been demonstrated in a number of studies [39, 40], although the translocated fraction of the dose is usually less than 1% in studies of single pulmonary exposure to model particles . However, there are a number of variables that may have caused increased translocation of particles in our study: 1) i.t. instillation of CB has been shown to induce lung inflammation and increased alveolar-capillary permeability in wild type mice , 2) apoE -/- mice have compromised vascular permeability [43, 44], 3) lipopolysaccharide-induced pulmonary inflammation has been shown to increase the translocation of subsequent particle exposure , 4) i.t. instillation of CB has been associated with a larger inflammatory response in apoE -/- mice than in wild type mice . It is thus possible that inflammation of the lungs caused by the first exposure to CB particles might in a similar manner have increased the translocation of the second dose of particles into the bloodstream leading to a significant effect on vasomotor function. Previously, we have shown that i.t. instillation of 18 or 54 μg/mouse of CB in apoE -/- mice was associated with increased expression of MIP-1, MCP-1, and IL-6 inflammatory markers in lung tissue after 3 hours and influx of neutrophils in bronchoalveolar fluid 24 hours after the exposure . The MCP-1 expression levels were 18 and 38-fold increased in lung tissue 24 hours after the instillation . In the present study, the same doses were associated with 10 and 23-fold increased MCP-1 expression levels in the lung tissue. The doses of 18 and 54 μg/mouse correspond to the doses of 0.9 and 2.7 mg/kg used in the present study. Alternatively, pulmonary inflammation has been demonstrated to induce systemic effects such as promoting the development of atherosclerosis . However, in the present study we found increased expression of MCP-1 only in the young mice exposed to the two highest doses of CB for 24 hours and not in the mice exposed to the low doses or exposed twice. This suggests that the effects on endothelial function cannot in this case be attributed to pulmonary inflammation.
In contrast to earlier studies on diesel exhaust particles and C60 fullerenes [17, 18], we did observe altered function of phenylephrine-induced vasocontraction. The effect was a relatively small shift towards an increased responsiveness for the mice exposed for 24 hours to the two lowest doses of CB. However, this effect was not seen for any of the other exposure groups. The observed effect is in agreement with the hypothesis that oxidative stress could have altered the signalling pathways of the cells and decreased the bio-availability of NO. This would increase the ability of the blood vessels to contract. Printex 90 does indeed generate high levels of reactive oxygen species [48–50]. However, we did not detect any increases in HO-1 (oxidative stress) in the lung tissue of any of the exposure groups. The vasomotor impairment is therefore unlikely to have been caused by systemic effects secondary to oxidative stress in the lungs.
The expression of adhesion molecules on the surface of endothelial cells is considered a hallmark in atherogenesis where they are localized to sites for plaque formation . VCAM-1 is expressed mainly in plaques and is considered particularly important in early foam cell formation, whereas ICAM-1 is more widely expressed both in plaques and in non-plaque areas [52, 53]. Still, we found no convincing evidence of increased gene or protein expression of VCAM-1 and ICAM-1 in the CB exposed animals. Studies on microarray analysis of endothelial cell cultures exposed to CB have shown upregulation of both ICAM-1 and VCAM-1 . Increased ICAM-1 and VCAM-1 expression has also been observed in rabbit aorta tissue after exposure to air pollution particles by i.t. instillation . Another study has shown increased VCAM-1 staining in BCA vessels of apoE -/- mice after pulmonary exposure to single-walled carbon nanotubes . Interestingly, both studies used repeated pulmonary exposures and also observed accelerated progression of atherosclerosis. In the present study, the staining for ICAM-1 and VCAM-1 was more pronounced in blood vessels of the aged apoE -/- mice compared to the young mice, although it should be emphasized that it was not the same type of blood vessel that was investigated in the two age groups. Still, we take these observations as evidence proving technical ability to detect expression of ICAM-1 and VCAM-1. The unaltered expression of ICAM-1 and VCAM-1 corresponds well with the unaltered ICAM-1 and VCAM-1 mRNA levels in the CB exposed mice of either age group as well as the unchanged progression of atherosclerosis in the aged CB exposed mice. This suggests that the doses may have been too small to elicit changes in progression of atherosclerosis. However, the aged mice did exhibit a significant increase in MCP-1 in the lungs indicating that, 5 weeks after the last CB instillation, pulmonary inflammation persisted. Our original aim was to use the same exposure scenario as Li et al. used in their study of single-walled carbon nanotubes, which was one instillation every other week for eight weeks . However, a number of the apoE -/- mice died after each i.t. instillation and the exposures were therefore discontinued after the second instillation, corresponding to 5 and 7 weeks prior to sacrifice. It is possible that pulmonary exposure to CB in younger apoE -/- mice on chow or Western diet would have been associated with progression of plaques as accelerated plaque progression has been shown in LDLr knockout mice after expose to CB by i.t. dispersion once a week for ten weeks .
Here we show that exposure to CB particles with a primary nano-size diameter is associated with modest vasomotor impairment in dyslipidemic apoE -/- mice. Repeated exposures of small doses of CB is more important that a single large dose in the generation of endothelial impairment in apoE -/- mice. The vasomotor impairment is associated neither with nitrosative stress nor with obvious increases in expression of cell adhesion proteins on endothelial cells or in plaque progression. Evidence of pulmonary inflammation was observed, but it was only for animals exposed to higher doses. Even though a direct comparison to humans cannot be drawn, these findings could indicate that pulmonary exposure to CB nanoparticles may be associated with vasomotor impairment in susceptible individuals.
The apoE-/- (C57BL/6-Apoe tm1) mice were purchased from Taconic MB (Ejby, DK) at the age of 5-8 weeks and were all female. They were housed in cages with a 12 hour day-night cycle and were provided with unlimited access to standard mouse chow (Standard Altromin no.1314, Lage, DE) and tap water. The apoE-/- mice were exposed to CB at the age of 11-13 (young) or 48-49 (aged) weeks. Institutional guidelines for animal welfare were followed and the Danish Ethical Committee for Animal Studies approved the animal experiments.
The nanosized CB particles were chosen for this study because they are well characterized and have been used in research of other end points than vascular function. These include inflammation and DNA damage in the lungs of apoE -/- mice following instillation  as well as apoptosis, cytokine release, and genotoxicity in cell culture [57–59]. The CB (Printex 90) was a gift from Evonik Degussa GmbH (Frankfurt, DE) (primary particle size 14 nm; surface area 300 m2/g). For the i.t. instillations, the particles were suspended by sonication in vehicle using a Branson Sonifier S-450D (Branson Ultrasonics Corp., Danbury, CT, USA) equipped with a disruptor horn (Model number: 101-147-037). The vehicle consisted of 90% sterile, isotonic saline and 10% bronchoalveolar lavage fluid. The latter was prepared by flushing the lungs of unexposed apoE-/- mice twice with 0.6 ml isotonic saline. The particle suspensions were sonicated on ice. The Branson Sonifier was operated under the following settings: total sonication time 15 min, alternating with a 55 s pulse ON and a 5 s pause and amplitude of 10%. Control solutions were prepared containing 90% isotonic saline and 10% bronchoalveolar fluid from apoE-/- mice. The suspensions were divided in aliquots and immediately frozen at -80°C until use. The suspensions were thawed at room temperature prior to use. We have used the same type of suspension of CB in this and an earlier study on pulmonary toxicity of particles in apoE -/- mice; the suspension of CB in the instillation solution exhibited a bimodal size-distribution with frequent peaks at 1.2 and 5.5 μm by dynamic light scattering . The animals that were used in the present study were different than the mice that were used in the study by Jacobsen et al , but the preparation and instillation of the particle suspensions were carried out using the same protocol.
The young apoE-/- mice were exposed to CB by i.t. instillation. One group received 0, 0.05, 0.5, 0.9 or 2.7 mg/kg bodyweight of CB and was sacrificed 24 hours later (n = 8-17). The second group received either 0 or 0.9 mg/kg bodyweight of CB and was sacrificed 2 hours later (n = 5-9) or two doses of 0 or 0.5 mg/kg bodyweight of CB 24 hours apart and was sacrificed 2 hours after the second exposure (n = 4-7). The aged mice received two doses of 0 or 0.5 mg/kg bodyweight of CB two weeks apart and were sacrificed 7 weeks after the first exposure (n = 11). After administration of CB, the mice were euthanized under general anaesthesia with Hypnorm-Dormicum by opening the thoracic cavity. The heart and aorta were carefully removed and placed in ice cold oxygenated physiological saline solution (PSS) and the surrounding connective tissue was removed.
We used the doses of CB in the range of 0.05-2.7 mg/kg because we have previously shown that exposures to other types of particulate matter, especially diesel exhaust particles, generate oxidatively damaged DNA in lung tissue by i.t. instillation or inhalation [60, 61]. In addition, we used 0.5 mg/kg as daily dose because this dose had been used in a previous study on plaque progression in mice exposed to single walled carbon nanotubes . In perspective, the daily dose of CB in the working environment can be as large as 0.12 mg/kg, assuming a threshold limiting value (TLV) for respirable CB of 2.5 mg/m3, 60% deposition, an average weight of a person of 70 kg, an 8 hour work day, and a respiratory volume of 0.7 m3 pr. hour. The lowest of the applied doses was below this calculated value, and the remaining doses were increasingly above it.
To the best of our knowledge, no threshold limit value for CB in ambient air exists. However, the future air quality standard in the European Union for PM2.5 (25 μg/m3) indicates that the daily dose would be 3.6 μg/kg, which is more than one order of magnitude lower than the lowest dose in our study.
The aorta from each of the young mice was cut in segments of approximately 1.5 mm in length starting from immediately after the three large side branches of the aortic arch. Three segments were obtained from each of the apoE-/- mice exposed to the different concentrations of CB. The segments were mounted on steel pins with a diameter of 150 μm in the organ baths of the multi myograph 610M (Danish Myo Technology, Aarhus, DK) containing 5 ml cold oxygenated PSS continuously perfused with a 95% O2 and 5% CO2 gas mixture. The order in which the aorta segments were mounted in the organ baths was randomized with regard to exposure-group. The myograph was connected to a computer and the data were processed by the PC-program Myodaq (Danish Myo Technology, Aarhus, DK). The measurements of vasomotor function were carried out as previously described .
X is the logarithm of concentration and Y is the response. Y starts at Bottom and goes to Top with a sigmoid shape. The data points on each curve are expressed as mean ± SEM.
The aorta extending from the heart to the iliac arteries from each of the aged mice was cut longitudinally and placed with the intimal surface facing upwards on an objective glass with a few drops of PSS. The aorta was then carefully flattened by adding a cover slip while avoiding any folds or overlap of the vascular tissue. Digital images were obtained of the intimal surface of the aorta by means of an Olympus SZX7 stereo microscope and an Olympus Color View I camera. The level of atherosclerosis in the aorta was measured on the digital images with the public domain Java image processing program ImageJ.
The heart and aortic root from each of the young mice and a segment of the brachiocephalic artery (BCA) from each of the aged mice were embedded in Tissue-Tek® O.C.T.™ Compound (Sakura Finetek, Værløse, DK) and frozen on dry ice. Frozen 4 μm sections of the aortic root or BCA from the young or aged mice, respectively, were obtained on a CM3050 S-Cryostat (Leica Microsystems Nussloch GmbH, DE) and mounted on Super Frost + slides (Hounisen Laboratory Equipment, Risskov, DK). The mounted sections were fixed in 100% acetone and the endogenous peroxidase activity was blocked with Dako REAL™ Peroxidase-Blocking Solution (Dako, Glostrup, DK). ICAM-1 and VCAM-1 protein expression and the presence of 3-nitrotyrosine was visualized by means of biotin-conjugated antibodies, streptavidin horse radish peroxidase (HRP) (1:500) (Dako, Glostrup, DK) and 3,3'-diaminobenzidine (DAB) (1:50) (Dako, Glostrup, DK). The antibodies used were purified hamster anti-mouse CD54 (ICAM-1) monoclonal antibody (1:100) (BD Biosciences, Brøndby, DK) and biotin-conjugated mouse anti-hamster cocktail (1:100) (Biosciences, Brøndby, DK), biotin-conjugated rat anti-mouse CD106 (VCAM-1) monoclonal antibody (1:100) (BD Biosciences, Brøndby, DK) and biotin-conjugated goat anti-Nitro tyrosine polyclonal antibody (1:100) (Abcam, Cambridge, UK). Furthermore the sections were counterstained with Mayer's Haematoxylin. Finally the slides were fixed with cover slips using pertex mounting medium (Sakura Finetek, Værløse, DK). Sections of wild type rat spleen or aged apoE-/- aorta, incubated with or without primary antibody, were used as positive and negative controls, respectively.
The slides were examined by means of an Olympus BX41TF-5 microscope and digital images were obtained with a ColorView I camera (Olympus Denmark A/S, Ballerup, DK) at 10× magnification.
The digital images were coded before being scored by an investigator who had not carried out the experiments and had no knowledge of which groups the depicted blood vessels belonged to. A semiquantative analysis of the images was carried out by visually scoring the intensity of the staining. The intensity of ICAM-1 and VCAM-1 staining in the young mice was scored as follows: 1) little staining, 2) few spots of staining in the endothelium, 3) strong staining of spots or long patches of staining in the endothelium, 4) strong staining of long patches of the endothelium. The blood vessels of the old mice were generally more intensively stained in both endothelium and intima; these images were scored according to the intensity in the endothelium. The 3-nitrotyrosine staining was scored as follows: 1) little staining, 2) slight staining near the endothelium, 3) staining in the intima, 4) strong staining in the intima. The images of at least 2-4 sections of blood vessels for each animal were scored and a mean score for each animal was calculated. The data are reported as the ranked intensity. Because there was overt difference in the staining of tissue from the young and old animals, the staining of the blood vessels from the respective ages were scored separately. The slides that were used for staining of ICAM-1, VCAM-1 and 3-nitrotyrosine were also used to determine the level of atherosclerosis in the BCA vessel by means of the program ImageJ.
The mRNA was extracted from lung tissue samples using the TRIzol reagent (Invitrogen, Carlsbad, CA, USA). Approximately 50-100 μg frozen tissue from each sample was added to 1 ml TRIzol and homogenized. The samples were incubated at room temperature for 5 min before adding 0.2 ml chloroform and centrifuging at 12.000 rcf for 15 min. The supernatant was transferred to a new tube and the mRNA was precipitated with 0.5 ml isopropanol. The samples were incubated at room temperature for 10 min before centrifuging at 12.000 rcf for 10 min. The supernatant was discarded and the pellet was washed in ice cold 75% ethanol followed by centrifugation at 7.600 rcf for 5 min. The ethanol was discarded and the pellet was allowed to air dry shortly. The pellet was resuspended in 30 μl RNase free water by incubation at 55°C for 10 min.
The extracted mRNA samples were DNase treated using the RQ1 RNase-Free DNase kit (Promega, Madison, WI, USA). For each sample of 4 μl mRNA a stock solution containing 10 μl RNase free water, 4 μl DNase and 2 μl DNase buffer was added and the samples were incubated at 37°C for 30 min. 2 μl stop buffer was added and the samples were incubated at 65°C for 10 min.
The total mRNA was converted into cDNA by reverse transcriptase polymerase chain reaction by using the High Capacity cDNA Transcription Kit (Applied Biosystems, Calsbad, CA, USA). For each sample containing 150 ng mRNA in 10 μl, a stock solution containing 2 μl RT buffer, 0.8 μl dNTP mix, 2 μl Random Primers, 4.2 μl RNase free water and 1 μl Reverse Transcriptase was added. The samples were cycled at 25°C for 10 min, 37°C for 120 min, 85°C for 5 min and maintained at 4°C for a short period until storage at -20°C. A negative control with no Reverse Transcriptase was included in each run.
The quantification of gene expression was determined by real-time PCR using the Taqman® gene expression assay. The primers used were: VCAM-1 (NM_011693.3), ICAM-1 (NM_010493.2), HO1 (NM_010442.2), MCP-1 (NM_011333.3) and as endogenous control: eukaryotic 18S rRNA (X03205.1), (Applied Biosystems). All samples were determined as triplicates of a stock solution containing 14.88 μl RNase free water, 18.75 μl Taqman® Fast Universal PCR Master Mix (Applied Biosystems), 1.8 μl cDNA and 1.8 μl primer.
The standard curves for the primers were generated with 10 steps of 2× dilution starting from 10 μl cDNA.
The level of mRNA expression normalized to the level of 18S rRNA was calculated as 2-ΔCt. The relative mRNA levels in the exposure groups were standardized in order to obtain fold increases in mRNA level relative to the level in the control groups.
The data on vasomotor function were analyzed by ANOVA with unequal variance, as the exposure groups did not exhibit homogeneity of variance. The curve fittings were carried out in GraphPad Prism 4 and the Emax and EC50 with corresponding 95% confidence intervals (CI) were calculated. Differences between groups with non-overlapping 95% CI were considered statistically significant at P < 0.05 level. The data on plaque progression, expression of adhesion molecules and presence of 3-nitrotyrosine, and expression of mRNA were assessed by non-parametric one-way ANOVA (Mann-Whitney U-test or Kruskall-Wallis test) with post-hoc Tukey-type multiple comparison test for effects showing statistical significance in the overall ANOVA test. Statistical significances were tested at P < 0.05 level. The differences in relative precontraction tension between exposure groups were analyzed by One-Way ANOVA (24 hours) or Two-Sample t-Test (2 hours and 24+2 hours). The association between relative precontraction tension and the maximal acetylcholine-induced vasorelaxation was assessed by Spearman correlation. The statistical analyses were performed in Statistica version 5.5 (StatSoft Inc., Tulsa, OK, USA) and SAS version 9.2 (SAS Institute Inc., Cary, NC, USA).
apolipoprotein E knockout
endothelial nitric oxide synthase
heme oxygenase 1
horse radish peroxidase
inter-cellular adhesion molecule 1
macrophage/monocyte chemoattractant protein 1
physiological saline solution
standard error of the mean
vascular cell adhesion molecule 1
This work was supported by The European Union (grant FP6-012912, NEST), Particle Risk and The Danish Research Council (grant 2052-03-0016), Air pollution in a life time health perspective (Airpolife).
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