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Challenges 2013, 4(2), 188-200; doi:10.3390/challe4020188
Published: 29 August 2013
Abstract: Chronic exposure to particulate pollution is suspected to exacerbate inflammatory respiratory diseases such as asthma characterized by an airway remodelling involving fibrosis. Our study aims to investigate whether the secretome from human bronchial epithelial (HBE) cells exposed to fine particulate matter (PM) induces fibroblast proliferation. Primary HBE cells grown on air liquid interface were repeatedly exposed to fine PM at 5 and 10 µg/cm² (four treatments, 48 hours apart) and maintained in culture for five weeks. Collected basolateral culture medium was used as a conditioned medium for the subsequent treatment of fibroblasts. We observed that the conditioned medium collected from HBE cells treated with fine PM increased the growth rate of fibroblasts compared to the conditioned medium collected from control HBE cells. Fibroblast phenotype assessed by the observation of the vimentin network was well preserved. The mitogenic effect of conditioned medium was reduced in the presence of anti-epidermal growth factor receptor (EGFR), anti-amphiregulin or anti-TGFα, underlining the role of EGFR ligands in fibroblast proliferation. When fibroblasts were co-cultured with HBE cells treated once with fine PM, they exhibited a higher growth rate than fibroblasts co-cultured with non-treated HBE cells. Altogether these data show that the exposure of HBE cells to fine PM induced the production of EGFR ligands in sufficient amount to stimulate fibroblast proliferation providing insight into the role of PM in airway remodelling.
For several decades, air pollution has been considered a serious public health threat requiring the implementation of regulations to limit gaseous and particulate pollution. Particularly, in the European population, fine particulate matter (PM2.5) has been responsible for the reduction of life expectancy of more than 8 months  due to cardiovascular and respiratory diseases. Long term exposure to PM is suspected to exacerbate pre-existing diseases such as asthma that are characterized by chronic inflammation and airway remodeling consisting of airway wall thickening due to excessive mucus production, collagen deposition and hyperplasia of smooth muscle cells. Airway epithelium is considered to play a critical role in asthma pathogenesis due to alteration in its physical and functional barrier properties .
Our previous studies showed that bronchial epithelium responds to fine and ultrafine PM exposure by releasing pro-inflammatory mediators as well as epidermal growth factor receptor (EGFR) ligands such as amphiregulin and transforming growth factor alpha (TGFα) [3,4], that are also found in high amounts in the sputum of asthmatics . Moreover we demonstrated that EGFR ligands have an autocrine effect on the epithelium leading to a sustained pro-inflammatory response and mucus production [6,7]. The increased EGFR ligands expression induced by PM exposure could also act as a potent mitogenic factor for fibroblasts as some experimental studies have implicated EGFR signaling in pulmonary fibrosis . Amphiregulin have been shown to induce fibroblast proliferation [9,10].
Altogether these data led us to hypothesize that the epithelial secretion induced by PM exposure could trigger fibroblast proliferation and differentiation, supporting assumptions that airway epithelium could play a key role in PM-induced airway remodeling. Evidence of the induction of airway remodeling by PM is scarce but it was demonstrated that the exposure of tracheal explants to PM increased the expression of genes involved in fibrogenesis such as pro-collagen 1, hydroxyproline and TGFβ . Contributing to airway remodeling, chronic exposure to PM could favor airflow obstruction in compromised people living in cities with high levels of PM. We took advantage of an experimental model, the primary culture of normal bronchial epithelial (HBE) cells grown at the air-liquid interface (ALI), which we developed for repeated exposures to PM , to investigate the effects of the epithelial secretome on fibroblasts. For this purpose two different approaches were used. Fibroblasts were either exposed to conditioned media coming from HBE cells repeatedly exposed to fine PM or were co-cultured with HBE cells that were exposed to fine PM.
2. Results and Discussion
2.1. Effects of Repeated Exposure to Fine Particles on the Release of EGFR Ligands by Bronchial Epithelium
In order to test our hypothesis of a potential paracrine effect of epithelial secretome on lung fibroblasts, Wi-38 cells were exposed to basal culture media recovered when HBE cells were repeatedly exposed to fine PM as well as to basal culture media recovered in the weeks following the end of treatments. Figure 1 continues with part of the results we previously showed  and, is shown to remind us of the characteristics of the conditioned culture media we used in the present study. Treatments were performed on undifferentiated HBE cells just after they started to be grown at the air-liquid interface (ALI). Four treatments, 48 hours apart, were done on the apical side of HBE cells and the release of EGFR ligands in the basal medium was measured by ELISA 48 hours after each treatment. We observed an increased and a dose-dependent release of two EGFR ligands (amphiregulin and TGF α) in PM-exposed cells compared to control cells after each treatment. The basal media collected during this treatment period were pooled for every condition in order to provide enough conditioned culture media to perform experiments with fibroblasts. At the end of the treatment period, cultures were maintained for the five following weeks and basal culture media were recovered and pooled for every week. We noticed no difference between control and PM-treated cultures considering the amphiregulin (Figure 1a) and TGFα (Figure 1b) release that were also less important as the culture was differentiating.
2.2. Effect of Conditioned Medium on Fibroblast Proliferation
The ability of the secretome produced by PM-treated HBE cells to promote lung fibroblast proliferation was investigated by counting cells after 48‑72 hours of treatment with conditioned culture media from control and PM-treated HBE cells as well as with fresh bronchial epithelial growth medium (BEGM), the culture medium used to cultivate HBE cells. In Figure 2 we only reported results obtained with Wi-38 cells exposed to conditioned media from HBE cells recovered during the treatment period, as those recovered during the post-treatment period had no effect. Wi-38 cells exposed to conditioned medium from control HBE cells exhibited two doublings of the cell population at 48 hours but the growth rate decreased at 72 hours compared to cells exposed to fresh BEGM medium suggesting that the proliferation cannot be sustained due to nutrient depletion (Figure 2a). Wi-38 cells exposed to conditioned medium from fine PM-treated HBE cells showed a significantly higher growth rate than Wi-38 cells exposed to conditioned medium from control HBE cells suggesting the presence of a sufficient amount of growth factors to promote cell proliferation. The growth rate was similar to the one induced by fresh BEGM medium for all used concentrations of fine PM-treatment at 48 hours. But it decreased at 72 hours with a significant effect only for the conditioned medium from HBE cells treated with fine PM at 10 µg/cm². These data suggest a growth factor/nutrient depletion over time (Figure 2a). The decrease of growth rate for fibroblasts grown in conditioned medium recovered from HBE cells treated with fine PM at 5 µg/cm² was not associated with cell death as viability was 88% whereas for cells grown in conditioned medium recovered from control HBE cells it was lower (76%) (Figure 2b).
Moreover immunolabeling of vimentin network was performed on fibroblasts exposed to conditioned media for 72 hours in order to appreciate fibroblast phenotype. Figure 3 shows the characteristic vimentin network in fibroblasts when grown with fresh BEGM (Figure 3a and b), while it was disrupted in fibroblasts grown with the conditioned medium from control HBE cells (Figure 3c and d), likely reflecting nutrient deficiencies in this conditioned medium emphasized by the decrease of growth rate (Figure 2a). By contrast, fibroblasts grown with conditioned medium from treated-HBE cells (Figure 3e to 3h) exhibited an intermediate situation.
Altogether these experiments showed that conditioned media from fine PM-treated HBE cells improved the growth rate and preserved vimentin cytoskeleton of lung fibroblasts suggesting the presence of growth factors in conditioned media that could contribute to fibroblast proliferation.
2.3. Role of EGFR Ligands on Fibroblast Proliferation
Among growth factors with a mitogenic effect on fibroblasts, EGFR ligands such as amphiregulin have been shown to induce fibroblast proliferation [9,10]. To determine whether EGFR ligands, especially TGFα and amphiregulin, which we had proved to be present in conditioned media, were involved in fibroblast proliferation, we exposed WI-38 cells to conditioned media supplemented or not with anti-EGFR (preventing the binding of EGFR ligands to the receptor), anti-amphiregulin, anti-TGFα or an anti-mouse IgG as an unspecific antibody. As shown in Figure 4, the presence of any of these antibodies modulated the growth rate of WI-38 cells treated with conditioned medium from control HBE cells. The significant increase of growth rate for Wi-38 cells exposed to conditioned media from fine PM-treated HBE cells at 5 and 10 µg/cm² was abolished when anti-EGFR was added in conditioned media but not when a control antibody (IgG) was used, underlying the involvement of EGFR and its ligands in fibroblast proliferation. In order to identify which EGFR ligand could be involved in Wi-38 proliferation, the experiment was also performed in the presence of anti-TGFα or anti-AREG in the conditioned medium. The mitogenic effect was significantly reduced whatever the antibody used and whatever the conditioned medium from fine PM treated HBE cells.
Altogether these results suggest that amphiregulin and TGFα present in the secretome of treated HBE cells could contribute to fibroblast proliferation.
2.4. Effect of Different Particle Size on Fibroblast Proliferation
Health effects of ambient PM are related to their size: the finest ones can go deeper in the lungs and their chemical composition is different according to the size fraction (the finest one have a larger carbonaceous content) . Our previous studies performed on bronchial epithelial cell lines demonstrated a higher pro-inflammatory effect of fine and ultrafine particles compared to coarse ones for particles coming from rural sites, traffic or background urban sites in France as well as African cities [14,15,16]. This was also observed for HBE cells repeatedly exposed to fine, ultrafine and coarse PM . In order to determine whether such differences could also be observed on proliferation of fibroblasts, we compared the effects of conditioned media recovered during repeated treatments of HBE cells to either coarse, fine or ultrafine PM at 5 µg/cm². As shown in Figure 5, a significant increase of fibroblast number was observed for Wi-38 cultures treated with conditioned media from HBE cultures exposed to either fine PM or ultrafine PM. By contrast the number of Wi-38 cells when grown with conditioned medium from HBE cultures exposed to coarse PM, was not significantly different from the one of cultures treated with conditioned media from control HBE cultures. However, the proliferative potential of these conditioned media was lower compared to fresh BEGM medium.
2.5. Effect of Epithelial Secretion on Fibroblast Proliferation in Co-Culture
To alternatively evaluate the paracrine effect of epithelial secretome on lung fibroblasts, co-cultures allowing the attainment of more realistic exposure conditions were carried out. Moreover it enables investigation of whether a paracrine effect can be also observed using differentiated NHBE cells. HBE cells were grown at ALI on inserts and fibroblasts were grown on the bottom of the culture plate where the inserts are placed and were submerged in BEGM medium. HBE were apically treated with fine PM at 5 µg/cm² and Wi-38 cells proliferation was measured over four days following the treatment. The experiment was firstly performed on undifferentiated HBE cells in the first week of ALI culture condition and renewed on differentiated HBE cells in the sixth week of ALI culture condition in order to assess whether fibroblast response was dependent on HBE differentiation.
Firstly we measured the amphiregulin release by HBE cells induced by fine PM exposure, whether HBE cells were grown alone or in co-culture with fibroblasts for 48 hours or 72 hours. Constitutive amphiregulin release was higher when HBE cells were cultured with Wi-38 (2,500 pg/mL at 48 hours and 3,000 pg/mL at 72 hours) than when cultured alone (1,500 pg/mL at 48 and 72 hours) (Figure 6a). After exposure to fine PM, a significant increase of amphiregulin release (compared to control cells) was observed when HBE were grown alone but not when co-cultured with fibroblasts (Figure 6a), confirming results shown in Figure 1. This could be explained by the consumption of amphiregulin by Wi-38 cells. This hypothesis was strengthened by the observation of a significant increase of fibroblast growth rate at 72 hours (Figure 6c).
For differentiated HBE cell cultures (sixth week in ALI), here again we observed that the constitutive release of amphiregulin is higher in co-culture conditions and that the PM-induced amphiregulin release at 72 hours was only significant when HBE cells were grown alone (Figure 6b). As for undifferentiated HBE cells, the number of fibroblasts was more important when co-cultured for 96 hours with HBE cells exposed to PM compared to co-culture with control HBE cells (Figure 6d).
In order to determine whether the epithelial secretome could also influence cell differentiation in addition to promoting proliferation, we studied the mRNA expression of pro-collagen I and α-smooth muscle actin and did not find significant induction using either conditioned media or co-culture (data not shown).
Altogether these results suggest that the proliferation of lung fibroblasts is associated with the mitogenic effect of the epithelial secretome. However we cannot exclude a direct effect of particles on fibroblast cells. It has been reported in in vivo studies that particles in the nanosized range could quickly translocate through pulmonary epithelium reaching the bloodstream . For our cultures, we used inserts with membranes of a low porosity (0,4 µm) that are essential to obtain an accurate differentiation of HBE cells, however other studies from our laboratory  showed it unlikely that fine PM could cross a porous membrane. However to avoid a possible direct effect of particles, conditioned media were centrifuged before treatment of Wi-38 cells in order to eliminate possibly present particles. In addition, to determine whether soluble compounds of PM could contribute to fibroblast proliferation, we investigated the effect of an aqueous extract of fine PM and found that it had no effect on Wi-38 proliferation (data not shown).
Our demonstration of the role of EGFR ligands in fibroblast proliferation is in line with in vivo experiments performed on transgenic adult mice over-expressing TGFα that developed pulmonary fibrosis in the absence of any inflammation or activation of TGFβ, a well-known and powerful fibrotic factor . This fibrosis is characterized by an increased fibroblast proliferation and collagen deposition that was reduced when mice were treated with inhibitors of the tyrosine kinase activity of EGFR .
Thanks to our in vitro approach, we demonstrated that the epithelial secretome from particle-treated epithelium exhibited a fibrotic potential underlining that the epithelium can contribute to the fibrotic process by stimulating fibroblast hyperplasia. Fibrosis can also result from epithelial to mesenchymal transition . It was very recently demonstrated that ultrafine particles containing radicals initiate such a transition in airway epithelial cells . Our further investigations will explore such a possibility.
3. Experimental Section
Ambient particles (PM) were sampled in Paris (site of background pollution in 13th district) in spring 2010 (from 20 May to 22 June) with a 13-stage low pressure Dekati impactor (Dekati, Tampere, Finland) in order to collect particles with an aerodynamic diameter between 30 nm and 10 µm on polycarbonate filters. Mass size distribution was obtained using gravimetric (filter weighing) prior and after sampling as reported in details by Sciare et al. (2007) . Coarse (C, PM10-1 µm), Fine (F, PM1-0.17 µm) and UltraFine (UF, PM0.17-0.03 µm) fractions were reconstituted by particle detachment from sampling filters in DMEM/F12 medium as previously described . Their mean chemical composition was described in .
3.2. NHBE Cell Culture and Exposure
Normal human bronchial epithelial (NHBE) cells (Lonza, Levallois-Perret, France) were seeded at 10,000 cells/cm2 on polycarbonate or polyester transwells inserts with 0.4 µm pore size diameter (Costar, Illkirch, France) with bronchial epithelial basal medium (BEBM, Lonza) supplemented with 5 μg/mL insulin, 0.5 ng/mL hEGF, 0.5 μg/mL hydrocortisone, 0.5 μg/mL epinephrine, 50 μg/mL gentamycin, 50 μg/mL amphotericin B, 10 μg/mL transferrin, 6.5 ng/mL triiodothyronin, and 0.13 mg/mL bovine pituitary extract (all supplied by Lonza : singleQuot Kit Lonza) to obtain bronchial epithelial growth medium (BEGM). Once cells had reached confluency, the air-liquid interface (ALI) was established by removing the apical medium and retinoic acid (10-7 M) was added to the basal medium that was changed every two days. Four treatments (spaced by 48 hours: T1, T2, T3 and T4) of four hours (at 5 and 10 µg/cm2) were applied on NHBE cells . Basal media were collected 48 hours after each treatment as well as in the following weeks after the end of the treatments in order to measure growth factor release and to be used as conditioned media for fibroblasts.
3.3. WI 38 Cell Culture and Exposure
The human embryonic lung fibroblast cell line Wi-38 purchased from Sigma (Sigma-Aldrich, Saint-Quentin Fallavier, France) was cultured in DMEM high glucose (4.5 g/L D-glucose) (Life Technologies, Saint Aubin, France) supplemented with 10% fetal calf serum (FCS, Life Technologies), 1% Glutamax. 24 hours after seeding at 6,000 cells/cm2 WI 38 cells were exposed from 24‑96 hours to NHBE conditioned media collected during treatment to PM size-fractions. These conditioned media were supplemented with D-glucose (1 g/L), peni-streptomycin (100 µg/mL, Sigma), fungizone (1µg/mL, Life Technologies) and Glutamax 1%. In some experiments, Wi 38 cells were treated with or without different antibodies: Anti-human EGFR (LA1) at 0.5 µg/µL, anti-human amphiregulin at 20 µg/mL, and anti-human TGFα at 1µg/mL (R&D systems, Lille, France). Antibodies were added at the same time as the conditioned media.
3.4. Co-Culture NHBE/Wi-38 and Exposure
NHBE cells were grown on the upper surface of the Transwell and once NHBE cells reached confluency, ALI was established with retinoic acid (10-7) added to the basal medium supplemented with D-glucose (1 g/L). Transwell filters were placed in 12-well plates (Corning, Illkirch, France), that were previously seeded with fibroblasts (6 × 103/cm²) fed with BEGM media supplemented with D-glucose (1 g/L). 24 hours after seeding, NHBE cells were exposed to fine PM (5 or 10 µg/cm2) for 4 hours and fibroblast proliferation was measured over the following days. PM treatment was performed on one week old NHBE cells as well as at six week old NHBE cells.
3.5. WI 38 Cells Proliferation
Fibroblast proliferation was assessed each day from 24‑96 hours after exposure with NHBE conditioned media collected during treatment period or during co-culture. It was performed by cell counting in a hemocytometer in the presence of Trypan Blue to evaluate cell viability.
3.6. Quantification of Growth Factor Release by NHBE Cells and WI 38 Cells
The basal media recovered 48 hours after each of the four treatments and those recovered in the post-treatment period were assessed for their content in amphiregulin and TGFα using a commercially available human enzyme-linked immunosorbent assay (ELISA) kit (R&D Systems Europe; Abingdon, United Kingdom) according to the manufacturer’s recommendations. Color development was measured at 450 nm with a microplate photometer MRX 5000 (Dynex Technology, Issy les Moulineaux, France).
At the end of the incubation, cells were rinsed with phosphate buffer saline and fixed in 4% paraformaldehyde for 20 min. Cells were permeabilized with 1% Triton X100 for 5 min and further incubated with mouse anti Vimentin (Sigma-Aldrich, Saint-Quentin Fallavier, France) in blocking solution, over night at 4 °C. After rinsing, cells were incubated with the fluorescent secondary antibodies Alexa 546 anti-mouse (Invitrogen, Saint Aubin, France) for 1 hour. Confocal images were captured with a Zeiss LSM700 Exciter laser scanning confocal microscope (Thornwood, NY) using sequential imaging to prevent interchannel cross-excitation between fluorochromes.
Data were analyzed by analysis of variance (ANOVA) followed by Dunnet’s t-test to examine the differences between the different groups treated with respect to the controls. A value of p < 0.05 was considered statistically significant. Data are represented as mean ± standard deviation (SD).
In this study using two different methodological approaches, we provided evidence that the epithelial secretome induced by exposure of bronchial epithelial cells to fine PM had a paracrine effect on fibroblasts promoting their proliferation. EGFR ligands, likely amphiregulin and TGFα, were among the growth factors involved in this mitogenic effect. This highlights that the airway epithelium, beyond its role of physical barrier, acts as a functional barrier interacting with surrounding cells. These experimental data contribute to strengthen the hypothesis that chronic exposure to PM could promote airway remodeling or exacerbate it in compromised people.
The authors thank the French ANR (Agence Nationale pour la Recherche) for funding the MEGATOX project (ANR CESA 2008-009-02), and the doctoral school ABIES (Agriculture Biologie Environnement Santé). The authors thank the Ministère de l'enseignement supérieur et de la recherche which supported LB PhD.
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