Inducible expression of beta defensins by human respiratory epithelial cells exposed to Aspergillus fumigatusorganisms
© Alekseeva et al; licensee BioMed Central Ltd. 2009
Received: 29 July 2008
Accepted: 11 February 2009
Published: 11 February 2009
Aspergillus fumigatus, a saprophytic mould, is responsible for life-threatening, invasive pulmonary diseases in immunocompromised hosts. The role of the airway epithelium involves a complex interaction with the inhaled pathogen. Antimicrobial peptides with direct antifungal and chemotactic activities may boost antifungal immune response.
The inducible expression of defensins by human bronchial epithelial 16HBE cells and A549 pneumocyte cells exposed to A. fumigatus was investigated. Using RT-PCR and real time PCR, we showed an activation of hBD2 and hBD9 defensin genes: the expression was higher in cells exposed to swollen conidia (SC), compared to resting conidia (RC) or hyphal fragments (HF). The kinetics of defensin expression was different for each one, evoking a putative distinct function for each investigated defensin. The decrease of defensin expression in the presence of heat-inactivated serum indicated a possible link between defensins and the proteins of the host complement system. The presence of defensin peptide hBD2 was revealed using immunofluorescence that showed a punctual cytoplasmic and perinuclear staining. Quantification of the cells stained with anti hBD2 antibody demonstrated that SC induced a greater number of cells that synthesized hBD2, compared to RC or HF. Labelling of the cells with anti-hBD-2 antibody showed a positive immunofluorescence signal around RC or SC in contrast to HF. This suggests co-localisation of hBD2 and digested conidia. The HBD2 level was highest in the supernatants of cells exposed to SC, as was determined by sandwich ELISA. Experiments using neutralising anti-interleukine-1β antibody reflect the autocrine mechanism of defensin expression induced by SC. Investigation of defensin expression at transcriptional and post-transcriptional levels demonstrated the requirement of transcription as well as new protein synthesis during A. fumigatus defensin induction. Finally, induced defensin expression in primary culture of human respiratory cells exposed to A. fumigatus points to the biological significance of described phenomena.
Our findings provide evidence that respiratory epithelium might play an important role in the immune response during Aspergillus infection. Understanding the mechanisms of regulation of defensin expression may thus lead to new approaches that could enhance expression of antimicrobial peptides for potential therapeutic use during aspergillosis treatment.
Aspergillus fumigatus (A. fumigatus) is a saprophytic mould that is responsible for life-threatening invasive pulmonary diseases in immunocompromised hosts. In general, A. fumigatus is propagated through airborne conidia . Despite the availability of new antifungal drugs, the number of deaths due to invasive aspergillosis has progressively increased in the last decades with a rise in the number of immunosuppressed patients in modern clinical practices . Therefore, a better understanding of the mechanisms responsible for resistance to Aspergillus infection is required. The respiratory epithelium plays an important role in the innate immune defence against various inhaled pathogens by sensing the signal from the external environment and stimulating the synthesis of the antimicrobial molecules directly affecting the microbes . The defensin family of antimicrobial peptides is an evolutionary conserved group of small cationic peptides involved in the innate immune system of plants and animals. They are divided into α-, β- and θ-defensins, which differ from one another by the spacing and connectivity of their six cystein residues . It was found that α-defensins are generally stored in the azurophilic granules of neutrophils and Peneth cells of the small intestine . Defensins isolated from rhesus monkey neutrophils are referred to as θ-defensins because of their circular molecular structure . Human β-defensins (hBD) are characteristic of epithelial tissue; they have been identified by traditional peptide purification, genomics-based searches [7–9] and an ORFeome-based peptide database search . Some of these defensins are tissue-specific, whereas others are expressed in the epithelium of different origins: hBD1 is expressed in most epithelial cells [11, 12], while hBD2 is most commonly expressed in the lung and thymus [13, 14]. Newly discovered defensin hBD9 was found to be ubiquitously expressed in most tissues . Inducible hBD2 expression by the epithelial cells exposed to microbial pathogens is well documented . The direct killing of microorganisms has been ascribed to human defensins . It was recently recognised that defensins have additional activities such as the chemoattraction of immature dendritic cells, T cells and monocytes, as well as activation of the professional antigen-presenting cells [16–18]. Killing of A. fumigatus by rabbit neutrophil cationic peptides , as well as antifungal activities of hBD2 against A. fumigatus , has been reported in in vitro experiments. Moreover, the expression of human drosomycin-like defensins, which display a broad spectrum of activity against Aspergillus spp, was found in several human tissues .
The role of the airway epithelium is not limited to the first mechanical barrier, but instead involves a complex interaction with A. fumigatus [22–24]. We hypothesized that various defensins may be expressed by the respiratory epithelium exposed to A. fumigatus. Taking the possibility into account that some host immunological reactions are A. fumigatus morphotype-specific [25, 26], the present study has been designed to investigate the expression of defensins by human pneumocytes and bronchial epithelial cells exposed to different forms of A. fumigatus: RC, SC or HF. The expression of previously studied hBD1  and hBD2 [14, 15], as well as recently discovered hBD8, hBD9 and hBD18 , were analysed. Since hBD2 and hBD9 were found to be highly expressed by cells exposed to A. fumigatus, those defensins were chosen for further analysis in the current study. The inducible expression of hBD2 and hBD9 was revealed by RT-PCR in airway epithelial cells exposed to A. fumigatus organisms. Real time PCR demonstrated that the expression was higher in cells exposed to SC, compared to RC or HF. The presence of the intracellular hBD2 peptide was demonstrated using immunofluorescence. The HBD2 level was highest in the supernatants of cells exposed to SC, as determined by sandwich ELISA. Furthermore, it was found that transcriptional and post-transcriptional mechanisms are involved in the regulation of defensin expression. Detection of inducible defensin expression in human airway primary culture epithelial cells was proof of the biological significance of obtained results. Our finding that hBD2 and hBD9 are expressed and produced (hBD2) in human respiratory epithelial cells exposed to A. fumigatus is novel and indicates that respiratory epithelium might play an important role in the early immune response during Aspergillus infection.
Expression of defensins by human pneumocytes and bronchial epithelial cells exposed to A. fumigatus
Primer sequences, annealing temperatures and product size (RT-PCR).
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Role of serum in defensin expression by human pneumocytes and tracheal epithelial cells exposed to A. fumigatus
Taking the lower basal level of defensin expression into account in untreated control cells maintained in the medium containing human serum compared to FCS, all of the following experiments, unless otherwise specified, were performed with human respiratory cells incubated in the presence of 5% human serum.
The identities of hBD2 and hBD9 defensins were confirmed by direct sequencing of the products of predicted molecular weight generated by PCR amplification using upstream PCR primers.
Effect of heat inactivation of serum on inducible defensin expression
The mechanisms of regulation of beta defensin expression by airway epithelial cells exposed to A. fumigatus organisms are unknown; the autocrine mechanism of defensin induction by cytokines cannot be ruled out. It was reported that Aspergillus induced cytokine production whereas heat inactivation of serum decreased cytokine production [28, 29]. We therefore checked to see of the heat-labile serum factor was required for defensin expression. To do this, human 16HBE cells were incubated either with heterologous FCS or autologous human serum (previously heated or not at 56°C for 30 min) and simultaneously exposed for 18 hours either to A. fumigatus conidia, HF or the latex beads.
As shown in Figure 2, a high level of hBD2, as well as hBD9 expression, was observed in the cells incubated either with FCS (Figure 2A) or human serum (Figure 2B). Heat inactivation of any of the serums led to the partial decrease of the expression of both of the tested defensins by cells exposed either to A. fumigatus conidia, HF, or to Il-1β (Figure 2C, D).
Kinetics of defensin expression by cells exposed to A. fumigatusorganisms
Similar kinetics of hBD2 and hBD9 expression was observed with A549 cells (data not shown).
Real time PCR
Neutralising anti-interleukine-1β antibody decreased defensin expression in cells exposed to swollen conidia
Since A. fumigatus has been shown to induce IL-1β in airway epithelium, and since the analysis of kinetic of defensin expression showed that the Il-1β-induced response was faster than the one induced by fungi (Figure 3), we investigated whether or not observed A. fumigatus-induced defensin expression was related to Il-1 β synthesized during anti-fungal response. For this reason, neutralising anti-interleukine-1β antibody was added to the cells before exposure to A. fumigatus organisms. One of the defensins, hBD-9, was chosen for real time PCR analysis of the role of Il-1 β in defensin expression. The results of real time PCR revealed that relative gene expression was statistically significantly decreased in the cells treated with anti-Il-1 β antibody before exposure to SC, compared to the cells only exposed to SC (120 ± 5 versus 143 ± 10 respectively). Relative gene expression was also decreased in the cells treated with anti-Il-1 β antibody before exposure to RC or HF, but the difference did not reach a statistically significant level. The pre-treatment of the cells with normal mouse immunoglobulin before exposure to A. fumigatus organisms had no effect on defensin expression.
Analysis of defensin expression by human primary airway epithelial cells exposed to A. fumigatusconidia or hyphal fragments
Detection of the hBD2 peptide in human airway epithelial cells by immunofluorescence
Co-localisation of hBD-2 and different A. fumigatusmorphotypes
Quantification of hBD2 in cells supernatants by sandwich ELISA
Analysis of hBD2 expression by airway epithelial cells exposed to live A. fumigatus
In order to determine if hBD2 expression was induced in the respiratory cells by live A. fumigatus organisms, RT-PCR and immunofluorescence analysis of cells exposed to unfixed 106 live conidia was performed. Using microscopic observation, we first examined the development of A. fumigatus in the environment of the epithelial A549 or 16HBE cells. When the RC were added to the epithelial cells, they settled onto the cells within 30 minutes and began to swell after 3–4 hours; after 8 hours of infection, the SC became polarised and began to germinate. The germ tubes then progressively elongated, forming the hyphae: after 18 hours of infection, the hyphae had completely covered the epithelial cells (data not shown).
Transcriptional and post-transcriptional mechanisms of defensin expression regulation
A better understanding of the mechanisms responsible for the defence against invasive Aspergillus infection is required to develop strategies aimed at boosting the antifungal actions of the immune system. Defensins, or antimicrobial peptides, which are implicated in potentiating innate and adaptive immunity [16–18] in addition to direct antimicrobial activities , would be a good candidate as a therapeutic agent for enhancing host defence mechanisms. Since the invasion of the airway epithelium by A. fumigatus conidia may play an important role in the development of aspergillosis, we therefore investigated the involvement of defensins in the response of pneumocytes A549 and bronchial epithelial cells 16HBE exposed to A. fumigatus in this study. The expression of human defensins hBD1, hBD2, hBD8, hBD9 and hBD18 was analysed. In agreement with earlier findings , constitutive expression of hBD1 by the epithelial cells 16HBE and A549 was observed in our experiments. It was found that hBD2 and hBD9 are highly expressed by the epithelial respiratory cells exposed to SC, RC or HF of A. fumigatus, while hBD8 and hBD18 gene expression was not observed in the current study. Previous investigations revealed that hBD2 was induced by various stimuli including microbes, cytokines and growth factors [33, 35]. Inducible expression of hBD2 defensins by airway epithelial cells exposed to A. fumigatus, observed in the present work, is therefore in agreement with earlier observations. The role of the recently discovered hBD9 in innate antimicrobial defence is not well determined; however, hBD9 gene regulation in gingival keratinocytes exposed to Candida albicans has been described . Additional investigations are essential for a better understanding of its role in direct antimicrobial activity and its contribution to innate immunity. The role of hBD8 and hBD18 in innate immunity of respiratory epithelium exposed to A. fumigatus cannot be ruled out before evaluation of other epithelial respiratory cells or other induction conditions. Further analysis of those defensins is recommended.
We have shown that the maintenance of the human epithelial cells in the presence of preheated serum (56°C for 30 min) resulted in the partial decrease of defensin expression. Involvement of the heat-labile serum factor suggests the potential role of the complement for defensin expression. The possible link between the proteins of the complement system and defensin expression may be anticipated since the interaction between the defensins and proteins of the complement system was demonstrated. It was found that HBD2 inhibits the classical pathway of the complement system . Moreover, the interrelationship between the respiratory tract and the complement system was studied in an animal model . The origin of complement proteins present in the lining fluid of the respiratory tract is thought to result mainly from plasma that exudes into the bronchoalveolar space. However, it was shown that human bronchial epithelial cells generate complement protein C3: the modulation of its expression by proinflammatory cytokines might be an additional regulatory mechanism of local airway defence during infection .
Furthermore, the kinetics of the expression of human beta defensins, hBD2 and hBD9, by airway epithelial cells exposed to the deferent morphotypes of A. fumigatus was analysed. Analysis of the kinetics of hBD2 and hBD9 defensin expression by cells exposed to A. fumigatus showed the prompt inducible expression of hBD9, following by delayed hBD2 expression. This could allow us to hypothesize that the host immune system may react against A. fumigatus by using the cascade of newly synthesized defensins that probably possess the different functions. However, this hypothesis would require further investigation at the protein level. Our data are in agreement with the analysis of kinetics of hBD2 expression by A549 cells exposed to Mycobacterium tuberculosis; infection of A549 cells resulted in hBD2 gene expression as early as 6 hours postinfection, while maximum expression was detected at 18 and 24 hours postinfection .
Several lines of evidence eliminated the possibility that observed inducible defensin expression was related to endotoxin contamination of A. fumigatus organisms. First, the addition of Polymixin B (known for its endotoxin-neutralising activity) to the cells prior to exposure to A. fumigatus organisms did not have any effect on defensin expression. Second, rigorous measures were undertaken to keep endotoxin out of the experimental system, including washing of A. fumigatus organisms with the solution containing Polymixin B during preparation, utilisation of endotoxin-free plasticware and solutions in experiments, and washing of fungal organisms in endotoxin-free PBS prior to use.
The expression of hBD2 and hBD9 was found to be higher in A549, 16HBE and primary culture HNT cells exposed to SC compared to RC or HF, as shown by quantitative PCR. During asexual growth, the morphological form of A. fumigatus changes from resting to swollen conidia, which then form germ tubes that continue growing in hyphal form. These transformations are accompanied by the modification of surface structures. The RC are covered with a proteinoceous layer that is disrupted during swelling, exposing the inner layer. Therefore, the surfaces of various A. fumigatus morphotypes differ form each other and, consequently, the reaction of host cells may vary towards divergent A. fumigatus growth forms . Our findings suggest that infected hosts can discriminate between inactive RC and active potentially-invasive SC. The data are consistent with findings showing that SC (the mature form of A. fumigatus), but not RC-activated NF-kβ, stimulated pro-inflammatory cytokines and the production of reactive oxygen by host macrophages .
Moreover, the presence of the hBD2 peptide in the respiratory cells was investigated. Detection of the hBD2 peptide by immunofluorescence in A549 and 16HBE cells exposed to the different forms of A. fumigatus confirmed its inducible expression in the infected cells. The presence of the negatively-stained cells in the infected culture may be due to defensin synthesis in the subpopulation of the epithelial cells or because of the release of synthesized defensins by the activated cells. The detection of the beta-defensin hBD2 peptide in the individual unstimulated control cells is in agreement with the observation made for the alpha-defensins; it has been reported that individual untreated HL-60 cells may contain variable amounts of alpha defensin, as assessed by immunostaining . Undoubtedly, inducible expression of defensin by cells exposed to A. fumigatus may represent the recruitment of additional cells that would synthesize antimicrobial peptides and further upregulation of defensin synthesis in cells that originally contained defensin. Punctuated distribution of peptide in the cytoplasm of A549 and 16HBE cells with a concentration in the perinuclear region was similar to the staining of defensin expressed by human gingival epithelial cells exposed to cell wall extract of the gram-negative periodontal bacteria, Fusobacterium nucleatum , suggesting that the mechanism of defensin expression may be universal for the different infectious agents. The punctuated perinuclear pattern of immunostaining may be related to the localisation of hBD2 in the endoplasmic reticulum and Golgi apparatus, which is in agreement with the previous observations of Rahman et al., showing that the hBD2 peptide was expressed in rough endoplasmic reticulum, the Golgi complex and cytoplasmic vesicles of human colon plasma cells . Quantification of the cells stained with anti-hBD2 antibody revealed that SC induced a greater number of cells that synthesized hBD2, compared to RC and HF. Analysis of hBD2 levels in the supernatants of A549, 16 HBE and primary culture HNT cells confirmed this observation; significantly higher hBD2 levels were detected in all tested cell supernatants exposed to SC, compared to those exposed to RC, HF or latex beads. The level of hBD2 detected in the cell supernatants does not exceed 200 pg/ml and was comparable to the level of hBD2 in cell supernatants exposed to other pathogens . Since Okamoto et al. showed that the effective dose of synthetic hBD2 was 1.5 μg/ml, we can hypothesize that the chemotactic activity of hBD2 rather then its direct antifungal activity plays a more important role in the protection of the infected host . However, antifungal activity of defensins in synergy with other antifungal factors in vivo cannot be excluded.
Co-localisation analysis of hBD2 and A. fumigatus morphotypes allow us to detect RC or SC stained with hBD2 antibody in contrast to HF; these observations confirm the different mechanism of hBD2 induction by various morphotypes. Our findings are in agreement with the observations of Lopez Bezzera et al. who found that A. fumigatus conidia and hyphae injure endothelial cells via different mechanisms . This difference between the different growth phases of A. fumigatus could be due to the discrepancy of the mechanisms of defensin induction, which may possibly be related to the diverse types/numbers of molecules involved in this process. Immunofluorescence analysis of inducible hBD2 expression by cells exposed to live A. fumigatus organisms revealed the perinuclear staining of peptide, similar to the staining observed in cells exposed to fixed A. fumigatus, pointing to the biological significance of our findings. Given the fact that conidia germinate and form hyphae after epithelial cells are exposed to live A. fumigatus conidia for 18 hours, in agreement with previous observation , we can then hypothesize that defensin expression is possibly induced by different morphotypes in this experiment.
Our observations of the induced defensin expression in the airway epithelial cells treated with Il-1 β or TNF-α, the cytokines that play an important role during Aspergillus infection [45, 46], suggest that defensin expression in infected cells may be induced by A. fumigatus organisms, as well as by the cytokines involved in the infectious process. Therefore, the regulation of defensin expression during Aspergillus infection may possibly depend on a variety of factors.
Significant decrease of defensin expression by neutralising anti-IL-1β antibody, added to the cells prior exposure to SC, reflects the autocrine mechanism of defensin induction. A statistically insignificant decrease of defensin expression in the cells treated with anti-IL-1β antibody and exposed to RC or HF supported the hypothesis that the host immune system may distinguish and react differently towards divers Aspergillus morphotypes.
Finally, to better understand defensin synthesis, we investigated the involvement of transcriptional and post-transcriptional mechanisms in the regulation of defensin synthesis. The inducible expression of hBD2 and hBD9 by cells exposed to all morphotypes of A. fumigatus was inhibited by pre-treatment with actinomycin D, implying that defensin genes are regulated at the transcriptional level. The inhibitory effect of cycloheximide on defensin induction substantiates the requirement for new protein synthesis, which may include cell receptors, transcription factors or proteins that enhance mRNA stability. Thus, post-transcriptional mechanisms of regulation were involved in the inducible expression of defensins as well.
While the direct fungicidal activity of hBD2 against A. fumigatus was revealed in the in vitro model , this is the first study, according to our knowledge, showing hBD2 and hBD9 defensin expression by host airway epithelial cells exposed to A. fumigatus. Defensin expression was higher in the cells exposed to SC than to RC or HF. Moreover, the HBD2 level was elevated in the supernatants of cells exposed to SC, compared to other Aspergillus morphotypes. Our findings suggest that identification of the most invasive fungal form by the host may be beneficial for anti-fungal host response.
Autocrine regulation of defensin expression in cells exposed to A. fumigatus was established in the experiments with neutralising anti-Il-1β antibody. Investigation of defensin expression at transcriptional and post-transcriptional level demonstrated the requirement of transcription as well as new protein synthesis during A. fumigatus defensin induction. The presence of defensin peptide hBD2 was revealed using immunofluorescence that showed a punctual cytoplasmic and perinuclear staining, suggestive of endoplasmic reticulum and Golgi apparatus localisation. The discovery of inducible hBD2 and hBD9 defensin expression by human primary respiratory culture cells is indicative of the biological significance of the observation. Our finding provides evidence that respiratory epithelium might play an important role in the early immune response during Aspergillus infection. Taking the antimicrobial activity of defensins together with their capacity to induce the migration of cells involved in the immune response into account, we can hypothesize that defensins may link innate and acquired immunities of the host infected by A. fumigatus. Future study of the regulation of defensin expression might provide new approaches that may enhance expression of antimicrobial peptides for potential therapeutic use during aspergillosis treatment.
Human serum, actinomycin D and cycloheximide were obtained from Sigma. Actinomycin D and cycloheximide were dissolved in dimethyl sulfoxide (DMSO) (Sigma). In all the experiments, the concentration of DMSO was always less than 0.1% (vol/vol). Interleukun-1β (Il-1 β) was purchased from Sigma. Lyophilised powder of Il-1β was reconstituted to the stock concentration of 10 μg/ml with sterile phosphate buffered saline (GIBCO BRL). Twenty ng/ml of IL-1β solution was used as a positive control for defensin expression in all experiments. Monoclonal anti human Il-1 β antibody (I3642) were obtained from Sigma. Recombinant human Tumor Necrosis Factor alpha (TNF-α) was obtained from Sigma; 10 ng/ml of TNF solution was used in the experiments.
Anti-hBD-2 polyclonal antibody was purchased from Peptide International, Inc (Louisville, Kentucky, USA). Lyophilised powder of anti-hBD-2 antibody was reconstituted to the stock concentration of 10 mg/ml with sterile phosphate buffered saline (GIBCO BRL). Bronchial epithelium medium (BEGM) was obtained from Lonza Group Ltd (Basel, Switzerland).
Maintenance of endotoxin-free conditions
Experiments were designed to minimise endotoxin contamination by using purchased endotoxin-free plasticware and heating all glassware at 180°C for 4 hours. All solutions used in the experiments contained less then 0.007 endotoxin unit/ml (minimal detectable level) when tested with Limulus amebocyte lysate assay (Sigma). A. fumigatus organisms were washed in the solution containing Polymixin B during preparation.
Human nasal turbinates of patients undergoing turbinectomy (Pr. G. Lamas, La Pitié-Salpêtrière University Hospital Centre, Paris, France) were used for the preparation of the primary epithelial cells. All patients signed an informed consent form before participating in this research protocol, which was approved by the Institutional Ethics Committee.
Fungal strain and growth conditions
The A. fumigatus strain, CBS 144.89 (Institut Pasteur, Paris, France), was used throughout this study. A. fumigatus conidia were prepared as previously described . Briefly, conidia of A. fumigatus were obtained from cultures grown on YM agar (0.3% yeast extract, 2% malt extract, 0.5% peptone and 0.5% agar) for three days at 37°C. Conidia were harvested by flooding the plates with sterile distilled water and then suspending the hydrophobic conidia in 0.01% Tween 20 in phosphate-buffered solution (PBS). To remove hyphae and debris, the conidial suspension was filtered through four levels of gauze. The RC obtained were maintained at 4°C.
Preparation of swollen conidia and hyphal fragments
SC were prepared as described . Briefly, 5 × 109 of resting A. fumigatus conidia were incubated in 200 ml of Sabouraud medium for 5 hours at 37°C in order to obtain the isodiametric swelling of the conidium resulting in the development of SC. As demonstrated by microscopic examination, the majority of the organisms were single conidia, with a few small clumps containing two to four organisms. To obtain a homogeneous preparation, the suspension was gently sonicated for 10 seconds using a Branson Sonifier 450 (output level 2; Branson Ultrasonics, Danbury, CT, USA). Before exposure of the cells to conidia, the solution was vigorously vortexed and observed microscopically to ensure the absence of clumps.
Hyphal fragments (HF) were prepared by incubating 2 × 108 of resting conidium in 200 ml of Sabouraud medium for 18 hours at 37°C with shaking in order to obtain a homogenous solution of the small HF. The tubes were then centrifuged in order to spin down the pellet. For the purpose of standardising the hyphal inoculum by weight, the pellet, which almost exclusively contained mycelium, was washed twice with Hanks balanced saline solution without Ca2+ and Mg2+ (HBSS w/o), followed by filtration through the gauze that was weighed beforehand. The gauze containing HF was dehydrated at 60°C overnight and weighed . The difference between the weight of the gauze alone and the gauze containing the dry mycelium corresponds to the weight of the dry mycelium. 700 mg of dry weight of mycelial mass was obtained during experiments under the conditions described above. Twenty ml of PBS were then added to the dry mycelial mass and vigorously resuspended. All A. fumigatus morphotypes were prepared so as to minimise endotoxin contamination as described . To eliminate potential endotoxin contamination, RC, SC or HF were washed in PBS containing 50 μg/ml of Polymixin B, known for its capacity to drastically decrease endotoxin activity, followed by four additional washings in endotoxin-free PBS. Since human cells have to be exposed to the different forms of A. fumigatus for various periods of time (including 18 hours to allow the RC to germinate), all A. fumigatus morphotypes were fixed in ethanol. The different solutions, containing RC, SC or HF, were centrifuged and resuspended in a 70% solution of ethanol in PBS and stored in a refrigerator for 24 hours as described in the literature . After centrifugation, either conidium or HF were vigorously resuspended in PBS containing 10 mg of RNAse A per ml (Sigma Aldrich) and incubated for 30 min at 37°C to remove intracellular RNA . After several washings in PBS, the different forms of A. fumigatus were viewed under the microscope; homogeneous solutions containing single resting or SC were obtained. The morphology of the mycelium was not altered. After being fixed in ethanol, mycelia (700 mg of dry weight in 20 ml of PBS) were used as a standard HF solution. In experiments with ethanol-fixed A. fumigatus organisms, the equivalent volume of the supernatant from the last washing was added to the human cells to check for the release of any toxic material as a result of the ethanol treatment. There was no induction of the defensin expression in the cell culture incubated in the presence of the supernatants from the last washing.
Human cell lines and growth conditions
A type II pneumocyte cell line A549 derived from a human lung carcinoma was obtained from the American Type Culture Collection [ATCC CCL 185 ] and maintained in Kaighn's modification of HAM's F12 medium supplemented with 10% FCS (Invitrogen, Cergy Pontoise, France), pen/strep (16 mg/ml penicillin and 100 mg/l streptomycin), 2 mM L-glutamine and 1.5 g/l sodium bicarbonate. The cells were grown until confluent at 37°C in an incubator with a humidified atmosphere of 5% CO2. Trypsin/EDTA (Invitrogen) was used to release adherent cells for subculturing when this was required.
Human bronchial epithelial SV40-transformed cells (16HBE) were kindly provided by Dr. D.C. Gruenert (Research Facility, California Pacific Medical Center, San Francisco, CA, USA). 16HBE cells were maintained in DMEM/F12 medium (Invitrogen) with 10% FCS (Invitrogen), pen 100 U/ml/strep 100 μg/ml, 2 mM L-glutamine (Sigma) and 1 Ug/ml de fungizone and 1.5 g/l sodium bicarbonate (Sigma), and were grown until confluent .
Establishment and maintenance of human airway epithelial primary culture cells
Primary epithelial cells were obtained from human nasal turbinates (HNT) of patients undergoing turbinectomy as previously described . Briefly, HNT were washed in Dulbecco's modified Eagle medium DMEM/F12 (Invitrogen) and incubated with 2 mg/ml pronase (Protease XIV; Sigma,) in DMEM/F12 supplemented with pen/strep, at 4°C for 16–20 h under slow rotary agitation (80 rpm.). After washing, aggregates were discarded and dissociated cells were filtered using a 30-μm pore filter. The cell suspension was then plated for 2 h at 37°C on plastic dishes (Falcon) to eliminate contaminating fibroblasts. After centrifugation, the supernatant containing the epithelial cells was cultivated in a 1:1 mix (vol:vol) of bronchial epithelium medium BEGM (Lonza Ltd): DMEM/F12 supplemented with Clonetics singlequots (5 μg/mL insulin, 0.5 μg/mL hydrocortisone, 0.5 μg/mL epinephrine, 6.5 ng/mL triiodothyronine, 10 μg/mL transferrin, 0.5 ng/mL human epidermal growth factor, 50 μg/mL gentamicin-amphotericinB, 0.13 mg/mL bovine pituitary extract), 50 U/mL of penicillin-streptomycin and 0.5% fungizone.
Heat inactivation of the serum
In the experiments devoted to the investigation of the role of the heat-labile component of serum in the production of defensins by the human airway epithelium, heat inactivation of the serum, the recognised method for serum decomplementation, was performed as described . Briefly, either human autologous serum or heterologous FCS was heated at 56°C for 30 min. After cultivation of the human respiratory cells under the conditions described above, the cells were exposed to A. fumigatus in the medium containing serum that was either heat-inactivated or not.
Exposure of the cells to A. fumigatusconidia or hyphal fragments
5 × 106 of A549, 16HBE or primary culture cells were placed in six well plates in 1.5 ml of the corresponding medium described above and grown until confluence. Following washing of A549, 16HBE or primary culture cells with PBS, 106 of A. fumigatus conidia per millilitre of medium were added to the cells for 4, 8 or 18 hours. Exposure to HF was carried out by incubation of the cells for 4, 8 or 18 hours with 20 μl of the standard solution (35 mg of dry weight/ml) obtained from 2 × 108 of resting conidium as described above. All A. fumigatus morphotypes were washed an additional four times in endotoxin-free PBS prior to use to eliminate potential endotoxin contamination.
After incubation, unbound conidia were removed by washing wells with PBS prior to RNA purification.
Primary epithelial cells were seeded at 5 × 106 cells per well and grown for 48 h before exposure to A. fumigatus.
In some experiments, the cells were exposed to 106 unfixed live conidia for 18 hours.
To be sure that the inducible expression of defensins was specific to A. fumigatus and did not simply reflect a phagocytosis response, latex beads were used as a control, since it was shown that the respiratory cells are capable of internalising nonspecific particles such as latex beads . Compared to the concentration of conidia, up to a five-fold higher concentration of latex beads was used in the experiments, as suggested .
Before exposing the cells to the A. fumigatus organisms, the solutions were vigorously vortexed and observed microscopically to ensure that they did not contain clumps.
RNA isolation and analysis of defensin expression by RT-PCR
In order to ensure that the cells were exposed to different morphotypes of A. fumigatus organisms (conidia or HF) during the incubation period, the cell culture was observed microscopically at the beginning and at the end of the exposure. The medium was discarded, the wells were briefly washed with PBS solution, and TRIzol reagent was added to the cells.
Total RNA was isolated with TRIzol Reagent (Invitrogen, Cat N 15596-026) according to the manufacturer's instructions. RNA was precipitated with ethanol and resuspended in diethyl pyrocarbonate H20. The RNA concentration was measured by spectroscopy, and the integrity of RNA was assessed on an agarose gel. cDNA was synthesized from 1 μg of purified RNA, using 50 nM of Oligo dT, 16 mer, (Operon Biotechnologies SP230), 30 units of AMV Reverse Transcriptase (Promega M5108) and RNA-se free H20 in a reaction volume of 25 μl, according to the manufacturer's recommendations. Identical reactions devoid of reverse transcriptase (-RT) were carried out in parallel and did not lead to any DNA amplification of predicted molecular weight in contrast to reverse transcriptase-containing reactions. Reactions containing H20 instead of cDNA were also used in negative controls (data not shown).
A RT-PCR approach was used for the analysis of defensin expression in A549 and 16HBE human respiratory cell lines, as well as in primary culture of human respiratory cells exposed to RC, SC, or HF. Gene-specific primers for hBD1 and hBD2 were designed according to the sequences available at the National Center for Biotechnology Information http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/ in order to amplify specific cDNA sequences and avoid genomic DNA amplification. In this respect, primer sequences were designed to cover at least two subsequent exons, the human beta-defensin (HBD) -1 and -2 (NCBI accession # NM 005218.3 and NM 004942.2, respectively). It should be observed that hBD2 is now referred to as hBD-4 in the NCBI database. However, we decided to use the term, hBD2, since it is widely used in scientific literature today . For the analysis of hBD8, hBD9 and hBD18, we relied on previous studies; the primers and PCR conditions were used as described in .
The PCR-amplified cDNA band of glyceraldehyde-3-phosphate dehydrogenase (GAPDH, NCBI accession # NM 2046.3) was used as an internal control with the predicted size of 473 bp. In each reaction, the initial denaturing step was 94°C for 8 min, followed by 32–38 cycles [denaturation at 94°C for 40 seconds, annealing at 56–61°C (according to primer melting temperature) for 40 s and elongation at 72°C for 1 minute]. The final elongation step was 72°C for 7 min. The primer annealing temperatures, cycles and predicted PCR product sizes for the transcripts investigated are summarised in Table 1. The PCR-amplified cDNA products were separated by electrophoresis on a 2% agarose gel and visualised by ethidium bromide after staining. The forward primers (f) and reverse primers (r) used are presented in Table 1. Identification of each defensin was confirmed by direct sequencing of respective PCR products, using upstream PCR primers (DNA Sequencing Facility, Qiagen, France).
Quantitative Real Time PCR
Primer sequences and annealing temperatures (Real Time PCR)
40 cycles, 55°C,
40 cycles, 55°C
40 cycles, 55°C
In order to amplify specific cDNA sequences and to avoid genomic DNA amplification, all primer sequences were designed to cover at least two subsequent exons (Table 2). Relative quantification relates the PCR signal of the target transcript in a treatment group to that of an untreated control. For each primer-pair, the amplification efficiency was determined by serial dilution experiments and the resulting efficiency coefficient was used for quantification of the products . Each 25 μl Quantitative PCR mixture included 5 microl of DNA, 0.08 μl of primers (300 nM), 12.5 μl of CYBR green IQ supermix (2×) (ABgene) and H2O. Quantitative PCR amplification was carried out on an iCycler iQ system (Bio-Rad, Marne la Coquette, France) with the following parameters: 15 min at 95°C and 40 cycles of two steps consisting of 30s at 95°C, 30 s at 55°C. The relative quantification of the mRNA levels of the target genes was determined using the deltaCT – method . Briefly, the amount of target was normalised to the endogenous reference gene GAPDH: deltaCT = CT (target gene) – CT (GAPDH) where CT represents the cycle number required to reach a defined threshold target abundance. The relative mRNA level was calculated as × deltaCT (x = Primer efficiency) (Pfaffl, 2001). All reactions were performed in triplicate and included a negative (-RT) control without reverse transcriptase.
Neutralising anti-IL-1β antibody
Experiments designed to analyse the role of IL-1 β in A. fumigatus-induced defensin expression were performed using real time PCR. 5 × 106 of A549 or 16HBE cells were placed in six well plates in 1.5 ml of the corresponding medium and grown until confluence. The cells were divided into three groups. The cells of the first group were exposed to either A. fumigatus morphotypes or beads for 18 hours as described above. Neutralising anti-IL-1β antibody (10 μg/ml) was added to the cells of the second group prior exposure to A. fumigatus organisms or beads for the same period. The amount of neutralising antibody was equal to that used in the experiments devoted to the study of the role of Il-1β synthesized by the monocytes infected with Streptococci . Normal mouse immunoglobulin (10 μg/ml) was used instead of neutralising antibody for the third group of cells. After collection of cells, RNA were isolated using TRIzol reagent and real time PCR was performed as described above.
Either A549 or 16HBE cells were seeded at 5 × 105 cells per well in 1 ml of DMEM/F12 on 18-mm-diameter cover slips (Marienfeld, Germany) in 12 well plates (Nunc, NuclonTM Surface) in triplicate and grown for 16 h at 37°C. After washing the cover slips with 5% BSA/PBS (BSA, Fraction V, Sigma), the cells were exposed to either 106 fixed conidia or to 20 μl of the fixed HF solution (20 mg of dry weight/ml), or 5 × 106 latex beads for 24 hours. The untreated cell culture was used as a negative control. The treatment with 20 ng of Il-1β, a well-known inductor of defensins , was used as a positive control. In some experiments, the cells were treated with 10 ng/ml of TNF-α. The cells were then fixed with freshly prepared 4% solution of paraformaldehyde for 30 min at 37°C, followed by permeabilisation in 0.05% of Triton/PBS solution. The slides were then incubated in 5% BSA/PBS, and then in a solution of 10% normal goat serum (Sigma). After washing, rabbit anti-human hBD2 (Peptide Institute 234) at a dilution of 1:250 was applied as a primary antibody overnight at 4°C, followed by incubation with FITC-labelled goat anti-rabbit secondary antibody (Sigma, Ac35-FITC) at a dilution of 1:300 for 4 hours at room temperature . After washing, the cover slips were mounted on slides with ProLong antifade Vectashield (Vectashield, Biovalley). Samples were viewed with a Zeiss fluorescence microscope using ×400 magnification. For each sample, cells from five random fields were counted and the percentage of the cells stained with anti-defensin-2 antibody was calculated as the number of stained cells divided by the total number counted, multiplied by 100. The epithelial cells incubated with normal rabbit serum at a dilution of 1:250 (Sigma, 10 mg/ml) as a negative control showed no reactivity.
Analysis of co-localisation of intracellular hBD-2 and A. fumigatusconidia or hyphal fragments
Co-localisation experiments were performed according to the method described by Botterel at al. with modifications . After exposing the cells to 106 per millilitre of medium of RC, SC or 20 μl of the standard HF solution (35 mg of dry weight/ml) for 18 hours, the cells were fixed and permeabilised as indicated above. The cells were then labelled with primary rabbit anti-hBD2 antibody (Peptide Institute 234) at a dilution of 1:250 overnight at 4°C, followed by incubation with Tex Red-labelled goat anti-rabbit secondary antibody (Sigma) at a dilution of 1:300 for 1 hour at 37°C. After washing in PBS, the cover slips were mounted on slides with ProLong antifade Vectashield (Vectashield, Biovalley, USA). Samples were viewed with a Zeiss fluorescence microscope using ×400 magnification and the images were compared to the phase-contrast images in order to identify stained internalised A. fumigatus organisms.
Detection of hBD2 in cell supernatants
Analysis of the hBD2 in cell supernatants was performed by sandwich-ELISA. Either A549 or 16HBE cells were seeded at 106 cells per well in 1 ml of DMEM/F12 in 12 well plates in triplicate and grown for 24 h at 37°C. Primary culture HNT cells were grown for 48 hours in BEGM medium as described above. The cells were then exposed to 106 per millilitre of medium of RC, SC or 20 μl of the standard HF solution (35 mg of dry weight/ml) for 18 hours. Cell supernatants were then centrifuged at 9000 g for 10 min at 4°C and analysed for the presence of hBD2 with a commercial ELISA kit (Antigenix America, Inc., NY, USA) according to the manufacturer's instructions. Briefly, a 96-well ELISA plate (Nunc, NY, USA) was coated with 100 μl of 0.5 μg/ml of capture anti-hBD2 antibody. The plate was sealed and incubated overnight at room temperature. After washing with phosphate buffer solution (PBS) containing 0.05% Tween 20, non-specific binding sites of the wells were blocked with 200 μl of 0.1% Bovine Serum Albumin (BSA)/PBS solution for 1 hour at room temperature. The wells were then washed again and 100 μl of cell supernatants or standard recombinant hBD2 in duplicate were added to the wells for 2 hours at room temperature. Serial dilutions of standard hBD2 from 10 ng/ml to 0.01 ng/ml were performed in diluent containing 0.1 BSA in 0.05% Tween 20/PBS. After washing, 100 μl of tracer biotinilated antibody was added to the wells at a concentration of 0.25 μg/ml for 2 hours at room temperature. The wells were then washed again and streptavidin-horse radish peroxidise solution at a concentration of 1 μg/ml was added for 30 minutes at room temperature, followed by intensive washing. Liquid chromogenic substrate (3, 3', 5, 5'-Tetramethyl-Benzidine) solution was used for colour development. The ELISA plate was read using a 96-well plate reader IEMS, THERMO LABSYSTEMS (Thermo Fisher Scientific, Cergy-Pontoise, France) at 450 nm (correction set at 650 nm) with 5 min intervals for 20 minutes. The sensitivity of ELISA for hBD2 was 10 pg/ml.
Analysis of defensin expression by cells treated with inhibitors of protein synthesis and gene transcription
To examine the mechanism(s) for inducible defensin expression in response to A. fumigatus, human airway epithelial cells A549 or 16HBE were pre-treated with either 2.5 μg of cycloheximide (an inhibitor of protein synthesis) per ml, 0.5 μg of actinomycin D (an inhibitor of RNA transcription) per ml, or DMSO (vehicle control), 1 h before exposure to A. fumigatus for an additional 6 or 18 hours. In this study, we used lower doses of actinomycin D and cycloheximide than were previously described , in order to avoid their toxic effect during incubation of the cells for 18 hours. The viability of human cells as assessed by trypan blue and total RNA yield were checked after each treatment, and no differences were found between experimental and untreated control cells.
The differences in the percentage of the cells positively stained with anti-defensin antibody in the cell cultures exposed or not to A. fumigatus were assessed by analysis of variance. P-values <0.05 were considered to be significant. Tukey's honestly significant difference test was applied for comparison of means between groups. The values are expressed as mean ± SEM. At least three different assays were performed per experiment
This work was supported by a grant from INRA (French National Institute of Agricultural Research), a bi-lateral collaboration. Ludmila Alekseeva was a recipient of a post-doctoral fellowship from MRI INRA. Mahdia Abdeluahab was the recipient of a fellowship from the Animal Health Department of INRA. We are grateful to Dr. S. Dutertre, the head of the microscopy platform of the Institut Fédératif de Recherche 140, Rennes, France, for assistance in immunostaining analysis. We gratefully acknowledge Pr. G. Lamas (La Pitié-Salpêtrière University Hospital Centre, Paris, France) for his help in the preparation of patient material. We would also like to thank Dr. Tom Ganz (Department of Medicine at the Will Rogers Institute for Pulmonary Research, University of California School of Medicine, Los Angeles, CA, USA) for his helpful suggestions for the experiments and the critical reading of the manuscript. We are grateful to Mr. Bernard Charpentier and Ms. Aline Jeannel (MRI, INRA, Paris) for their assistance in the organisation of this work. We thank Gail Wagman for revising the English.
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