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. 2016 Jan 8;48(1):e202. doi: 10.1038/emm.2015.96

Aspirin induces IL-4 production: augmented IL-4 production in aspirin-exacerbated respiratory disease

Su-Kang Kong 1, Byung Soo Kim 1, Tae Gi Uhm 2, Hun Soo Chang 3, Jong Sook Park 4, Sung Woo Park 4, Choon-Sik Park 4, Il Yup Chung 1,2,*
PMCID: PMC4686698  PMID: 27534531

Abstract

Aspirin hypersensitivity is a hallmark of aspirin-exacerbated respiratory disease (AERD), a clinical syndrome characterized by the severe inflammation of the respiratory tract after ingestion of cyclooxygenase-1 inhibitors. We investigated the capacity of aspirin to induce interleukin-4 (IL-4) production in inflammatory cells relevant to AERD pathogenesis and examined the associated biochemical and molecular pathways. We also compared IL-4 production in peripheral blood mononuclear cells (PBMCs) from patients with AERD vs aspirin-tolerant asthma (ATA) upon exposure to aspirin. Aspirin induced IL-4 expression and activated the IL-4 promoter in a report assay. The capacity of aspirin to induce IL-4 expression correlated with its activity to activate mitogen-activated protein kinases, to form DNA–protein complexes on P elements in the IL-4 promoter and to synthesize nuclear factor of activated T cells, critical transcription factors for IL-4 transcription. Of clinical importance, aspirin upregulated IL-4 production twice as much in PBMCs from patients with AERD compared with PBMCs from patients with ATA. Our results suggest that IL-4 is an inflammatory component mediating intolerance reactions to aspirin, and thus is crucial for AERD pathogenesis.

Introduction

Aspirin-exacerbated respiratory disease (AERD) refers to chronic rhinosinusitis, nasal polyposis and bronchoconstriction in asthmatics following the ingestion of aspirin or other cyclooxygenase-1 (COX-1) inhibitors.1 AERD is an acquired metabolic inflammatory disorder with adult onset that affects ~10% of all patients with asthma.2, 3 Aspirin hypersensitivity is the most specific marker for AERD and has aggressive airway manifestations, such as chronic rhinosinusitis, nasal polyps, frequent exacerbation and severe asthma. Moreover, the entire respiratory tract mucosa in patients with AERD is intensely infiltrated with eosinophils, mast cells and activated T cells.4, 5, 6 A distinguishing feature of AERD is the overproduction of and hyperreactivity to cysteinyl leukotrienes (CysLTs). The CysLT level is elevated both at baseline7 and following aspirin exposure in patients with AERD.8 Patients with AERD also express more LTC4 synthase9 and CysLT receptors on their inflammatory cells and respiratory tract mucosa compared with healthy controls.10 Platelet adherence to leukocytes has been implicated in excessive CysLT production in patients with AERD.11 In addition, inhibition of COX-1 decreases the production of inflammatory suppressive mediators such as prostaglandin E2 (PGE2).12 AERD is therapeutically responsive to agents that block CysLT receptors or inhibit CysLT synthesis.13 Nonetheless, the precise role of CysLT overproduction/hyperreactivity in AERD has been questioned. Variable therapeutic responses have been observed among asthmatics treated with CysLT receptor 1 antagonists.14, 15 Zileuton, a 5-lipoxygenase inhibitor, and montelukast and zafirlukast, inhibitors of CysLT receptor 1, are only partially effective at inhibiting the reaction to aspirin in patients with AERD.16, 17, 18, 19 Moreover, their therapeutic effects may not even be related to aspirin hypersensitivity.20

Interleukin-4 (IL-4) is abundantly produced by a subset of leukocytes including T-helper type 2 cells, mast cells and eosinophils.21 Increased IL-4 levels have been found in the nasal mucosa of patients with chronic rhinosinusitis.6, 22 IL-4 potentiates many pathophysiological features of AERD, including the upregulation of LTC4 synthase23 on mast cells and of CysLT receptors 1 and/or 2 on immune cells.24, 25, 26, 27 IL-4 also induces vascular adhesion molecules to facilitate eosinophil extravasation,28 decreases PGE2 production by inhibiting COX-2 and microsomal PGE227 and activates T-helper type 2 differentiation and inflammation.29 Thus, IL-4 is an important mediator of the AERD phenotype.

Aspirin is believed to exert its anti-inflammatory effect, which has typically been evaluated in the presence of potent proinflammatory mediators such as phorbol myristate acetate, calcium ionophores, cytokines and LPS.30, 31, 32, 33 In these conditions, the anti-inflammatory effects of aspirin are shown to be mediated by the inhibition of PGE2 synthesis and other inflammatory signaling molecules34 such as NF-κB (nuclear factor-κB),30 AP-1 (activator protein-1),35 ERK1/2 (extracellular signal-regulated kinase 1/2)36 and STAT6 (signal transducer and activator of transcription 6).31, 32 These effects appear to be independent of COX inhibition. Moreover, aspirin has been reported to inhibit IL-4 transcription in activated CD4+ T cells via an unknown mechanism.33 Aspirin-mediated inhibition of IL-4 synthesis has been hypothesized to explain the therapeutic benefit of aspirin desensitization treatment.37 However, the effect of aspirin itself on inflammatory responses in the absence of inflammatory stimuli has rarely been evaluated. We previously demonstrated that aspirin stimulates IL-4 transcription in some leukemic cell lines.38 This result was surprising, as aspirin-induced IL-4 expression is in sharp contrast to the reported inhibitory effect on IL-4 production.33 However, our results may provide an important perspective on aspirin hypersensitivity, given the multifaceted roles of IL-4 in generating the pathophysiological characteristics of AERD, a T-helper type 2-type disease. In the present study, we investigated whether aspirin induced IL-4 production and examined the associated biochemical and molecular mechanisms. We also found that peripheral blood mononuclear cells (PBMCs) from patients with AERD produce more IL-4 upon exposure to aspirin compared with those from patients with aspirin-tolerant asthma (ATA).

Materials and methods

Cell cultures

HMC-1, EoL-1, Jurkat and human cord blood (CB) eosinophils and mast cells were cultured as described previously.39, 40 The identity of CB eosinophils was confirmed by intracellular staining with anti-human MBP antibody (BD Pharmingen, San Diego, CA, USA), which indicated >90% purity. The purity of the CB mast cells was also >90%, as determined by staining with anti-human FcɛRIα (Millipore, Bedford, MA, USA). The PBMCs were isolated using Ficoll-Paque Premium 1.073 (GE Healthcare, Uppsala, Sweden).

Measurement of IL-4 mRNA expression

The cells were treated with aspirin (A2093) or celecoxib (PZ0008) from Sigma-Aldrich (St Louis, MO, USA) for the indicated time intervals. cDNA synthesis from total RNA and quantitative real-time PCR (qPCR) were performed as described previously.39 The IL-4 mRNA levels were normalized to the PP1A mRNA levels. The relative expression was evaluated using the comparative cycle threshold (2−ΔΔCt) method. The mean normalized gene expression±s.e.m. was calculated from independent experiments. The following primers were used: IL-4—forward, 5′-AACAGCCTCACAGAGCAGAAGAC-3′ reverse, 5′-GCCCTGCAGAAGGTTTCCTT-3′ PP1A—forward, 5′-TCCTGGCATCTTGTCCATG-3′ reverse, 5′-CCATCCAACCACTCAGTCTTG-3′. The PCR product of the IL-4 gene was confirmed by sequencing.

Flow cytometry

The cells were fixed in 4% paraformaldehyde (Sigma-Aldrich) for 15 min at 4 °C, stained intracellularly with either phycoerythrin-conjugated mouse anti-human IL-4 monoclonal antibodies (mAbs) (BioLegend, San Diego, CA, USA) or mouse IgG1 Abs (BD Pharmingen), and analyzed with a FACSCalibur flow cytometer and CellQuest software (Becton Dickinson, San Jose, CA, USA).

Western blot analysis

Cell lysates were prepared in RIPA buffer as described previously.39 The blots were probed with anti-phospho-ERK1/2, anti-ERK, anti-phospho-p38, anti-p38, anti-phospho-JNK (c-Jun N-terminal kinase) and anti-JNK Abs (Cell Signaling Technology, Beverly, MA, USA). Expression of nuclear factor of activated T cells (NFAT), which has a crucial role in immune function, was monitored with anti-NFAT1 and anti-NFAT2 Abs (Abcam, Cambridge, UK). The blots were probed with anti-glyceraldehyde 3-phosphate dehydrogenase Abs (Santa Cruz Biotechnology, Santa Cruz, CA, USA) as a loading control. Secondary anti-rabbit horse radish peroxidase-conjugated Abs and anti-mouse horse radish peroxidase-conjugated Abs were obtained from Cell Signaling Technology. Immunoreactive bands were visualized using an ECL detection system (Amersham Biosciences, Buckinghamshire, UK).

Luciferase reporter assay

The luciferase reporter vector consisting of the IL-4 promoter sequence (from −649 to −1 relative to the translation start site) subcloned into pGL3-Basic (Promega, Madison, WI, USA) has been described previously.38 IL-4 promoter deletion constructs were generated by PCR using the primers listed in Supplementary Table S1. Transfection was performed with Lipofectamine 2000 (Invitrogen Life Technologies, Waltham, MA, USA) for HMC-1 cells and Jurkat cells or with an Amaxa 4D-nucleofector (Lonza, Köln, Germany) for EoL-1 cells. The luciferase activity was measured and expressed as described previously.39

Nuclear extract preparation and EMSA

Nuclear extracts were subjected to electrophoretic mobility shift assay (EMSA) analysis as described previously,39 using probes for six P elements41 and for an aspirin-targeted region (ATR), which was previously implicated in the aspirin-induced inhibition of IL-4 production in activated T cells.33 The ATR extends from nucleotides −164 to −200 in the IL-4 promoter. For supershift analysis, the extracts were incubated with anti-NFAT Abs or control Abs (Sigma-Aldrich) before reaction with the radiolabeled P4 probe.

Subjects

Written informed consent was obtained from all subjects. The protocols used in this study were approved by the Ethics Committees of Hanyang University (HYG-11-019-1), Soonchunhyang University Bucheon Hospital (SCHBC_IRB_05_02 and schbc-biobank-2012-004) and the Korean Red Cross, Korea. Patients with AERD (n=11) or ATA (n=12) were recruited from the outpatient clinics of Soonchunhyang University Bucheon Hospital. All patients were diagnosed by physicians and met the definition of asthma from the Global Initiative for Asthma guidelines.42 Questionnaires covered the five specific elements of aspirin hypersensitivity (dyspnea, wheezing, nasal blockage, skin eruption and loss of consciousness after aspirin ingestion). To confirm aspirin hypersensitivity, oral aspirin challenges with increasing doses of aspirin were performed with all asthmatics as described.43, 44 The oral aspirin challenge reactions were categorized into two groups: a 15% or greater decrease of forced expiratory volume in 1 s or the appearance of naso-ocular reactions (AERD) and a decrease of <15% of forced expiratory volume in 1 s1 without naso-ocular or cutaneous reactions (ATA). The clinical characteristics of the AERD and ATA groups are compared in Table 1. Blood samples for the control subjects were provided by the Korean Red Cross. These subjects had no history of drug allergy, including aspirin hypersensitivity. Therefore, the clinical parameters were considered not be to be applicable because no measurement of these parameters was made.

Table 1. Clinical characteristics of the study subjects.

  ATA AERD P-valuea
N 12 11 −
Age (years)b 53.4±14.0 42.6±14.8 0.089
Gender (male, %) 27.3 25.0 0.901
Smoking status (smoker, %) 9.1 8.3 0.865
Height (cm)b 159.6±10.3 164.0±10.4 0.317
Weight (kg)b 63.6±9.1 63.6±11.4 0.990
Body mass index (kg m−2)b 25.0±2.5 23.7±3.7 0.354
Decline in FEV1 by aspirin provocation (%)b 5.3±5.3 26.5±8.0 <0.001
Blood eosinophils (%)b 8.3±17.4 6.8±4.7 0.785
FEV1 (% predicted)b 87.7±14.6 84.7±29.3 0.760
PC20 methacholine (mg ml−1)b 11.0±11.1 5.5±7.6 0.218
Total IgE (IU ml−1)b 175.0±279.7 391.3±463.2 0.191
Skin test (positive, %) 54.5 50.0 0.827
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Abbreviations: AERD, aspirin-exacerbated respiratory disease; ATA, aspirin-tolerant asthma; FEV1, forced expiratory volume in 1 s; Ig, immunoglobulin.

a

The P-values were obtained using χ2 test and independent t-test.

b

Presented as mean±s.d.

Statistical analysis

All statistical analyses were performed using SPSS software, version 12.0 (SPSS, Chicago, IL, USA). Independent t-test was used to compare the relative reporter activities between the experiments. The Kruskal–Wallis and post hoc Mann–Whitney tests were used to analyze the differences between the IL-4 mRNA levels in PBMCs in the control, ATA and AERD groups. Differences with a P-value <0.05 were considered statistically significant. The results are expressed as the means±s.e.m.

Results

Aspirin-mediated induction of IL-4 mRNA expression and protein production

We first examined whether primary cells, including PBMCs, CB eosinophils and CB mast cells, expressed IL-4 in response to aspirin. Aspirin induced IL-4 mRNA in a dose-dependent manner (Figure 1). Next, we examined IL-4 expression in HMC-1 mast cells, EoL-1 eosinophilic cells and Jurkat T cells, which were chosen because they are representative of cells that express high levels of IL-4 in vivo21 and are relevant to AERD pathogenesis.4, 5, 6 Aspirin induced a similar, dose-dependent pattern of IL-4 transcription in each cell line (Figure 2a). Kinetic experiments showed that IL-4 expression reached a peak 2–4 h after stimulation and declined thereafter (Figure 2b). Aspirin also activated the IL-4 promoter in all three cell lines (Figure 2c). The intracellular IL-4 protein levels also increased in a dose-dependent manner upon exposure to aspirin for 24 h (Figure 2d). No cytotoxic effects of 0.2–5 mM aspirin were observed in any of these cells for the indicated period of time, as evaluated by Trypan blue exclusion. Celecoxib, a selective COX-2 inhibitor,3 which has no crossreactivity with aspirin and thus is tolerated,1, 3 did not induce IL-4 expression at concentrations within or above its respective COX-inhibitory range (1–100 μM)45 in any cell type examined (Supplementary Figure S1). In summary, aspirin induced IL-4 production in all of the cell types examined.

Figure 1.

Figure 1

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Aspirin induces interleukin-4 (IL-4) mRNA expression in cord blood (CB) eosinophils, CB mast cells and peripheral blood mononuclear cells (PBMCs). CB eosinophils and CB mast cells were differentiated from CD34+ CB cells for 24 and 42 days, respectively. PBMCs were isolated from normal subjects. The cells were treated with aspirin for 4 h, and IL-4 mRNA expression was measured by quantitative real-time PCR (qPCR). The data are presented as the mean±s.e.m. for eosinophils (n=3), mast cells (n=3) and PBMCs (n=6; **P<0.01 compared with unstimulated cells at 4 h).

Figure 2.

Figure 2

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Aspirin induces interleukin-4 (IL-4) mRNA expression and protein production. (a) HMC-1, EoL-1 and Jurkat cells were treated with various concentrations of aspirin for 4 h. IL-4 expression was measured by quantitative real-time PCR (qPCR); n=4–6. The IL-4 mRNA levels (means±s.e.m.) are expressed relative to the PP1A expression levels (**P<0.01 compared with unstimulated cells at 4 h). (b) Kinetics of IL-4 expression in the presence of 5 mM aspirin; n=2. (c) Cells were transfected with an IL-4 promoter reporter (−649). After 24 h, the transfected cells were stimulated with aspirin for 4 h; n=4 (*P<0.05 and **P<0.01 compared with unstimulated cells at 4 h). (d) Cells were treated with aspirin for 24 h, and the levels of intracellular IL-4 were analyzed by FACS (fluorescence activated cell sorting).

Activation of ERK, p38 and JNK in aspirin-induced IL-4 expression

Aspirin can activate, inhibit or have no effect on mitogen-activated protein kinase (MAPK) family members.34 Thus, we examined the effects of aspirin on various MAPK family members. The treatment of HMC-1 cells with aspirin for 4 h resulted in a dose-dependent activation of ERK1/2 (Figure 3a). Aspirin at 5–20 mM concentrations has been shown to inhibit ERK1/2 activation in cells under stress conditions.46, 47 Because the latter observation conflicted with our findings, we used U0126, an ERK inhibitor. In the presence of U0126, ERK1/2 phosphorylation (Figure 3b) and IL-4 mRNA levels (Figure 3c) were decreased. Moreover, phospho-p38 and phospho-JNK levels were elevated with increased concentrations of aspirin, and the inhibitors of these two MAPKs almost completely blocked IL-4 transcription in a dose-dependent manner (Figure 3d). In contrast, celecoxib did not activate ERK1/2 or p38; in fact, the compound reduced JNK phosphorylation at high doses (Figure 3a). These results indicate that activation of each MAPK member is necessary for aspirin-induced IL-4 expression.

Figure 3.

Figure 3

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Interleukin (IL-4) mRNA expression requires the activation of mitogen-activated protein kinases (MAPKs). (a) HMC-1 cells were treated with aspirin or celecoxib for 4 h. Activation of MAPKs was then assessed by western blotting. The blots were probed with anti-phospho-MAPK antibodies (Abs). Replica blots were probed for total MAPKs as loading controls. (b) HMC-1 cells were treated with aspirin (5 mM) for 4 h following pretreatment with U0126 (10 μM), SB203580 (10 μM) or SP600125 (20 μM) for 30 min. The blots were probed with anti-phospho-ERK1/2 Ab and reprobed with anti-total ERK Ab as a loading control. (c) HMC-1 cells were treated with aspirin (5 mM) for 4 h following pretreatment with increasing doses of U0126 or for 30 min. IL-4 expression was then assessed by quantitative real-time PCR (qPCR). (d) HMC-1 cells were pretreated with U0126 (10 μM), SB203580 (10 μM) or SP600125 (20 μM) for 30 min before treatment with aspirin for 4 h. IL-4 expression was then quantified by qPCR. The data (mean±s.e.m., n=3) are expressed relative to the PP1A mRNA levels (**P<0.01 compared with aspirin-treated cells). ERK1/2, extracellular signal-regulated kinase 1/2; JNK, c-Jun N-terminal kinase.

Aspirin responsiveness does not map to any particular region within the IL-4 proximal promoter

We next investigated which cis-acting elements or sequences within the IL-4 promoter are aspirin-responsive. At least six P elements (P0–P5) and other sequence elements in the IL-4 proximal promoter have been shown to have a critical role in IL-4 transcriptional activation.48 NFAT binds to most, if not all, P elements through interactions with AP-141 or other transcription factors.49 To study the responsiveness of the P elements, serially deleted IL-4 promoter reporters were constructed (Figure 4a). HMC-1 cells were transfected with these constructs and then treated with aspirin. Aspirin responsiveness was well conserved in the three largest constructs (−649, −584 and −330), which retained all or most of the P elements. The −210 promoter reporter, which lacked the P5, P4 and P3 elements, was no longer aspirin-responsive. The −177 construct, which lacked two-thirds of the ATR but contained the P0 and P1 elements, retained aspirin responsiveness (Figure 4b). Identical response patterns were observed in Jurkat and EoL-1 cells (data not shown). These results suggest that the aspirin-responsive sequence of the IL-4 proximal promoter is not confined to a particular region.

Figure 4.

Figure 4

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Aspirin augments interleukin (IL-4) promoter activity. (a) The IL-4 proximal promoter. (b) HMC-1 cells were transfected with reporter constructs. After 24 h, the cells were stimulated with aspirin (5 mM) for an additional 4 h. Reporter activity was then analyzed. The data (mean±s.e.m., n=3) are presented as fold increase compared with unstimulated cells (**P<0.01 compared with unstimulated cells). ATR, aspirin-targeted region.

Aspirin alters DNA–protein complex formation at the IL-4 proximal promoter

HMC-1 cells were treated with aspirin or celecoxib for 4 h. Nuclear extracts were generated and subjected to EMSA analysis. In unstimulated cells, few or no protein complexes were formed with the P0, P2 and ATR probes. In contrast, the P1, P3, P4 and P5 probes all bound to protein(s) (Figure 5a). The treatment of HMC-1 cells with aspirin resulted in a slightly increased amount of DNA–protein complexes with the P0, P2 and ATR probes and a substantial increase with the P1 and P3 probes. Moreover, a slower-migrating species appeared with the P4 and P5 probes. Each cold probe efficiently outcompeted the augmented or newly formed DNA–protein complexes (data not shown), indicating that these bands are specific. In contrast, celecoxib failed to induce DNA–protein complex formation with the P0, P1, P2 or ATR probes. Furthermore, this compound considerably reduced DNA–protein complex formation with the P3, P4 and P5 probes.

Figure 5.

Figure 5

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Aspirin induces the formation of DNA–protein complexes on P elements in the interleukin-4 (IL-4) promoter. (a) HMC-1 cells were treated with aspirin or celecoxib for 4 h. Nuclear extracts were incubated with 32P-labeled oligonucleotides, as indicated. Representative results are shown (n=3). (b) Nuclear extracts from aspirin-treated HMC-1 cells were incubated with the 32P-labeled P4 probe in the presence or absence of its cold probe. (c) Nuclear extracts from aspirin-treated HMC-1 cells were incubated with the 32P-labeled P4 probe following reaction with anti-NFAT1, anti-NFAT2 or isotype-control antibodies (Abs). The arrow and the arrowhead indicate the major DNA–protein complex and the supershifted band, respectively. ATR, aspirin-targeted region; NFAT, nuclear factor of activated T cell.

Synthesis of NFATs by aspirin and celecoxib

NFAT1 and NFAT2 are both required for IL-4 expression in T cells.50 Treatment of HMC-1 cells for 4 h with aspirin, but not celecoxib, stimulated NFAT1 and NFAT2 production (Figure 6). EMSA analysis showed that the P4–protein complex that disappeared following treatment with a P4 cold probe (Figure 5b) and was increased by aspirin treatment was supershifted by incubation with anti-NFAT1 or anti-NFAT2 Abs but not with isotype-control Abs (Figure 5c). This result indicates that aspirin induces IL-4 expression at least, in part, through the increased synthesis of NFATs. This conclusion is also supported by a collection of the IL-4 promoter deletion experiments, the formation of DNA–protein complex and the upregulation of NFAT synthesis. The −330 or longer constructs, all of which contain most P elements, were aspirin-responsive. This could be because aspirin increased or induced the formation of the DNA–protein complexes, presumably including NFAT1 or NFAT2, on these elements. The −210 construct, which contains P0, P1 and the ATR, was not aspirin-responsive (Figure 4). In this construct, the ATR represses IL-4 expression in a dominant manner, despite the presence of P1, which appears to act as a positive element. Finally, the −177 construct, which contains P0 and P1 but lacks the ATR, restored the aspirin response because of the presence of P1, which has previously been shown to interact with NFAT1 and NFAT2.51 Thus, both P elements and the ATR appear to regulate the aspirin-mediated expression of IL-4.

Figure 6.

Figure 6

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Aspirin induces the synthesis of nuclear factor of activated T cells (NFATs). HMC-1 cells were treated with aspirin or celecoxib for 4 h. The levels of NFAT1 and NFAT2 were then analyzed by western blotting. Images are representative of three independent experiments. GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

The effects of aspirin on IL-4 expression in PBMCs from patients with AERD or ATA

We next examined IL-4 expression in PBMCs from patients with AERD or ATA (Table 1). Aspirin upregulated IL-4 expression in PBMCs from both groups compared with the untreated controls. Of particular note, aspirin upregulated IL-4 mRNA expression twice as much in PBMCs from patients with AERD compared with those from patients with ATA (4.50±0.32, n=11 vs 2.25±0.18, n=12, respectively; P=0.00004), as seen in Figure 7a. In contrast, celecoxib did not upregulate IL-4 expression in any group. Aspirin, also induced IL-4 expression in PBMCs from control subjects (Figure 7a). The fold induction in control PBMCs (1.94±0.17) was significantly lower compared with that in PBMCs from patients with AERD (P=0.00003) but was comparable with that in the PBMCs of patients with ATA (Figure 7a). Similarly, a significantly higher IL-4 protein expression was observed in aspirin-treated PBMCs from AERD patients compared with that in ATA patients (P=0.0002; Figure 7b).

Figure 7.

Figure 7

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Aspirin upregulates interleukin-4 (IL-4) production to a greater extent in peripheral blood mononuclear cells (PBMCs) from patients with aspirin-exacerbated respiratory disease (AERD) compared with those from patients with aspirin-tolerant asthma (ATA). (a) PBMCs were treated with aspirin (5 mM) or celecoxib (100 μM) for 4 h. IL-4 expression was then measured by quantitative real-time PCR (qPCR). The data are presented as the mean±s.e.m. (patients with AERD, n=11; patients with ATA, n=12; control subjects, n=8; **P<0.01 compared with unstimulated cells within each group at 4 h). (b) PBMCs were treated with the two compounds for 24 h, and the levels of intracellular IL-4 were analyzed by FACS (fluorescence activated cell sorting). The data are presented as the mean±s.e.m. (patients with AERD, n=11; patients with ATA, n=12; **P<0.01 compared with unstimulated cells within each group at 4 h). †Comparisons of aspirin-treated PBMCs from patients with AERD vs patients with ATA.

Discussion

The primary mechanism of AERD pathogenesis is believed to be the aspirin-mediated relief of negative inhibition of CysLT production. However, agents that modify or blunt CysLT metabolism partially eliminate respiratory reactions in patients with AERD,14, 15, 16, 17, 18, 19 suggesting alternative and/or complementary pathways driving AERD pathogenesis. IL-4 potentiates many pathophysiological aspects of AERD.6, 22, 23, 24, 25, 26, 27, 28, 29 We have previously demonstrated that aspirin induces IL-4 transcription in some leukemic cells,38 raising the possibility that IL-4 is an inflammatory mediator of aspirin hypersensitivity. This observation is intriguing considering that AERD is considered to be a T-helper type 2-mediated disorder. The present study indicates that aspirin is directly linked with IL-4 production in the context of AERD pathogenesis as (i) aspirin induced IL-4 expression and activated the IL-4 promoter in cell types relevant to AERD pathogenesis, indicating that IL-4 may be a direct target of aspirin; (ii) aspirin-induced IL-4 production was accompanied by the activation of biochemical and molecular pathways leading to IL-4 transcription; (iii) aspirin-induced higher levels of IL-4 transcription in PBMCs from patients with AERD compared with those from patients with ATA. Based on these results, we suggest that IL-4 serves as an important inflammatory mediator for intolerance reactions to aspirin.

The aim of the present study is threefold: to examine aspirin-induced IL-4 production, to analyze its biochemical and molecular mechanisms and to corroborate the differential response to aspirin by comparing IL-4 production in primary cells from patients with AERD and ATA. We used both human leukemic cell lines and their primary counterparts, which are more relevant to the pathogenesis of aspirin sensitivity. We found that aspirin induced IL-4 expression in nearly all of the cells examined, whereas celecoxib did not. Their ability or inability to induce IL-4 expression was consistent with their ability to activate the three MAPK members, form DNA–protein complexes with P elements and the ATR in the IL-4 promoter, and upregulate production of NFATs, which are critical transcription factors for IL-4.48 EMSA analysis showed that the DNA–protein complexes included both NFAT1 and NFAT2. Notably, aspirin itself has been shown to increase intracellular Ca2+ levels, transiently upregulate protein kinase C in T cells52, 53 and activate p38 and JNK,34, 54, 55 all of which are required for IL-4 production by CD4+ T cells.48 Our data are in agreement with these findings. In contrast, aspirin has also been reported to suppress ERK1/2 activity;46, 47 however, ERK1/2 was activated by UV or phorbol myristate acetate before treatment with aspirin in these studies. Our data demonstrate unequivocally that aspirin activates ERK1/2, supporting the involvement of ERK1/2 in aspirin-mediated IL-4 induction (Figure 3). Overall, aspirin-induced IL-4 production appears to rely on signaling pathways and their subsequent molecular events (see below). Celecoxib can also mobilize these signaling molecules in some epithelial cells.56, 57 However, this inhibitor did not activate pathways associated with IL-4 expression, at least in the cell types examined in our study. We therefore conclude that the capacity of aspirin to induce IL-4 expression is consistent with its ability to initiate biochemical and molecular processes leading to the induction of IL-4 production.

Our data conflict with a previous report concluding that aspirin inhibits IL-4 transcription in phorbol myristate acetate/ionomycin-stimulated peripheral blood CD4+ T cells,33 a result that has not been confirmed to date. Additionally, aspirin has been shown to mediate anti-inflammatory responses by inhibiting numerous signaling molecules, including NF-κB.30, 31, 32, 35, 36 These studies all involved placing cells under strong inflammatory conditions. However, there are also a few studies demonstrating the proinflammatory effects of aspirin itself, including the upregulation of nuclear NFAT expression58 and the activation of NF-κB.59 Thus, aspirin can exert both proinflammatory and anti-inflammatory functions depending on the inflammatory context.

We found that IL-4 mRNA and protein levels were significantly higher in aspirin-treated PBMCs from AERD patients compared with that in aspirin-treated PBMCs from ATA patients (Figure 7). This result is consistent with a previous study, in which lysine aspirin induced Ca2+ mobilization in eosinophils isolated from AERD patients.60 Furthermore, Steinke et al.61 showed that nasal polyps from patients with AERD had significantly elevated IL-4 and interferon-γ expression compared with polyps from patients with an aspirin-tolerant disease. However, it is not yet known whether high IL-4 concentrations induced by aspirin elicit the characteristic phenotypes of AERD, including CysLT overproduction/hyperreactivity and reduced PGE2 synthesis. Nonetheless, as our data show that aspirin induces IL-4 production at a much higher level in PBMCs from AERD compared with that in ATA patients, it would be critically informative for the diagnosis of AERD to compare aspirin-induced IL-4 production between larger cohorts of patients.

It has been shown that aspirin has both inhibitory and stimulatory effects on notable signaling molecules, especially at high doses. These include NF-κB,30 ERK1/2,36 STAT6,31, 32 p38,45 and JNK.62 These effects are exerted by single- to two-digit millimolar concentrations of aspirin. It has recently been shown that lysine aspirin at 3–10 mM provokes Ca2+ mobilization and degranulation of eosinophil-derived neurotoxin in peripheral blood eosinophils from AERD patients and in CB eosinophils.60 Therefore, the concentrations of aspirin used in this study appear to be comparable to those in most other in vitro studies.

In summary, here, we reveal a previously unrecognized transcriptional target of aspirin, IL-4. Aspirin-induced IL-4 production exploits known biochemical and molecular pathways involved in IL-4 transcription. Of particular note, much higher IL-4 levels are produced in aspirin-treated PBMCs from patients with AERD compared with those from patients with ATA. Thus, IL-4 functions as a new inflammatory mediator that might drive AERD pathogenesis.

Acknowledgments

This work was supported by a grant from the Korea Healthcare Technology R&D Project, Ministry of Health, Welfare and Family Affairs and Republic of Korea (HI13C0319). SKK was supported by BK21 Plus, Korea Research Foundation. Whole blood was obtained from the Biobank in Soonchunhyang University, Bucheon Hospital (Republic of Korea) after obtaining written consent from the subjects. We thank Drs Tae Wook Yoo and Woo Sung Lim (Woosung Women's Hospital, Ansan, Republic of Korea) for providing CB.

The authors declare no conflict of interest.

Footnotes

Supplementary Information accompanies the paper on Experimental & Molecular Medicine website (http://www.nature.com/emm)

Supplementary Material

Supplementary Information
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Supplementary Figure S1
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Supplementary Table S1
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