Abstract
Patients with late-onset asthma (LOA) have poor clinical outcomes. Osteopontin (OPN) is associated with airway inflammation and remodeling. To investigate the role of OPN in LOA compared to early-onset asthma (EOA), serum OPN levels were compared between 131 adult asthma patients (48 LOA and 83 EOA patients) and 226 healthy controls (HCs). BALB/c mice were sensitized with ovalbumin with/without polyinosinic-polycytidylic acid (poly(I:C)) from week 6 (A6 mice) or week 12 (A12 mice) after birth. Airway hyperresponsiveness (AHR), bronchoalveolar lavage fluid (BALF), cell counts, histology, and Spp1 expression were assessed. The levels of OPN, transforming growth factor β1 (TGF-β1), chitinase 3-like 1 (CH3L1), and interleukin (IL) 5 were measured by ELISA. The expression of Smad3 phosphorylation and tissue transglutaminase 2 (TGM2) was evaluated by Western blot. The serum OPN levels were significantly higher in asthma patients than in HCs and in LOA patients than in those with EOA (P < 0.05) and were positively correlated with serum TGF-β1 and CH3L1 (r = 0.174, r = 0.264; P < 0.05). A12 mice showed elevated AHR with increased levels of OPN/TGF-β1/IL-5 in BALF and Spp1 compared to A6 mice. Poly(I:C) induced remarkable TGF-β1, CH3L1, Th2 cytokine, and OPN levels in BALF and the expression of phosphorylated Smad3, TGM2, and Spp1 in the lungs. OPN triggered TGF-β1/Smad3 signaling in the lungs, which was suppressed by dexamethasone and anti-IL5 antibody. In conclusion, aging and exposure to viral infections may induce OPN release and consequently modulate inflammation and TGF-β1/Smad3-related remodeling, contributing to the development of LOA.
Similar content being viewed by others
Introduction
The prevalence of asthma in the aged populations is increasing, causing an economic burden in Korea and worldwide. Asthma is characterized by chronic inflammation of the respiratory tract and consists of various phenotypes1. Late-onset asthma (LOA) is a phenotype that results in the development of asthma symptoms after 40 years of age and is characterized as being less eosinophilic, with a female predominance and more severe clinical features associated with a progressive decline in lung function2,3. Non-T helper (Th)2-LOA is usually corticosteroid-resistant and requires special treatment strategies2. Additionally, age-related changes in the immune system could complicate the pathophysiology of LOA4,5. The increasing prevalence and poor prognosis of LOA pose a challenge in the management of adult asthma. Attempts to elucidate the pathogenic mechanisms of LOA are warranted.
Airway remodeling consists of changes in the components and organization of the airway wall, which occurs in the epithelium, subepithelial layer, extracellular matrix (ECM) proteins, smooth muscle, and blood vessels6. The airway epithelium contributes to epithelial–mesenchymal transition, which leads to epithelial damage7. In subjects with LOA, airway remodeling can be either pathological or physiological due to aging-related structural changes in the airway2,8. Additionally, viral respiratory infections can worsen airway remodeling in adult asthma9. Respiratory viral infections induce the release of proinflammatory cytokines such as interleukin (IL)-6 and IL-8 from human airway epithelial cells (HAECs) and initiate cell recruitment, which amplifies airway inflammation and subsequent airway remodeling, such as long-term alterations in airway structures and functions in asthma10,11. A history of upper and lower respiratory infections, including acute bronchitis, the common cold and sinusitis, strongly increases the risk of asthma development in adults12. Furthermore, individuals with atopic asthma have been found to have an impaired response to viral infection13. Therefore, in addition to the aging process, respiratory viral infection may be an important risk factor that regulates airway remodeling in LOA.
Recently, osteopontin (OPN), a noncollagenous ECM protein, has been shown to be widely expressed in various cells, including HAECs, and is known as a multifunctional cytokine, as it drives Th1, Th2, and Th17 immunity14,15,16. OPN is known to act as a dual-regulatory cytokine—a proinflammatory cytokine during primary sensitization while having an anti-inflammatory effect on Th2 responses during a secondary antigen challenge16. More importantly, OPN is upregulated and remains a key component in allergen-induced airway remodeling in mouse models of asthma17,18. In patients with severe refractory asthma, OPN levels were shown to be associated with increased levels of transforming growth factor-β1 (TGF-β1)19. Epithelial OPN has been found to increase with IL-6/soluble IL-6 receptor stimulation in individuals with asthma20. Eosinophil-derived OPN was shown to contribute to fibrosis through the IL-33/amphiregulin (Areg)/epidermal growth factor receptor (EGFR) axis in the context of Th2 inflammation21. Recent functional studies demonstrated that OPN presents as the polymerized form due to the effect of tissue transglutaminase 2 (TGM2) in the human airways, which increases its collagen-binding activity22,23. Accumulating evidence suggests that OPN is a key cytokine in the modulation of inflammation and fibrotic events in asthmatic airways. Nevertheless, the role of OPN in the LOA phenotype has not yet been investigated. A subgroup of adults with asthma with high chitinase 3-like 1 (CH3L1, also called YKL-40) was prone to have adult-onset and frequent asthma exacerbations, suggesting an association between OPN and CH3L124.
In the present study, we hypothesized that respiratory viral infection as well as aging could induce OPN release, thereby contributing to airway inflammation and remodeling in the pathogenesis of LOA. In addition, relationships with various inflammatory cytokines, including Th1/Th2 cytokines (IL-4, IL-5, IL-13, interferon [IFN]-γ) and epithelial and ECM cytokines (IL-8, IL-33, TGF-B1 and CH3L1), were evaluated in in vitro and in vivo models. Two different mouse models of asthma representing younger and older onset times were established. The effects of exposure to respiratory viruses on innate immunity and asthma severity were investigated using in vitro and in vivo models. Moreover, the downstream effects of OPN on fibrosis-associated pathways were explored.
Materials and methods
Study population
This study was approved by the Ethics Committee of Ajou University Institutional Review Board (AJIRB-GEN-SMP-13-108). In this study, 131 adults with asthma, including 48 with LOA and 83 with early onset-onset asthma (EOA), and 226 non-atopic healthy controls (HCs), were enrolled at the Department of Allergy and Clinical Immunology, Ajou University Hospital (Suwon, South Korea). The individuals with asthma were diagnosed and treated following the Global Initiative for Asthma (GINA) 2019 guideline25. Patients with primary eosinophilic diseases, including eosinophilic granulomatosis with polyangitis and hypereosinophilic syndrome, were excluded. We obtained written consent from each subject. The demographic data were recorded regarding age, sex, asthma onset time, asthma duration and smoking status. A diagnosis of atopy was based on positive skin test results for at least one or more common inhalant allergens (tree mixture, grass mixture, mugwort, ragweed, cat fur, dog fur, Dermatophagoides farinae (Der F), Dermatophagoides pteronyssinus (Der P) and Alternaria spp. [Bencard Co., Bredford, UK]). Patients with asthma underwent spirometry (FEV1%, FVC% predicted values) and methacholine (Mct) challenge tests to evaluate airway hyperresponsiveness (AHR) according to the European Respiratory Society standard26. The concentration of Mct required to produce a 20% decrease in FEV1 from baseline (MctPC20) was recorded. Severe asthma was defined according to the American Thoracic Society/European Respiratory Society guidelines27. Serum samples from patients and HCs were collected, stored at −70 °C and thawed before use. Total IgE levels in serum were measured by the ImmunoCAP system (Thermo Fisher Scientific, Waltham, MA, USA) in the detection range of 2–5000 kU/L.
Classification of asthma phenotype
LOA and EOA were defined when asthma had been diagnosed at the age of ≥40 years and <40 years, respectively28. To identify eosinophilic asthma, we used blood eosinophil counts with the cutoff at 300 cells/µl as previously described29.
HAEC cultures and treatment
HAECs, including A549 cells and primary small airway epithelial cells (SAECs), were purchased from the American Type Culture Collection (ATCC) (Manassas, VA, USA). A549 cells were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum, penicillin G sodium (100 UI/mL) and streptomycin sulfate (100 μg/mL) (all from Gibco, Grand Island, NY, USA). SAECs were cultured in basal medium supplemented with a bronchial epithelial cell growth kit (ATCC), penicillin G sodium (10 UI/mL), streptomycin sulfate (10 μg/mL) (Gibco), and amphotericin B (25 ng/mL) (Sigma Aldrich, St. Louis, MO, USA) according to the manufacturer’s protocol. Cells were grown at 37 °C in humidified air with 5% CO2. For treatment, cells (2 × 105) were seeded onto a 12-well plate and stimulated with polyinosinic:polycytidylic acid (poly(I:C)) (Sigma Aldrich) at 1 and 10 μg/mL. After 24-h incubation, the supernatant was collected; cells were lysed in radioimmunoprecipitation assay (RIPA) buffer supplemented with protease inhibitor (Thermo Fisher Scientific) and stored at −70 °C for further experiments.
Establishment of an LOA mouse model
Female BALB/c mice at 6 and 12 weeks old (weight 20 ± 2 and 21 ± 2 g, respectively) were purchased from the Jackson Laboratory (Bar Harbor, ME, USA), housed under specific pathogen-free conditions, maintained on a 12-h light/dark cycle and fed ad libitum. Asthma was induced at two time points, modified from a previous protocol30. Briefly, on days 0 and 14, mice were intraperitoneally sensitized with ovalbumin (OVA)/aluminum hydroxide (Alum) solution at 10 µg/1 mg. On days 28–30, the mice were challenged with 2% OVA for 30 min using an ultrasonic nebulizer (NE-SM1; Ktmed Inc., Seoul, South Korea). To establish the mouse model of virus-induced asthma exacerbation, mice were administered intranasal poly(I:C) (10 µg/mouse) prior to sensitization/challenge. To investigate the effects of OPN on asthma, mice were treated intranasally with 4 μg of mouse recombinant OPN protein (rOPN, 763606, Biolegend, San Diego, CA, USA) for 1 h prior to sensitization on days 0 and 14. In some experiments, mice were given dexamethasone 21-phosphate disodium salt (D1159) (Dex, 1 mg/kg), montelukast sodium hydrate (Mon, 10 mg/kg) or anti-IL-5 antibody (504302) (anti-IL5, 20 mg/kg) for 3 consecutive days prior to the challenge. Mice were assayed at 24 h after the last challenge. All animal experiments were approved by the Institutional Animal Care and Use Committee of Ajou University (IACUC 2018-0041). OVA, Dex and Mon were from Sigma Aldrich, Alum was from Thermo Fisher Scientific, and the anti-IL-5 antibody was from Biolegend.
Measurement of AHR
AHR to acetyl-β-methylcholine chloride was recorded using the FlexiVent system (Scireq, Montreal, QC, Canada). Mice were anesthetized with pentobarbital sodium, intubated with a cannula and ventilated with a tidal volume of 10 mL/kg at a frequency of 150 breaths/min. The airway resistance (RL) at baseline and a dilution series of MC from 1.56 to 25 mg/mL were noted.
Analysis of differential cell count and histology
To collect bronchoalveolar lavage fluid (BALF), 1 mL of 1x phosphate buffered saline (PBS) plus 1% bovine serum albumin (Sigma Aldrich) was used to wash the trachea. The BALF was centrifuged at 1200 revolutions per minute for 5 min at 4 °C, and the supernatant was harvested and stored at −70 °C until further experiments. Total and differential cell counts were determined by using a hemocytometer and hematoxylin–eosin (HE)-stained slides as previously described30.
Consecutively, lung tissues were perfused and divided in half; the left parts were fixed in 4% paraformaldehyde, while the right lung tissues were divided for the isolation of RNA (immersed in RNAlater® solution, Thermo Fisher Scientific) and proteins. The fixed tissues were embedded in paraffin and sectioned at 5-μm thickness. To visualize infiltrated cells, mucus-containing cells, and collagen deposition, tissues were stained with HE, periodic acid-Schiff, and Masson’s trichrome, respectively. The number of cells in the peribronchial, perivascular, and mucus-secreting cell areas, as well as smooth muscle thickness and collagen deposition were counted.
Measurement of inflammatory cytokines
The levels of inflammatory cytokines in the serum, cell-free supernatant and BALF were measured by enzyme-linked immunosorbent assay (ELISA) according to the manufacturer’s protocol. ELISA kits for human TGF-β1/CH3L1/OPN, mouse TGF-β1/IL-33 and CH3L1 were purchased from R&D Systems, Inc. (Minneapolis, MN, USA). The human IL-8 ELISA kit was purchased from Endogen (Woburn, MA, USA). For mouse BALF, the ELISA kits used to measure the levels of mouse OPN and eotaxin-2 were purchased from Ray Biotech, Inc. (Norcross, GA, USA), and mouse IL-4, IL-5, IL-13 and IFN-γ were purchased from Thermo Fisher Scientific.
Immunohistochemistry
Briefly, tissue antigen retrieval was performed with sodium citrate buffer (pH 6.0), followed by incubation with blocking buffer (0.05% PBS-Tween 20 containing 5% bovine serum albumin and 10% normal donkey serum) for 1 h at room temperature. Tissues were then incubated with rabbit anti-mouse TGM2 antibody (3357S, Cell Signaling Technology, Inc., Danvers, MA, USA) at 4 °C overnight in a humidified chamber. Subsequently, tissues were incubated with Alexa Flour 488-conjugated donkey anti-rabbit antibody (Thermo Fisher Scientific) for 1 h at room temperature, followed by counterstaining with 4',6-diamidino-2-phenylindole (1 μg/mL) for 10 min and finally mounting with a mounting solution (Biodema Corp, Foster City, CA, USA). All reagents were purchased from Sigma Aldrich unless indicated otherwise.
Analysis of gene expression by real-time PCR
Lung tissues were homogenized and harvested for total RNA using TRIzol® (Thermo Fisher Scientific). Total RNA was synthesized for cDNA by the SuperScriptTM First Strand Synthesis System (Thermo Fisher Scientific). Gene expression analysis using cDNA as templates was conducted using the KAPA SYBR® FAST qPCR Master Mix (2x) kit (Boston, MA, USA). The sequences of the primers are displayed in Table S1. The annealing temperature was 60.6 °C for all genes.
Detection of Smad3 intermediate signaling by Western blotting
Proteins were isolated from the right lung tissues by lung homogenate, followed by incubation with RIPA buffer. Aliquots of 35 μg of protein were loaded onto 10% sodium dodecyl sulfate polyacrylamide gels and transferred to polyvinylidene difluoride membranes (Bio-Rad, Hercules, CA, USA). After blocking in 5% skim milk (Sigma Aldrich) in Tris buffered saline containing 0.05% Tween 20 (TBS-T) for 1 at room temperature, membranes were incubated with primary antibodies against OPN (R&D Systems), Smad3, phosphorylated Smad3 (pSmad3) (Abcam, Cambridge, UK), and TGM2 overnight at 4 °C with gentle shaking. Then, membranes were washed three times with TBS-T for 10 min each and incubated with horseradish peroxidase conjugated with anti-goat or anti-rabbit antibody for 1 h at room temperature. Anti-β-actin antibody (Thermo Fisher Scientific) was used as an internal control. Signals were detected using ECL Plus Western Blotting Detection Reagents (GE Healthcare, Little Chalfont, UK). The intensity of bands was analyzed using a gel doc system (Bio-Rad Laboratories, Inc., Hercules, CA, USA).
Statistical analysis
The normality test of data was checked with the Kolmogorov–Smirnov test. Comparisons between the two groups were performed by the Mann–Whitney U test for continuous variables and Pearson’s chi-squared test for categorical variables. Bivariate correlations were analyzed with Spearman's rank correlation coefficient test and are presented as scatter plots. Multiple comparisons of data from multiple groups were approached by one-way ANOVA with the Tukey post hoc test. A receiver operating characteristic (ROC) curve analysis was applied to estimate the diagnostic values of serum cytokines. Data analysis and graph preparation were performed by using the statistical software packages IBM SPSS 20.0 (Armonk, NY, USA) and GraphPad Prism 6 (San Diego, CA, USA), respectively. Heatmap graphs were drawn by R (R Core Team 8, Vienna, Austria). Significance levels for all analyses were set at P < 0.05.
Results
Clinical characteristics of the study subjects
The demographic characteristics of the study subjects enrolled are summarized in Table 1. Subjects with asthma were older than the HCs (P < 0.001), and there were more females in the asthma group than in the HC group (P = 0.023). Compared to patients with EOA, those with LOA were older and less atopic (P < 0.001 and P < 0.001, respectively). There were no significant differences in peripheral eosinophil counts, FEV1% predicted values or serum total IgE levels between the two phenotypes. Subjects with asthma showed significantly higher serum levels of IL-8, CH3L1, and TGF-β1 than HCs (all P < 0.01). The serum levels of CH3L1 remained significantly increased in patients with LOA compared to those with EOA (P < 0.05).
Increased levels of serum OPN with age
The serum levels of OPN were significantly higher in subjects with asthma than in HCs (3.41 ± 0.54 vs. 2.99 ± 0.83 pg/mL) (Fig. 1a) and in patients with LOA compared to those with EOA (3.57 ± 0.41 vs. 3.31 ± 0.59 pg/mL) (Fig. 1b and Table 1). The serum OPN levels in subjects with asthma were positively correlated with age (r = 0.396, P < 0.001) (Fig. 1c).
Diagnostic values of OPN in the discrimination of individuals with asthma and patients with LOA from HCs
The ROC curve analysis of serum OPN was performed for differentiating individuals with asthma from HCs with an area under the curve (AUC) value of 0.757 (P < 0.001) and an optimal cutoff of 1488.51 pg/mL (log-transformed data as 3.17) at 75.4% sensitivity and 66.1% specificity (Fig. 1d). Based on the given cutoff value, subjects were divided into high-OPN and low-OPN responders. Additionally, the serum OPN levels were significantly different between patients with LOA and HCs, with an AUC value of 0.853 (P < 0.001) at 93.3% sensitivity and 66.1% sensitivity (Fig. 1e).
Association of serum OPN with clinical characteristics and other inflammatory cytokines
Differences in clinical characteristics between high-OPN and low-OPN responders are displayed in Table 2. High-OPN responders were older and had a higher prevalence of atopy than low-OPN responders (both P < 0.05). There were no significant differences between high-OPN and low-OPN responders in sex, total IgE level, and baseline values of FEV1/FVC and MctPC20. For inflammatory cytokines, high-OPN responders displayed significantly higher serum levels of IL-8, CH3L1, and TGF-β1 (all P < 0.05).
Significantly positive correlations were noted between serum OPN and IL-8/TGF-β1/CH3L1 (r = 0.282, r = 0.174, r = 0.264; all P < 0.05), while a negative correlation between OPN and eotaxin-2 was noted (r = −0.337, P < 0.05) (data not shown).
Characteristics of LOA and EOA mouse models
The induction of asthma led to significantly higher AHR and total cell/eosinophil counts in the BALF of older mice at 12 weeks after birth (A12 mice) than in younger mice with asthma at 6 weeks after birth (A6 mice) (Fig. 2a–c). Changes in Th2 cytokines were observed as decreased levels of IL-4 but increased levels of IL-5 and IL-13 (Fig. 2d). Genes associated with ECM remodeling and fibrosis (Spp1, Areg, Egfr, Tgfβ1, Ch3ll) and epithelial inflammation (IL33) were differentially expressed in A12 mice. Spp1 was upregulated, and the levels of OPN and TGF-β1 were increased in BALF (A6 vs. A12 mice, P < 0.05 for all, Fig. 2d–f). Histological analysis revealed a tendency toward an increase in infiltrated cells, mucus secretion, and collagen deposition (Figs. S2 and S3). These findings led us to investigate whether exogenous factors, including environmental factors, may worsen asthma severity.
Effect of respiratory virus on airway inflammation in mouse models of asthma: comparison between younger and older mice with asthma
Given that respiratory viruses, especially RNA viruses such as rhinovirus, can cause asthma exacerbation, we administered poly(I:C) to C12 (Poly(I:C)) and A12 (A12 w Poly(I:C)) mice (Fig. 3a). Treatment with poly(I:C) alone increased AHR, total cell counts and OPN levels, although there were no significant differences between the groups. The administration of poly(I:C) to A12 [A12 w Poly(I:C)] mice robustly aggravated AHR and induced mixed cellular (including neutrophils and eosinophils) infiltration in BALF (Fig. 3b, c, P < 0.05 for all). In the A12 w Poly(I:C) group, poly(I:C) enhanced the expression of most of the genes investigated (Spp1, Egfr, Il33, Tgfb1) as well as Th2 cytokines (IL-4, IL-5, IL-13) and epithelial cell/ECM-derived cytokines such as OPN, TGF-β1, IL-33, TSLP, and CH3L1 (Fig. 3d, e). In histological examinations, A12 w Poly(I:C) strongly enhanced inflammatory cell infiltration and mucus secretion as well as collagen deposition (Figs. S2 and S3).
Regulatory function of OPN on TGF-β1/Smad3 signaling pathways
The simultaneous increase in OPN and TGF-β1 raised the question of whether OPN has any regulatory effect on TGF-β1 secretion. The administration of rOPN to the A12 w Poly(I:C) group (w OPN) during the sensitization period significantly increased AHR compared to the nontreated group (without OPN) (Fig. 4a, b, P < 0.05); however, neutrophil/eosinophil counts were elevated in the BALF of the two groups, but without any statistical significance (Fig. 4c). There were no significant changes in the levels of inflammatory genes/cytokines, except for Tgfb1 expression, but the TGF-β1 levels in BALF were significantly higher in the OPN-treated group than in the nontreated group (P < 0.05) (Fig. 4d). Interestingly, the phosphorylation of Smad3 was upregulated with age (A12 vs. A6 mice) in the A12 w Poly(I:C) group (P < 0.05, Fig. 4e, f). TGF-β1 gene expression, release, and activity were enhanced as OPN levels increased.
Effects of anti-asthmatic drugs on OPN regulation
Mice were treated with Dex, Mon, and anti-IL5 antibody to evaluate whether these anti-asthmatic medications and type 2 biologics may downregulate OPN levels. Dex, Mon, and anti-IL5 antibody significantly suppressed AHR and neutrophil/eosinophil counts in BALF (Fig. 3b, c). Dex and anti-IL5 antibody were effective in attenuating Spp1, OPN, and TGF-β1 in BALF, while Mon was effective in reducing the levels of CH3L1 in BALF and Ch3l1 expression (Fig. 3d, e). In an in vitro assay, exposure to Poly(I:C) released OPN, TGF-β1, and IL-8 from HAECs and CH3L1 from SAECs. Dex, Mon, and anti-IL5 antibody significantly suppressed epithelial-cell-derived OPN release (Figs. 3f and S1).
Viral infection increases polymerization of OPN by TGM2 in A12
To elucidate the association between OPN and epithelial TGM2, the expression levels of TGM2 were compared in the lung tissues of mice with age and virus infection status. The A12 w Poly(I:C) group showed the highest expression of TGM2, which was highly localized in the epithelial layer and the peribronchial/perivascular area compared to the three other groups (P < 0.05) (Fig. 5a–c). TGM2 is known to polymerize OPN22, as shown in Fig. S3. Interestingly, in mouse BALF, Western blot analysis revealed the polymerized form of OPN with bands ranging from >55 to 200 kDa in the A6, A12, and A12 w Poly(I:C) groups (Fig. 5d). All anti-asthmatic drugs used in this study could not significantly suppress the increased TGM2 level.
Discussion
This study demonstrated the role of OPN as a central mediator in the pathogenesis of LOA rather than EOA. The upregulation of OPN may be attributed to the aging process and viral infections in older subjects with asthma, which can accelerate airway remodeling by enhancing TGF-β1/Smad3-related pathways in the pathogenesis of LOA. In the milieu of aging and viral exposure, the structure of OPN was modified due to increased TGM2, subsequently enhancing fibrosis. This is the first investigation identifying higher serum OPN levels in patients with LOA and revealing the role of OPN using in vitro and in vivo models of LOA. LOA is considered a distinct phenotype of adult asthma presenting less eosinophilia and more severe clinical features with poorer prognosis than EOA2,4. Until now, serum CH3L1 and eotaxin-2 have been found to be upregulated in patients with LOA, although the age cutoff for LOA was variable among studies24,31,32. The present study demonstrated that the serum level of OPN among screened cytokines was upregulated in patients with LOA compared to those with EOA. Serum OPN level was found to have the potential to discriminate patients with LOA and those with adult asthma from HCs at 93.3% sensitivity. Several studies supported higher serum and sputum OPN levels in adults with asthma19,33. Bronchial OPN levels were correlated with impaired lung function in patients with severe refractory asthma, while sputum OPN levels were associated with the degree of neutrophilic inflammation33,34,35. The present study demonstrated a significant association between serum OPN and IL-8 levels in adults with asthma. IL-8 is a potent mediator inducing neutrophil migration and activation, which can additionally recruit eosinophils36. Thus, increased serum OPN levels have been shown to induce mixed neutrophilic/eosinophilic inflammation in adults with asthma. Serum OPN may be a potential, noninvasive biomarker for the early diagnosis of LOA in adults.
Attempts have been made to elucidate the mechanism underlying airway remodeling in LOA. In addition to environmental exposure, aging-related changes in airway structure and morphology may impact lung function and fibrosis in asthmatic airways2,37. Age at the initial time of allergen sensitization is critical for dictating the response upon subsequent exposure, as older mice showed increased expression of a steroid-resistant cascade of wingless/integrase and TGM2, which aggravated airway inflammation and remodeling38,39. OPN is known as a major ECM-inducing cytokine that modulates collagen deposition and fibrosis in asthma17,21,33. In this study, older mice with asthma showed increased airway inflammation and AHR compared to younger mice with differential expression of cytokines at the genetic and protein levels. T cell and innate immunity were upregulated by Spp1/OPN, Th2 cytokines (IL-5, IL-13), and ECM cytokines (TGF-β1 and CH3L1), while IL-4, IFN-γ, and epithelial cytokines (IL-33, TSLP) were downregulated. These findings were in partial agreement with those of previous studies using older mice with asthma40,41. Moreover, exposure to viral dsRNA poly(I:C) worsened AHR and induced mixed eosinophil/neutrophil infiltration in older mice with asthma, which might resemble the phenotype of LOA. Robust changes in gene/cytokine profiles were induced through the upregulation of OPN/Spp1 and inflammatory cytokines. In addition, the administration of rOPN during sensitization greatly amplified AHR, inflammatory cells, and fibrosis in our virus-infected asthma mouse model. Interestingly, compared with younger mice with asthma, older mice with asthma displayed a higher expression of pSmad342, an important pathway of TGF-β1-mediated fibrosis43, which was also strongly enhanced by poly(I:C). Chronic poly(I:C) stimulation can stimulate NF-κB expression and epithelial–mesenchymal transition, fibrosis, and airway remodeling44. Taken together, these findings suggest that viral exposure could amplify the age-dependent increase in OPN, which enables airway inflammation and TGF-β1-mediated remodeling and contributes to presenting a more severe phenotype of asthma of LOA.
Associations of serum OPN with TGF-β1 and CH3L1 led us to further investigate the role of OPN in the regulation of these ECM cytokines. Increasing evidence suggests that both TGF-β1 and CH3L1 are crucial for modulating airway remodeling and fibrosis in severe asthma19,24,45,46. In this study, viral exposure triggered direct activation of HAECs by the release of OPN, TGF-β1, and CH3L1 (mostly from primary small airway epithelial cells). Exposure to rOPN could induce the expression of Tgfβ1 and the release of TGF-β1, IL-5, IL-13, and phosphorylated Smad3 in a mouse model of virus-induced asthma exacerbation. The latter was in line with the results of a previous study that showed that OPN-deficient mice had reduced TGF-β118. TGF-β1 produces OPN through transcriptional regulation in osteosarcoma cells47. These findings show the bidirectional effects between OPN and TGF-β1 and suggest that OPN can trigger TGF-β1/Smad3-induced fibrosis in the airway of LOA. Regarding CH3L1, there were no observed causal relationships between OPN and CH3L1 in this context. However, TGF-β1 could stimulate chitinase-like 2, the closest homolog to CH3L1, in cultured macrophages48. Conversely, YKL-40 was found to induce TGF-β1 gene expression in fibroblasts49. Thus, we hypothesized that increased OPN enhances TGF-β1/Smad3-dependent fibrosis; consequently, TGF-β1 modulates CH3L1, which contributes to amplifying TGF-β1 expression. Further studies on the TGF-β1/CH3L1 axis are warranted.
The multiple functions of OPN have been extensively studied in various kinds of inflammation mechanisms. In addition to TGF-β1-dependent fibrosis, two other fibrosis-related downstream effects of OPN have been demonstrated in asthmatic airways. The polymerization of OPN leads to increased collagen binding under the effect of TGM222. The latter has been found to be upregulated with aging38. OPN could be released from eosinophils reprogrammed by the Areg/IL33/EGFR pathway and initiated fibrosis21. In the present study, we could not detect any changes in Areg/IL33/EGFR. Instead, we found that TGM2 was highly upregulated by virus infection in older mice with asthma. Concomitantly, polymerized forms of OPN (similar to the structure of OPN, which was polymerized by TGM2) were detected in mice with asthma and enhanced after exposure to viruses. In addition, the polymerized form of OPN was found in asthmatic airways, while fragmented forms were found in the airway secretion of patients with asthma23. Although we could not find a direct effect of OPN on TGM2 formation, the current findings led us to speculate that viral infection and aging may stimulate TGM2 polymerization, which further enhances collagen binding. Moreover, an age-dependent increase in TGM2 has been reported to facilitate steroid insensitivity38. Thus, novel therapies targeting the TGM2/OPN axis could help prevent the development of steroid insensitivity and airway remodeling in LOA.
Finally, we aimed to investigate the potential therapies for the modulation of OPN in LOA, and, on the basis of our findings, we suggest that Dex and anti-IL5 antibody are potential drugs to suppress OPN-mediated airway inflammation and remodeling in the older mouse model of virus-induced asthma exacerbation. Regarding the effects of glucocorticoids on OPN release, there are some conflicting results showing that steroids increased OPN expression in cardiac myocytes and microvascular endothelial cells, while Dex suppressed OPN expression in a mouse model of allergic asthma50,51. Glucocorticoid receptors recognize an element on the promoter sequence of the OPN gene; thus, glucocorticoids may exert various responsiveness to the OPN promoter52. The increased level of OPN in LOA can be a potential target of glucocorticoid treatment. With respect to the association of OPN with IL-5, it has been suggested that OPN suppresses plasmacytoid dendritic cells, resulting in enhanced Th2 cytokines16. IL-5 induces eosinophil-derived OPN, which leads to angiogenesis in asthma53. Reslizumab, an anti-IL5 antibody, is effective in treating LOA patients with increased eosinophilia54. Our findings help elucidate mechanisms by which anti-IL5 antibody could effectively modulate the elevated OPN in the LOA phenotype. Therefore, Dex and anti-IL5 antibody could be beneficial in the treatment of LOA.
There is a limitation in this study. No direct associations were found among serum OPN levels, FEV1% predicted values, and MctPC20 levels. Longitudinal follow-up studies are necessary to clarify the exact role of OPN in the process of age-dependent changes in lung function and in the development of LOA. Taken together, respiratory viral infection and aging may induce OPN release, which induces TGF-β1/Smad3 signaling pathways, consequently enhancing airway inflammation and fibrosis in patients with LOA. Therefore, the serum OPN level may be a potential biomarker for the diagnosis of patients with LOA.
References
Yoo, K. H. et al. Burden of respiratory disease in Korea: an observational study on allergic rhinitis, asthma, COPD, and rhinosinusitis. Allergy Asthma Immunol. Res. 8, 527–534 (2016).
Hirano, T. & Matsunaga, K. Late-onset asthma: current perspectives. J. Asthma Allergy 11, 19–27 (2018).
Ilmarinen, P., Tuomisto, L. E. & Kankaanranta H. Phenotypes, risk factors, and mechanisms of adult-onset asthma. Mediators Inflamm. 2015, 514868 (2015).
Ulrik, C. S. Late-onset asthma: a diagnostic and management challenge. Drugs Aging 34, 157–162 (2017).
Ulambayar, B., Lee, S. H., Yang, E. M., Ye, Y. M. & Park, H. S. Association between epithelial cytokines and clinical phenotypes of elderly asthma. Allergy Asthma Immunol. Res. 11, 79–89 (2019).
Hur, G. Y. & Broide, D. H. Genes and pathways regulating decline in lung function and airway remodeling in asthma. Allergy Asthma Immunol. Res. 11, 604–621 (2019).
Hackett, T. Epithelial–mesenchymal transition in the pathophysiology of airway remodelling in asthma. Curr. Opin. Allergy Clin. Immunol. 12, 53–59 (2012).
Bai, T. R., Cooper, J., Koelmeyer, T., Paré, P. D. & Weir, T. D. The effect of age and duration of disease on airway structure in fatal asthma. Am. J. Respir. Crit. Care Med. 162, 663–669 (2000).
Seo, K. H. et al. Prevalence of respiratory viral infections in Korean adult asthmatics with acute exacerbations: comparison with those with stable state. Allergy Asthma Immunol. Res. 9, 491–498 (2017).
Kelly, J. T. & Busse, W. W. Host immune responses to rhinovirus: mechanisms in asthma. J. Allergy Clin. Immunol. 122, 671–684 (2008).
Becnel, D., You, D., Erskin, J., Dimina, D. M. & Cormier, S. A. A role for airway remodeling during respiratory syncytial virus infection. Respir. Res. 6, 122–122 (2005).
Rantala, A., Jaakkola, J. J. K. & Jaakkola, M. S. Respiratory infections precede adult-onset asthma. PLoS ONE 6, e27912 (2011).
Moskwa, S. et al. Innate immune response to viral infections in primary bronchial epithelial cells is modified by the atopic status of asthmatic patients. Allergy Asthma Immunol. Res. 10, 144–154 (2018).
Ashkar, S. et al. Eta-1 (Osteopontin): an early component of type-1 (cell-mediated) immunity. Science 287, 860–864 (2000).
Renkl, A. et al. Osteopontin functionally activates dendritic cells and induces their differentiation toward a Th1-polarizing phenotype. Blood 106, 946–955 (2005).
Xanthou, G. et al. Osteopontin has a crucial role in allergic airway disease through regulation of dendritic cell subsets. Nat. Med. 13, 570–578 (2007).
Kohan, M. et al. Enhanced osteopontin expression in a murine model of allergen-induced airway remodelling. Clin. Exp. Allergy 37, 1444–1454 (2007).
Kohan, M., Breuer, R. & Berkman, N. Osteopontin induces airway remodeling and lung fibroblast activation in a murine model of asthma. Am. J. Respir. Cell. Mol. Biol. 41, 290–296 (2009).
Delimpoura, V. et al. Increased levels of osteopontin in sputum supernatant in severe refractory asthma. Thorax 65, 782–786 (2010).
Jevnikar, Z. et al. Epithelial IL-6 trans-signaling defines a new asthma phenotype with increased airway inflammation. J. Allergy Clin. Immunol. 143, 577–590 (2019).
Morimoto, Y. et al. Amphiregulin-producing pathogenic memory T helper 2 cells instruct eosinophils to secrete osteopontin and facilitate airway fibrosis. Immunity 49, 134–150. e6 (2018).
Kaartinen, M. T., Pirhonen, A., Linnala-Kankkunen, A. & Mäenpää, P. H. Cross-linking of osteopontin by tissue transglutaminase increases its collagen binding properties. J. Biol. Chem. 274, 1729–1735 (1999).
Arjomandi, M. et al. Secreted osteopontin is highly polymerized in human airways and fragmented in asthmatic airway secretions. PLoS ONE 6, e25678 (2011).
Gomez, J. L. et al. Characterisation of asthma subgroups associated with circulating YKL-40 levels. Eur. Respir. J. 50, 50 (2017).
Global strategy for asthma management and prevention. Global Initiative for Asthma 2019. https://ginasthma.org/gina-reports/ (2019).
Coates, A. L. et al. ERS technical standard on bronchial challenge testing: general considerations and performance of methacholine challenge tests. Eur. Respir. J. 49, 49 (2017).
Chung, K. F. et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur. Respir. J. 43, 343–373 (2014).
Sood, A. et al. Adult-onset asthma becomes the dominant phenotype among women by age 40 years. The longitudinal CARDIA Study. Ann. Am. Thorac. Soc. 10, 188–197 (2013).
Ortega, H. G. et al. Mepolizumab treatment in patients with severe eosinophilic asthma. N. Engl. J. Med. 371, 1198–1207 (2014).
Trinh, H. K. T. et al. Characterization of cysteinyl leukotriene-related receptors and their interactions in a mouse model of asthma. Prostaglandins Leukot. Essent. Fatty Acids 141, 17–23 (2019).
Coleman, J. M. et al. Epithelial eotaxin-2 and eotaxin-3 expression: relation to asthma severity, luminal eosinophilia and age at onset. Thorax 67, 1061–1066 (2012).
Guerra, S. et al. The relation of circulating YKL-40 to levels and decline of lung function in adult life. Respir. Med. 107, 1923–1930 (2013).
Samitas, K. et al. Osteopontin expression and relation to disease severity in human asthma. Eur. Respir. J. 37, 331–341 (2011).
Hillas, G. et al. Increased levels of osteopontin in sputum supernatant of smoking asthmatics. Cytokine 61, 251–255 (2013).
Kanemitsu, Y. et al. Osteopontin and periostin are associated with a 20-year decline of pulmonary function in patients with asthma. Am. J. Respir. Crit. Care Med. 190, 472–474 (2014).
Norzila, M. Z., Fakes, K., Henry, R. L., Simpson, J. & Gibson, P. G. Interleukin-8 secretion and neutrophil recruitment accompanies induced sputum eosinophil activation in children with acute asthma. Am. J. Respir. Crit. Care Med. 161, 769–774 (2000).
Dunn, R. M., Busse, P. J. & Wechsler, M. E. Asthma in the elderly and late-onset adult asthma. Allergy 73, 284–294 (2018).
Dietz, K. et al. Age dictates a steroid-resistant cascade of Wnt5a, transglutaminase 2, and leukotrienes in inflamed airways. J. Allergy Clin. Immunol. 139, 1343–1354. e6 (2017).
Gelfand, E. W. et al. Induction and maintenance of airway responsiveness to allergen challenge are determined at the age of initial sensitization. J. Immunol. 173, 1298–1306 (2004).
Kang, J. et al. Effect of aging on airway remodeling and muscarinic receptors in a murine acute asthma model. Clin. Interv. Aging 8, 1393–1403 (2013).
Mack, S. et al. Age-dependent pulmonary reactivity to house dust mite allergen: a model of adult-onset asthma? Am. J. Physiol. Lung Cell. Mol. Physiol. 316, L757–L763 (2019).
Le, A. V. et al. Inhibition of allergen-induced airway remodeling in Smad 3-deficient mice. J. Immunol. 178, 7310–7316 (2007).
Lee, H. Y. et al. Inhibitory effects of Resveratrol on airway remodeling by transforming growth factor-β/Smad signaling pathway in chronic asthma model. Allergy Asthma Immunol. Res. 9, 25–34 (2017).
Tian, B. et al. NFΚB mediates mesenchymal transition, remodeling and pulmonary fibrosis in response to chronic inflammation by viral RNA patterns. Am. J. Respir. Cell. Mol. Biol. 56, 506–520 (2016).
Tang, H. et al. YKL-40 induces IL-8 expression from bronchial epithelium via MAPK (JNK and ERK) and NF-kappaB pathways, causing bronchial smooth muscle proliferation and migration. J. Immunol. 190, 438–446 (2013).
Volck, B. et al. YKL-40, a mammalian member of the chitinase family, is a matrix protein of specific granules in human neutrophils. Proc. Assoc. Am. Physicians 110, 351–360 (1998).
Noda, M., Yoon, K., Prince, C. W., Butler, W. T. & Rodan, G. A. Transcriptional regulation of osteopontin production in rat osteosarcoma cells by type beta transforming growth factor. J. Biol. Chem. 263, 13916–13921 (1988).
Gratchev, A. et al. Expression of osteoarthritis marker YKL-39 is stimulated by transforming growth factor beta (TGF-beta) and IL-4 in differentiating macrophages. Biomark. Insights 3, 117727190800300003 (2008).
Park, S. J. et al. Increased expression of YKL-40 in mild and moderate/severe persistent allergic rhinitis and its possible contribution to remodeling of nasal mucosa. Am. J. Rhinol. Allergy 27, 372–380 (2013).
Kurokawa, M. et al. Effects of corticosteroids on osteopontin expression in a murine model of allergic asthma. Int. Arch. Allergy Immunol. 149(Suppl. 1), 7–13 (2009).
Singh, K., Balligand, J. L., Fischer, T. A., Smith, T. W. & Kelly, R. A. Glucocorticoids increase osteopontin expression in cardiac myocytes and microvascular endothelial cells. Role in regulation of inducible nitric oxide synthase. J. Biol. Chem. 270, 28471–28478 (1995).
Wang, D., Yamamoto, S., Hijiya, N., Benveniste, E. N. & Gladson, C. L. Transcriptional regulation of the human osteopontin promoter: functional analysis and DNA–protein interactions. Oncogene 19, 5801–5809 (2000).
Puxeddu, I. et al. Osteopontin is expressed and functional in human eosinophils. Allergy 65, 168–174 (2010).
Brusselle, G., Germinaro, M., Weiss, S. & Zangrilli, J. Reslizumab in patients with inadequately controlled late-onset asthma and elevated blood eosinophils. Pulm. Pharmacol. Ther. 43, 39–45 (2017).
Acknowledgements
This study was supported by a grant from the Korean Health Technology R&D Project, Ministry of Health & Welfare, (H16C0992), Republic of Korea. In addition, we would like to express our gratitude to Prof. Yoo Seob Shin, M.D., Ph.D., for his support in preparing the proposals of animal studies and to Thuong-Khanh Tran for his guidance of R software.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Trinh, H.K.T., Nguyen, T.V.T., Kim, SH. et al. Osteopontin contributes to late-onset asthma phenotypes in adult asthma patients. Exp Mol Med 52, 253–265 (2020). https://doi.org/10.1038/s12276-020-0376-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/s12276-020-0376-2
- Springer Nature Limited
This article is cited by
-
MMP-3 mediates copper oxide nanoparticle-induced pulmonary inflammation and fibrosis
Journal of Nanobiotechnology (2024)
-
Osteopontin: A Novel Therapeutic Target for Respiratory Diseases
Lung (2024)
-
The miR-9-5p/KLF5/IL-1β Axis Regulates Airway Smooth Muscle Cell Proliferation and Apoptosis to Aggravate Airway Remodeling and Inflammation in Asthma
Biochemical Genetics (2024)
-
S100A9 in adult asthmatic patients: a biomarker for neutrophilic asthma
Experimental & Molecular Medicine (2021)