- Open Access
Airway hyperresponsiveness is associated with airway remodeling but not inflammation in aging Cav1 -/- mice
© Gabehart et al.; licensee BioMed Central Ltd. 2013
Received: 9 August 2013
Accepted: 14 October 2013
Published: 21 October 2013
Airway inflammation and airway remodeling are the key contributors to airway hyperresponsiveness (AHR), a characteristic feature of asthma. Both processes are regulated by Transforming Growth Factor (TGF)-β. Caveolin 1 (Cav1) is a membrane bound protein that binds to a variety of receptor and signaling proteins, including the TGF-β receptors. We hypothesized that caveolin-1 deficiency promotes structural alterations of the airways that develop with age will predispose to an increased response to allergen challenge.
AHR was measured in Cav1-deficient and wild-type (WT) mice 1 to 12 months of age to examine the role of Cav1 in AHR and the relative contribution of inflammation and airway remodeling. AHR was then measured in Cav1 -/- and WT mice after an ovalbumin-allergen challenge performed at either 2 months of age, when remodeling in Cav1 -/- and WT mice was equivalent, and at 6 months of age, when the Cav1 -/- mice had established airway remodeling.
Cav1 -/- mice developed increased thickness of the subepithelial layer and a correspondingly increased AHR as they aged. In addition, allergen-challenged Cav1 -/- mice had an increase in AHR greater than WT mice that was largely independent of inflammation. Cav1 -/- mice challenged at 6 months of age have decreased AHR compared to those challenged at 2 months with correspondingly decreased BAL IL-4 and IL-5 levels, inflammatory cell counts and percentage of eosinophils. In addition, in response to OVA challenge, the number of goblet cells and α-SMA positive cells in the airways were reduced with age in response to OVA challenge in contrast to an increased collagen deposition further enhanced in absence of Cav1.
A lack of Cav1 contributed to the thickness of the subepithelial layer in mice as they aged resulting in an increase in AHR independent of inflammation, demonstrating the important contribution of airway structural changes to AHR. In addition, age in the Cav1 -/- mice is a contributing factor to airway remodeling in the response to allergen challenge.
Asthma is a major public health problem, affecting patients of all ages from infants to older adults. Morbidity and mortality are greater in older patients (> 65 yrs) despite a similar prevalence as that in younger asthmatics, and yet there is limited evidence on how age can influence the pathogenesis of asthma [1, 2]. Older patients have a larger than predicted reduction in pulmonary function parameters even though physician-assessed severity, duration of diagnosed asthma, and smoking status were not different compared to younger adults. A significant increase in the comorbid diagnosis of chronic obstructive pulmonary disease is associated with asthma in older patients suggesting that long-standing asthma may lead to irreversible airflow obstruction . Asthma is characterized by airway hyperresponsiveness (AHR), an exaggerated narrowing of the airway in response to stimuli. AHR can reflect asthma severity, and has been associated with a variety of contributing factors [4–7]. AHR has two distinct components. First, a transient component occurring after an allergen exposure that is linked to acute inflammation, second, a more persistent component, associated with the chronicity of the disease causing structural changes in the airways known as airway remodeling. Several features of airway remodeling can contribute to AHR, including: increased sensitivity, hypertrophy and hyperplasia of smooth muscle cells (SMCs), as well as increased subepithelial fibrosis characterized by increased collagen deposition . The development of structural changes persists during and after acute inflammation in allergic asthma subjects and in allergen challenge animal models with low inflammation [9–11]. Some asthma patients develop AHR in association with airway remodeling . Furthermore, severe asthmatic patients under anti-inflammatory treatments will present loss in lung function despite inflammation being controlled . These facts illustrate that underlying non-inflammatory mechanisms regulate airway structure and function, which include epithelial thickening and subepithelial collagen deposition.
Caveolin 1 (Cav1) is the main structural and functional protein of caveolae. These are 10 to 100 nm wide invaginations of the plasma membrane found in many cell types. Cav1 acts as a scaffolding protein, as well as a regulatory protein in many signaling cascade protein complexes. Cav1 inhibits the activity of these signaling proteins by binding and releasing them in a controlled fashion . Cav1 has been shown to be involved in the regulation of both inflammation and fibrosis [15–19]. One of the important pathways that Cav1 regulates is the Transforming Growth Factor (TGF)-β pathway. Cav1 binds to and inhibits the TGF-β type II receptor thus preventing downstream signaling including the phosphorylation of Smad2/3. Others and our group have demonstrated that Cav1 -/- mice have enhanced Smad2 phosphorylation and altered ECM deposition notably in the lungs [18, 19]. We have shown that aged Cav1 -/- mice have decreased lung function (i.e. increased elastance and decreased compliance) mainly due to an increase in ECM deposition of collagen and elastin . The regulation of Cav1 has also been shown to be important in allergic airway disease [20, 21]. We have previously shown that TGF-β signaling is enhanced in ovalbumin (OVA) challenged Cav1 -/- mice leading to enhanced airway remodeling .
TGF-β1 is a pleiotrophic growth factor that participates in resolution of inflammation, as well as promotion of airway remodeling, especially promoting extracellular matrix (ECM) deposition. Anti-TGF-β1 antibody treatment prevents the progression of airway remodeling following allergen challenge in mice . More surprisingly, enhanced AHR has been reported in anti-TGF-β antibody treated OVA challenged mice associated with reduced Smad2 phosphorylation, marker of canonical TGF-β signaling pathway activation . The regulation of TGF-β signaling activity has been the focus of intensive studies as a potential therapeutic target but it has not yet been fully characterized.
This study was designed to evaluate the relationship between inflammation, structural changes, and lung function in aged and OVA-challenged mice. We hypothesized that structural alterations of the airways that develop with age in Cav1 deficient mice will predispose them to an increased response to allergen challenge. The effect of Cav1-deficiency on airway structure was investigated, and AHR was associated to change in airway structures.
Material and methods
Animals and OVA-allergen challenge
Wild type C57Bl/6 J (WT) and Cavtm1Mls/J (Cav1 -/- ) mice were purchased from The Jackson Laboratory (Bar Harbor, Maine) to establish our colonies and obtained the appropriate number of animals needed for our experiment. Animal experiments were conducted using a protocol approved by the Institutional Animal Care and Use Committee of the University of Hawaii.
Two- or 6-month-old Cav1 -/- and WT female mice were sensitized by 2 intraperitoneal (IP) injections of OVA absorbed on alum 12 days apart, followed 2 weeks later by intranasal challenge with OVA three times over a week. Measurement of acetylcholine induced AHR and sacrifice were performed 24 h after the last challenge as described previously . A group of 2-month old mice was treated with the Cav1 scaffolding domain or scrambled peptide for 4 weeks as previously described .
Measurement of airway hyperresponsiveness (AHR)
AHR was measured using a Flexivent instrument (Scireq Inc., Montreal, Quebec, Canada) as previously described . Briefly, mice were anesthetized with ketamine (100 mg/kg IP) and xylazine (10 mg/kg IP). The trachea was then surgically exposed and cannulated to allow ventilation via the Flexivent at 150 breaths/min and a tidal volume of 7.5 ml/kg. Pancuronium bromide was administered IP to induce paralysis. Mice were then given increasing doses of acetylcholine (0.03, 0.1, 0.3, 1.0, 3.2 μg/g) in volume of 2 μl/g of body weight by tail vein administration at three-minute intervals and total lung resistance was measured to generate a dose-response curve. Log PC200 is the log of the dose required to increase resistance 200% over saline baseline. The lower the LogPC200 value the greater the reactivity .
After completion of the AHR measurement, mice were disconnected from the animal ventilator and exsanguinated by cardiac puncture. Immediately after, bronchoalveolar lavage (BAL) was performed. Right side lobes were used for histology and electron microscopy (EM), and sections were cut longitudinally. EM preparation was carried out as previously described . The left side lobes was reserved for RNA and protein extraction.
Photomicrograph images were captured using a Spot Cooled Color Digital camera (Q Imaging, Burnaby, BC, Canada). Briefly, a minimum of 5 bronchi, measuring 150–350 μm in luminal diameter with a continuous smooth muscle layer, were analyzed per mouse for the parameters described below, using Image Pro-Discovery software (Media Cybernetics, Silver Spring, MD), calibrated with a reference micrometer slide [10, 26, 27]. The thickness of the bronchial epithelial layer and subepithelial deposition of collagen were measured in sections stained with Masson’s trichrome.
Morphometric α-SMA detection
Formalin-fixed paraffin-embedded sections were stained for α-smooth muscle actin (α-SMA) using immunohistochemistry and analyzed morphometrically. Primary antibody, mouse monoclonal anti α-SMA (Dako, Glostrup, Denmark), and a FITC labeled secondary antibody was used to detect α-SMA. The thickness of labeled α-SMA per length of basement membrane measured in a minimum of 5 bronchi, measuring 150–350 μm in luminal diameter, were analyzed per mouse for the parameters described below, using Image Pro-Discovery software (Media Cybernetics, Silver Spring, MD). Airways were selected and analyzed morphometrically for airway smooth muscle thickness using the method described above.
Determination of airway inflammation
BAL was collected by injecting and withdrawing one ml cold phosphate-buffered saline (PBS). Recovered BAL (70–80%) was centrifuged at 300 g for 10 min. The fluid was collected for cytokine analyses. Cells were resuspended in 0.5 ml of PBS and an aliquot was removed to determine cell concentration using a hemocytometer. The remaining cells were adhered to glass slides using cytocentrifugation. Slides were stained using Wright-Giemsa stain and differential cell counts (minimum of 300 total cells) were obtained using a Zeiss light microscope. Cytokine levels were measured in BAL fluid using a Mouse Th1/Th2 Cytokine Kit Cytometric Bead Array™ (BD Biosciences Pharmingen) according to the manufacturer’s instructions.
Airway remodeling assessment
Detection of goblet cells: Paraffin-embedded sections were deparafinized and stained using the standard procedure of periodic acid Schiff staining as described by the manufacturer (NovaUltra PAS Stain Kit, IHC WORLD, Woodstock, MD). We selected airways of approximately 100-200 μm in diameter and counted goblet cells in each airway. Five airways per animals were counted and a total of 3 animals per group were randomly selected.
Detection of collagen deposition: Paraffin-embedded lung sections were stained with picrosirius red (PSR) stain. Briefly, sections were deparafinized and hydrated to distilled water, then placed in phosphomolybdic acid 0.2% (cat. No 26356-01 Electron Microscopy Science, Hatfield, PA 19440) for 5 minutes, and placed directly in sirius red 0.2% in saturated picric acid (cat. No 26357-02; Electron Microscopy Science) for 90 minutes. Slides were washed in 0.01 N hydrochloric acid for 2 minutes and then placed in 70% ethanol for 45 seconds. Sections were dehydrated, cleared and mounted. PSR stained slides were quantified to determine the percent of collagen in the pulmonary tissue with Image Pro (Meyer Instruments Houston, TX 77084), a computer based analytical software. For each group, the quantification was performed on the entire upper right lobe of 5 mice.
Detection of activation of the canonical TGF-β signaling pathway. For analyses of levels of phospho-Smad2 (pSmad2) and total Smad2, whole lung homogenates were prepared in RIPA buffer in the presence of HALTTM protease and phosphatase inhibitor cocktail (#78430 and # 78420, Thermo Fisher Scientific, Rockford, IL). All antibodies were purchased from Cell Signaling (Danvers, MA), except for β-actin (Cytoskeleton Inc; Denver, CO). Western blot analysis was carried out using the standard protocol as described previously . Densitometric quantification was carried out by Image J software to represent the semi-quantitative protein levels. Relative levels of activated proteins were obtained as the ratio of phosphorylated protein: total protein levels. For detection of pSmad2 expression in allergen challenged lung tissue sections, non-inflated lung tissues were fixed in a solution of phosphate-buffered saline (PBS) containing 4% paraformaldehyde. Lungs were embedded in paraffin and sectioned. Following routine techniques of deparaffinization, antigen retrieval and quenching of peroxidase activity, the slides were incubated with primary pSmad2/3 antibody (cat# 9510S, Cell signaling, Danvers, MA) at a 1:500 dilution for 12 h, then biotinylated secondary antibody from VectaStain Elite ABC Mouse kit (PK-6102, Vector Laboratories Burlingame, CA 94010). We selected airways of approximately 100-200 μm in diameter and counted pSmad2/3 positive cells in each airway. Five airways per animals were counted and a total of 3 animals per group were randomly selected.
Cav1-deficient mice developed age-dependent airway hyperresponsiveness
Structural changes in the airways in aging Cav1-/-mice compared to WT animals
The α-SMA stained SMC layer increased in thickness as both Cav1 -/- and WT mice aged, peaking at 6 months of age, as measured by morphometric analysis (Figure 3C). However, the thickness of SMC layer surrounding the airway between Cav1 -/- and WT animals was never significantly different at any time point, indicating that the change in SMC development is a part of normal growth. This suggests that an increase in airway smooth muscle mass is not the cause of increased AHR in the aging Cav1-/- mice.
This data indicate that cumulative thickening of the subepithelial matrix layer, but not an increase in smooth muscle mass, may contribute to the increase in AHR in Cav1 -/- mice over time.
AHR after a 1-week OVA challenge in 2- and 6-month-old in Cav1-/-and WT mice
After it was established that 6-month-old Cav1 -/- mice had increased AHR and increased subepithelial matrix thickness, an OVA allergen challenge was carried out to examine the effect of previously established airway structural changes on AHR, airway remodeling and inflammation triggered by allergen challenge. Two-month old Cav1 -/- and WT mice received a 1-week OVA allergen challenge before airway remodeling is established. In addition, another group of mice, at 6 months of age, also received a 1-week OVA allergen challenged after we established the occurrence of airway remodeling in the knockout mice.
Treatment of 2-month-old OVA-challenged Cav1 -/- mice with the Cav1 scaffolding domain (CSD) over a 4-week period prior to challenge was able to partially attenuate the exaggerated AHR in the Cav1 -/- mice, demonstrating the reversibility of these changes and the specific role of Cav1 (Figure 4D).
Reduced inflammation after a 1-week OVA challenge in 6-month old Cav1-/-compared to WT mice
BAL cytokine level comparisons between 2- and 6-month-old mice after a one-week PBS or OVA challenge
2 M old
10.5 ± 2
921 ± 446*
16 ± 7
1273 ± 1251###
94 ± 7
1711 ± 2596
128 ± 34
4434 ± 7265
13 ± 3
31 ± 12***
16 ± 3
25 ± 11
19.5 ± 9.5
122 ± 95
15 ± 5
129 ± 180**
36.5 ± 2
63 ± 24
38 ± 4
59 ± 24
42 ± 74
49 ± 85
6 M old
75 ± 13
341 ± 244
71 ± 10
520 ± 780
22 ± 3
903 ± 176
21 ± 5
542 ± 788
27 ± 3.5†
24 ± 14
24 ± 5
21 ± 5
34 ± 5.5
176 ± 121**
36 ± 5
45 ± 21##
84 ± 19
96 ± 16
82 ± 8
67 ± 14 ##
1.8 ± 1.3
53 ± 68.9
BAL inflammatory cell comparison between 2- and 6-month-old mice after a one-week PBS or OVA challenge
BAL Cells Cell/ml
0.8 ± 0.2
6.6 ± 1.5*
0.5 ± 0.2*
17.1 ± 5.3*
0.3 ± 0.1
3.4 ± 0.6*
0.3 ± 0.04
5.2 ± 2.5
6.1 ± 2
32.2 ± 2.4*
8.4 ± 1.6
38 ± 2.5*
1.3 ± 0.3
29.5 ± 7.1*
1.5 ± 0.7
19.4 ± 3.4*
Enhanced collagen deposition and reduced mucus cells in aged OVA-challenged Cav1 -/- compared to WT mice
As expected based on our previous studies, the level of activation of the canonical TGF-β signaling pathway was increased in 2-month Cav1 -/- mice after OVA challenge compared to WT mice as measured by immunohistology detection of pSmad2. Interestingly, the level of activation stayed similar in the OVA challenged WT mice compared to PBS controls but was dramatically reduced in the 6-month Cav1 -/- mice after OVA challenge (Figure 5G, H).
Overall, important differences in airway remodeling after OVA-challenge were measured between WT and Cav1 -/- mice and they appear to be diminished with age.
Murine models have been useful in studying the mechanisms that contribute to AHR [22–25]. The relative contribution of airway remodeling to AHR is difficult to assess as most of these models involve an allergic response triggering both inflammation and airway remodeling. In this study, we explored the inflammatory responses before and after airway remodeling was established. Our main finding was that Cav1 -/- mice develop AHR as they age. At 6 months of age, the AHR was significantly increased compared to WT mice, but not at an earlier age. Furthermore, there was also a significantly increased thickening of the subepithelial matrix layer in Cav1 -/- mice as compared to WT mice at 6 months of age. In previous studies, we have demonstrated by trichrome and picrosirius red staining that subepithelial collagen deposition is increased in Cav1 -/- mice by the time they are 6 months of age . This suggests that AHR is related to collagen deposition in the bronchial subepithelial layer. Mathematical modeling has demonstrated that relatively minor increases in the thickness of the small airways can decrease the size of the airway caliber enough during muscle contraction to physiologically affect AHR, further supporting our findings . We have also previously demonstrated that subepithelial collagen deposition contributes to increased AHR in a chronic OVA allergic airways disease model and that reversal of subepithelial and total lung collagen by relaxin treatment can reduce AHR .
The mechanisms for increased collagen deposition in the setting of Cav1 deficiency are incompletely understood. TGF-β promotes airway remodeling, especially promoting ECM deposition . In asthmatics, TGF-β regulated by leukotrienes, can activate lung fibroblasts and increase collagen deposition [29, 30]. We have previously established that Cav1 was involved in the regulation of TGF-β signaling in murine lungs and that over time, the absence of Cav1 leads to increased TGF-β signaling and collagen deposition in the parenchyma . In this study we confirmed the increase in pSmad2 signaling in OVA challenged Cav1 -/- lungs. For the first time, we demonstrate the association of Cav1 deficiency with the development of increased AHR and thickening of the subepithelial layer. Cav1 interacts with and regulates a number of proteins in addition to TGF- β that are potentially important for regulation of AHR that we did not investigate in this study. For example, it has been well documented that Cav-1 participates in SMC contractility via Ca2+-dependent mechanisms. Indeed, SMC expressed Cav-1 and the caveolae contain a number of proteins that participate in the regulation of Ca2+[31–34]. Importantly, Sathish and al.  recently showed that Cav-1 regulates proteins (Orai1) that are important for calcium regulation. They also showed that an association between Cav1, calcium and inflammation.
After it was established that Cav1 -/- mice develop AHR and subepithelial thickness at 6 months of age, an OVA allergen sensitization and challenge was carried out at 2 months of age (before airway remodeling is established) and at 6 months of age (after airway remodeling is established) to explore differences in the inflammatory response. OVA challenge induced markedly elevated BAL cytokine levels in 2-month old WT and Cav1 -/- mice, but reduced cytokine levels in 6-month Cav1 -/- mice after the OVA allergen challenge. In a similar fashion, 6-month Cav1 -/- mice had a decreased number of inflammatory cells and percentage of eosinophils in the BAL after the OVA allergen challenge compared to 2-month Cav1 -/- mice. Increased number of mucous cells has been associated with increased IL-13, inflammation and eosinophilia . Importantly, both age and Cav1 expression influence these parameters of response to allergen challenge. In our study, eosinophilia and levels of IL-5 decreased in older mice and correlated with reduced mucous cell metaplasia. Six-month-old OVA challenged Cav1 -/- mice reduced IL-13 in the BAL corresponding to few mucous cells. Few reports investigating airway inflammation in aged sensitized and challenged mice are available and even less on airway remodeling. The decrease in eosinophilia and overall cytokine level in aged mice both WT and Cav1 -/- mice was consistent with 2 of 3 previous studies using similar allergen challenge protocols [36–38]. Our findings suggest that the AHR observed in 6-month-old Cav1 -/- mice is independent of inflammation and more closely related to increased collagen around the airways. The work from Busse et al. also argues against a direct relationship between pulmonary inflammation or eosinophils and increased AHR, even though a different OVA sensitization and challenge protocol was used .
In asthmatic patients, the persistence of AHR can be associated with airway remodeling after the resolution of inflammation . In addition, in mouse models, prolonged allergen challenge leads to persistent changes in the airways despite discontinuation of the allergen challenge [7, 8]. These studies demonstrate a role of airway remodeling in AHR beyond the immediate inflammatory response. Other genetically engineered mouse models also point toward the importance of airway remodeling independent of inflammation [7, 8]. For example, relaxin-deficient mice also show similar results, where an increase in airway remodeling leads to increased AHR [7, 8, 26].
The timing of airway remodeling development in asthma is an area of increasing interest. Evidence suggests that remodeling of airways may develop long before symptoms of asthma and inflammation appear . In our study, older mice in both groups had less AHR and the BAL cytokines tended to be present at lower levels after the OVA allergen challenge. This suggests that some alterations in lung response to allergen challenge as the mice age were independent of the presence or absence of Cav1. Nevertheless, the reduction in inflammation was more prominent in the Cav1 -/- mice with greater reductions in eosinophils and IL-13. The decrease in inflammation in 6-month-old mice can account for the decrease in AHR seen in these mice compared to 2-month-old mice. Indeed, we demonstrated a decrease in the IL-4 levels in 6-month-old mice versus 2-month-old mice, and other studies have shown that treatment of sensitized mice with anti-IL-4 antibody prior to antigen stimulation reduces antigen-induced AHR, eosinophilia, and goblet cell metaplasia . In addition, IL-4 can induce AHR and goblet cell metaplasia independent of IL-13 . Despite the greater decrease in inflammation in the Cav1 -/- mice as they aged, the AHR of the Cav1 -/- remained greater than age-matched WT indication that remodeling rather than inflammation may play a role in the elevated AHR in 6-month-old OVA-challenged Cav1 -/- mice.
These findings have important implications, as they open avenues for possible therapeutic interventions to prevent the development of airway remodeling. Our data are supportive of the beneficial effects on airway remodeling after treatment with Cav1 scaffolding domain peptide. In addition, in other studies using relaxin-deficient mice, it has been demonstrated that treatment with relaxin is capable of reversing established airway remodeling and AHR . These studies suggest that the development of anti-fibrotic therapies that could potentially prevent lung function decline associated with airway remodeling is warranted. This approach may be especially relevant in severe asthma, where well-established treatments with inhaled corticosteroids have limited efficacy in the control of airway remodeling development and reversibility [10, 29].
Even though subepithelial fibrosis is an established characteristic in airway remodeling, other studies have demonstrated that changes in myocytes and globet cells may also induce AHR. In this murine model, we identified an increase in subepithilial thickening as the main contributor of AHR in Cav1 -/- mice, but because asthma is a heterogeneous disease, other cellular components may still play an important role in airway remodeling and AHR.
In conclusion, our findings demonstrate that Cav1 deficiency is associated with airway remodeling and the development of AHR. The airway remodeling progressed with age. Inflammation appears not to be required for the development of these age-related changes in Cav1 deficient mice. Cav1 may play a role, possibly through the TGF-β pathway, in the prevention of the development of subepithelial fibrosis and airway remodeling.
This work was supported by the National Institutes of Health Grants P20RR016467, the American Lung Association of Hawaii, the Hawaii Community Foundation (Leahi and Perry Funds) and the Janey Briscoe Center of Excellence in cardiovascular Research.
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