Role of Abl in airway hyperresponsiveness and airway remodeling
© Cleary et al.; licensee BioMed Central Ltd. 2013
Received: 8 September 2013
Accepted: 9 October 2013
Published: 11 October 2013
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© Cleary et al.; licensee BioMed Central Ltd. 2013
Received: 8 September 2013
Accepted: 9 October 2013
Published: 11 October 2013
Asthma is a chronic disease that is characterized by airway hyperresponsiveness and airway remodeling. The underlying mechanisms that mediate the pathological processes are not fully understood. Abl is a non-receptor protein tyrosine kinase that has a role in the regulation of smooth muscle contraction and smooth muscle cell proliferation in vitro. The role of Abl in airway hyperresponsiveness and airway remodeling in vivo is largely unknown.
To evaluate the role of Abl in asthma pathology, we assessed the expression of Abl in airway tissues from the ovalbumin sensitized and challenged mouse model, and human asthmatic airway smooth muscle cells. In addition, we generated conditional knockout mice in which Abl expression in smooth muscle was disrupted, and then evaluated the effects of Abl conditional knockout on airway resistance, smooth muscle mass, cell proliferation, IL-13 and CCL2 in the mouse model of asthma. Furthermore, we determined the effects of the Abl pharmacological inhibitors imatinib and GNF-5 on these processes in the animal model of asthma.
The expression of Abl was upregulated in airway tissues of the animal model of asthma and in airway smooth muscle cells of patients with severe asthma. Conditional knockout of Abl attenuated airway resistance, smooth muscle mass and staining of proliferating cell nuclear antigen in the airway of mice sensitized and challenged with ovalbumin. Interestingly, conditional knockout of Abl did not affect the levels of IL-13 and CCL2 in bronchoalveolar lavage fluid of animals treated with ovalbumin. However, treatment with imatinib and GNF-5 inhibited the ovalbumin-induced increase in IL-13 and CCL2 as well as airway resistance and smooth muscle growth in animals.
These results suggest that the altered expression of Abl in airway smooth muscle may play a critical role in the development of airway hyperresponsiveness and airway remodeling in asthma. Our findings support the concept that Abl may be a novel target for the development of new therapy to treat asthma.
Asthma is a chronic airway disease characterized by airway hyperresponsiveness (AHR) and airway remodeling, which lead to impaired respiratory air flow in patients with asthma. However, the underlying mechanisms for the pathological processes are not fully understood.
AHR is largely attributed to hyperreactivity of airway smooth muscle . The contractile properties of human asthmatic airway smooth muscle cells are distinctive from normal human airway smooth muscle cells [2, 3]. In addition, the hyperreactivity of airway smooth muscle tissues occurs in animal models of asthma [4, 5]. Furthermore, increased airway smooth muscle cell proliferation contributes to the progression of airway remodeling in asthma [6, 7]. Airway smooth muscle hyperplasia may facilitate the thickening of the bronchial wall and promote AHR to a variety of stimuli [7, 8].
Abl (Abelson tyrosine kinase, c-Abl) is a non-receptor tyrosine kinase that participates in the regulation of a range of cellular functions including migration and adhesion of nonmuscle cells [9, 10]. Recent studies have implicated Abl in the regulation of vascular smooth muscle contraction in vitro. Contractile activation induces Abl phosphorylation, an indication of Abl activation [10, 11], in smooth muscle. Knockdown of Abl attenuates smooth muscle force development in response to contractile activation [11–13]. Moreover, Abl has been implicated in regulating smooth muscle cell proliferation. Activation of Abl occurs in smooth muscle cells in response to stimulation with growth factors. Silencing of Abl inhibits smooth muscle cell proliferation induced by growth factors [14, 15]. Nevertheless, the role of Abl in asthma pathology in vivo is largely unknown.
In this study, we generated smooth muscle-specific conditional knockout mice, and determined whether smooth muscle-specific knockout of Abl affects AHR and airway remodeling in a mouse model of chronic asthma. Our results suggest that the altered expression of Abl in airway smooth muscle is critical for the development of AHR and airway remodeling.
To assess the effects of inhibitors, BALB/c mice (6–7 weeks old) were purchased from The Jackson Laboratory. They were sensitized and challenged by OVA as described above. In addition, animals were intranasally instilled with 10 mg/kg GNF-5 or imatinib, or PBS 1 h before OVA instillation and 5 h after OVA instillation for last three weeks (Figure 2). Airway resistance in these mice was then assessed on Day 77.
Mice were euthanized by injection of pentobarbital (140 mg/kg). A segment of tracheas (4–5 mm in length) was immediately removed and placed in physiological saline solution (PSS) containing 110 mM NaCl, 3.4 mM KCl, 2.4 mM CaCl2, 0.8 mM MgSO4, 25.8 mM NaHCO3, 1.2 mM KH2PO4, and 5.6 mM glucose. The solution was aerated with 95%O2-5%CO2 to maintain a pH of 7.4. Two stainless steel wires were passed through the lumen of tracheal rings. One of the wires was connected to the bottom of organ baths and the other was attached to a Grass force transducer that had been connected to a computer with A/D converter (Grass). Tracheal segments were then placed in PSS at 37°C. Passive tension with 0.5 g was applied to each segment for 60 min. Contractile force in response to various treatments was then measured.
Human airway smooth muscle (HASM) cells were prepared from human bronchi and adjacent tracheas obtained from the International Institute for Advanced Medicine . Human tissues were non-transplantable and consented for research. This study was approved by the Albany Medical College Committee on Research Involving Human Subjects. Briefly, muscle tissues were incubated for 20 min with dissociation solution [130 mM NaCl, 5 mM KCl, 1.0 mM CaCl2, 1.0 mM MgCl2, 10 mM Hepes, 0.25 mM EDTA, 10 mM D-glucose, 10 mM taurine, pH 7, 4.5 mg collagenase (type I), 10 mg papain (type IV), 1 mg/ml BSA and 1 mM dithiothreitol]. All enzymes were purchased from Sigma-Aldrich. The tissues were then washed with Hepes-buffered saline solution (composition in mM: 10 Hepes, 130 NaCl, 5 KCl, 10 glucose, 1 CaCl2, 1 MgCl2, 0.25 EDTA, 10 taurine, pH 7). The cell suspension was mixed with Ham’s F12 medium supplemented with 10% (v/v) fetal bovine serum (FBS) and antibiotics (100 units/ml penicillin, 100 μg/ml streptomycin). Cells were cultured at 37°C in the presence of 5% CO2 in the same medium. The medium was changed every 3–4 days until cells reached confluence, and confluent cells were passaged with trypsin/EDTA solution [15, 18, 19]. Smooth muscle cells within passage 5 were used for the studies.
Cells were lysed in SDS sample buffer composed of 1.5% dithiothreitol, 2% SDS, 80 mM Tris–HCl (pH 6.8), 10% glycerol and 0.01% bromophenol blue. The lysates were boiled in the buffer for 5 min and separated by SDS-PAGE. Proteins were transferred to a nitrocellulose membrane. The membrane was blocked with bovine serum albumin or milk for 1 h and probed with use of primary antibody followed by horseradish peroxidase-conjugated secondary antibody (Fisher Scientific). Proteins were visualized by enhanced chemiluminescence (Fisher Scientific) using the LAS-4000 Fuji Image System. Abl antibody was purchased from BD Biosciences and Santa Cruz Biotechnology. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) antibody was purchased from Fitzgerald (Acton, MA). The levels of proteins were quantified by scanning densitometry of immunoblots (Fuji Multigauge Software). The luminescent signals from all immunoblots were within the linear range.
Mouse lungs were placed in frozen tissue-embedding medium (Neg 52, Richard-Allen Scientific) and cryosectioned using Cryostats (Richard-Allen Scientific). Tissue sections were fixed for 15 min in 4% paraformaldehyde, and were then washed three times in PBS buffer followed by permeabilization with 0.2% Triton X-100 dissolved in PBS for 5 min. These tissues were incubated with α-smooth muscle actin antibody (Sigma) or proliferating cell nuclear antigen (PCNA) antibody (Thermo Scientific) followed by appropriate secondary antibody conjugated to Alexa-488 or Alex-543 (Molecular Probes/Life Technologies). The sections were also counterstained with 4',6-diamidino-2-phenylindole to visualize the nucleus. The samples were viewed and digitally captured using a Leica microscope system (MDI 6000). All immunohistochemical measurements were performed by using the NIH ImageJ software.
Lungs from sacrificed mice were lavaged three times with 1 mL sterile Hanks balanced salt solution (HBSS) containing 3 mM EDTA. Bronchoalveolar lavage fluid (BALF) was collected after centrifugation and, the supernatant was removed and frozen at −80°C for cytokine/chemokine measurements (See below). The cell pellet was resuspended in HBSS, and total number of inflammatory cells in the BALF was counted by using a hemocytometer. Differential cell counts (macrophages, neutrophils, lymphocytes, and eosinophils) were performed by counting 100 cells from cytospin preparations stained with DiffQuick stain. The levels of IL-13 and CCL2 in the BALF were determined using ELISA kits (R&D systems) according to the manufacturer’s instructions.
All statistical analysis was performed using Prism 4 software (GraphPad Software, San Diego, CA). Comparison among multiple groups was performed by one-way analysis of variance followed by Tukey’s multiple comparison test. Differences between two groups were analyzed by Student-Newman-Keuls test or Dunn's method. Values of n refer to the number of experiments used to obtain each value. P < 0.05 was considered to be significant.
Our previous studies demonstrate that Abl regulates vascular smooth muscle contraction [11–13]. To determine the role of Abl in airway smooth muscle, we generated SM22creAbl-lox mice, a mouse model with smooth muscle cell–specific disruption of the abl gene (Figure 1A). Genotyping and immunoblot analysis verified knockout of Abl in airway smooth muscle (Figure 1B and C). Previous studies by others demonstrate that SM22 is expressed in airway smooth muscle tissues [20–22], which suggests that SM22 promoter is functional in airway smooth muscle. Our results are consistent with these studies.
We also evaluated acute effects of the Abl pharmacological inhibitors imatinib (Gleevec, STI-571) [11, 23] and GNF-5  on airway smooth muscle contraction. Treatment of mouse tracheal rings with imatinib significantly attenuated force development induced by ACh (Figure 3B). Likewise, GNF-5 had inhibitory effects on contraction of tracheal segments with slightly stronger potency (Figure 3B). Furthermore, treatment with imatinib or GNF-5 induced relaxation of tracheal rings precontracted by ACh (Figure 3C).
We also assessed the effects of Abl knockout on airway smooth muscle hyperreactivity in vitro. Contractile force in isolated tracheal rings from OVA-treated Abl-lox mice was greater compared to naïve Abl-lox mice. However, active force of isolated tracheal rings from OVA-treated Ablsm−/− mice was reduced compared to OVA-treated Abl-lox mice. Contractile response of tracheal rings from naïve Ablsm−/− mice was also lower compared to naïve Abl-lox mice (Figure 5B).
We noticed that airway resistance in response to MCh inhalation was slightly higher in BALB/c mice than in Abl-lox mice sensitized and challenged by OVA (Figure 5A and Figure 6A). This is not surprising because BALB/c mouse strain is known to have skewed Th2 response compared to other mouse strains [25, 26].
To determine the role of Abl in the remodeling of airway smooth muscle, we assessed whether conditional knockout of Abl in smooth muscle affects the allergen-induced airway smooth muscle mass by determining the area of α-smooth muscle actin (a smooth muscle marker) staining in the airways of Abl-lox and Ablsm−/− mice sensitized and challenged with OVA.
We also evaluated whether the knockout of Abl influences allergen-induced airway smooth muscle cell proliferation. Proliferating cell nuclear antigen (PCNA) is a critical protein that is expressed by proliferating cells in S phase of the cell cycle. Thus, it has been widely used as a marker of cell proliferation in the airways [8, 27]. The fluorescent intensity of PCNA colocalized with α-smooth muscle actin was greater in the airways of Abl-lox mice treated with OVA compared with Abl-lox mice treated with PBS. However, the intensity of PCNA costained with actin in the airways of Ablsm−/− mice treated with OVA was lower than that in the airways of Abl-lox mice treated with OVA (Figure 7A and C). Moreover, treatment with the Abl inhibitors imatinib or GNF-5 diminished the fluorescent intensity of PCNA in BALB/c mice treated with OVA (Figure 7C). These results indicate that Abl has a role in the allergen-induced airway smooth muscle proliferation.
As a consequence of allergic sensitization and challenge, inflammatory cells enter into the lungs and cytokine/chemokine levels are increased in the bronchoalveolar space of asthmatic patients and animal models, which are characteristic features of allergic airway inflammation [7, 28, 29]. To determine whether the smooth muscle-specific depletion of Abl affects recruitment of inflammatory cells, we determined total and differential cell counts of BALF in lungs of naïve and OVA-treated Abl-lox mice and Ablsm−/− mice.
We also evaluated the effects of the Abl inhibitors imatinib and GNF-5 on cell counts of BALF from mice treated with PBS or OVA. OVA sensitization and challenge increased total and differential cell counts of BALF from BALB/c mice. Treatment with imatinib and GNF-5 reduced the OVA-induced increase in inflammatory cell numbers (Figure 8C and D).
Abl is a non-receptor tyrosine kinase that has a role in regulating smooth muscle contraction and smooth muscle cell proliferation in vitro. The role of Abl in the pathogenesis of asthma in vivo is largely unknown. In this study, Abl expression is upregulated in asthmatic airways. More importantly, conditional knockout of Abl in smooth muscle inhibits airway resistance and airway smooth muscle growth in the animal model of chronic asthma. The results suggest that Abl plays a critical role in the progression of AHR and airway remodeling in chronic asthma.
Our previous studies demonstrate that Abl is essential for vascular smooth muscle force development [10–13]. In this report, conditional knockout of Abl in smooth muscle diminished contractile response of tracheal rings. Moreover, acute inhibition of Abl by the pharmacological agents attenuated contraction in tracheal rings. The results suggest that Abl is necessary for airway smooth muscle contraction. Abl may regulate the functional states of several proteins including Crk-associated substrate and Abi1, which in turn regulate actin dynamics and smooth muscle contraction [11–13, 32, 33].
AHR largely stems from hyperreactivity of airway smooth muscle . The pathological mechanisms that mediate airway smooth muscle hyperreactivity and AHR in asthma are not completely elucidated. Th2 cytokines including IL-13 has been implicated in smooth muscle hypercontractility and AHR [34–36]. In this study, the expression of Abl was upregulated in airway tissues of the animal model of asthma as well as in smooth muscle cells of patients with severe asthma. Furthermore, conditional knockout of Abl in smooth muscle attenuated airway smooth muscle hyperreactivity in vitro and airway resistance in mice sensitized and challenged by the allergen. To rule out the potential effects by compensation in genetically-modified mice, we also determined the acute effects of the Abl pharmacological inhibitors imatinib [11, 23] and GNF-5  on airway resistance in vivo and airway smooth muscle hyperreactivity in vitro. Treatment with the inhibitors also diminished the OVA-sensitized airway resistance in vivo and tracheal contraction in vitro. The results suggest that Abl has a critical role in the development of AHR in asthma.
Airway remodeling is a characteristic feature of severe asthma. In addition to fibrosis, enhanced deposition of extracellular matrix protein, epithelial injury and airway smooth muscle hypertrophy, proliferation of airway smooth muscle cells markedly contributes to the pathogenesis of airway remodeling [6, 8, 29, 37]. Our recent studies demonstrate that Abl is required for smooth muscle cell proliferation in in vitro studies [14, 15]. Abl may modulate cell proliferation by affecting actin polymerization and the Raf-1/MEK/ERK1/2 pathway [14, 15].
Growth factors such as epidermal growth factor and platelet-derived growth factor have been implicated in the progression of airway remodeling . In this report, smooth muscle mass in the airways was reduced in conditional knockout mice sensitized and challenged by ovalbumin. In addition, the cell proliferation marker PCNA was also diminished in conditional knockout mice treated with the allergen. Moreover, treatment with the pharmacological inhibitors had similar effects. Thus, the increased expression of Abl in smooth muscle may contribute to the development of airway remodeling in chronic asthma.
In response to allergic sensitization and challenge, inflammatory cells enter into the lungs and cytokine/chemokine levels are increased in the bronchoalveolar space of asthmatic patients and animal models [4, 30, 34]. Because airway smooth muscle cells have ability to secret cytokines in vitro, we assessed whether Abl knockout in smooth muscle affects airway inflammation. Conditional knockout of Abl did not affect the increase in inflammatory cell numbers, IL-13 and CCL2 in animals sensitized and challenged by the allergen. The results lead us to suggest that Abl expression in smooth muscle does not modulate inflammatory cell infiltration and production of IL-13 and CCL2 in asthma.
On the contrary, treatment with imatinib and GNF-5 reduced the OVA-induced increase in inflammatory cell numbers, and levels of IL-13 and CCL2. The results suggest that global inhibition of Abl diminishes airway inflammation in chronic asthma, which is consistent with the findings that Abl may regulate migration and synthetic functions of immune cells in vitro[38–41].
Currently, β2 agonists are widely used to treat asthma. β2 agonists reduce symptoms of airway obstruction by inducing airway smooth muscle relaxation. However, this therapy has various limitations including β2 adrenergic receptor desensitization . In this study, we demonstrate that Abl in smooth muscle has a critical role in the pathogenesis of AHR and airway remodeling. Furthermore, global inhibition of Abl by pharmacological agents attenuates airway inflammation. Thus, our findings support the concept that Abl may be a novel target for the development of new therapy to treat asthma.
Abl is a non-receptor tyrosine kinase that has a role in regulating smooth muscle contraction and smooth muscle cell proliferation in vitro. The role of Abl in asthma pathogenesis in vivo is not well elucidated. Our present results suggest that the altered expression of Abl in smooth muscle plays a critical role in the progression of AHR and airway remodeling in chronic asthma. Furthermore, global inhibition of Abl attenuates airway inflammation. Thus, Abl may be a novel target for the development of new therapy to treat asthma.
Abelson tyrosine kinase
Bronchoaleolar lavage fluid
Chemokine (C-C motif) ligand 2
Glyceraldehyde 3-phosphate dehydrogenase
bcr-Abl inhibitor III
Human airway smooth muscle
This work was supported by NHLBI Grants HL-110951 and HL-113208 from the National Institutes of Health (to Dale D. Tang). We thank Orion P. Mercaitis for technical support. We thank Dr. Anthony Koleske of Yale University for providing Abl-floxed mice.
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