- Open Access
Activation of Src-dependent Smad3 signaling mediates the neutrophilic inflammation and oxidative stress in hyperoxia-augmented ventilator-induced lung injury
Respiratory Research volume 16, Article number: 112 (2015)
Mechanical ventilation and concomitant administration of hyperoxia in patients with acute respiratory distress syndrome can damage the alveolar epithelial and capillary endothelial barrier by producing inflammatory cytokines and reactive oxygen species. The Src tyrosine kinase and Smad3 are crucial inflammatory regulators used for ventilator-induced lung injury (VILI). The mechanisms regulating interactions between high-tidal-volume mechanical ventilation, hyperoxia, and acute lung injury (ALI) are unclear. We hypothesized that high-tidal-volume mechanical stretches and hyperoxia augment lung inflammation through upregulation of the Src and Smad3 pathways.
Wild-type or Src-deficient C57BL/6 mice, aged between 6 and 8 weeks, were exposed to high-tidal-volume (30 mL/kg) ventilation with room air or hyperoxia for 1–4 h after 2-mg/kg Smad3 inhibitor (SIS3) administration. Nonventilated mice were used as control subjects.
We observed that the addition of hyperoxia to high-tidal-volume mechanical ventilation further induced microvascular permeability, neutrophil infiltration, macrophage inflammatory protein-2 and matrix metalloproteinase-9 (MMP-9) production, malondialdehyde, nicotinamide adenine dinucleotide phosphate oxidase activity, MMP-9 mRNA expression, hypoxemia, and Src and Smad3 activation (P < 0.05). Hyperoxia-induced augmentation of VILI was attenuated in Src-deficient mice and mice with pharmacological inhibition of Smad3 activity by SIS3 (P < 0.05). Mechanical ventilation of Src-deficient mice with hyperoxia further reduced the activation of Smad3.
Our data suggest that hyperoxia-increased high-tidal-volume ventilation-induced ALI partially depends on the Src and Smad3 pathways.
Acute respiratory distress syndrome (ARDS) is a disorder of acute hypoxemic respiratory failure marked by increased microvascular permeability and capillary leak because of disruption of the epithelial-endothelial barrier, which consists of alveolar epithelium, capillary endothelium, and extracellular matrix (ECM) [1–3]. Mechanical ventilation with high levels of oxygen has been employed for life support in patients with ARDS; however, the potential for hyperinflation of the intact parts of the lungs and production of reactive oxygen species (ROS) is high [4–6]. Ventilator-induced lung injury (VILI) is characterized by noncardiogenic pulmonary edema, the release of cytokines and chemokines leading to recruitments of neutrophils [7–11]. Previous studies have demonstrated that high tidal volume (VT) mechanical ventilation may upregulate Src, Smads, and the production of inflammatory cytokines, including tumor necrosis factor-α (TNF-α), macrophage inflammatory protein-2 (MIP-2), and matrix metalloproteinase-9 (MMP-9) in acute lung injury (ALI) [4, 7–13]. However, the mechanisms regulating the interactions between mechanical ventilation and these inflammatory reactions remain unclear.
Prolonged exposure to hyperoxia causes the generation of ROS, including superoxide, hydrogen peroxide, and hydroxyl radical, which may overwhelm the protection of antioxidants in ALI . High-tidal-volume ventilation with hyperoxia has been shown in rat models to induce neutrophil migration into the alveoli and is dependent on MIP-2 production, a chemoattractant belonging to the cysteine-amino-cysteine family of cytokine [4, 6]. MMP-9, a 92-kDa proteolytic enzyme released from activated neutrophils, is required for their transendothelial migration [15, 16]. MMP-9 can cleave gelatin and type IV collagen present in basement membranes and causes disruption of the pulmonary alveolar-capillary integrity, contributing to high-permeability lung edema in ALI [15–17]. Moreover, Foda et al., in a rat model of high-tidal-volume mechanical ventilation, demonstrated that MMPs are crucial for the development of VILI .
The Src family is composed of non-receptor tyrosine kinases, which regulate cell proliferation, migration, apoptosis, and ECM adhesion functions . These protein kinases are expressed by macrophages, neutrophils, endothelial cells, alveolar epithelial cells, and fibroblasts in the lung . In addition to their roles in inducing fibrogenesis, Src and Smad2/3 phosphorylation are increased in mice after endotoxin treatment or in bronchial epithelial cells in response to endoplasmic reticulum stress [19, 20]. Previous studies of hyperoxia-mediated ALI have demonstrated the involvement of the Src pathway in the regulation of leukocyte infiltration, fibrin deposition, activation of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX), and MIP-2 and MMP-9 production [21–24]. Furthermore, recent studies of sepsis-induced ALI in rats have revealed that pharmacologic inhibition of transforming growth factor-β1 (TGF-β1) and the Smad3 signaling pathways substantially ameliorated epithelial and endothelial microvascular permeability [3, 13, 25]. Given the absence of a proven effective treatment for ALI and subsequent lung fibrogenesis, Src and Smad3 inhibition might provide an attractive target in the deteriorating process of patients with ARDS.
Using this murine model of hyperoxia-mediated VILI, we compared the relationships among high-tidal-volume ventilation with or without hyperoxia, the correlation of Src and Smad3 activations to neutrophil influx, oxidative stress, severity of lung injury, and MIP-2 and MMP-9 production by using a specific inhibitor of Smad3 (SIS3) and Src-deficient mice. We hypothesized that the addition of hyperoxia to high-tidal-volume mechanical ventilation would increase neutrophil infiltration, NADPH oxidase expression, and MIP-2 and MMP-9 production secondary to activating the Src and Smad3 pathways.
Materials and methods
Ethics of experimental animals
Wild-type or Src-deficient C57BL/6 mice, weighing between 20 and 25 g, aged between 6 and 8 weeks, were obtained from Jackson Laboratories (Bar Harbor, ME) and National Laboratory Animal Center (Taipei, Taiwan) [8, 26]. Src-deficient mice were generated by target gene disruption as previously described . The experiments were performed in accordance with the National Institutes of Health Guidelines on the Use of Laboratory Animals and approved by the Institutional Animal Care and Use Committee of Chang Gung Memorial Hospital (Permit number: 2011093005).
Animals were randomly distributed into 9 groups in each experiment: group 1, control, nonventilated wild-type mice with room air; group 2, control, nonventilated wild-type mice with hyperoxia; group 3, VT 30 mL/kg wild-type mice with room air; group 4, VT 30 mL/kg wild-type mice with hyperoxia; group 5, VT 30 mL/kg wild-type mice after SIS3 administration with hyperoxia; group 6, VT 30 mL/kg Src+/− mice with hyperoxia; group 7, control, nonventilated wild-type Src+/− mice with room air; group 8, VT 30 mL/kg wild-type mice after SIS3 administration with room air; and group 9, VT 30 mL/kg Src+/− mice with room air. In group 1–6, three mice underwent transmission electron microscopy and five mice underwent measurement for bronchoalveolar lavage (BAL) fluid total protein, cell counts, Evans blue dye (EBD) assay, gelatin zymography, histology, immunohistochemistry assay, lung edema, myeloperoxidase (MPO), malondialdehyde (MDA), total antioxidant capacity, NADPH oxidase assay, real-time polymerase chain reaction (PCR), Western blot, and MIP-2 and MMP-9. In group 7–9, four mice underwent measurement for EBD assay and lung edema.
We used our established mouse model of VILI, as previously described [4, 6]. Mean arterial pressure was monitored every hour during mechanical ventilation by using the data acquisition system (iWorx 214, iWorx Systems, Inc., Dover, NH) connected to a 0.61-mm outer diameter (0.28-mm inner diameter) polyethylene catheter ending in the common carotid artery. Our previous work has shown that activation of Src and increased mRNA expression of what occurred around 1 h of lung stretch, whereas changes in cytokine production and neutrophil infiltration occur later [8, 27]. One hour of mechanical ventilation was employed for gelatin zymography, real-time PCR, and Western blot analyses, and 4 h was applied for MIP-2 and MMP-9 production, BAL fluid total protein, cell counts, lung edema, EBD, and histologic staining analyses, transmission electron microscopy.
SIS3 is a Smad3 inhibitor (2-mg/kg; Calbiochem, La Jolla, CA), and was given intraperitoneally 1 h before mechanical ventilation, based on previous in vivo study that showed 2-mg/kg SIS3 inhibited Smad3 activity and lung injury .
Measurement of MIP-2 and MMP-9
At the end of the study period, the lungs were lavaged via tracheostomy with 20-gauge angiocatheter 3 times with 0.6 mL of 0.9 % normal saline. The effluents were pooled and centrifuged at 310 × g for 10 min. Supernatants were frozen at −80 °C for further analysis of cytokines. MIP-2 with a lower detection limit of 1 pg/mL and MMP-9 with a lower detection limit of 14 pg/mL were measured in bronchoalveolar lavage fluid using a commercially available immunoassay kit containing primary polyclonal anti-mouse antibody that was cross-reactive with rat and mouse MIP-2 and MMP-9 (Biosource International, Camarillo, CA). Each sample was run in duplicate according to the manufacturer’s instructions.
The activity of MMP-9 in lung tissues was measured using gelatin zymography, as previously described . Briefly, the lung tissue homogenates were matched for protein concentration and resolved on a 10 % bis-acrylamide gel copolymerized with 2-mg/mL of gelatin. After electrophoresis, gels were rinsed in 2.5 % Triton × −100 twice for 20 min to remove sodium dodecyl sulfate. The gels were then incubated in incubation buffer (50 mM Tris–HCl, 10 mM CaCl2, 150 mM NaCl, and 0.05 % NaN3) at 37 °C for 24 h. The gels were stained in 0.05 % Coomassie Brilliant Blue G-250 (Sigma, St. Louis, MO) in a mixture of methanol: glacial acetic acid: water (2.5:1:6.5), v: v) and destained in aqueous 4 % methanol: 8 % glacial acetic acid (v: v). Developed gels were then scanned through densitometry.
Measurement of malondialdehyde and total antioxidant capacity
The lungs were homogenized in phosphate buffered saline with or without containing butylated hydroxytoluene for MDA and total antioxidant capacity, respectively. The malondialdehyde and total antioxidant capacity in the protein extracts were measured using the Oxiselect TBARS assay kit containing thiobarbituric acid reactive substances and Oxiselect total antioxidant assay kit containing uric acid (Cell Biolabs, San Diego, CA). Each sample was run in duplicate and expressed as μmole/g protein for MDA and μmole Copper reducing equivalents/g protein for total antioxidant capacity according to the manufacturer’s instructions.
The lungs were homogenized in 3 mL of lysis buffer (20 mM HEPES pH 7.4, 1 % Triton × -100, 10 % glycerol, 2 mM ethylene glycol-bis (β-aminoethyl ether)-N, N, N’, N’-tetraacetic acid, 50 μM β-glycerophosphate, 1 mM sodium orthovanadate, 1 mM dithiotreitol, 400 μM aprotinin, and 400 μM phenylmethylsulfonyl fluoride), transferred to eppendorf tubes and placed on ice for 15 min. The above chemicals were purchased from Sigma-Aldrich (St. Louis, MO). Tubes were centrifuged at 15,350 × g for 10 min at 4 °C and supernatant was flash-frozen. Crude cell lysates were matched for protein concentration, resolved on a 10 % bis-acrylamide gel, and electrotransferred to Immobilon-P membranes (Millipore Corp., Bedford, MA). For assay of Src phosphorylation and Src, Smad3 phosphorylation and Smad3, NOX2, and glyceraldehydes-phosphate dehydrogenase (GAPDH) total protein expression, Western blot analyses were performed with phospho-Src, Src, phospho-Smad3, Smad3, NOX2, and GAPDH antibodies (New England BioLabs, Beverly, MA). Blots were developed by enhanced chemiluminescence (NEN Life Science Products, Boston, MA).
The lungs were paraffin embedded, sliced at 4 μm, deparaffinized, antigen unmasked in 10 mM sodium citrate (pH 6.0), incubated with rabbit phospho-Src and phosopho-Smad3 primary antibody (1:100; New England BioLabs, Beverly, MA), and biotinylated goat anti-rabbit secondary antibody (1:100) according to the manufacturer’s instruction for an immunohistochemical kit (Santa Cruz Biotechnology, Santa Cruz, CA). The specimens were further conjugated with horseradish peroxidase-streptoavidin complex, detected with a diaminobenzidine (DAB) substrate mixture, and counterstained by hematoxylin. A dark-brown DAB signal, identified by arrows, indicated positive staining of phospho-Src and phospho-Smad3 of epithelial cells, whereas shades of light blue signified nonreactive cells.
Real-time polymerase chain reaction
For isolating total RNA, the lung tissues were homogenized in TRIzol reagents (Invitrogen Corporation, Carlsbad, CA) according to the manufacturer’s instructions. Total RNA (1 μg) was reverse transcribed by using a GeneAmp PCR system 9600 (PerkinElmer, Life Sciences, Inc., Boston, MA), as previously described . The following primers were used for real-time PCR: MMP-9, forward primer 5’- CCTACTGCGGGCTCTTCTGA −3’ and reverse primer 5’- CCCTGTAATGGGCTTCCTCT −3’ and GAPDH as internal control, forward primer 5’- AATGCATCCTGCACCACC AA −3’ and reverse primer 5’- GTAGCCATATTCATTGTCATA −3’ (Integrated DNA Technologies, Inc., Coralville, IA) . All quantitative PCR reactions using SYBR Master Mix were performed on an ABI Prism 7000 sequence detector PCR system (Applied Biosystems, Foster City, CA). All PCR reactions were performed in duplicate and heated to 94 °C for 5 min followed by 30 cycles of denaturation at 94 °C for 30 s, annealing at 59 °C for 45 s, and extension at 72 °C for 1 min. The standard curves (cycle threshold values versus template concentration) were prepared for each target gene and for the internal control (GAPDH) in each sample.
Analysis of BAL fluid total protein, cell counts, EBD analysis, histopathologic grading of VILI, NADPH oxidase assay, lung edema MPO assay, transmission electron microscopy, and ventilator protocol were performed as previously described [6, 8].
The gelatin zymogrphy and Western blots were quantitated using a National Institutes of Health (NIH) image analyzer Image J 1.27z (National Institutes of Health, Bethesda, MD) and presented as arbitrary units. Values were expressed as the mean ± SD from at least 5 separate experiments. The data of BAL fluid total protein, cell counts, EBD assay, lung wet-to-dry weight ratio, MIP-2 and MMP-9, MMP-9 mRNA, MPO, NADP+/NADPH, histopathologic assay, and oxygenation were analyzed using Statview 5.0 (Abascus Concepts Inc. Cary, NC; SAS Institute, Inc.). All results of gelatin zymography, real-time PCR, and Western blots were normalized to the nonventilated control wild-type mice with room air. ANOVA was used to assess the statistical significance of the differences, followed by multiple comparisons with a Scheffe’s test, and a P value < 0.05 was considered statistically significant.
Suppression of the effects of hyperoxia on VILI by SIS3 and Src-deficient mice
High-tidal-volume (30 mL/kg) ventilation with room air or hyperoxia for 4 h was employed to induce VILI in mice. The injurious effects of hyperinflation and inhibitory effects of intraperitoneally delivered SIS3 were identified by measuring lung EBD leak, wet-to-dry weight ratio, and BAL fluid total protein and shown in Fig. 1. The physiological conditions at the beginning and end of mechanical ventilation are shown in Table 1. The stable hemodynamic statuses of mice were maintained by monitoring their mean artery pressures. The lung EBD leak, wet-to-dry weight ratio, and BAL fluid total protein were measured to determine the effects of high-tidal-volume ventilation with and without hyperoxia on microvascular permeability and lung edema in VILI (Fig. 1a, b, c). Furthermore, neutrophil counts, MPO activity, and MIP-2 protein production were examined to quantitate neutrophils, the main inflammatory cells and a potential source of ROS, and chemoattractants associated with VILI and concomitant hyperoxia (Fig. 1c, d, e). Additionally, the expression of an oxidant-generating enzyme, NOX2, the NADP+-to-NADPH ratio, the levels of oxidant loads and antioxidant capacity were measured to determine the level of oxidative stress in hyperoxia-induced ALI (Fig. 2). Increased levels of EBD, wet-to-dry weight ratio, BAL fluid total protein, neutrophil counts, MPO, MIP-2 protein, NADP+-to-NADPH ratio, activity of NOX2, and MDA but reduced production of total antioxidant capacity were observed in mice subjected to a tidal volume of 30 mL/kg with hyperoxia compared with those subjected to a tidal volume of 30 mL/kg with room air and nonventilated control mice. The increases of lung inflammation with a tidal volume of 30 mL/kg mechanical ventilation and hyperoxia were substantially suppressed by treatment with SIS3 or with Src-deficient mice. Reduced production of MDA, which is an aldehydic secondary product of lipid peroxidation, but increased production of total antioxidant capacity, was found after pharmacological inhibition with SIS3 or with Src-deficient mice. There were no statistically significant differences between EBD and wet-to-dry ratio in wild-type or Src-deficient non-ventilated control mice with room air, in wild-type mice subjected to a tidal volume of 30 mL/kg pretreated with SIS3 with or without hyperoxia, and in Src-deficient mice subjected to a tidal volume of 30 mL/kg with or without hyperoxia (the levels of EBD: control, nonventilated wild-type mice with room air = 23.6 ± 1.7 ng/mg lung weight versus control, nonventilated Src-deficient mice with room air 22.3 ± 1.2 ng/mg lung weight, P = 0.36; VT 30 mL/kg wild-type mice after SIS3 administration with room air = 61.7 ± 2.6 ng/mg lung weight versus VT 30 mL/kg wild-type mice after SIS3 administration with hyperoxia = 64.1 ± 2.3 ng/mg lung weight, P = 0.29; VT 30 mL/kg Src+/− mice with room air = 51.2 ± 3.2 ng/mg lung weight versus VT 30 mL/kg Src+/− mice with hyperoxia = 52.9 ± 2.5 ng/mg lung weight, P = 0.51; wet-to-dry weight ratio: control, nonventilated wild-type mice with room air = 4.2 ± 0.2 versus control, nonventilated Src-deficient mice with room air = 4.0 ± 0.1, P = 0.24; VT 30 mL/kg wild-type mice after SIS3 administration with room air = 5.0 ± 0.4 versus VT 30 mL/kg wild-type mice after SIS3 administration with hyperoxia = 5.3 ± 0.3, P = 0.71; VT 30 mL/kg Src+/− mice with room air = 4.5 ± 0.3 versus VT 30 mL/kg Src+/− mice with hyperoxia = 4.7 ± 0.2, P = 0.49).
Inhibition of the effects of hyperoxia on lung stretch-induced activation of MMP-9 by SIS3 and in Src-deficient mice
MMP-9 has been shown to play a crucial role in modulating neutrophil-related ALI [9, 10]. The gelatinase activity of MMP-9, MMP-9 mRNA expression associated with chemotactic factors for neutrophils, and MMP-9 protein production in mice subjected to a tidal volume of 30 mL/kg were measured to determine the effects of MMP-9 in VILI with hyperoxia. The elevation of stretch-induced MMP activity using hyperoxia was substantially lowered in Src-deficient mice and pharmacologic inhibition with SIS3 (Fig. 3).
Reduction of the effects of hyperoxia on mechanical ventilation-induced expression of Smad3 by Src-deficient mice and SIS3
Western blot analysis and immunohistochemical staining were performed to identify Smad3 expression and the cell types involved in the VILI model with hyperoxia (Fig. 4). Western blot analyses revealed increased Smad3 phosphorylation in mice subjected to a tidal volume of 30 mL/kg with hyperoxia compared with those subjected to a tidal volume of 30 mL/kg with room air and nonventilated control mice. Additionally, Western blot analyses showed that Src knockout and SIS3 attenuated the high-tidal-volume-induced phospho-Smad activation by 56 % (P < 0.05) and 40 % (P < 0.05), respectively (Fig. 4a). The expression of total nonphosphorylated proteins of Smad3 did not change significantly. Consistent with the Western blot results, the positive immunohistochemical staining for phospho-smad3 in the lung epithelium of mice after a tidal volume of 30 mL/kg mechanical ventilation with hyperoxia was significantly attenuated by Src-deficient mice and SIS3 (Fig. 4b). These data suggested the involvement of the Smad3 pathway in regulating VILI.
The effects of hyperoxia on the mechanical ventilation-induced Src pathway were diminished in Src-deficient mice
To further examine the roles of Src and Smad3 in hyperoxia-related ALI, Western blot analysis and immunohistochemical assay were performed to identify Src expression (Fig. 5). Western blot analyses revealed increased Src phosphorylation in mice subjected to a tidal volume of 30 mL/kg with hyperoxia compared with those subjected to a tidal volume of 30 mL/kg with room air and nonventilated control mice. Moreover, high-tidal-volume ventilation plus hyperoxia-induced phospho-Src activation was attenuated by Src-deficient mice but not inhibited by SIS3 (Fig. 5a). The expression of total nonphosphorylated proteins of Src did not change significantly. Additionally, the airway epithelial cells positively stained for phospho-Src were substantially increased in mice subjected to a tidal volume of 30 mL/kg and concurrent administration of hyperoxia compared with those subjected to a tidal volume of 30 mL/kg with room air and nonventilated control mice (Fig. 5b). Consistent with the Western blot results, the increases of Src phosphorylation after mechanical ventilation were substantially lowered in Src-deficient mice but not inhibited by SIS3, suggesting that Src was the upstream regulator of Smad3 signaling involved in both VILI and hyperoxia.
Inhibition of hyperoxia-augmented stretch-induced lung injuries and improved oxygenation by Src-deficient mice and SIS3
Histological examinations and transmission electron microscopy indicated that the animal lung injured by high-tidal-volume mechanical ventilation with hyperoxia displayed a hemorrhaging pattern, severe congestion, enlargement, neutrophil sequestration, and disruption of the airway ultrastructure: increased of secretory vesicles and epithelial apoptosis characterized by nuclear condensation (Fig. 6a, b). The lung injury score quantification confirmed that mechanical stretch induced severe lung damage during hyperoxia and the lung damage was substantially attenuated by treatment with SIS3 or in Src-deficient mice (Fig. 6c). Moreover, Src-deficient mice and pharmacologic inhibition with SIS3 improved the decreases of the gas exchange (PaO2/FiO2 ratio) in mice receiving a tidal volume of 30 mL/kg with hyperoxia (Fig. 6d).
Mechanical ventilation and concurrent hyperoxia, in the early and late fibroproliferative phases of ALI, is often required to prevent hypoxemia in patients with ARDS [1, 30]. Even while using the protective ventilatory strategy, pathologic lung over-distension may occur in the more compliant lung in patients with ARDS. Moreover, hyperoxia can mediate ALI characterized by disruption of the alveolar-capillary barrier, enhanced diffuse lung inflammation, pulmonary edema, and loss of lung compliance [4–6, 8, 14]. Although some recent improvements have been made in the prevention of VILI, it remains a crucial clinical problem, and the pathogenetic mechanisms must be further defined [14, 31]. Previous studies of murine model of VILI and endoplasmic reticulum stress in alveolar epithelial cells have shown the crucial roles of Src, Smad3, and MMP-9 pathways in the regulation of epithelial-mesenchymal transition [15, 20, 32]. Additionally, recent studies employing alveolar type II epithelial cells and rats have exhibited that cyclic mechanical stretch can induce ALI by activating the TGF-β/Smad pathway and inducing oxidative stress and MMP-9 production [5, 9, 13]. In the current mouse model of VILI, we demonstrated that high-tidal-volume ventilation plus hyperoxia further activated Src and Smad3 signaling pathways and exacerbated lung damage. Furthermore, pharmacologic inhibition with SIS3 and Src-deficient mice attenuated microvascular leak, neutrophil accumulation, upregulation of Src and Smad3, and MIP-2 and MMP-9 production.
A previous rat study of ALI showed that hyperoxia increased high-tidal-volume -induced production of MIP-2, a functional homolog of human interleukin-8 that is related to neutrophil sequestration . Neutrophils, mostly chemoattracted by MIP-2, are the predominant inflammatory cells involved in the process of VILI and are crucial for the generation of ROS [31, 33]. Previous studies have demonstrated that excessive ROS production in response to mechanical ventilation plus hyperoxia can act as direct cell toxins and as secondary messengers by inducing pulmonary epithelium to secrete chemoattractants and proinflammatory cytokines that causes an influx of neutrophils to the lung [5, 24, 33]. The potential sources of oxidant-generating enzymes include NADPH oxidase, xanthine oxidase, and nitric oxide synthase . The NADPH oxidase, a multimeric enzyme complex comprising NOX1-5 and two larger dual oxidases, DUOX1 and DUOX2, has been implicated as a major source for increased superoxide production in response to mechanical ventilation in pulmonary epithelial cells [5, 8, 34]. A recent isolated and perfused rat lung model of VILI also showed that pharmacologic inhibition with apocycin, a NADPH oxidase inhibitor, reduced high-tidal-volume ventilation-induced NADPH oxidase activity and the production of ROS . In vitro, Src protein tyrosine kinases can be activated by TGF-β1 through NADPH oxidase-dependent redox signaling in H358 cells, a small cell lung carcinoma cell line . Recently, we have revealed that the up-regulation of NOX2 occurred in mice subjected to a tidal volume of 30 mL/kg with hyperoxia compared with those subjected to a tidal volume of 30 mL/kg with room air and the control mice. However, no substantial differences on NOX1 expression occurred between mice subjected to a tidal volume at 30 mL/kg with or without hyperoxia . In the current study, we demonstrated that administering hyperoxia augmented stretch-induced neutrophil infiltration, MIP-2 production, MDA level, NOX2 expression, and NADPH oxidase activity, which can be suppressed by Src-deficient mice. Additionally, increased level of total antioxidant capacity in this murine model of VILI was observed after using Src-deficient mice.
MMP-9, a gelatinase B granule stored in the neutrophils, has been shown to participate in both collagen turnover and growth factor activation . It is secreted by many cells, including neutrophils, macrophages, fibroblasts, and endothelial and epithelial cells. Importantly, MMPs are crucial in angiogenesis, tissue remodeling, the restoration of functional connective tissue in the wound-healing process . The migration of activated neutrophils through the basement membrane is aided by digestion of alveolar epithelial ECM by MMP-9, which is considered crucial in the pathogenesis of ALI [15, 36]. Previous rat models of VILI have revealed that pharmacologic inhibition with CMT-3 or doxycycline attenuated high-tidal-volume mechanical ventilation-induced neutrophil accumulation, MMP-9 activation, and lung injury [9, 10]. It is known that Src or Smad3 can activate the promoter of MMP-9 indirectly by p300/nuclear factor-κB (NF-κB) binding or forming a complex with activator protein-1 [37, 38]. Moreover, a previous murine study of hyperoxia-mediated ALI also demonstrated that serine/threonine kinase/protein kinase B (Akt) and NF-κB regulated MPO activity, lipid peroxidation, and the releases of MIP-2 and MMP-9 [16, 17, 24]. We observed that hyperoxia mediated lung damage by generating free radicals. Additionally, we found that mice exposed to hyperoxia would be more susceptible to the deleterious effects of high-tidal-volume mechanical ventilation through upregulation of NOX2, MMP-9 mRNA expression, production of MIP-2 and MMP-9, and influx of neutrophils.
Lipopolysaccharide-induced and ischemia-reperfusion-mediated ALI in rodents have revealed pharmacologic inhibition of Src phosphorylation by Src inhibitors suppressed neutrophil influx, upregulated MMP-9 mRNA expression, and MIP-2 production [21, 23]. Furthermore, a previous murine model of endotoxin-induced ALI also demonstrated that Src activation was crucial in the regulation of NF-κB and αvβ3 integrin signaling . Src-mediated activation of NADPH oxidase and superoxide production was related to phosphorylation of p47phox tyrosine, a major cytosolic subunits of NADPH oxidase in lung endothelial cells . These studies suggest that Src protein tyrosine kinase is a major regulator for the production of chemotactic factor, recruitment of neutrophils, and NADPH oxidase activation in ALI [12, 21–24]. Recently, mechanical stretch-induced activation of Src in rats was proven to increase intracellular signal transduction and regulate the expression of cell junction proteins . Src activation may promote the degradation of junctional proteins from their cytoskeletal anchors and cause endothelial gap formation, resulting in an increase in vascular permeability . Inhibition of Src phosphorylation is crucial in reducing cyclic stretching-induced lung injury, enhances barrier function, and attenuates intercellular signaling . Collectively, high-tidal-volume mechanical ventilation can modulate Src phosphorylation by activating Ca2+ entry through focal adhesion kinases, G protein-coupled receptors, integrin receptors, and stretch-activated cation channels . Our results demonstrated that mechanical ventilation with hyperoxia further induced oxidative stress, MMP-9 expression, and the phosphorylation of Src in murine lung tissue, which can be suppressed in Src-deficient mice. We further explored the roles of Src activation and its downstream signaling targets in the regulation of hyperoxia-augmented VILI.
In addition to playing a role in TGF-β1-mediated lung fibrogenesis, Smad3, a cytoplasmic signal transducer protein, was proven to be involved in the pathogenesis of ALI [3, 13, 19, 25]. Activation of Smad-2/3 signaling is associated with increased neutrophil sequestration in a murine model of LPS-induced ALI . Recent studies of LPS- or cecal ligation-induced ALI in rats have also demonstrated that Smad3 activation increases the level of malondialdehyde, an aldehydic secondary product of ROS, and induces the lung edema and ultrastructural damage of lung tissue [13, 25]. Moreover, oxidant stress is known to regulate tissue inflammation through activation of lipid peroxidation, protein peroxidation, DNA damage, and transcription factors such as NF-κB and Smad . Once activated, receptor-regulated Smads (R-Smads, Smad2, and Smad3) become phophorylated and form heteromeric complexes with common Smads (Co-Smad, Smad4). These complexes translocate to the nucleus, where they bind to TGF-β-responsive promoter DNA, either directly through the Smad-binding elements or in conjunction with other co-activators, and upregulate MMP-9 expression . Further, Src protein kinases can be activated by TGF-β and TGF-β-stimulated Src expression sustained the duration of Smad3 phosphorylation in vascular smooth muscle cells . However, the mechanisms by which Src regulates Smad3 in hyperoxia-augmented ALI are not well defined. Our data indicated that Src activation and Src-dependent phosphorylation of Smad3 were involved in the regulation of NADPH oxidase, intracellular ROS generation, and MMP-9 production in a mouse model of VILI. Furthermore, we observed that high-tidal-volume ventilation and hyperoxia enhanced the expression of Smad3, which was reduced by Src-deficient mice, suggesting that Src was upstream of Smad3 signaling pathway (Fig. 7).
This study had some limitations. There are other potential upstream signal molecules involved in the regulation of hyperoxia-augmented MMP-9 production. An in vitro study of human tracheal smooth muscle cells revealed that TNF-α-induced MMP-9 expression was regulated through phosphoinositide 3-OH kinase and Akt phosphorylation . Recent studies used murine models of hyperoxia-mediated ALI have also demonstrated that inhibition of DNA-binding activity of NF-κB reduced lung injury and MMP-9 production [22, 36]. Two time points for measurements were used based on our previous findings that upstream regulators occurs early in VILI and changes of lung microvascular permeability occurs later [8, 27]. Additional experiments are necessary to explore potential regulators of VILI with hyperoxia.
Using our in vivo mouse model of ALI, we have demonstrated that administration of hyperoxia aggravated high-tidal-volume ventilation-induced destruction of the alveolar-capillary barrier, resulting in increased lung microvascular permeability, neutrophil influx, oxidative stress, and MIP-2 and MMP-9 production. The injurious process caused by mechanical ventilation with or without hyperoxia partly depends on the activation of Src and Smad3. Knowledge of the effect of mechanical forces on Src and Smad3 signaling pathways allows clarification of the molecular and cellular mechanisms regulating acute exudative phase of ARDS. Therefore, inhibiting Src and Smad3 might serve as a novel therapeutic target in the management of mechanically ventilated patients with ARDS exposed to hyperoxia, whose mortality has remained substantially high with the present lung-protective ventilation strategy.
Acute lung injury
Acute respiratory distress syndrome
Evans blue dye
Macrophage inflammatory protein-2
Nicotinamide adenine dinucleotide phosphate
Reactive oxygen species
Polymerase chain reaction
Phosphoinositide 3-OH kinase
Specific inhibitor of Smad3
Transforming growth factor-β1
Tumor necrosis factor-α
Ventilator-induced lung injury
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This research was supported by a grant from the National Science Council (No. 101-2314-B-182A-088-MY3, 104-2314-B-182A-124). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank Chang-Hung Tien for his help with the experiment.
The authors declare that they have no competing interests.
Conceived and designed the experiments: L-LF, L-CW, Y-CT. Performed the experiments: L-LF. Analyzed the data: L-LF, C-NH. Contributed reagents/materials/analysis tools: L-CS, C-LC, K-KC, C-CH. Wrote the paper: L-LF, L-YY. All authors read and approved the final manuscript.
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Li, LF., Lee, CS., Liu, YY. et al. Activation of Src-dependent Smad3 signaling mediates the neutrophilic inflammation and oxidative stress in hyperoxia-augmented ventilator-induced lung injury. Respir Res 16, 112 (2015). https://doi.org/10.1186/s12931-015-0275-6
- Matrix metalloproteinase-9
- Nicotinamide adenine dinucleotide phosphate oxidase
- Ventilator-induced lung injury