Background
Fibrosis as a result of lung injury arising from various known or unknown etiologies, carries a high rate of morbidity and mortality [
1]. Idiopathic pulmonary fibrosis is usually diagnosed at a late stage of disease, and identification of the pathogenic steps leading to fibrosis has met with limited success [
2]. Various animal models of fibrotic diseases have shown a role for inflammatory cells, including macrophages and neutrophils, as well as their secreted proteases [
3‐
5] and superoxide-derived free radicals [
6,
7].
One way of understanding the cellular and inflammatory mechanisms associated with lung fibrosis has been the intratracheal application of bleomycin (BLM), an antineoplastic antibiotic, to induce a model of pulmonary fibrosis in mice [
8]. BLM-induced lung injury is characterized by early recruitment of neutrophils followed by extensive fibrosis that is self-limiting. Many other cells, including mast cells and macrophages, have also been implicated in establishing inflammation in this model.
Rac2 is a member of the Rho subfamily of
ras-related guanosine triphosphatase expressed primarily in hematopoietic cells, and is a crucial molecule regulating a variety of neutrophil and macrophage functions [
9‐
11]. Rac2 switches from a resting, inactive GDP-bound state to an active GTP-bound state in response to receptor stimulation. The GTP-bound form of Rac2 is essential for activation of the superoxide-generating NADPH oxidase complex in neutrophils [
10] and is required for exocytosis of primary azurophilic granules through polymerization of F-actin filaments required for propelling granules to the cell membrane [
9,
12]. Macrophages utilize Rac2, in addition to the ubiquitously expressed homolog Rac1, for maximal phagocytosis and oxidant production [
11]. Disruption of the gene encoding Rac2 led to attenuated lung inflammation and injury in a model of immune complex-mediated acute lung injury [
13]. Diminished lung injury in
rac2
-/-
mice with acute lung injury was associated with decreased neutrophil recruitment to the airways, reduced matrix metalloproteinase (MMP)-2 and -9 levels in bronchoalveolar lavage samples, and decreased MMP-2 and -9 immunoreactivity in airway and mucosal macrophages [
13]. A small molecule inhibitor of Rac1 and Rac2 also alleviates LPS-induced acute lung injury [
14].
Since neutrophils and macrophages have been shown to play an important role in the development of BLM-induced fibrosis, we hypothesized that Rac2 deficiency will protect mice from lung injury and fibrosis in response to BLM administration.
Materials and methods
Animals
Rac2-deficient mice (
rac2
-/-
) were established by gene disruption [
10] and were backcrossed for >11 generations on the C57BL/6 strain background. Rac2-deficient mice were bred in our animal facility and housed under specific virus antigen-free conditions on a 12:12-h light–dark cycle and fed autoclaved food and water as needed. Wild type (WT) C57BL/6 mice were purchased from Charles River Laboratories and were housed and maintained in the same manner as
rac2
-/-
mice. For our experiments, we used female
rac2
-/-
or C57BL/6 WT mice at 10–14 wk of age. Animal experiments were approved by the University of Alberta Health Sciences Laboratory Animal Ethics Committee (Edmonton, AB, Canada).
BLM-induced pulmonary fibrosis
After general anesthesia with 4% isoflurane inhalation, the trachea was exposed and a single intratracheal injection of BLM sulphate (0.125 U/100 g body weight dissolved in normal saline, Sigma-Aldrich Co., MO, USA) or saline as control was administrated to C57BL/6 WT and rac2
-/-
mice. Following the injection, mice were sutured, allowed to recover and daily monitored for morbidity and mortality.
Lung function measurements
On day 21 after BLM intratracheal instillation, mice were weighed and lung function was measured. Each mouse was anesthetized with 0.1 ml/10 g body weight of a mixture containing xylazine (1.6 mg/ml; Bayer) and ketamine (8 mg/ml; Parnell). Following anesthesia, a tracheotomy was performed, and a polyethylene cannula was inserted. Pancuronium amide (2 mg/kg) was administered intravenously before animals were attached to a ventilator. Mice were mechanically ventilated on a computed controlled piston ventilator FlexiVent® Systems (SCIREQ, Montreal, QC, Canada) with a tidal volume of 5.5 ml/kg at a rate of 150 breaths/min.
Lung histology, αSMA and TGFβ analysis
On days 7 or 21 after BLM administration, left lungs were cannulated, inflated with 10% neutral buffered formalin (Sigma-Aldrich, St. Louis, MO) for 5 min under a constant pressure of 20 cm of H
2O, removed from animals, and placed in fresh 10% neutral buffered formalin for 24 h. In the case of the 21 day group, lung resection was done after lung function testing. Tissues were then embedded in paraffin blocks, and sections were cut (4 μm) and stained with hematoxylin and eosin (H&E) and periodic acid-Schiff-diastase stain (PAS-D). Staining of lung sections with Masson’s trichrome, or with antibodies for α-smooth muscle actin (αSMA) and TGFβ were performed to obtain histological evidence of fibrotic activity. Lung fibrosis was scored according to Ashcroft’s criteria as previously published [
15].
Bronchoalveolar lavage (BAL) and evaluation of cellular infiltration, neutrophil myeloperoxidase (MPO) activity, MMP and cytokine/chemokine levels
Mice were euthanized on days 3 and 7 after saline or BLM intratracheal instillation. Following blood collection by cardiac puncture, the trachea was exposed and intubated with a polyethylene catheter. Lungs were lavaged twice with 1 ml of isotonic phosphate-buffered saline (pH 7.4) and the bronchoalveolar lavage (BAL) fluid was collected. The BAL fluid was centrifuged at 300
g for 5 min. Total cells in the resulting pellet were counted, and cytospins of 5000 cells/sample were prepared and stained with Diff-Quick (Fisher Scientific Co, Kalamazoo, MI). Airway inflammation was assessed by counting the number of inflammatory cells in the BAL fluid as previously described [
16]. BAL supernatants were kept frozen in -80°C for MMP and MPO evaluation. MMPs were evaluated by gelatin zymography as previously described [
17]. MPO activity was assessed using tetramethylbenzidine (TMB) as the substrate, as previously described [
9]. Cytokine and chemokine levels were also evaluated in BAL fluid at day 7 after BLM instillation.
Biochemical analysis of lung tissue
After lung function measurements, right lungs from each animal were removed, weighed and immediately frozen on liquid nitrogen and stored at -80°C for biochemical analysis as described below.
Hydroxyproline determination was done as described [
18]. In brief, lung tissue was thawed and homogenized in 1 ml of water. To precipitate protein, 125 μl of 50% trichloroacetic acid (Sigma-Aldrich) was added to the homogenate and samples were incubated on ice for 20 min. Samples were centrifuged at 300
g for 5 min at 4°C. Supernatants were discarded and 1 ml 12 N HCl was added to the pellet. The pellet was baked at 110°C for 24 h. The dried pellet was reconstituted with 2 ml of distilled water and 500 μl of chloramine T solution (1.4% chloramine T in 0.5 M sodium acetate and 10% isopropanol, Sigma-Aldrich) and incubated for 20 min at 24°C. Ehrlich’s/pDMAB (1 M p-diamethylaminobenzaldehyde in 70% isopropanol and 30% perchloric acid) was also added and incubated at 65°C for 15 min. A sample of 100 μl of the final reaction solution was transferred to a 96-well plate, and the absorbance for each sample was read at 550 nm in a Power Wave XS (BioTek Instruments Inc., Winooski, VT) ELISA reader. The concentration of lung hydroxyproline was calculated from a hydroxyproline standard curve and expressed as μg/gram of lung tissue.
The total collagen content of lungs was determined using homogenized right lungs and a Sircol™ Soluble Collagen Assay kit (Biocolor, Carrickfergus, UK) according to manufacter’s instructions. Data are expressed as the collagen content of the entire right lung.
Statistical analysis
Values are expressed as mean ± SEM. Statistical differences in the mean values among treatment groups were determined by using a one-way ANOVA test with post-hoc analysis using Tukey’s multiple comparison test. In all cases, a value for p < 0.05 was considered statistically significant.
Discussion
Rac2 is a
ras-related guanosine triphosphatase expressed mainly in hematopoietic cells, and is a crucial molecule regulating a diversity of neutrophil functions. We have previously shown that disruption of the gene encoding Rac2 significantly attenuated lung inflammation and injury in an immune complex-mediated acute lung injury model [
13]. Injury in that model is mediated by Rac2 expression in hematopoietic cells. Although we did not identify the exact cell(s) mediating Rac2-dependent injury in that study, we speculated that neutrophils were primarily responsible. Accumulation of neutrophils in the BAL following immune complex-mediated acute lung injury was decreased, as it was also decreased in
rac2
-/-
mice in the BLM injury model we present here. We also showed here that there were differences in MMP-9 levels in the BAL between BLM-treated WT and
rac2
-/-
mice as well as differences in certain cytokine and chemokine levels. These inflammatory changes correlated with changes in lung physiology. There was however no significant difference in parenchymal inflammation seen by histology and in fibrotic markers between surviving BLM-treated WT and
rac2
-/-
mice on day 21 after BLM treatment. Our study also showed a large decrease in mortality of
rac2
-/-
mice compared to wild type mice following treatment with bleomycin. It is not clear whether the changes in inflammation or changes in lung physiology are responsible for this large decrease in mortality. Further work will be required to identify the mechanisms leading to Rac2-mediated mortality in the BLM model of lung injury. With the results presented here our group has shown that
rac2 gene deficiency prevents or attenuates tissue injury in both acute lung injury [
13] and chronic lung injury (data presented here) models.
BLM-induced lung injury develops in two phases in mice. The first phase takes place over the first 9 days after BLM administration, and is characterized by inflammation and accumulation of inflammatory cells in the parenchyma and airways. The second fibrotic phase starts on day 9, with the presence of pro-fibrotic mediators, and leads to the development of overt fibrosis [
22]. In our model, we have shown an increase in MMP-9 on day 3 along with an increase in the accumulation of neutrophils and macrophages in the airways on day 7 after BLM administration to WT mice. The MMP-9 and neutrophil increase, but not the increase in macrophage numbers, were absent from
rac2
-/-
mice treated with BLM. The exact reason for this is not clear at this time. Neutrophil chemotaxis [
23] and the subsequent accumulation in the airways require Rac2 function, and the lack of neutrophil accumulation may be an early event leading to these differences in
rac2
-/-
mice.
Neutrophil accumulation and mediator release have been implicated in the pathophysiology of BLM-induced lung injury. Lack of CXCR2, the receptor for CXCL3/KC, one of the main neutrophil chemotactic agents in mice, resulted in decreased lung fibrosis along with decreased accumulation of neutrophils in the airways [
24]. That study showed that CXCL3/KC levels increased 6 h after BLM treatment and returned to normal by day 8. This may explain why we did not see significant changes in CXCL3/KC levels in our mice when we analyzed them on day 7. It is interesting to note that in the same study the numbers of neutrophils in the parenchyma, as assessed by the levels of MPO in the lung, were not decreased, although tissue injury was decreased. In our study also we did not see a significant difference in inflammatory cell infiltration in the lung tissue on day 7 by histology between WT and
rac2
-/-
mice, although there was significant difference in the numbers of neutrophils in the BAL on day 7. Transmigration of neutrophils into the airways might facilitate fibrosis through the release of mediators that can activate TGFβ. For example it has been shown that lack of elastase prevented TGFβ activation in the airways and decreased the development of fibrosis following bleomycin administration [
20]. In our study we did not see significant differences in TGFβ positive cells on day 21, but we did not analyze TGFβ expression at earlier time points to know if there were any differences.
We showed significant differences in TNF and CCL3/MIP-1α between BLM-treated WT and
rac2
-/-
mice. Both of these mediators have been implicated in the pathophysiology of bleomycin-induced injury. The degree of bleomycin-induced injury correlates with TNF upregulation in the lungs of different strains of mice [
25] and the presence of soluble TNF has been shown to be required for the development of fibrotic lesions in the lungs following bleomycin administration [
26]. In addition TNF has been shown to be mediating the increased expression of CCL3/MIP-1α in the lungs of BLM-treated mice [
27]. CCL3/MIP-1α has been shown to be elevated throughout the time course of bleomycin-induced lung injury and is required for injury to develop [
28]. CCL3/MIP-1α recruits macrophages to the lung through the interaction with CCR5 and may increase the expression of TGFβ in the airways. Lack of these two inflammatory mediators in
rac2
-/-
mice may be responsible for the physiological and other changes described in this manuscript.
A number of other mediators may also be involved in the recruitment of neutrophils and the neutrophil-mediated effects in the BLM model. IL-1β is increased in the BAL of humans with idiopathic lung fibrosis [
29]. IL-1β was also induced by bleomycin in mouse lungs [
30] and lung injury was attenuated when IL-1β activity was decreased [
30]. In our study we only saw a trend towards decreased levels of IL-1β in
rac2
-/-
mice compared to WT mice following BLM treatment. Chemokines that activate CXCR3, such as CXCL10/IP-10 and CXCL9/MIG, have a protective role and can limit fibrosis in the lungs [
31,
32]. CCL11/eotaxin has also been shown to mediate another pathway that leads to BLM-induced lung fibrosis [
33]. Our data indicate that these pathways may not be affected in the absence of Rac2. There are finally also other cytokines that have been shown to mediate BLM-induced lung injury. For example, IL-17A is required for BLM-induced fibrosis [
29] and its main effect in the model may be recruitment of neutrophils. Neutrophils in the airways of mice with BLM injury produce IL-18, and inhibition of IL-18 can prevent fibrosis [
30]. IL-18 was also increased in the lungs of patients with lung injury after receiving BLM. It would be interesting to also study changes in these inflammatory mediators in BLM-treated Rac2 mice to better understand the mechanism of protection.
Other members of the Rho family of GTPases have also been implicated in lung fibrosis. A RhoA inhibitor decreased accumulation of macrophages and neutrophils in the airways of BLM-treated mice and also BLM-induced fibrosis [
34]. In this case the effect is more likely through inhibition of the proliferative effects of RhoA in lung fibroblasts [
35]. In addition Rac1 expression in cutaneous fibroblasts in required for the development of BLM-induced skin fibrosis [
36]. This is an important family of signaling molecules and there has been significant effort in identifying inhibitors for these GTPases. This fact increases the translational potential of these studies, since these inhibitors may be proven to be valuable as therapeutic options for lung fibrotic diseases.
The levels of MMP-2 and MMP-9 in the BAL fluid of WT mice given BLM correlate with the levels in lung tissues, and reportedly peak at day 4 [
37]. In our case we observed that the levels of MMP-9 were decreased compared to WT responses on day 3 in
rac2
-/-
mice, suggesting that MMP-9 production was lacking in the knockout mice. In our earlier study on acute lung injury, we determined that the main cell type responsible for generating MMP-2 and MMP-9 in lung tissues was the tissue macrophage [
13]. These findings indicate that macrophages may be responsible for elevated production of MMP-2 and MMP-9 in early stages of lung injury. Further studies are needed to determine if reduced Rac2 activity in macrophages leads to reduced secretion of MMPs, or if reduced recruitment of neutrophils to the airways of BLM-treated
rac2
-/-
mice results in decreased macrophage activation.
Macrophages have also been implicated in the pathophysiology of BLM-induced injury in mice [
21,
38]. In our study we did not see a difference in macrophage accumulation in the airways in the early stages of BLM-induced injury in
rac2
-/-
mice. However, Rac2 is important for macrophage function, and it is possible that decreased activity and or altered activation status of the recruited macrophages may have a role in the effects we describe. A role for Rac1 in the inflammatory, but not fibrotic, phase of asbestos-induced lung injury in mice has been shown in a mouse strain with conditional, myeloid-specific gene deletion of Rac1 [
39]. This observation suggests that granulocyte/macrophage-expressed Rac1 regulates inflammatory processes, but has little impact on fibrotic lesions arising from asbestos exposure. Although a different model was used in our study, our findings show an additional role for Rac2 in lung physiology and mortality associated with fibrosis, which has not been reported before.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
NA performed the experiments describing mortality and fibrosis in the BLM model and generated the first draft of the manuscript, LP and KC performed the histological analysis, BT advised on the use of animal models, DC and CD performed the experiments for analysis of MMP, PL and HV supervised the study and wrote the manuscript with input from the other authors. All authors read and approved the final manuscript.