Open Access

Rac2 is involved in bleomycin-induced lung inflammation leading to pulmonary fibrosis

  • Narcy Arizmendi1,
  • Lakshmi Puttagunta2,
  • Kerri L Chung2,
  • Courtney Davidson1,
  • Juliana Rey-Parra3,
  • Danny V Chao1,
  • Bernard Thebaud3,
  • Paige Lacy1Email author and
  • Harissios Vliagoftis1Email author
Respiratory Research201415:71

https://doi.org/10.1186/1465-9921-15-71

Received: 21 June 2013

Accepted: 16 June 2014

Published: 27 June 2014

Abstract

Background

Pulmonary fibrotic diseases induce significant morbidity and mortality, for which there are limited therapeutic options available. Rac2, a ras-related guanosine triphosphatase expressed mainly in hematopoietic cells, is a crucial molecule regulating a diversity of mast cell, macrophage, and neutrophil functions. All these cell types have been implicated in the development of pulmonary fibrosis in a variety of animal models. For the studies described here we hypothesized that Rac2 deficiency protects mice from bleomycin-induced pulmonary fibrosis.

Methods

To determine the role of Rac2 in pulmonary fibrosis we used a bleomycin-induced mouse model. Anesthetized C57BL/6 wild type and rac2 -/- mice were instilled intratracheally with bleomycin sulphate (1.25 U/Kg) or saline as control. Bronchoalveolar lavage (BAL) samples were collected at days 3 and 7 of treatment and analyzed for matrix metalloproteinases (MMPs). On day 21 after bleomycin treatment, we measured airway resistance and elastance in tracheotomized animals. Lung sections were stained for histological analysis, while homogenates were analyzed for hydroxyproline and total collagen content.

Results

BLM-treated rac2 -/- mice had reduced MMP-9 levels in the BAL on day 3 and reduced neutrophilia and TNF and CCL3/MIP-1α levels in the BAL on day 7 compared to BLM-treated WT mice. We also showed that rac2 -/- mice had significantly lower mortality (30%) than WT mice (70%) at day 21 of bleomycin treatment. Lung function was diminished in bleomycin-treated WT mice, while it was unaffected in bleomycin-treated rac2 -/- mice. Histological analysis of inflammation and fibrosis as well as collagen and hydroxyproline content in the lungs did not show significant differences between BLM-treated rac2 -/- and WT and mice that survived to day 21.

Conclusion

Rac2 plays an important role in bleomycin-induced lung injury. It is an important signaling molecule leading to BLM-induced mortality and it also mediates the physiological changes seen in the airways after BLM-induced injury.

Keywords

Lung injury Lung fibrosis Bleomycin Neutrophils Rac2

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 [35] 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 [911]. 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 H2O, 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.

Results

Rac2 mediates airway neutrophil infiltration and MMP-9 release in the airways following BLM-induced injury

Rac2 is expressed primarily in hematopoietic cells, and has an important role in cell motility, superoxide release and degranulation in neutrophils and macrophages [9, 10, 19]. Rac2 also mediates acute lung injury due to immune complexes in murine models [13]. The aim of this study was to understand the role of Rac2 in BLM-induced lung injury, a model with a more prolonged time course than immune complex-mediated injury. BLM induces reversible fibrosis over 2–3 weeks; early accumulation of neutrophils [20] and macrophages [21] has been shown to be important for the transition from inflammation to fibrosis in this model.

To understand the role of Rac2 in BLM-induced lung injury, we first examined the accumulation of inflammatory cells and inflammatory mediators in the airways of mice 3 and 7 days after induction of bleomycin-induced lung injury. To do that we performed BAL on days 3 and 7 after BLM administration, and evaluated the numbers of neutrophils and macrophages, and the presence of MPO, MMP-2 and MMP-9 activity, as well as cytokine and chemokine levels.

BAL performed on day 3 showed no significant differences in total cells, neutrophils, macrophages or lymphocytes between BLM- and saline-treated mice in WT and rac2 -/- groups (Figure 1A-D, n = 5). WT mice receiving BLM showed accumulation of inflammatory cells in the BAL on day 7 compared to saline-treated mice (Figure 1A). In contrast, BLM-treated rac2 -/- mice showed no significant accumulation of cells in BAL on day 7 (Figure 1A). While BLM induced the recruitment of neutrophils to the airways of WT mice o day 7, there were no increased numbers of neutrophils in BLM-treated rac2 -/- mice compared to saline treated mice on day 7 (Figure 1B). For both total cells and neutrophils there was a statistically significant difference between BLM-treated WT and rac2 -/- mice. The numbers of macrophages increased in BLM-treated WT and rac2 -/- mice on day 7 (Figure 1C) but the number of lymphocytes showed only a trend towards increase by BLM in both backgrounds (Figure 1D). There was no difference between BLM-treated WT and rac2 -/- mice in the number of macrophages and lymphocytes in the BAL, indicating that lack of Rac2 affects primarily neutrophil accumulation in the airways of BLM-treated mice.
Figure 1

Rac2 mediates BLM-induced airway neutrophil infiltration . (A) Total cell counts, (B) neutrophils, (C) macrophages and (D) lymphocytes in BAL samples at 3 and 7 days after intratracheal saline or bleomycin administration to WT and rac2 -/- mice (n.s. not significant, *p < 0.05, **p < 0.01, ***p < 0.001, n = 5).

We next measured MPO activity in BAL samples. WT mice treated with BLM showed higher levels of MPO in BAL on day 3 and day 7 compared to saline-treated mice (Figure 2A and B n = 5). Rac2 -/- mice exhibited increased MPO activity on day 3 but not on day 7 (Figure 2A and B). There was no statistically significant difference in MPO between BLM-treated WT and rac2 -/- mice on day 3 or day 7. Histological analysis of the lungs of saline and BLM-treated WT and rac2 -/- mice on day 7 showed diffuse inflammatory cell infiltration in both groups of BLM-treated mice, but there were no clear differences between the two groups in the pattern or degree of inflammation (Figure 3).
Figure 2

MPO and MMP in BAL fluid . MPO (A and B), MMP-9 (C and D) and MMP-2 (E and F) levels in the BAL fluid on day 3 (A, C, E) and 7 (B, D, F) after intratracheal saline or bleomycin administration to WT and rac2 -/- mice. (n.s. not significant, *p < 0.05, **p < 0.01, ***p < 0.001, n = 5).

Figure 3

Histological analysis of BLM-induced lung injury on day 7 . Representative images of H&E staining of lung sections 7 days after intratracheal saline or bleomycin administration to WT and rac2 -/- mice (in every condition 5 mice were analyzed by histology).

We also examined the levels of matrix metalloproteinases in the BAL samples from these mice. BLM treatment increased MMP-9 levels in WT mice, but not in rac2 -/- mice, on day 3 (Figure 2C). MMP-9 levels returned to baseline by day 7 (Figure 2D). In contrast MMP-2 levels were increased in both WT and rac2 -/- mice on day 7, but not day 3, and there was no difference in MMP-2 levels between BLM-treated WT and rac2 -/- mice on day 3 (Figure 2E and F).

In order to further understand the mechanisms for the defect in neutrophil migration to the airways in rac2 -/- mice treated with BLM, we evaluated the levels of various cytokines and chemokines in the BAL fluid. TNF was increased in WT mice following BLM administration, but not in rac2 -/- mice (Figure 4A, n = 5). IL-1β and CXCL3/KC showed a trend towards an increase in WT mice following BLM administration, but there were no statistically significant differences between any of the groups studies (Figure 4B and C, n = 5). CCL3/MIP-1α showed similar pattern with TNF (Figure 4D, n = 5). Finally CCL11/eotaxin and CXCL10/IP-10 were increased in both WT and rac2 -/- mice following BLM treatment and there was no difference between BLM-treated WT and rac2 -/- mice (Figure 4E and F, n = 5).
Figure 4

Cytokine/chemokine levels in BAL fluid . Levels of TNF (A), IL-1β (B), CXCL3/KC (C), CCL3/MIP-1α (D), CCL11/Eotaxin (E) and CXCL10/IP-10 (F), were determined in BAL fluid 7 days after intratracheal saline or bleomycin administration to WT and rac2 -/- mice. (n.s. not significant, *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, n = 5).

Rac2 deficiency attenuates biological long-term consequences of BLM-induced lung injury

BLM-induced lung injury in mice is characterized by the development of extensive reversible fibrosis 15–20 days after a single treatment [22]. Fibrosis alters lung physiology and leads to significant morbidity and mortality in this model, before the process resolves. Since rac2 -/- mice showed altered early inflammatory response after lung injury, we next studied whether later events of BLM injury, including mortality and fibrosis, were also affected.

To understand the function of Rac2 in the long-term effects of BLM-induced lung injury, WT and rac2 -/- mice were given BLM intratracheally and followed for 21 days. WT mice showed 70% mortality by day 21, while rac2 -/- mice showed significantly lower mortality (p < 0.005) (Figure 5). In order to further understand the functional role of Rac2 in BLM-induced lung injury, we analyzed lung physiology and markers of fibrosis in the mice that survived until day 21.
Figure 5

Rac2 deficiency decreases mortality in bleomycin-induced pulmonary fibrosis . Survival curves shown over 21 days for WT and rac2 -/- mice receiving BLM or saline (n = 13-22 per group).

WT mice that received BLM showed significantly increased airway resistance and elastance compared to saline-treated mice (p < 0.05) (Figure 6A and B, n = 8). In contrast, rac2 -/- mice that received BLM showed resistance and elastance levels that were similar to rac2 -/- mice receiving saline. There was also significant difference in resistance and elastance between BLM-treated WT and rac2 -/- mice.
Figure 6

Rac2 deficiency prevents BLM-included changes in pulmonary physiology . (A) Resistance and (B) elastance 21 days after intratracheal saline or bleomycin administration to WT and rac2 -/- mice (*p < 0.05, **p < 0.01, n = 5-8).

The mortality and pulmonary physiology results indicate that BLM-induced injury is attenuated in rac2 -/- mice, and that in contrast to WT mice surviving to day 21, the injury still present in the rac2 -/- mice still surviving to day 21 does not affect lung physiology.

Rac2 deficiency had no significant effect inflammation in BLM-treated mice surviving to day 21

We also performed histological analysis of lungs from surviving BLM-treated and saline-treated mice on day 21. Lungs were excised, fixed and then stained with H&E for morphology and inflammatory cell infiltration and PAS-D to identify mucin.

Saline-treated WT and rac2 -/- mice (Figure 7A) showed normal architectural pattern of airways and alveoli, with an apparent increase in interstitial leukocytes evident in rac2 -/- mice. We hypothesize that the latter observation is the result of the modest peripheral neutrophilia that has been described in these animals [10], but we have no data to support this conclusion. Lung parenchyma of WT BLM-treated mice exhibited prominent perivascular, peribronchiolar and intra-alveolar inflammation, with increased numbers of alveolar macrophages (Figure 7A). The lungs of rac2 -/- BLM-treated mice showed a similar picture except that interstitial inflammation often had a more focal distribution. A semi-quantitative analysis (perivascular, peribronchial and intra-alveolar infiltrates were graded on a score of 0–3 for all the mice and these 3 numbers of every mouse were averaged and are presented as the inflammation score) showed no significant difference in inflammatory infiltrates between BLM-treated WT and rac2 -/- mice (Figure 7B).
Figure 7

Histological analysis of BLM-induced lung injury . (A) Representative images from H&E staining of 21 days after intratracheal saline or bleomycin administration to WT and rac2 -/- mice (B) Inflammation score for saline and BLM-treated WT and rac2 -/- mice 21 days following saline or BLM administration (n.s. non-significant, *p < 0.05, n = 5-8).

We also stained the lungs with PAS-D to identify mucin (Figure 8). WT BLM-treated mice displayed airway epithelium exhibiting increased numbers of mucin-containing epithelial cells consistent with goblet cell hyperplasia (arrow, fuchsia colored cells). In contrast, rac2 -/- BLM-treated mice showed airway epithelium with reduced numbers of mucin-containing epithelial cells compared to WT mice treated with BLM. In control saline-treated mice, there were essentially no mucin-containing epithelial cells in WT and rac2 -/- airway epithelia.
Figure 8

Analysis of mucin expression following BLM-induced lung injury . PAS-D staining of lung sections 21 days after intratracheal saline or bleomycin administration to WT and rac2 -/- mice (in each condition, 5–8 mice were analyzed by histology).

Effect of Rac2 deficiency on fibrosis in BLM-treated mice surviving to day 21

To further assess the degree of fibrosis histologically, we analyzed lung sections from WT and rac2 -/- mice after Masson’s Trichrome staining to evaluate collagen deposition and measured total collagen in the lungs of these mice. We also performed immunohistochemical analysis with staining for αSMA and TGFβ.

WT and rac2 -/- saline-instilled mice presented with normal lung parenchyma with an expected minimal level and distribution of collagen fibrils. In contrast, the lung parenchyma of WT and rac2 -/- BLM-treated mice showed increased collagen deposition compared saline-treated controls (arrows, Figure 9A lower panels). In general, BLM-treated rac2 -/- mice showed smaller patchy regions of collagen deposition compared to BLM-treated WT mice. However, evaluation of fibrosis by Ashcroft scoring as done before [15] showed no significant difference between BLM-treated WT and rac2 -/- mice (Figure 9B).
Figure 9

Rac2 deficiency and BLM-induced fibrosis . (A) Representative images of Masson’s trichrome staining of lung sections 21 days after intratracheal saline or bleomycin administration to WT and rac2 -/- mice (in every condition 5–8 mice were analyzed by histology). (B) Quantitation of lung fibrosis using Ashcroft’s criteria (5–8 mice were analyzed per group). Total collagen (C) and hydroxyproline content (D) of lungs 21 days were determined after intratracheal saline or bleomycin administration to WT and rac2 -/- mice (n.s. not significant, *p < 0.05, n = 5-8).

In order to determine fibrosis using biochemical approach, we estimated total lung collagen content using the Sircol Dye Reagent and hydroxyproline content using lung homogenates from saline and BLM-treated WT and rac2 -/- mice. We detected a significant increase in total lung collagen content and in hydroxyproline content in BLM-treated WT mice compared to saline-treated mice (p < 0.05, n =6), while rac2 -/- BLM-treated mice did not show significant increase in lung collagen or hydroxyproline content compared to saline-treated rac2 -/- animals (Figure 9C and D, n = 7-8 per group). However, BLM-treated rac2 -/- mice also showed no statistically significant difference in collagen or hydroxyproline content compared to BLM-treated WT mice.

To further study the role of Rac2 in pulmonary fibrosis was also performed immunohistochemistry for αSMA and TGFβ. As shown in Figure 10, there were no differences in αSMA and TGFβ staining between BLM-treated WT and rac2 -/- mice on day 21.
Figure 10

αSMA and TGFβ immunohistochemistry . Representative images showing immunostaining of αSMA, with arrows indicating the presence of myofibroblasts (A), and TGFβ with arrows indicating TGFβ-positive leukocytes (B), in lung sections 21 days after intratracheal saline or bleomycin administration to WT and rac2 -/- mice (in every condition 5–8 mice were analyzed by histology).

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.

Conclusions

This manuscript shows that rac2 deficiency decreases BLM-induced mortality from 70% in wild type mice to less than 30% in Rac2 knockout mice. Rac2 activation also plays an important role in BLM-induced alterations in respiratory physiology and may also mediate the development of early airway inflammation in response to inhaled BLM. We conclude that Rac2 mediates many physiological changes seen in the lungs that may be related to BLM-induced mortality.

Abbreviations

αSMA: 

α-smooth muscle actin

BAL: 

Bronchoalveolar lavage

BLM: 

Bleomycin

H&E: 

Hematoxylin and eosin

MMP: 

Matrix metalloproteinases

PAS-D: 

Periodic-acid Schiff diastase

Rac2: 

ras-related C3 botulinum toxin substrate 2

WT: 

Wild type.

Declarations

Acknowledgements

This study was funded by grants from The Lung Association of Alberta and NWT, Alberta Innovates Health Solutions (formerly Alberta Heritage Foundation for Biomedical Research) and CIHR.

Authors’ Affiliations

(1)
Pulmonary Research Group and Department of Medicine, University of Alberta
(2)
Department of Laboratory Medicine and Pathology, University of Alberta
(3)
Department of Pediatrics and Women and Children’s Health Research Institute, University of Alberta

References

  1. Olson AL, Swigris JJ, Lezotte DC, Norris JM, Wilson CG, Brown KK: Mortality from pulmonary fibrosis increased in the United States from 1992 to 2003. Am J Respir Crit Care Med. 2007, 176 (3): 277-284.PubMedView ArticleGoogle Scholar
  2. Noble PW, Barkauskas CE, Jiang D: Pulmonary fibrosis: patterns and perpetrators. J Clin Invest. 2012, 122 (8): 2756-2762.PubMedPubMed CentralView ArticleGoogle Scholar
  3. Tan RJ, Fattman CL, Niehouse LM, Tobolewski JM, Hanford LE, Li Q, Monzon FA, Parks WC, Oury TD: Matrix metalloproteinases promote inflammation and fibrosis in asbestos-induced lung injury in mice. Am J Respir Cell Mol Biol. 2006, 35 (3): 289-297.PubMedPubMed CentralView ArticleGoogle Scholar
  4. Pardo A, Barrios R, Gaxiola M, Segura-Valdez L, Carrillo G, Estrada A, Mejia M, Selman M: Increase of lung neutrophils in hypersensitivity pneumonitis is associated with lung fibrosis. Am J Respir Crit Care Med. 2000, 161 (5): 1698-1704.PubMedView ArticleGoogle Scholar
  5. Taooka Y, Maeda A, Hiyama K, Ishioka S, Yamakido M: Effects of neutrophil elastase inhibitor on bleomycin-induced pulmonary fibrosis in mice. Am J Respir Crit Care Med. 1997, 156 (1): 260-265.PubMedView ArticleGoogle Scholar
  6. Yang J, Tan Y, Zhao F, Ma Z, Wang Y, Zheng S, Epstein PN, Yu J, Yin X, Zheng Y, Li X, Miao L, Cai L: Angiotensin II plays a critical role in diabetic pulmonary fibrosis most likely via activation of NADPH oxidase-mediated nitrosative damage. Am J Physiol Endocrinol Metab. 2011, 301 (1): E132-E144.PubMedView ArticleGoogle Scholar
  7. Fattman CL, Tan RJ, Tobolewski JM, Oury TD: Increased sensitivity to asbestos-induced lung injury in mice lacking extracellular superoxide dismutase. Free Radic Biol Med. 2006, 40 (4): 601-607.PubMedPubMed CentralView ArticleGoogle Scholar
  8. Moore BB, Hogaboam CM: Murine models of pulmonary fibrosis. Am J Physiol Lung Cell Mol Physiol. 2008, 294 (2): L152-L160.PubMedView ArticleGoogle Scholar
  9. Abdel-Latif D, Steward M, Macdonald DL, Francis GA, Dinauer MC, Lacy P: Rac2 is critical for neutrophil primary granule exocytosis. Blood. 2004, 104 (3): 832-839.PubMedView ArticleGoogle Scholar
  10. Roberts AW, Kim C, Zhen L, Lowe JB, Kapur R, Petryniak B, Spaetti A, Pollock JD, Borneo JB, Bradford GB, Atkinson SJ, Dinauer MC, Williams DA: Deficiency of the hematopoietic cell-specific Rho family GTPase Rac2 is characterized by abnormalities in neutrophil function and host defense. Immunity. 1999, 10 (2): 183-196.PubMedView ArticleGoogle Scholar
  11. Yamauchi A, Kim C, Li S, Marchal CC, Towe J, Atkinson SJ, Dinauer MC: Rac2-deficient murine macrophages have selective defects in superoxide production and phagocytosis of opsonized particles. J Immunol. 2004, 173 (10): 5971-5979.PubMedView ArticleGoogle Scholar
  12. Mitchell T, Lo A, Logan MR, Lacy P, Eitzen G: Primary granule exocytosis in human neutrophils is regulated by Rac-dependent actin remodeling. Am J Physiol Cell Physiol. 2008, 295 (5): C1354-C1365.PubMedPubMed CentralView ArticleGoogle Scholar
  13. Dooley JL, Abdel-Latif D, St Laurent CD, Puttagunta L, Befus D, Lacy P: Regulation of inflammation by Rac2 in immune complex-mediated acute lung injury. Am J Physiol Lung Cell Mol Physiol. 2009, 297 (6): L1091-L1102.PubMedPubMed CentralView ArticleGoogle Scholar
  14. Yao HY, Chen L, Xu C, Wang J, Chen J, Xie QM, Wu X, Yan XF: Inhibition of Rac activity alleviates lipopolysaccharide-induced acute pulmonary injury in mice. Biochim Biophys Acta. 2011, 1810 (7): 666-674.PubMedView ArticleGoogle Scholar
  15. Ashcroft T, Simpson JM, Timbrell V: Simple method of estimating severity of pulmonary fibrosis on a numerical scale. J Clin Pathol. 1988, 41 (4): 467-470.PubMedPubMed CentralView ArticleGoogle Scholar
  16. Ebeling C, Forsythe P, Ng J, Gordon JR, Hollenberg M, Vliagoftis H: Proteinase-activated receptor 2 activation in the airways enhances antigen-mediated airway inflammation and airway hyperresponsiveness through different pathways. J Allergy Clin Immunol. 2005, 115 (3): 623-630.PubMedView ArticleGoogle Scholar
  17. Vliagoftis H, Schwingshackl A, Milne CD, Duszyk M, Hollenberg MD, Wallace JL, Befus AD, Moqbel R: Proteinase-activated receptor-2-mediated matrix metalloproteinase-9 release from airway epithelial cells. J Allergy Clin Immunol. 2000, 106 (3): 537-545.PubMedView ArticleGoogle Scholar
  18. Edwards CA, O’Brien WD: Modified assay for determination of hydroxyproline in a tissue hydrolyzate. Clin Chim Acta. 1980, 104 (2): 161-167.PubMedView ArticleGoogle Scholar
  19. Didsbury J, Weber RF, Bokoch GM, Evans T, Snyderman R: rac, a novel ras-related family of proteins that are botulinum toxin substrates. J Biol Chem. 1989, 264 (28): 16378-16382.PubMedGoogle Scholar
  20. Chua F, Dunsmore SE, Clingen PH, Mutsaers SE, Shapiro SD, Segal AW, Roes J, Laurent GJ: Mice lacking neutrophil elastase are resistant to bleomycin-induced pulmonary fibrosis. Am J Pathol. 2007, 170 (1): 65-74.PubMedPubMed CentralView ArticleGoogle Scholar
  21. Baran CP, Opalek JM, McMaken S, Newland CA, O’Brien JM, Hunter MG, Bringardner BD, Monick MM, Brigstock DR, Stromberg PC, Hunninghake GW, Marsh CB: Important roles for macrophage colony-stimulating factor, CC chemokine ligand 2, and mononuclear phagocytes in the pathogenesis of pulmonary fibrosis. Am J Respir Crit Care Med. 2007, 176 (1): 78-89.PubMedPubMed CentralView ArticleGoogle Scholar
  22. Chaudhary NI, Schnapp A, Park JE: Pharmacologic differentiation of inflammation and fibrosis in the rat bleomycin model. Am J Respir Crit Care Med. 2006, 173 (7): 769-776.PubMedView ArticleGoogle Scholar
  23. Carstanjen D, Yamauchi A, Koornneef A, Zang H, Filippi MD, Harris C, Towe J, Atkinson S, Zheng Y, Dinauer MC, Dinauer MC, Williams DA: Rac2 regulates neutrophil chemotaxis, superoxide production, and myeloid colony formation through multiple distinct effector pathways. J Immunol. 2005, 174 (8): 4613-4620.PubMedView ArticleGoogle Scholar
  24. Russo RC, Guabiraba R, Garcia CC, Barcelos LS, Roffe E, Souza AL, Amaral FA, Cisalpino D, Cassali GD, Doni A, Bertini R, Teixeira MM: Role of the chemokine receptor CXCR2 in bleomycin-induced pulmonary inflammation and fibrosis. Am J Respir Cell Mol Biol. 2009, 40 (4): 410-421.PubMedView ArticleGoogle Scholar
  25. Ortiz LA, Lasky J, Lungarella G, Cavarra E, Martorana P, Banks WA, Peschon JJ, Schmidts HL, Brody AR, Friedman M: Upregulation of the p75 but not the p55 TNF-alpha receptor mRNA after silica and bleomycin exposure and protection from lung injury in double receptor knockout mice. Am J Respir Cell Mol Biol. 1999, 20 (4): 825-833.PubMedView ArticleGoogle Scholar
  26. Oikonomou N, Harokopos V, Zalevsky J, Valavanis C, Kotanidou A, Szymkowski DE, Kollias G, Aidinis V: Soluble TNF mediates the transition from pulmonary inflammation to fibrosis. PLoS One. 2006, 1: e108-PubMedPubMed CentralView ArticleGoogle Scholar
  27. Smith RE, Strieter RM, Phan SH, Lukacs N, Kunkel SL: TNF and IL-6 mediate MIP-1alpha expression in bleomycin-induced lung injury. J Leukoc Biol. 1998, 64 (4): 528-536.PubMedGoogle Scholar
  28. Ishida Y, Kimura A, Kondo T, Hayashi T, Ueno M, Takakura N, Matsushima K, Mukaida N: Essential roles of the CC chemokine ligand 3-CC chemokine receptor 5 axis in bleomycin-induced pulmonary fibrosis through regulation of macrophage and fibrocyte infiltration. Am J Pathol. 2007, 170 (3): 843-854.PubMedPubMed CentralView ArticleGoogle Scholar
  29. Wilson MS, Madala SK, Ramalingam TR, Gochuico BR, Rosas IO, Cheever AW, Wynn TA: Bleomycin and IL-1beta-mediated pulmonary fibrosis is IL-17A dependent. J Exp Med. 2010, 207 (3): 535-552.PubMedPubMed CentralView ArticleGoogle Scholar
  30. Hoshino T, Okamoto M, Sakazaki Y, Kato S, Young HA, Aizawa H: Role of proinflammatory cytokines IL-18 and IL-1beta in bleomycin-induced lung injury in humans and mice. Am J Respir Cell Mol Biol. 2009, 41 (6): 661-670.PubMedView ArticleGoogle Scholar
  31. Tager AM, Kradin RL, LaCamera P, Bercury SD, Campanella GS, Leary CP, Polosukhin V, Zhao LH, Sakamoto H, Blackwell TS, Luster AD: Inhibition of pulmonary fibrosis by the chemokine IP-10/CXCL10. Am J Respir Cell Mol Biol. 2004, 31 (4): 395-404.PubMedView ArticleGoogle Scholar
  32. Jiang D, Liang J, Hodge J, Lu B, Zhu Z, Yu S, Fan J, Gao Y, Yin Z, Homer R, Gerard C, Noble PW: Regulation of pulmonary fibrosis by chemokine receptor CXCR3. J Clin Invest. 2004, 114 (2): 291-299.PubMedPubMed CentralView ArticleGoogle Scholar
  33. Huaux F, Gharaee-Kermani M, Liu T, Morel V, McGarry B, Ullenbruch M, Kunkel SL, Wang J, Xing Z, Phan SH: Role of Eotaxin-1 (CCL11) and CC chemokine receptor 3 (CCR3) in bleomycin-induced lung injury and fibrosis. Am J Pathol. 2005, 167 (6): 1485-1496.PubMedPubMed CentralView ArticleGoogle Scholar
  34. Shimizu Y, Dobashi K, Iizuka K, Horie T, Suzuki K, Tukagoshi H, Nakazawa T, Nakazato Y, Mori M: Contribution of small GTPase Rho and its target protein rock in a murine model of lung fibrosis. Am J Respir Crit Care Med. 2001, 163 (1): 210-217.PubMedView ArticleGoogle Scholar
  35. Zhou Y, Huang X, Hecker L, Kurundkar D, Kurundkar A, Liu H, Jin TH, Desai L, Bernard K, Thannickal VJ: Inhibition of mechanosensitive signaling in myofibroblasts ameliorates experimental pulmonary fibrosis. J Clin Invest. 2013, 123 (3): 1096-1108.PubMedPubMed CentralView ArticleGoogle Scholar
  36. Liu S, Kapoor M, Shi-wen X, Kennedy L, Denton CP, Glogauer M, Abraham DJ, Leask A: Role of Rac1 in a bleomycin-induced scleroderma model using fibroblast-specific Rac1-knockout mice. Arthritis Rheum. 2008, 58 (7): 2189-2195.PubMedView ArticleGoogle Scholar
  37. Kim JY, Choeng HC, Ahn C, Cho SH: Early and late changes of MMP-2 and MMP-9 in bleomycin-induced pulmonary fibrosis. Yonsei Med J. 2009, 50 (1): 68-77.PubMedPubMed CentralView ArticleGoogle Scholar
  38. Trujillo G, O’Connor EC, Kunkel SL, Hogaboam CM: A novel mechanism for CCR4 in the regulation of macrophage activation in bleomycin-induced pulmonary fibrosis. Am J Pathol. 2008, 172 (5): 1209-1221.PubMedPubMed CentralView ArticleGoogle Scholar
  39. Murthy S, Adamcakova-Dodd A, Perry SS, Tephly LA, Keller RM, Metwali N, Meyerholz DK, Wang Y, Glogauer M, Thorne PS, Carter AB: Modulation of reactive oxygen species by Rac1 or catalase prevents asbestos-induced pulmonary fibrosis. Am J Physiol Lung Cell Mol Physiol. 2009, 297 (5): L846-L855.PubMedPubMed CentralView ArticleGoogle Scholar

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© Arizmendi et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.

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