Attenuation of lung inflammation and fibrosis in CD69-deficient mice after intratracheal bleomycin
© Yamauchi et al; licensee BioMed Central Ltd. 2011
Received: 27 June 2011
Accepted: 5 October 2011
Published: 1 December 2011
Cluster of differentiation 69 (CD69), an early activation marker antigen on T and B cells, is also expressed on activated macrophages and neutrophils, suggesting that CD69 may play a role in inflammatory diseases. To determine the effect of CD69 deficiency on bleomycin(BLM)-induced lung injury, we evaluated the inflammatory response following intratracheal BLM administration and the subsequent fibrotic changes in wild type (WT) and CD69-deficient (CD69-/-) mice.
The mice received a single dose of 3 mg/kg body weight of BLM and were sacrificed at 7 or 14 days post-instillation (dpi). Lung inflammation in the acute phase (7 dpi) was investigated by differential cell counts and cytokine array analyses of bronchoalveolar lavage fluid. In addition, lung fibrotic changes were evaluated at 14 dpi by histopathology and collagen assays. We also used reverse transcription polymerase chain reaction to measure the mRNA expression level of transforming growth factor β1 (TGF-β1) in the lungs of BLM-treated mice.
CD69-/- mice exhibited less lung damage than WT mice, as shown by reductions in the following indices: (1) loss of body weight, (2) wet/dry ratio of lung, (3) cytokine levels in BALF, (4) histological evidence of lung injury, (5) lung collagen deposition, and (6) TGF-β1 mRNA expression in the lung.
The present study clearly demonstrates that CD69 plays an important role in the progression of lung injury induced by BLM.
Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial pneumonia of unknown causes and has poor prognosis [1, 2]. Patients with IPF could be treated with steroids or immunosuppressants to ameliorate the inflammation that occurs early in the course of the disease, but these drugs do not improve their survival . Hence, the discovery of a target that could be useful in the therapeutic intervention of IPF is desirable.
Bleomycins (BLMs) are a family of glycopeptide antibiotics  with potent anti-tumor activity against a wide range of lymphomas, head and neck cancers, and germ-cell tumors . However, the therapeutic efficacy of BLM is limited by the development of pulmonary fibrosis in patients using it [6, 7]. BLM-induced pulmonary fibrosis in mice is the most common experimental model of human IPF. In this model, intratracheal administration of BLM induces acute alveolitis and interstitial inflammation, which are characterized by the recruitment of leukocytes within 1 week  and pulmonary edema. Subsequently, during the second week, fibrotic responses, such as fibroblast proliferation and synthesis of extracellular matrix, occur . Various types of cells, including macrophages and neutrophils have been the immune cells primarily implicated as playing potential roles in the development of pulmonary fibrosis .
Cluster of differentiation 69 (CD69) is a C-type lectin expressed as a disulfide-linked homodimeric membrane protein . The CD69 gene is located within the natural killer (NK) gene complex on mouse chromosome 6 and human chromosome 12 [12, 13]. CD69 was initially detected on the surface of activated lymphocytes and is known as a very early activation marker antigen [14–16]. However, CD69 expression is not restricted to these cells, since activated macrophages, neutrophils, and eosinophils can also express CD69 [17–19]. Moreover, antibody crosslinking of CD69 induces several cellular responses, including nitric oxide (NO) production and release of tumor necrosis factor α (TNF-α) in murine macrophages , NO production in human monocytes , neutrophil degranulation , T cell proliferation and production of TNF-α [21, 22], and NK cell cytotoxicity . These facts indicate that CD69 exerts a potential proinflammatory function and may be involved in the pathogenesis of inflammatory diseases such as pulmonary fibrosis. To determine the effects of CD69 deficiency on BLM-induced lung injury, we evaluated the inflammatory response to intratracheal BLM administration and the subsequent fibrotic changes in wild-type (WT) and CD69-deficient (CD69-/-) mice.
Materials and methods
Eight-week-old male C57BL/6J mice were purchased from Clea Japan (Tokyo, Japan). CD69-/- mice  were backcrossed with C57BL/6J 10 times. Male CD69-/- and WT mice (8-10 weeks) were used in this study. All mice used in this study were bred in the Animal Resource Facility at Chiba University under pathogen-free conditions and cared for according to the animal care guidelines of Chiba University.
Induction of lung injury by bleomycin
Prior to experimentation, mice were weighed and anaesthetized with an intraperitoneal injection of tribromoethanol. Subsequently, the animals were given a single intratracheal injection of BLM hydrochloride (3 mg⋅kg-1; Nippon Kayaku, Tokyo, Japan) dissolved in phosphate-buffered saline (PBS) by using a Microsprayer® atomizer (PennCentury, Philadelphia, PA). Control mice received a sham treatment of PBS.
Measurement of fluid content in lung
The right lung was carefully excised, and then its wet weight was measured. Subsequently, the lung was dried for 24 h at 60°C, and then its dry weight was measured. The ratio between wet and dry lung weight is a measure of edema formation.
Collection of bronchoalveolar lavage fluid
Seven days after BLM administration, mice were anesthetized with pentobarbital (Schering-Plough, Kenilworth, NJ) and sacrificed. The trachea was exposed and lavaged 3 times with 1 mL of PBS by using a 20-gauge catheter. The lavage fluids were pooled and then centrifuged at 300 × g for 5 min at 4°C. The resulting supernatants were stored at -80°C for chemokine and cytokine measurements. The pellets were resuspended in PBS to determine the total and differential cell counts of the bronchoalveolar lavage fluid (BALF). The total cell count was measured by using a hemocytometer. The differential cell count was determined by manually counting 200 cells per mouse that were stained with Diff-Quick (Sysmex Corporation, Kobe, Japan) and fixed on glass slides.
Measurement of cytokine levels
The level of cytokines in the BALF was measured by a RayBio mouse inflammation antibody array 1 (RayBiotech, Norcross, GA). This assay employs a qualitative westernblot (WB) screening technique that can detect 80 cytokines. We precisely followed the manufacturer's protocol. Briefly, the membranes were placed in an 8-well tissue culture tray and incubated with blocking buffer at room temperature for 30 min. One milliliter of BALF sample was added to each membrane and incubated for 2 h. After the samples were removed and washed, the membranes were incubated with the biotin-conjugated antibodies specific for cytokines overnight at 4°C. After washing, the membranes were incubated with 1:1,000 diluted horseradish peroxidase-conjugated streptoavidin for 2 h at room temperature. Next, the membranes were incubated with chemiluminescent detection buffer, wrapped in plastic wrap, and exposed to radiographic film (Kodak X-Omat; Kodak; Rochester, NY) for 40 s. The visualized signals on the developed film were quantified by an image-processing and analysis program (Fuji Image Gauge software version 3.0; Fujifilm, Tokyo, Japan).
Lung biopsies were taken at 14 dpi with BLM or PBS. Lung tissues were inflated and fixed in 4% paraformaldehyde, embedded in paraffin, and cut into 8-μm-thick sections. Sections were subjected to hematoxylin and eosin (H-E) or Masson trichrome stain (Sigma-Aldrich, St. Louis) according to the manufacturer's instructions. The severity of the fibrosis was semi-quantitatively assessed according to the method proposed by Ashcroft and coworkers . Briefly, the grade of lung fibrosis was scored on a scale from 0 to 8 by examining random sections at 100 × magnification. The general scoring criteria were as follows: grade 0, normal lung; grade 1, minimal fibrous thickening of the alveolar or bronchiolar walls; grade 3, moderate thickening of the walls without obvious damage to lung architecture; grade 5, significant fibrosis with obvious damage to lung structure and formation of fibrous bands or small fibrous masses; grade 7, severe distortion of lung structure and large fibrous masses; grade 8, total fibrous obliteration of the field. The Ashcroft score of each lung section was reported as the mean score of at least 20 microscopic fields.
Desiccated caudal lobes from the right lung 14 d after BLM administration were homogenized with 0.1 mg/mL pepsin (Wako chemicals, Osaka, Japan) in 0.5 mol/L acetic acid and incubated for 24 h at 4°C while stirring constantly. Subsequently, the samples were centrifuged at 10000 × g for 5 min at 4°C. The total lung collagen content of the supernatant was measured by using the Sircol Collagen Assay kit (Biocolor, Belfast, Northern Ireland).
Expression of TGF-ß1 in bleomycin-treated lung
Mice were sacrificed at 7 dpi, and the lung was dissected out. The RNA of the lung was isolated using ISOGEN (Wako chemicals) according to the manufacturer's instructions. Single-stranded cDNA was synthesized from prepared RNA (1 μg) with Moloney murine leukemia virus reverse transcriptase (Invitrogen, Carlsbad, CA) using an oligo(dT) primer (Invitrogen) in a total volume of 20 μL. The resultant cDNA sample (1 μL) was subjected to PCR for the amplification of mouse TGFß-1 cDNA using specific primers (sense primer, 5'-CAACAACGCCATCTATGAGA-3'; antisense primer, 5'-TATTCCGTCTCCTTGGTTC-3'). As an internal control, mouse glyceraldehyde-3-phosphate dehydrogenase (GAPDH) cDNA was amplified using specific primers (sense primer, 5'-GACCACAGTCCATGACATCACT'-3; antisense primer, 5'-TCCACCACCCTGTTGCTGTAG-3'). The settings of the thermal cycler were 30 cycles of 45 s at 94°C, 1 min at 52°C, and 1 min at 72°C for mouse TGFß-1 and 25 cycles of 40 s at 94°C, 1 min at 60°C, and 1 min at 72°C for mouse GAPDH. The amplified products were separated on a 1.2% agarose gel and visualized with ethidium bromide staining under UV radiation. Specific amplification of the expected sizes (mouse TGFß-1, 295 bp; mouse GAPDH, 452 bp) was observed.
The lung fixed in 4% paraformaldehyde/0.1M sodium phosphate buffer (pH 7.4) was embedded in OCT (SAKURA Finetek, Tokyo) and cut into 10-μm-thick sections, which were placed on poly-L lysine-coated slides. The sections were subjected to double staining with hamster anti-CD69 monoclonal antibody (Biolegend, San Diego, CA) in combination with rabbit anti-Iba1 polyclonal antibody (Wako chemicals, Tokyo) followed by a reaction with Alexa Fluor 594-conjugated anti-hamster antibody or Alexa Fluor 488-conjugated anti-rabbit antibody. The sections were simultaneously stained with 4',6-diamino-2-phenylindole (DAPI). To confirm the precise localization of Iba1-positive cells, the sections were stained with hamster anti-podoplanin/gp36 monoclonal antibody, which detects alveolar epithelial cells and thereby clearly visualizes the alveolar structure.
The Student's t-test or analysis of variance (ANOVA) with the Newman-Keuls test was used to determine whether results were statistically significant (P < 0.05). All statistical analyses were performed with GraphPad PRISM software (Version 5.0 for Windows; GraphPad, San Diego, CA).
Body weight change
Differential cell counts in bronchoalveolar lavage fluid and lung edema
Inflammatory cytokine levels in bronchoalveolar lavage fluid
Histological and biochemical changes in lung
Predominant localization of CD69 in lung
The ability of CD69 to function as a signal transducing molecule in various types of cells, together with its upregulation in certain inflammatory diseases, suggests a possible pathogenic role for CD69 . Indeed, CD69 is persistently expressed in the infiltrates of leukocytes produced during the course of chronic inflammatory diseases such as chronic hepatitis  and rheumatoid arthritis . Recently, Miki et al. demonstrated that CD69 expressed on CD4-positive T cells plays a critical role in the development of allergen-induced eosinophilic inflammation . These findings led us to consider that the gene disruption of CD69 could affect the pathogenesis of pulmonary inflammatory diseases. To address to this notion, we investigated the development of BLM-induced lung injury in CD69-/- mice.
The importance of a profibrotic inflammatory process in the pathogenesis of pulmonary fibrosis has been suggested in a number of studies that have found that lung injury leads to an inflammatory reaction characterized by the production of inflammatory cytokines and the recruitment of leukocytes . In this study, we showed that inflammatory responses such as an accumulation of inflammatory cells in the BALF and lung edema occur after instillation with BLM. These parameters were significantly reduced in CD69-/- mice compared with WT mice (Figures 2 & 3). The differences in the inflammatory parameters between the CD69-/- and WT mice were consistent with the differences in the body weight profiles reflecting a pathological state in the mice (Figure 1). These results suggest that CD69-/- mice are more resistant to BLM-induced lung inflammation than WT ones. This conclusion was supported by the WB array analysis for cytokines/chemokines. The expression of BLM-induced cytokines/chemokines (e.g., MCP-1, IL-6, TIMP-1) in the WT mice was significantly reduced in CD69-/- mice (Figure 4). Likewise, these cytokines/chemokines have been reported to play an important role in the pathogenesis of pulmonary fibrosis [31–34]. Thus, the reduced expression of these cytokines/chemokines appears to be at least partly responsible for the suppression of the BLM-induced lung inflammation that leads to fibrosis in CD69-/- mice.
TGF-β1 plays a critical role in the pathogenesis of lung fibrosis through the stimulation of collagen and fibronectin production in fibroblasts . Likewise, it is well established that the initial elevation of pro-inflammatory cytokines leads to an increase in the expression of pro-fibrotic markers involving TGF-β1. This increased expression appears to occur in the following manner: 1) MCP-1 may act as a profibrotic mediator by promoting fibroblast procollagen gene expression through the up-regulation of TGF-β1 ; and 2) TNF signaling through sTNF-receptors contributes to the regulation of TGF-β1 expression during BLM-induced lung fibrosis, as mice lacking sTNF-receptors have been shown to be resistant to BLM-induced lung fibrosis . These facts strongly suggest the possibility that the expression of cytokines/chemokines involving MCP-1 and sTNF-receptors in the lung can affect the extent of TGF-β1 expression and the fibrotic tissue profiles. As expected, BLM-induced expression of TGF-β1 mRNA prior to fibrosis was suppressed in the lungs of CD69-/- mice relative to that in WT mice (Figure 6C). Furthermore, lung fibrosis was markedly attenuated in the CD69-/- mice (Figures. 5, 6A & 6B).
By immunohistochemical analysis, CD69 was predominantly expressed in macrophages after BLM administration in WT mice at an earlier stage (Figure 7). At this time point, the infiltration of T cells and neutrophils was not observed. These results suggest that CD69 on macrophages may play an important role in the initial step of BLM-induced lung injury. Macrophages are thought to play a pivotal role in the pathogenesis of pulmonary fibrosis. Activated macrophages secrete a variety of enzymes, complement components, cytokines, and other mediators of inflammatory and fibroblast cell function . It has been also reported for in vitro and in vivo studies that alveolar macrophages release proinflammatory cytokines after BLM administration . Furthermore, it is thought that alveolar macrophages, following stimulation by BLM-induced injury, secrete a large quantity of TGF-β1 and thereby induce the lung fibroblasts in the alveolar interstitium to synthesize collagen, resulting in pulmonary fibrosis [39, 40]. These suggest that BLM-activated macrophages may function as one of major sources of chemical mediators in the pulmonary inflammation/fibrosis loop. Indeed, the majority of inflammatory cells recovered by BAL were macrophages, which were of an order of magnitude higher in number than those of neutrophils and lymphocytes (Figure 2).
An important question is the role of CD69 on macrophages in the induction of IPF. Previous studies have reported the ability of the CD69 antigen to act as a potent trigger of murine macrophage activation . The stimulation of macrophages with anti-CD69 mAb has been shown to induce both NO production and TNF-α release. Likewise, it has been found that CD69 cross-linking induces TGF-β1 production in macrophages as well as in T cells and NK cells [41, 42]. We also confirmed a clear difference between macrophages from WT mice and those from CD69-/- mice in the secretion of LPS-induced cytokines/chemokines (unpublished data). Hence, it is indisputable that CD69 can participate in the activation and regulation of macrophages in the inflammatory process. Although the signaling loop of CD69/TGF-β in activated macrophages may contribute to IPF in a direct manner, it is of interest as to whether BLM-associated tissue injury induces the expression of the putative CD69 ligand on certain cells, such as epithelial cells, especially from the standpoint of epithelial mesenchymal transition (EMT). Further study will be necessary to determine the precise molecular mechanisms of CD69-mediated development in IPF.
We have shown for the first time that CD69 plays a key role in promoting inflammation and fibrosis in the BLM-injured lung. The present study suggests that CD69 may be a potentially useful target in the therapeutic intervention of IPF.
This work was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture of Japan ((B), 21390172 to Y.K.) and a grant to the Respiratory Failure Research Group from the Ministry of Health, Labour and Welfare, Japan. The authors wish to thank Dr. Masahiko Hagihara for helpful discussions.
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