ATP serves an anti-inflammatory role by enhancing β-defensin-2 response in acute pneumonia of rat.

The aim of the current study was to evaluate the effect of ATP on the expression of rat β-defensin-2 (rBD-2) in a time-dependent manner, as well as its therapeutic value in an acute pneumonia rat model. A total of 30 rats as a treatment group and 30 as a control group were treated with the same dose of ATP and normal saline, respectively, lung tissues were isolated from rat and expression of rBD-2 mRNA was assessed with reverse transcription-quantitative polymerase chain reaction (RT-qPCR) at 12, 24 and 36 h following treatment. Rats were divided into five groups: The control group treated with normal saline, the Pseudomonas aeruginosa (PA) infected group, group treated with ATP, group treated with cephalosporins, and the group treated with both ATP and cephalosporins. At 24 h following treatment, rat serum and lung tissues were collected for assessment of histological changes, and alterations to expression of the rBD-2 protein by immunohistochemistry, expression of tumor necrosis factor (TNF)-α and interleukin (IL)-6 proteins by ELISA. RT-qPCR results indicated that the expression of rBD-2 mRNA was upregulated in response to ATP stimulation in lung tissues of rat, reaching its highest peak at 24 h. Immunohistochemistry demonstrated that ATP treatment enhanced the expression of rBD-2 protein in rat lungs. Ceftazidime and ATP protected lungs from infection of PA and reduced the pathological damage of the lung. Overexpression of rBD-2 by ATP led to decreased protein expression of TNF-α and IL-6 in lung tissues and serum. ATP upregulates the expression of rBD-2 and serves an anti-inflammatory role in the acute pneumonia of a rat model.

Introduction

β-defensins (BDs) are cationic peptides which present broad-spectrum antimicrobial activities against bacteria, fungi and viruses (1). To date, 6 BDss, human BD (hBD)-1 (2), hBD-2 (3), hBD-3 (4,5), hBD-4 (6), hBD-5 and hBD-6 (7) have been identified and characterized in humans. hBD-2 is expressed in a wide range of cell types, such as epithelial cells, keratinocytes and monocytes/macrophages (8,9). It is expressed rarely or lowly under normal circumstances, and is upregulated in response to infectious and inflammatory stimuli through multiple signaling pathways, such as the NF-κB pathway (10,11). Previous studies have indicated that BD2 has multiple functions in the immune system, including antibacterial activity (12–14), connection between epithelial innate and adaptive immunity (15,16), as well as chemotactic function (16,17).

ATP is a well-known energy source inside cells, it also functions as an essential messenger between cells. Activation of P2 receptors, P2X and P2Y, by ATP may initiate the release of sodium and calcium ions, producing different cellular effects (18). ATP has a wide range of functions in the human body, including the development of pain, the heart and blood vessel disorders, secretion of digestive enzymes, as well as tumor-killing effects (18). In addition, ATP serves an important role in inflammation and infection. ATP activation of the P2×7 receptor results in the processing and secretion of mature interleukin (IL)-1β, which is a potent cytokine capable of inducing inflammation (19,20). Moreover, active ATP release and adenosine receptor signaling are required for activation of the NLR pyrin domain containing 3 (NLRP3) inflammasome that is a major component of the innate immune system (21). Nonetheless, little is known regarding the relationship between BD2 and ATP, as well as their roles in the acute pneumonia of rats.

In the present study, the authors evaluated the impact of ATP on the expression of rat BD-2 (rBD-2) in a time-dependent manner, as well as their protective effect in the acute pneumonia of rat caused by Pseudomonas aeruginosa (PA) (Xinjiang Uygur Autonomous Region Food and Drug Administration, Urumqi, China). The completion of the study provides some novel findings on rBD-2 in acute pneumonia which will be useful to guide further investigation and targeted therapy for this disease.

Materials and methods

Animal housing and treatment

Given the homology between rBD-2 and hBD-2, such as 6 cysteine and other lysine and arginine residues (22), the rat was chosen as a model to study the function of hBD-2 in vivo. BALB/c rats (4–6 weeks old, male/female ratio, 1:1; 20–30 g), provided by Medical School of Tongji University (Shanghai, China), were housed under controlled conditions. Procedures involving animals and their care were approved in accordance with the guidelines of the Experimental Animal Ethics Committee of Medical School of Tongji University (Shanghai, China; no. 2010–1-1). A total of 60 rats were randomly divided into treatment and control groups with 30 rats in each. A control group was administrated with normal saline at 250 µl/100 g body weight, treatment group was injected with ATP at 0.12 mg/10 g body weight through the tail vein. Rats were sacrificed at 12, 24 and 36 h, respectively after treatment, and the lung tissues were isolated from each rat and stored in liquid nitrogen.

Determination of rBD-2 mRNA in rat lungs by RT-qPCR

Total RNA was isolated from the whole lung tissue using TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA) and reversely transcribed into cDNA using M-MLV Reverse Transcriptase (Takara Bio, Inc., Otsu, Japan). The following primers were used for PCR amplification of rBD-2: Forward, 5′-GAACTTGACCACTGCCACACC-3′; and reverse, 5′-GCTCTAGATTATCATTTCATGTACTTGCACC-3′. β-actin was used as a reference to normalize rBD-2 mRNA expression levels using the 2−∆∆Cq method (23). The RT-qPCR primers used for β-actin in the present study were: Forward, 5′-AACAGTCCGCCTAGAAGCAC-3′; and reverse, 5′-GGTTGACATCCGTAAAGACC-3′. Each RNA sample was run in triplicate. PCR parameters were set as follows: 39 cycles of denaturation at 95°C for 20 sec, annealing at 59°C for 30 sec and extension at 72°C for 30 sec.

Establishment of acute pneumonia model of rat, animal grouping and treatment

Rats were randomly divided into four treatment groups and one control group, with eight rats each. Rats were anesthetized with ether, 1 cm skin incisions were made along the middle of the mouse's neck, and muscle tissues were bluntly dissected exposing the trachea and thyroid. A total of 0.2 ml PA (6×108 CFU/ml, Xinjiang Uygur Autonomous Region Food and Drug Administration) was injected into each rat trachea in treatment groups, while, the control group was injected with the same dose of sterile phosphate buffered saline, then incisions were sutured. After three days, treatment groups were divided into four different groups: PA infected group, group treated with ATP at 16 mg/kg or cephalosporins at 0.4 g/kg through the tail vein, group treated with both ATP at 16 mg/kg and cephalosporins at 0.4 g/kg through tail vein. Rats were sacrificed 24 h following treatment, lung tissues and serum were collected and stored in liquid nitrogen for subsequent experiments.

Pathological examination

The grouping and treatment were the same as described above, lung tissues were isolated from rats 24 h following ATP and cephalosporin intervention. Fresh lung specimens were fixed in 4% paraformaldehyde, embedded in paraffin, cut and heated, and subjected to hematoxylin and eosin (H&E) staining. The morphological changes of H&E-stained tissues were analyzed by Leica digital microscopy.

Immunohistochemistry

Formalin-fixed, paraffin-embedded tissue sections of lung tissues were obtained from treatment and control groups as described above in animal grouping and treatment. The expression of rBD-2 was detected following the immunohistochemistry protocol of Sigma-Aldrich; Merck KGaA (Darmstadt, Germany). The sections were incubated with primary rabbit polyclonal antibody rBD-2 (YY3068R; Santa Cruz Biotechnology, Inc., Dallas, TX, USA) at 1:200 dilution overnight at 4°C and secondary antibody [SP9000D; DAB Detection kit (Streptavidin-biotin); ZSGB-BIO, Beijing, China] for another 2 h at room temperature. Finally, visualization of the sections was conducted and images were taken with a Leica confocal laser scanning microscope (Leica Microsystems, Wetzlar, Germany).

Determination of IL-6 and tumor necrosis factor (TNF)-α expression in lung tissues and peripheral blood. At 24 h following ATP and cephalosporin intervention, rats from control and treatment groups were sacrificed and lung tissues were isolated, centrifuged at 2,045 × g for 20 min at room temperature followed by collection of supernatants. The peripheral blood samples were also collected. IL-6 and TNF-α expression was evaluated using ELISA assay kits in accordance with the instructions (Invitrogen; Thermo Fisher Scientific, Inc.).

Statistical analyses

Data were presented as mean ± standard deviation. Student's t-test or SNK-q test was used to determine the statistical significance between each two groups, differences among multiple groups were analyzed using an analysis of variance (ANOVA). The SNK-q test was used for multiple comparisons. P<0.05 was considered to indicate a statistically significant difference.

Results

ATP enhanced expression of rBD-2 mRNA in rat lungs

Expression of rBD-2 in lung tissues of rats in response to ATP has not yet been investigated. Therefore, the authors determined induction of rBD-2 expression by ATP in the lung tissues of rat. RT-qPCR was conducted to analyze the expression pattern of rBD-2 following ATP stimulation. The expression of rBD-2 gene was upregulated in ATP-treated groups at 12 h (0.5921±0.3007 vs. 0.9029±0.3136, P=0.001, t-test), 24 h (0.6031±0.2943 vs. 1.3867±0.3011, P<0.001, t-test) and 36 h (0.5273±0.3211 vs. 1.0912±0.2591, P<0.001, t-test; Fig. 1). It increased greatly at 12 h, reached highest peak at 24 h and gradually declined by ~20% at 36 h following ATP treatment, however, significant differences of the expression of rBD-2 were observed between each control and treatment group at 12, 24 and 36 h. Therefore, the authors confirmed that ATP could upregulate rBD-2 mRNA expression in rat lungs.

Figure 1.

β-defensin-2 mRNA expression measured by reverse transcription-quantitative polymerase chain reaction in rat lungs. Data are presented as mean ± standard deviation.

ATP increases expression of rBD-2 protein in rat lungs

As expression of rBD-2 mRNA was upregulated by ATP in rat lungs, the next question concerned whether ATP promotes the production of rBD-2 protein in vivo. In the present study, the authors reported that the expression of the rBD-2 protein was slightly increased in the PA infected group, an enhanced expression of the rBD-2 protein was observed in the ATP or cephalosporin treatment group and the cephalosporin and ATP treatment group, in comparison with that in PA infected group and control group, suggesting ATP could induce rBD-2 expression at both mRNA and protein levels in rat lungs (Fig. 2).

Figure 2.

Expression of β-defensin-2 protein of rat lungs detected by immunohistochemistry in different groups (magnification, ×200): (A) Control group treated with normal saline, (B) Pseudomonas aeruginosa infected group, (C) group treated with ATP, (D) group treated with ceftazidime, and (E) group treated with ceftazidime and ATP.

ATP alleviates histological changes in rat lungs

Microcopy indicated that alveolar and interstitial lung structures were normal, alveolar inflatable was good, no exudation of red blood cells was observed, part of bronchial and alveolar walls were infiltrated with a small amount of inflammatory cells in the lung tissues of the control group. The PA infected group presented alveolar wall edema, infiltration of a large number of inflammatory cells (neutrophils and lymphocytes) on bronchial and alveolar walls, red blood cells and cellulose exudation in the alveolar space. ATP or ceftazidime intervention groups presented an improved lung edema, less inflammatory cell infiltration, thicker partial alveolar wall and a small amount of red blood cells as compared with the PA infected group. The results demonstrated that ceftazidime, ATP and ceftazidime + ATP treatment groups improved the histological destruction of lung tissues caused by PA (Fig. 3).

Figure 3.

Histopathological changes of rat lungs in different groups (magnification, ×200): (A) Control group treated with normal saline, (B) Pseudomonas aeruginosa infected group, (C) group treated with ATP, (D) group treated with ceftazidime, and (E) group treated with ceftazidime and ATP.

ATP decreases expression of TNF-α and IL-6 levels in rat lungs

Following this, the authors next investigated mechanisms by which enhancement of rBD-2 by ATP presented a beneficial effect on the PA infection in rat lungs. In order to clarify whether rBD-2 regulated the secretion of proinflammatory cytokines, IL-6 and TNF-α expression was analyzed by ELISA. Significant differences of IL-6 and TNF-α expression were identified in both lung and serum among five groups (F: 12.4864–28.3971, v=4, P=0.0000, ANOVA), PA induced a significant increase in TNF-α and IL-6 expression levels in rat lungs and serum of treatment groups as compared with the control group (TNF-α, 44.1250±6.6235 vs. 33.9750±1.0403; IL-6, 125.2813±38.7227 vs. 11.8438±4.2075 in serum; TNF-α, 59.3000±17.1713 vs. 17.5438 ±3.4582; IL-6, 47.3875±12.8895 vs. 25.7250±3.3139 in rat lung, P<0.05 for all cases, SNK-q test). Moreover, IL-6 and TNF-α expression in the rat lung and serum was reduced in ceftazidime, ATP and ceftazidime + ATP treatment groups relative to the PA-infected group (P<0.05 for all cases, SNK-q test). No significant difference was observed for TNF-α expression in serum and IL-6 in lungs among ceftazidime, ATP and ceftazidime + ATP treatment groups (P>0.05 for all cases, SNK-q test). However, the ceftazidime + ATP treatment group presented a decreased expression of TNF-α in lungs and IL-6 in serum relative to ceftazidime or ATP treatment groups (P<0.05 for all cases, SNK-q test; Fig. 4).

Figure 4.

Changes of TNF-α and IL-6 protein production measured by ELISA in rat lung and serum. Data are presented as mean ± standard deviation. TNF-α, tumor necrosis factor-α; IL, interleukin.

Discussion

There has been an increasing body of evidence that ATP serves a protective role in the immune system. ATP promotes a wide range of epithelial responses through the activation of P2X and P2Y receptors in response to infectious stimuli and injuries. For instance, ATP mediates the activation of the NADPH oxidase DUOX1 through the P2Y receptor, phospholipase C and intracellular calcium signaling in the airway epithelium, leading to the activation of ERK1/2 and NF-κB pathways, IL-8 release and the production of H2O2 in response to bacterial stimulations or tissue injury (24,25). In addition, ATP modulates the activities of the NLRP3 inflammasome during bacterial infection by activation of the purinergic receptor P2X7, resulting in IL-1β maturation and secretion of chemokines (26,27). Here, believed to be for the first time, the authors reported that ATP upregulated the expression of rBD-2 mRNA and enhanced the production of rBD-2 protein in response to the bacterial stimulation of PA in rat lungs. A possible mechanism underlying this process is that ATP activates the NF-κB pathway, which is critical to the production of rBD-2 (11,28) through either the P2X or P2Y receptor, however, further studies are still required in the future.

In addition, enhanced rBD-2 expression by ATP reduced inflammatory damage was caused by PA in lung tissues, indicating that rBD-2 ameliorates the infection of PA. These findings are consistent with studies conducted by Wu et al (12) and Hu et al (29). The primary reasons may lie in the antibacterial function of increased rBD-2 and its regulation of inflammatory factors during bacterial infection and inflammation. Therefore, the authors analyzed the secretion of cytokines, TNF-α and IL-6 following stimulation of ATP and ceftazidime. It was identified that PA infection significantly increased pro-inflammatory factors, such as TNF-α and IL-6 in the rats, and overexpression of rBD-2 by ATP inhibited the increase of these inflammatory factors. These results are in line with a previous report by Wu et al (12), indicating that rBD-2 accelerated the weakening process of inflammation.

In summary, these results demonstrated that ATP induces rBD-2 mRNA and rBD-2 protein expression in rat lungs and decreases the expression of proinflammatory cytokines TNF-α and IL-6, suggesting ATP has protective effects against infection of PA. These results may provide a better understanding of the therapeutic values of ATP and hBD-2 in infectious diseases.