Background
Pulmonary fibrosis is a progressive disorder characterized by the excessive proliferation of fibroblasts and deposition of extracellular matrix, which destroy normal tissue architecture and function. The mechanisms of pulmonary fibrosis are not completely understood, and the effects of drugs on idiopathic pulmonary fibrosis (IPF), a fatal respiratory disease in humans, are not satisfactory [
1]. Therefore, it is crucial to find new therapeutic strategies for pulmonary fibrosis.
Clara cells are secretory cells that are mainly distributed in terminal respiratory bronchioles and the respiratory bronchiole epithelium. Clara cell secretory protein (CCSP) is mainly secreted from Clara cells. CCSP is often called uteroglobin (UG) because UG/CCSP was initially found in the endometrium of early-pregnancy-phase rabbits. UG/CCSP is a small secretory protein that has a variety of pharmacological and physiological effects
in vitro and
in vivo. UG/CCSP has potent anti-inflammatory, antichemotactic and immunomodulatory properties [
2,
3] and also inhibits the proliferation of various cell lines [
4‐
6]. In our previous study, we found that after bleomycin treatment, Clara cell-ablated mice that were exposed to naphthalene vapor exhibited more severe lung pathology and collagen deposition [
7]. Lee and colleagues also reported that UG knockout mice were extraordinarily sensitive to bleomycin and were highly susceptible to developing pulmonary fibrosis [
8]. These results suggest that UG, as an endogenous protective factor, plays an important role in inhibiting pulmonary fibrosis.
Antiflammin-1 (AF-1), a peptide with the sequence methionine - glutamine - methionine - lysine - lysine - valine - leucine - aspartic acid - serine (MQMKKVLDS), is equivalent to the carboxyl-terminal part of the third α-helix of uteroglobin and has biological characteristics similar to those of its parent protein [
9,
10]. AF-1 has a wide range of functions. For example,
in vitro, AF-1 can inhibit leukocyte adhesion and function, suppress macrophage activation, reduce platelet aggregation, prevent mast cell degranulation, block lymphatic vessel contraction and decrease inflammatory mediator production and release [
11‐
15].
In vivo, AF-1 has highly potent anti-inflammatory activity in different animal models, tissues and organs [
9,
16‐
18]. Despite progress in recent decades, our understanding of the biological properties of AF-1 remains incomplete. Although AF-1 has been explored by numerous groups, there is no research on this molecule in the field of fibrosis.
Because UG plays an important role in inhibiting pulmonary fibrosis, we sought to determine whether AF-1 could also protect against pulmonary fibrosis. We found that AF-1 attenuated bleomycin-induced pulmonary fibrosis. Our findings suggest that AF-1 has potential as a new therapeutic tool for pulmonary fibrosis.
Materials and methods
Ethics statement
The Ethics Committee Institute of Clinical Pharmacology of the Central South University (Changsha, China) approved the experiments, which were performed in accordance with National Institutes of Health guidelines. All surgery was performed using anesthesia, and all efforts were made to minimize suffering.
Animal treatment protocol
Adult male C57BL/6 mice were obtained from the laboratory animal unit of Central South University. After being anesthetized, mice were intratracheally injected with 50 μL of bleomycin (5 mg · kg-1) on Day 0. For time course experiments, lung samples were collected on Days 0, 3, 7, 10, 14, 21 and 28 for further analysis.
AF-1 was synthesized according to the standard solid-phase method by the Shanghai Shenggong Bioengineering Company (China) and stored at -20°C until use [
19]. To investigate the antifibrotic effect of AF-1, mice were randomly divided into four groups: (1) intratracheal saline plus intraperitoneal saline (control group); (2) intratracheal saline plus intraperitoneal AF-1 (AF-1 group); (3) intratracheal bleomycin (BLM) plus intraperitoneal saline (BLM group); (4) intratracheal BLM plus intraperitoneal AF-1 (BLM + AF-1 group). For the preventive antifibrotic treatment, AF-1 (2 mg · kg
-1 · day
-1) was administered from Day 0 to Day 27, and lung samples were collected on Day 28. For the therapeutic antifibrotic treatment, AF-1 (2, 5 or 10 mg · kg
-1 · day
-1) was administered from Day 11 to Day 27, and mice were sacrificed on Day 28. To determine whether continuous treatment with AF-1 (2 mg · kg
-1 · day
-1) could inhibit the inflammatory response in the bleomycin mouse model, AF-1 was injected from Day 0 to Day 6, and mice were sacrificed on Day 7.
ELISA for cytokine measurements
An enzyme-linked immunosorbent assay (ELISA) was used to determine the concentrations of several cytokines (tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β) and IL-6) in the lungs. After a thoracotomy, the lungs were removed and homogenized in phosphate-buffered saline (PBS, pH 7.4) containing protease inhibitors (Roche, Germany). The lung homogenates were centrifuged at 10,000 × g to remove insoluble debris. The supernatants were assayed with ELISA kits according to the manufacturer’s instructions (Invitrogen, CA).
Bronchoalveolar lavage
The mice were anesthetized, and after exposure of the trachea, a plastic cannula was inserted into the trachea. A syringe was used to inject 1 mL of 0.9% saline solution into the lungs and was then withdrawn. This injection procedure was repeated five times. After the number of cells in the bronchoalveolar lavage fluid (BALF) was counted, BALF samples were centrifuged, and the cell pellets were resuspended in PBS. Then, the cells were cytospun onto glass slides and stained with Wright’s-Giemsa Stain for cell classification.
Hydroxyproline assay
The collagen content in the lung homogenates was examined by a hydroxyproline (HYP) assay (HYP kit from Nanjing Jiancheng Bioengineering Company, China). All steps of the HYP assay were performed according to the manufacturer’s instructions. The absorbance of each sample at 550 nm wavelength was read by a microplate reader (Thermo Fisher Scientific, USA).
Histopathology
The lung samples were fixed in 4% buffered paraformaldehyde and embedded in paraffin. Sections were stained with hematoxylin-eosin and Masson’s trichrome. The Ashcroft score was used for the quantitative histologic analysis [
20].
Wet/Dry weight ratio assay
The wet/dry (W/D) method was used to measure pulmonary edema. After a thoracotomy, the lungs were collected and weighed before and after drying in the incubator at 60°C for 72 h.
Cell line
Murine lung fibroblasts (NIH3T3) were obtained from the National Genetics Laboratory (Changsha, China). The cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) (Gibco) supplemented with 2 mM L-glutamine (Sigma, USA) and 10% fetal bovine serum (FBS) (Gibco).
Antibody preparation
The peptides corresponding to mouse UG receptor (Accession No.AY052398.1, GI:23707077) were synthesized with free N and C terminus according to the standard solid phase method by Jingmei bioengineering company (Beijing, China) for experimental immunization [
19]. Adult New Zealand white rabbits were injected subcutaneously with 2.5 mg peptides in Complete Freund’s Adjuvant (CFA) (Sigma, USA) six times, every 3 weeks. Animals were bled before immunization and 8–10 days after each injection, and the serological response of immunized rabbits was tested by ELISA. The absorbance (optical density) at 405 nm (OD 405 nm) was measured using a microplate reader. The animals were sacrificed 60 days later (when a strong serological response was detected), and the specific antisera were finally obtained. The antisera were further purified using CNBr-activated Sepharose 4B (Pharmacia, USA) according to protocol provided by the manufacturer. Purity and reactivity of the antisera were checked by SDS-PAGE and ELISA, respectively. The antisera were then stored at -70°C until use, as described for UG receptor antibody.
Bromodeoxycytidine (BrdU) incorporation assay
NIH3T3 cells were seeded in 48-well plates and grown for 24 h. Before the experiments, the medium was changed to the incubation medium containing transforming growth factor-β1 (TGF-β1) (10 ng · mL-1) (RD Systems, USA) in the absence or presence of AF-1 (10 μM) and with or without anti-UG receptor antibody (50 μg · mL-1). Then, cells were cultured for an additional 12 h and were pulsed with BrdU for 2–6 h. Cell proliferation was assessed using a BrdU colorimetric cell proliferation ELISA kit (Roche, Germany). Similar experimental conditions were used in the following methods.
Cell cycle analysis
The stages of the cell cycle were determined by flow cytometry. In brief, NIH3T3 cells were resuspended in a mixture of 0.3 mL of PBS and 0.7 mL of ice-cold ethanol. Propidium iodide (50 μg · mL-1) and ribonuclease A (20 μg · mL-1) were added to the mixture, which was then incubated overnight at 4°C. The cell cycle histograms were acquired on a FACSCalibur instrument using CELLQUEST software (Becton Dickinson) and were analyzed using ModFit LT V3.1 software (Verity Software House).
Cyclin measurements
The protein levels of cyclin D1 and p27 were detected by flow cytometry. In brief, cells were resuspended in 0.5 mL of PBS, mixed with 0.5 mL of 4% paraformaldehyde and then permeabilized with Triton X-100 (Promega, USA). The permeabilized cells were stained with the phycoerythrin-conjugated antibody of anti-cyclin D1 or anti-p27 (Santa Cruz, USA). Single-color histograms were acquired on the FACSCalibur and analyzed using CELLQUEST software.
Statistics
Comparisons were made using one-way analysis of variance followed by the Student-Newman-Keuls (SNK) test for multiple comparisons or using the nonparametric test (Mann–Whitney U test), depending on the distribution of the data. Survival rates were evaluated with a log-rank test over a period of 28 days. P ≤ 0.05 was considered significant.
Discussion
The present study showed a role for AF-1 in the suppression of pulmonary fibrosis. This report is the first to demonstrate that AF-1 prevented bleomycin-induced inflammation and fibrosis in lungs. Furthermore, AF-1 significantly inhibited the TGF-β1-induced proliferation of NIH3T3 cells in vitro by interacting with the UG receptor.
The bleomycin animal model is the best available experimental tool for studying the pathophysiology of IPF and testing novel pharmaceutical compounds for IPF [
23]. However, the IPF progression in humans differs the development of pulmonary fibrosis in the bleomycin-induced mouse model. In the mouse model, bleomycin first induces gross inflammation in the rodent lung, and this sustained damage leads to the initiation of fibrosis [
24,
25]. Numerous anti-inflammatory agents inhibit fibrosis in bleomycin animal models, but none of them has shown a comparable effect against IPF in humans [
26]. Therefore, it is important to distinguish the anti-inflammatory and antifibrotic actions of test drugs in this model. If compounds only work when administered over the entire experimental period but are ineffective when administered after most of the inflammatory response is resolved, these compounds should only have anti-inflammatory activity. However, if drugs work irrespective of the treatment regimen, the drugs should have antifibrotic activity. In our study, we first performed a time course experiment to determine the duration of the inflammatory and fibrotic phases. After Day 10, the inflammatory cytokines significantly decreased, accompanied by a significant increase in collagen deposition (Figure
1). Therefore, we speculated that the course of pulmonary fibrosis in this bleomycin model changed from the inflammatory phase to the fibrotic phase after Day 10. Our results show a process of inflammatory and fibrotic phase development that is similar to previously published data, and our results further confirm that the bulk of the inflammatory response was resolved by approximately Day 10 after bleomycin injection [
21]. Therefore, comparison of the preventive treatment, which began at the initiation of the inflammatory response (i.e., starting on Day 0), with the therapeutic treatment, which commenced after most of the inflammatory response was resolved (i.e., starting at Day 11), allowed us to distinguish the anti-inflammatory and antifibrotic actions of AF-1.
As a novel antiinflammatory peptide, AF-1 has highly potent anti-inflammatory activity in different animal models, tissues and organs [
16‐
18]. In the present study, continuous treatment with AF-1 (2 mg · kg
-1) starting on Day 0 significantly alleviated the inflammation on Day 7 and the collagen deposition on Day 28 in the bleomycin-induced model of lung injury (Figures
2 and
3). The anti-inflammatory activity of AF-1 in this model may be due to its blockade of neutrophil trafficking, suppression of the activation of macrophages and reduction of the production and release of inflammatory mediators [
11,
12].
Next, we examined the antifibrotic effects of AF-1 in the bleomycin mouse model. When therapeutic treatment with AF-1 began on Day 11, AF-1 (10 mg · kg
-1 but not 2 mg · kg
-1 or 5 mg · kg
-1) (5 mg · kg
-1 data not shown) significantly attenuated the collagen deposition on Day 28 (Figure
4). Our results clearly show that AF-1 alleviated pulmonary fibrosis significantly by both anti-inflammatory and antifibrotic actions, which were independent of the treatment regimen. However, the effective AF-1 dose for the therapeutic treatment was higher than that for the preventive treatment.
The proliferation and extracellular matrix (ECM) production of fibroblasts constitute the final common pathogenic factor in fibrotic diseases. Numerous antifibrotic strategies aim to target the activation, proliferation and/or recruitment of fibroblasts, which occur in response to the strengthened actions of profibrotic cytokines. TGF-β is one of the most important profibrotic cytokines and is produced by various types of cells, including macrophages, epithelial cells and fibroblasts. After being activated, TGF-β becomes a pleiotropic cytokine with proliferative and chemotactic properties [
27]. As mentioned above, any drugs that successfully ablate the activation and/or proliferation of fibroblasts
in vitro might have antifibrotic activity
in vivo. Therefore, to further research the underlying mechanisms of AF-1, we observed the effect of AF-1 on TGF-β1-induced proliferation in NIH3T3 cells. We found that AF-1 inhibited the TGF-β1-induced proliferation in NIH3T3 cells in a concentration-dependent manner, and the inhibition induced by AF-1 might have been due to its regulation of the expression of cyclin D1 and p27 (Kip1) (Figure
5), which determine the transition from G0/G1 phase to S phase [
28‐
30].
The mechanism responsible for the antiproliferative effect of AF-1 on TGF-β1-induced proliferation in NIH3T3 cells is not clear. Recently, we found that AF-1 specifically binds to a saturable membrane receptor, the UG receptor, and activates the MAPK signaling pathway [
22]. Kundu and coworkers first identified the UG receptor in several types of cells; treating the cells expressing the UG receptor with UG dramatically suppressed cell growth and ECM invasion, but such treatment had no effect on cells lacking the UG receptor [
5,
31‐
33]. Subsequently, molecular cloning and analysis of the UG receptor cDNA indicated that it encodes a 55-kDa protein; on the basis of amino acid similarity, the UG receptor was classified in the lipocalin receptor family, which has remarkable functional diversity [
34,
35].
As a synthetic peptide derived from UG, AF-1 has similar activities to UG [
10]. Because UG can inhibit cell growth and ECM invasion by interacting with the UG receptor, we sought to determine whether the antiproliferative activity of AF-1 was also related to the UG receptor. Our results show that the antiproliferative effect of AF-1 was reversed by pretreatment with anti-UG receptor antibody (Figure
6). Therefore, AF-1 might suppress TGF-β1-induced NIH3T3 proliferation by interacting with the UG receptor.
According to our studies, the antifibrotic effect of AF-1 in bleomycin-treated mice may be related to its antiproliferative activity, which is mediated by the UG receptor. Of course, the roles of the UG receptor in the development of pulmonary fibrosis
in vivo require further rigorous investigation. Similarly to most drugs or the UG protein itself, AF-1 has an antifibrotic effect that is difficult to explain by a simple mechanism of action. Moreno reported that AF-1 can inhibit the activity of transglutaminase-2 (TG-2) [
36]. TG-2 is a multifunctional protein that plays an important role in bleomycin-induced pulmonary fibrosis [
37,
38]. Overexpression of TG-2 increases fibronectin deposition and matrix organization
in vitro. In contrast to wild-type mice, TG-2 knockout mice develop markedly less severe pulmonary fibrosis [
37]. Therefore, inhibiting the activity of TG-2 by AF-1 may also be helpful in alleviating pulmonary fibrosis.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
ZQL, SJY and DDF designed the study. WL, JW, YHH, YC, QMC and YL performed the experiments. WL, JW, JZH and CL performed the statistical analysis. WL wrote the manuscript. All authors read and approved the final manuscript.