Polydatin up-regulates clara cell secretory protein to suppress phospholipase A2 of lung induced by LPS in vivo and in vitro
© Shiyu et al; licensee BioMed Central Ltd. 2011
Received: 27 December 2010
Accepted: 25 July 2011
Published: 25 July 2011
Lung injury induced by lipopolysaccharide (LPS) remains one of the leading causes of morbidity and mortality in children. The damage to membrane phospholipids leads to the collapse of the bronchial alveolar epithelial barrier during acute lung injury (ALI)/acute respiratory distress syndrome (ARDS). Phospholipase A2 (PLA2), a key enzyme in the hydrolysis of membrane phospholipids, plays an important traumatic role in pulmonary inflammation, and Clara cell secretory protein (CCSP) is an endogenous inhibitor of PLA2. Our previous study showed that polydatin (PD), a monocrystalline extracted from a traditional Chinese medicinal herb (Polygonum cuspidatum Sieb, et Zucc), reduced PLA2 activity and sPLA2-IIA mRNA expression and mitigated LPS-induced lung injury. However, the potential mechanism for these effects has not been well defined. We have continued to investigate the effect of PD on LPS-induced expression of CCSP mRNA and protein in vivo and in vitro.
Our results suggested that the CCSP mRNA level was consistent with its protein expression. CCSP expression was decreased in lung after LPS challenge. In contrast, PD markedly increased CCSP expression in a concentration-dependent manner. In particular, CCSP expression in PD-pretreated rat lung was higher than in rats receiving only PD treatment.
These results indicated that up-regulation of CCSP expression causing inhibition of PLA2 activation may be one of the crucial protective mechanisms of PD in LPS-induced lung injury.
Acute lung injury (ALI), or its severe form, acute respiratory distress syndrome (ARDS), induced by sepsis is still a major cause of morbidity and mortality in children . ALI is characterized by an extensive neutrophil influx into the lung, the expression of proinflammatory mediators and damage to the lung epithelium and endothelium. Current clinical and experimental research on the treatment of lung injury is aimed at inhibiting different stages of this process with drugs or therapy, along with enhancing the body's own resistance, to delay or mitigate lung injury. However, the outcome of sepsis and septic shock cases has not been improved significantly. Mortality in ALI is still as high as 18%-27%, and the mortality rate of (ARDS) is even higher to 29%-50% . Therefore, improved treatments and prevention strategies are needed to minimize the mortality associated with ALI.
It is generally acknowledged that damage to membrane phospholipids leads to the collapse of the bronchial alveolar epithelial barrier during ALI/ARDS. Phospholipase A2 (PLA2), a key enzyme that hydrolyzes membrane phospholipids, plays a critical traumatic role in pulmonary inflammation through its influence on membrane signal transduction, biomembrane stability, activation of lipid mediators and leukocyte-endothelial cell adhesion cascade formation. PLA2 hydrolyzes the fatty acid from the sn-2 position of phospholipids to release arachidonic acid, prostaglandins, platelet-activating factor and other inflammatory mediators . In mammals, PLA2 forms a large family of enzymes that can be schematically divided into two major classes: high-molecular-weight intracellular PLA2 (cPLA2) and low-molecular-weight secretory PLA2(sPLA2), including sPLA2-IIA. The former (cPLA2) is now generally considered to be a central enzyme mediating generation of eicosanoids and hence many inflammatory processes. The latter (sPLA2) is found at high levels in the circulation and locally in the tissues and has been suggested to play a role in a number of inflammatory diseases by regulating the synthesis of prostaglandins, leukotrienes and platelet activating factor. Especially, recent study showed that sPLA2-IIA catalyzes the hydrolysis of surfactant phospholipids and suggested that this process can contribute to the loss of surface tension-lowering properties of surfactant . Clinically, sPLA2-IIA offers new possibilities as an early marker for severe inflammation and predicting systemic complications in severely ill patients. Thus, PLA2 is regarded as the core and rate-limiting enzyme of inflammation and plays an important role in the pathogenesis of LPS-induced acute lung injury. Specific inhibitors can be used to elucidate the roles of PLA2 in cellular processes or to develop new potential therapeutics . Sato R reported  that LY37 4388, an exogenous inhibitor of sPLA2, may exert a protective effect on LPS-induced acute lung injury in male C57BL/6J mice.
Clara cell secretory protein (CCSP; also known as CC16, CC10 and uteroglobin) is a 16-kDa homodimeric protein that is secreted by non-ciliated bronchiolar (Clara) cells into the mucus lining the bronchial epithelium of the mammalian lung. It is one of the most abundant proteins in the airway mucus of mammals . As a biomarker of Clara cells and lung health, CCSP has been proposed as a useful diagnostic marker of toxicant exposure or airway epithelial damage. Some studies have reported that administration of exogenous CCSP such as recombinant human CCSP to the lungs mitigates inflammation [9–11]. Although evidence points to antioxidant , anti-inflammation, immunomodulation, anti-cytokine, pollutant clearance, anti-fibrosis, anti-tumor invasion and anti-protease activity , its endogenous mechanism is not known. Studies on CCSP-deficient mice have indicated that CCSP acts as an endogenous inhibitor of PLA2[14, 15] by binding calcium, a cofactor for secretory PLA2 activation, or phosphatidylcholine, a substrate of PLA2.
Our previous experimental results indicate that polydatin has prophylactic and therapeutic effects (the former is more distinct than the latter) on acutely injured lungs in rats with endotoxic shock by inhibiting phospholipase A2 activity and the gene expression of secretory phospholipase A2 type II A (sPLA2-IIA) . Phospholipase A2 activity and sPLA2-IIA expression are increased by endotoxin injection, but treatment with polydatin inhibits these increases. In our preliminary experiments, obvious morphological evidence was found in pathological lung sections, and the protective effect of PD was most obvious in lung from rats pretreated with PD. These early results suggest that PD may act as a phospholipase A2 inhibitor to inhibit the activation and activity of PLA2. However, the potential mechanism is not yet fully understood. Therefore, the purpose of this study was to determine whether polydatin can up-regulate the expression of CCSP and inhibit PLA2 to suppress LPS-induced lung injury.
In vivo experiments
Animals and grouping
Ninety-eight healthy, male, 7-week-old Sprague-Dawley rats (clean grade) weighing 200-250 g were purchased from the Animal Experiment Center of Chongqing Medical University (Chongqing, China). They were housed in a regulated environment (24 ± 2°C), with a 12 hours dark and 12 hours light cycle. All animal treatments were strictly in accordance with international ethical guidelines and the National Institutes of Health Guide for the Care and Use of Laboratory Animals, and the experiments were carried out with the approval of the Committee of Experimental Animal Administration of the University.
Animal grouping and drug injection
PD was administered as a 0.5% solution (0.2 ml per kg body weight) with a final concentration of 1 mg PD per kg body weight.
The PD treatment and pretreatment groups were each further divided into four subgroups (n = 6 each) that received 1 mg·kg-1, 5 mg·kg-1, 10 mg·kg-1 or 30 mg·kg-1 PD, respectively.
Rats were fasted overnight but given free access to water, then anesthetized with 20% urethane (5-6 ml·kg-1 body weight) intraperitoneally. The left common carotid artery was separated and catheterized. The canal was connected to an MS302 biology signal recording and analyzing system (provided by Guangdong Pharmacological Institute in Guangzhou, China) to measure the mean arterial pressure (MAP). The right cervical vein was then separated and catheterized. LPS (Sigma, 10 mg per kg body weight) was injected from the right cervical vein. After injection, MAP fell from normal to shock levels (The blood pressure of rat and human being are almost same). After six hours' observation, they were sacrificed with cervical dislocation and their lung tissues and blood were collected for experiments.
Determining the expressions of CCSP/sPLA2/cPLA2 mRNA in rat lung with real-time PCR
PCR primer pairs used amplify CCSP, sPLA2, cPLA2 and β-actin cDNA fragments of rat lung
Determining the expression of CCSP mRNA in rat lung with RT-PCR
Total RNA was extracted from lung tissue using Trizol reagent, and the first strand of cDNA was synthesized using reverse transcriptase. The genes of interest were then amplified by PCR. Primers corresponding to the genes of interest were the same as those mentioned previously.
Determining the content of CCSP protein in rat lung with western blotting
Human CCSP (Biovendor) was used as the half-quantitation standard. Protein was isolated from tissues that were homogenized in a buffer (containing protein lysates). The quantity of protein from the lung homogenate depended on the size of lung issue we used. The concentration of total protein was 10 μg·μl-1. The total protein of each sample for measuring was 10 μg. Samples were then combined with loading buffer containing 10% glycerol, 10% 2-mercapthanol, 2% SDS, and bromophenol blue in 0.07 M Tris-HCL (pH 6.8, boiled for 5 minutes), resolved by SDS-PAGE and then transferred to a membrane for western blotting. The membrane was incubated with a blocking solution (5% skim milk) at 24°C for 2 hours. A primary antibody was then added to the solution and incubated at 4°C for 12 hours. A peroxidase-conjugated secondary antibody solution was used to incubate the membrane at 24°C for 1 hour. The membranes were then incubated with a chemiluminescent substrate (Thermo 34077) and exposed to film (Millipore IPVH00 10).
Determining the concentration of CCSP protein in rat serum with ELISA
Four milliliters of blood was collected from the aorta, mixed with 1% heparin to anticoagulate for 10-20 minutes and then centrifuged for 20 minutes (2000-3000 × g). Supernatant was carefully collected for determination. The concentration of CCSP protein was measured by ELISA according to the manufacturer's instructions (Rat CCSP ELISA kit, Westang, F15255; Rabbit polyclonal to Uteroglobin, ab4 0873, Abcam).
Measuring CCSP positive cells with immunohistochemistry
Biopsy samples were fixed by immersion in Bouin's fluid, paraffin-embedded and cut into 6-μm-thick sections. CCSP-immunoreactive cells were detected with the uteroglobin antibody (Abcam, ab40873) and the immunoperoxidase technique. The number of CCSP-positive and -negative bronchiolar cells was determined for each bronchiolar profile examined in the lung biopsies by counting all surface epithelial cells on the bronchial biopsy specimens. For each sample, the proportion of CCSP-positive cells was expressed as a percentage of the whole bronchiolar epithelium cell population examined.
In vitro experiments
All cell lines used in this study were purchased from the American Type Culture Collection (Manassas, VA). BEAS-2B cells are human bronchial epithelia cells transformed by the SV40 T-antigen. BEAS-2B cells were cultured in LHC-8 medium (Gibco, America) and incubated at 37°C in an atmosphere of 5% CO2 and 95% air. The medium was replaced every second day, and cells were passaged when > 85% confluent by washing with Ca2+- and Mg2+-free PBS and dislodging with 0.05% trypsin. MTT assay was used to determine the suitable concentrations of PD and LPS.
Cells were divided into five groups: the normal control group, containing cultured BEAS-2B cells under normal conditions for 28 hours; the LPS group, containing cultured BEAS-2B cells in LHC-8 medium treated with LPS (100 ng·ml-1) for 28 hours to mimic a LPS-induced inflammatory response model; the PD treatment group, containing cultured BEAS-2B cells challenged with LPS (100 ng·ml-1) in LHC-8 medium for 24 h, followed by PD treatment (0.5 m mol·L-1 in LHC-8 medium) for 4 h; the PD pretreatment group, containing cultured BEAS-2B cells that were pretreated with PD (0.5 m mol·L-1) in LHC-8 medium for 4 hours, followed by an LPS challenge (100 ng·ml-1) in LHC-8 medium under normal conditions for 24 hours; and the PD control group, containing cultured BEAS-2B cells treated with PD (0.5 m mol·L-1) in LHC-8 medium for 28 hours.
Determining the expression of CCSP mRNA in BEAS-2B cells
PCR primer pairs used amplify CCSP and β-actin cDNA fragments of BEAS-2B cells
F: 5'- GAAACTCGCTGTCACCCTCACC-3'
Determining the expression of CCSP protein in BEAS-2B
Cells were washed with phosphate-buffered saline and lysed in lysis buffer. Lysates were subjected to 4% to 15% SDS-PAGE and western blotting with anti-c-kit (1:100) antibody. Immunopositive bands were visualized by enhanced chemiluminescence (ECL, Amersham). Blots were stripped and reprobed with GAPDH antibody (1:2000) as a control to ensure equal loading.
All data were expressed as the mean ± SEM. Data were analyzed with SSPS for Windows 13.0 using one-way analysis of variance (ANOVA) and the Bonferroni correction for multiple comparisons, when appropriate. In all cases, P values less than 0.05 was considered statistically significant.
Polydatin up-regulates CCSP mRNA expression in rat lung
Polydatin down-regulates sPLA2 and cPLA2 mRNA expression in rat lung
Polydatin up-regulates CCSP protein expression in rat lung
Polydatin down-regulates serum CCSP level in rat
Polydatin increases the percentage of CCSP-positive cells
Percentage of CCSP-positive cells of lung tissue in each group ( ± s, n = 10).
The percentage of CCSP positive cells
20.3 ± 2.4
13.2 ± 1.3b
37 ± 4be
46 ± 6cf
53 ± 6cf
Percentage of CCSP-positive cells of lung tissue in each group ( ± s, n = 6).
Percentage of CCSP-positive cells
40.2 ± 2.3
54 ± 3b
63.5 ± 2.6f
79 ± 3i
37.4 ± 2.4
46 ± 3c
56.8 ± 2.4f
70 ± 4j
Polydatin up-regulates CCSP expression in BEAS-2B
There are many experimental models of acute lung injury, but none of them completely reproduces all the prominent features of human ALI/ARDS, such as alveolar neutrophilia (indicating inflammation), hyaline membrane deposition (indicating disruption of the alveolar-capillary barrier) and microthrombi (indicating endothelial injury). Hence, there is no single "best" model of lung injury; instead, the best model will be one that reproduces the features to be tested in the investigator's hypothesis.
We used one of the well-established rat models of acute lung injury, intravenous administration of LPS because it can lead to activation of various inflammatory mediators such as phospholipase A2. These mediators may cause epithelial lesions and increase the alveolocapillary barrier permeability. Therefore, this model met all the requirements for our purpose.
First, we observed a reduction of CCSP mRNA in parallel with decreased CCSP protein expression in rat lung tissue after LPS stimulation for five hours. Prior to this, we knew that different inflammatory stimuli result in different CCSP expression patterns in lung. Inhalation of O3 and injection of phenyl isothiocyanate can induce acute and chronic inflammation in humans and increase CCSP expression in lung . By contrast, CCSP production is decreased during acute and chronic lung injury caused by viral and bacterial infections, smoking  or chronic obstructive pulmonary disease. All of these factors make the role of CCSP in the inflammatory process more complex. Moreover, CCSP expression may result in tissue damage caused by inflammatory factors, rather than the inflammation itself . It is most likely that up-regulation of CCSP expression is a result of the body's self-protection mechanism in the early stages of the inflammatory response, but suppression of CCSP expression follows during the later inflammatory response. CCSP expression is down-regulated after acute lung inflammation induced by intratracheal or intravenous LPS administration [28, 31]. Our results are in agreement with these previous experimental observations. The finding that LPS reduces CCSP expression should provide an excellent foundation for future research.
Second, polydatin increased the CCSP-positive cell percentage and up-regulated CCSP mRNA and protein expression in lung tissue during acute lung injury induced by LPS. CCSP expression was increased along with PD increasing. There was a dose-effect relationship between PD and CCSP expression within our observational dose range. Additionally, CCSP protein expression was consistent with its mRNA level. Some possible mechanism by which PD promotes CCSP expression can be explained as follows: 1) PD can increase the number of CCSP-positive cells (i.e., Clara cells); 2) PD can promote the secretion of CCSP in individual Clara cells to increase total CCSP expression; and 3) most importantly, PD can enhance the stability of CCSP. The reduction of CCSP degradation is an important factor in increasing CCSP level. PD can help to keep the bronchoalveolar blood-gas barrier integrity and decrease the bronchoalveolar blood-gas barrier permeability induced by LPS so that CCSP will not be decomposed in serum. Berg et al  have reported that glucocorticoids regulate the CCSP promoter via C/EBP beta and -delta in lung cells. Ramsay et al.  have indicated that IFN-γ can up-regulate the expression of CCSP in rat and rabbit lung tissue. The reported mechanisms are as follows: 1) regulation of the Th1/Th2 cytokine network to increase CCSP mRNA expression; 2) hormone receptor and IFN-γbinding sites exist in the 5'-flanking region of the CCSP gene, which can directly promote the transcription of the CCSP gene and increase the synthesis and secretion of CCSP; and 3) increased stability of CCSP mRNA at the post-transcriptional level. Therefore, our future research will be focused on the effect of polydatin on the transcription of CCSP.
Third, CCSP expression in lung in the PD pretreatment group was greater than in the PD treatment group. This result suggests that a competitive inhibition of CCSP exists between PD and LPS. Therefore, we propose that PD and LPS have a common binding site in Clara cells that can influence the secretion of CCSP. However, the specific mechanism remains unclear, and the intrinsic link between PD and CCSP requires further investigation.
Fourth, based on animal experiments, the BEAS-2B cell line was chosen as the model to study the effect of PD on CCSP in vitro. BEAS-2B cells are clara cells that have been transformed by the SV40 T-antigen. BEAS-2B is the most commonly used model for CCSP research [34, 35]. The human CCSP gene exists as a single copy in BEAS-2B cells. Tumor necrosis factor-α (TNF-α) can induce a change in chromosome structure that enhances the stability of an RNA-binding protein involved in transcriptional regulation, which increases CCSP gene expression in BEAS-2B cells . Kim et al.  have reported that IL-13 and other indirectly acting proteins can promote the expression and activation of epidermal growth factor receptor (EGFR) so as to increase CCSP expression in airway epithelium. We found that CCSP can be expressed in and secreted by BEAS-2B cells in culture medium. LPS can decrease CCSP expression in BEAS-2B cells, while PD can promote the expression of CCSP in normal and LPS-stimulated cells, and the change in mRNA is consistent with CCSP protein expression. PD may enhance the proliferation of Clara cells and it may enhance the proliferation of CCSP-positive/pro-surfactant protein C pro-SPC-positive cells .
As far as the limitation of this research work was concerned, we just observed that polydatin suppressed PLA2 of lung induced by LPS through up-regulating Clara cell secretory protein. The intrinsic relationship between PD and CCSP need further investigation.
We have demonstrated that PD can modulate CCSP expression to inhibit PLA2. This inhibition is probably a crucial protection mechanism of PD in LPS-induced acute lung injury. These findings provide compelling evidence for the potential efficacy of PD in clinical use, although the molecular mechanisms of its action need further exploration.
We would like to thank Mrs Luo Qing (Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China) for the experiment technology and Mr Zhu Jin (Department of Pathology, Children's Hospital of Chongqing Medical University, China) for the microscopic observation technology.
This work was supported by grants from National natural science foundation of China (30700166) and Chongqing Medical University of China (XBYB2007050)
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