Skip to main content

Advertisement

Polydatin up-regulates clara cell secretory protein to suppress phospholipase A2 of lung induced by LPS in vivo and in vitro

BMC Cell Biologyvolume 12, Article number: 31 (2011) | Download Citation

Article metrics

  • 5766 Accesses

  • 24 Citations

Abstract

Background

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.

Results

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.

Conclusion

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.

Background

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 [1]. 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% [2]. 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 [3]. 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[4]. 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 [5]. 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 [6]. Sato R reported [7] 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 [8]. 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 [12], anti-inflammation, immunomodulation, anti-cytokine, pollutant clearance, anti-fibrosis, anti-tumor invasion and anti-protease activity [13], 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[16].

Polydatin (PD), also known as polygonin, is a type of polyphenolic phytoalexin with strong antioxidative activity that is isolated from a variety of plant species and also can be readily synthesized [17, 18]. One of the richest sources of this monocrystalline compound is the roots of Polygonum cuspidatum Sieb, a weed widely used in traditional Chinese and Japanese medicine. Its chemical name is 3, 4', 5-trihydroxystilbene-3-β-single-D-glucoside [19] (Figure 1). PD exhibits multiple biological activities and pharmacological effects, such as protection of the heart [19, 20], brain [21] and liver [22], improving microcirculation [23], inhibiting platelet aggregation [24], combating shock [25], anti-asthmatic, microbial resistance, and anti-cancer activities. In 2006, PD was evaluated by the State Food and Drug Administration of China and became one of the new drugs approved for further testing in phase II clinical trials.

Figure 1
figure1

The chemical structure of trans-polydatin (3,4',5-trihydroxystilbene-3-β-single-D-glucoside).

Full size image

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) [26]. 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.

Methods

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.

The rats were randomly divided into five groups (Table 1): the sham operation group (I), endotoxic shock group (II), PD treatment group (III), PD pretreatment group (IV) and PD control group (V) (n = 10 each). The rats in group I were injected with normal saline and served as the control; the rats in group II were injected with LPS (10 mg per kg body weight). For group III and group IV, LPS (10 mg per kg body weight) was injected, and PD solution was injected 1 hour later or 0.5 hours before, respectively. The rats in group V received PD solution only.

Table 1 Animal grouping and drug injection
Full size table

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.

Animal model

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

Total RNA was isolated from lung tissue using Trizol reagent (Invitrogen). RNA was further purified with the RNeasy Mini Kit, treated with DNase I (30 U·μg-1total RNA) (Qiagen), and then reverse transcribed using the SuperScript III First-Strand Synthesis System (Invitrogen) according to the manufacturer's recommended protocols. Quantitative gene expression analysis was performed using the ABI Prism 7000 Sequence Detection System (Applied Biosystems), with cDNA equivalent to 10 ng of total RNA and SYBR Green PCR Master Mix (Applied Biosystems) following the manufacturer's protocol. The following primers (Table 2) were used to amplify CCSP, sPLA2, cPLA2 and β-actin.

Table 2 PCR primer pairs used amplify CCSP, sPLA2, cPLA2 and β-actin cDNA fragments of rat lung
Full size table

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

Cells culture

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 grouping

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

Total RNA was isolated from cells using Trizol reagent (Invitrogen) according to the manufacturer's instructions. RNA was further purified with an RNeasy Mini Kit and treated with DNase I (30 U·μg-1 total RNA) then reverse-transcribed using the Super Script III First-Strand Synthesis System according to the protocols supplied by the manufacturer. Quantitative gene expression analysis was performed using the ABI Prism 7000 Sequence Detection System, with cDNA equivalent to 10 ng of total RNA and SYBR Green PCR Master Mix following the manufacturer's protocol. The following primers (Table 3) were used to amplify CCSP and β-actin.

Table 3 PCR primer pairs used amplify CCSP and β-actin cDNA fragments of BEAS-2B cells
Full size table

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.

Statistical analysis

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.

Results

Polydatin up-regulates CCSP mRNA expression in rat lung

A significant decrease CCSP mRNA expression was observed only in the endotoxic shock group five hours after LPS injection (Figure 2A/2B-group II). PD can increase CCSP mRNA expression not only in normal rat lung (Figure 2A/2B, group V vs. group I) but also in rat lung following endotoxic shock(Figure 2A/2B-group III/IV). Moreover, CCSP mRNA level in the PD pretreatment group was significantly higher (P < 0.05) than in the PD treatment group (Figure 2A/2B-group III/IV, group IV vs. group III). PD increased CCSP mRNA expression in a dose-dependent manner (Figure 3A-1, A-2, B-1 and 3B-2).

Figure 2
figure2

Effects of polydatin on the expression of CCSP mRNA in rat lung. A. Relative expression of CCSP, quantified by real-time PCR. B. Electrophoresis showing the RT-PCR results. I: sham operation group, injected with normal saline; II: endotoxic shock group, injected with LPS (10 mg·kg-1 body weight); III: PD treatment group, injected with LPS (10 mg·kg-1 body weight), then a 0.5% PD solution (0.2 ml·kg-1 body weight) 1 hour later; IV: PD pretreatment group, injected with a 0.5% PD solution (0.2 ml·kg-1 body weight), then LPS (10 mg·kg-1 body weight) 0.5 hours later; V: PD control group. cP < 0.01 vs. group I; eP < 0.05 and fP < 0.01 vs. group II; iP < 0.05 vs. group III.

Full size image
Figure 3
figure3

The dose-effect relationship between polydatin and CCSP mRNA expression in rat lung. A. CCSP mRNA expression in PD treatment groups with different doses by real-time PCR (A-1) and RT-PCR(A-2). B. CCSP mRNA expression in PD pretreatment groups with different doses by real-time PCR (B-1) and RT-PCR(B-2). bP < 0.05 vs. 1 mg·kg-1 PD group, eP < 0.05 vs. 5 mg·kg-1PD group, and jP < 0.01 vs. 10 mg·kg-1 PD group.

Full size image

Polydatin down-regulates sPLA2 and cPLA2 mRNA expression in rat lung

Because CCSP was the potential inhibitor of PLA2, we investigated the effects of PD on PLA2 along with CCSP. PD could down-regulate the levels of sPLA2 and cPLA2 mRNA expressions in normal rat lung (Figure 4A/4B, group V vs. group I). Not only that, PD could decrease the levels of sPLA2 and cPLA2 mRNA expressions of rat lung induced by LPS (Figure 4A/4B-group III/IV), in a dose-dependent manner (Figure 5A, B and Figure 6A, B). The expression of sPLA2 and cPLA2 in PD pretreatment group was lower than in PD treatment group (Figure 4A and 4B, group IV vs. group III, P < 0.05).

Figure 4
figure4

Effects of polydatin on the expression of sPLA 2 /cPLA 2 mRNA in rat lung. A. Relative expression of sPLA2, quantified by real-time PCR. B. Relative expression of cPLA2, quantified by real-time PCR. I: sham operation group, injected with normal saline; II: endotoxic shock group, injected with LPS (10 mg·kg-1 body weight); III: PD treatment group, injected with LPS (10 mg·kg-1 body weight), then a 0.5% PD solution (0.2 ml·kg-1 body weight) 1 hour later; IV: PD pretreatment group, injected with a 0.5% PD solution (0.2 ml·kg-1 body weight), then LPS (10 mg·kg-1 body weight) 0.5 hours later; V: PD control group. bP < 0.05 and cP < 0.01 vs. group I; fP < 0.01 vs. group II; iP < 0.05 and jP < 0.01 vs. group III.

Full size image
Figure 5
figure5

The dose-effect relationship between polydatin and sPLA 2 mRNA expression in rat lung. A. sPLA2 mRNA expression in PD treatment groups with different doses by real-time PCR and RT-PCR. B. sPLA2 mRNA expression in PD pretreatment groups with different doses by real-time PCR and RT-PCR. cP < 0.01 vs. 1 mg·kg-1 PD group, eP < 0.05 and fP < 0.01 vs. 5 mg·kg-1PD group, and iP < 0.05 vs. 10 mg·kg-1 PD group.

Full size image
Figure 6
figure6

The dose-effect relationship between polydatin and cPLA 2 mRNA expression in rat lung. A. cPLA2 mRNA expression in PD treatment groups with different doses by real-time PCR. B. cPLA2 mRNA expression in PD pretreatment groups with different doses by real-time PCR. cP < 0.01 vs. 1 mg·kg-1 PD group, eP < 0.05 and fP < 0.01 vs. 5 mg·kg-1PD group, and iP < 0.05 vs. 10 mg·kg-1 PD group.

Full size image

Polydatin up-regulates CCSP protein expression in rat lung

To investigate whether CCSP protein expression changed with its mRNA expression synchronously, we detected CCSP protein in lung by western blot. The results indicated that LPS not only inhibited the protein expression of CCSP but also that PD treatment and PD pretreatment increased the level of CCSP markedly (Figure 7A and 7B). In particular, CCSP protein in the pretreatment and PD control groups was significantly higher than in the sham operation group (Figure 7A/7B, group IV and V vs. group I). CCSP protein expression in the PD pretreatment group was higher than in PD treatment group (Figure 7A/7B, group IV vs. group III). Thus, PD increased CCSP protein expression in a dose-dependent manner (Figure 8A-1, A-2, B-1 and 8B-2).

Figure 7
figure7

Effects of polydatin on the expression of CCSP protein in rat lung. CCSP protein expression was examined by western blot. I: sham operation group; II: endotoxic shock group; III: PD treatment group; IV: PD pretreatment group; V: PD control group. A. The electrophoretogram of CCSP protein expression. B. Relative ratio of CCSP protein expression. bP < 0.05 and cP < 0.01 vs. group I; eP < 0.05 and fP < 0.01 vs. group II; iP < 0.05 vs. group III.

Full size image
Figure 8
figure8

Dose-effect relationship between polydatin and CCSP protein expression in rat lung. A.CCSP protein expression in PD treatment groups with different doses. B.CCSP protein expression in PD pretreatment groups with different doses. bP < 0.05 vs. 1 mg·kg-1 PD group, eP < 0.05 and fP < 0.01 vs. 5 mg·kg-1PD group, and iP < 0.05 vs. 10 mg·kg-1 PD group.

Full size image

Polydatin down-regulates serum CCSP level in rat

CCSP can transfer from lung tissue into the blood serum. Serum CCSP level is closely related to its synthesis and secretion by Clara cells in the respiratory tract, and serum CCSP level may act as a marker of the bronchoalveolar blood-gas barrier integrity and permeability [27, 28]. As shown in Figure 9, serum CCSP level in the endotoxin shock group was significantly higher than in the sham operation group(Figure 9, group II vs. group I). However, CCSP levels in the PD treatment and PD pretreatment groups were lower than in the endotoxic shock group (Figure 9, group III/IV vs. group II). Serum CCSP level decreased with increasing PD dose (Figure 10A/10B). Therefore, PD decreased CCSP transference from lung to serum in a dose-dependent manner.

Figure 9
figure9

Effects of polydatin on serum CCSP level in different groups of rats. I: Sham operation group; II: endotoxic shock group; III: PD treatment group; IV: PD pretreatment group; V: PD control group. bP < 0.05 vs. group I; fP < 0.01 vs. group II.

Full size image
Figure 10
figure10

Dose-effect relationship between polydatin and serum CCSP level in rat. A.Serum CCSP level in PD treatment groups with different doses. B. Serum CCSP level in PD pretreatment groups with different doses. bP < 0.05 and cP < 0.01 vs. 1 mg·kg-1 PD group, fP < 0.01 vs. 5 mg·kg-1PD group, and iP < 0.05 vs. 10 mg·kg-1 PD group.

Full size image

Polydatin increases the percentage of CCSP-positive cells

In rat lung slices, CCSP-positive cells are non-ciliated epithelial cells, namely, Clara cells. The relative CCSP-positive airway epithelial cell proportions were as follows. Compared with the sham operation group, CCSP-positive cells were decreased in the endotoxic shock model group and increased in the PD control group (Table 4). Compared with the LPS group, CCSP-positive cells were increased in the PD treatment and pretreatment groups (Table 4). Thus, PD increased CCSP-positive cells in lung tissue in a dose-dependent manner (Table 5).

Table 4 Percentage of CCSP-positive cells of lung tissue in each group ( ± s, n = 10).
Full size table
Table 5 Percentage of CCSP-positive cells of lung tissue in each group ( ± s, n = 6).
Full size table

Polydatin up-regulates CCSP expression in BEAS-2B

The MTT assay suggested that the most suitable concentration of PD to use in BEAS-2B cells was 0.5 mmol/L and the most suitable concentration of LPS was 10 ng·ml-1. In vitro, LPS led to reduced CCSP expression in BEAS-2B cells, while PD promoted CCSP expression, not only in normal BEAS-2B cells but also in LPS-induced BEAS-2B cells (Figure 11 and 12). In addition, CCSP expression in the PD pretreatment group was greater than in the PD treatment group (Figure 11 and 12).

Figure 11
figure11

Effects of polydatin on CCSP mRNA expression in LPS-induced BEAS-2B cells. A. Relative expression of CCSP quantified by real-time PCR. B. RT-PCR analysis shown by electrophoresis. bP < 0.05 vs. normal control group; eP < 0.05 and fP < 0.01 vs. LPS group; iP < 0.05 vs. LPS+PD group.

Full size image
Figure 12
figure12

Effects of polydatin on CCSP protein levels in LPS-induced BEAS-2B cells. A. The electrophoretogram of CCSP protein expression. B. Relative ratio of CCSP protein expression. cP < 0.01 vs. normal control group; eP < 0.05 and fP < 0.01 vs. LPS group; iP < 0.05 vs. LPS+PD group.

Full size image

Discussion

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 [27]. By contrast, CCSP production is decreased during acute and chronic lung injury caused by viral and bacterial infections, smoking [29] 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 [30]. 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 [32] have reported that glucocorticoids regulate the CCSP promoter via C/EBP beta and -delta in lung cells. Ramsay et al. [33] 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 [36]. Kim et al. [37] 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 [38].

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.

Conclusion

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.

References

  1. 1.

    Kneyber MC, Markhorst DG: Management of acute lung injury and acute respiratory distress syndrome in children: a different perspective. Crit Care Med. 2009, 37 (12): 3192-3193. 10.1097/CCM.0b013e3181be7b72.

  2. 2.

    Wheeler AP, Bernard GR: Acute lung injury and the acute respiratory distress syndrome: a clinical review. Lancet. 2007, 369 (9572): 1553-1564. 10.1016/S0140-6736(07)60604-7.

  3. 3.

    Burke JE, Dennis EA: Phospholipase A2 structure, function, mechanism and signaling. J Lipid Res. 2009, 50: S237-242.

  4. 4.

    Kitsiouli E, Nakos G, Lekka ME: Phospholipase A2 subclasses in acute respiratory distress syndrome. Biochim Biophys Acta. 2009, 1792 (10): 941-953.

  5. 5.

    Wu Y, Singer M, Thouron F, Alaoui-El-Azher M, Touqui L: Effect of surfactant on pulmonary expression of type IIA PLA(2) in an animal model of acute lung injury. Am J Physiol Lung Cell Mol Physiol. 2002, 282 (4): L743-750.

  6. 6.

    Cunningham TJ, Yao L, Lucena A: Product inhibition of secreted phospholipase A2 may explain lysophosphatidylcholines' unexpected therapeutic properties. J Inflamm (Lond). 2008, 22 (5): 17-

  7. 7.

    Sato R, Yamaga S, Watanabe K, Hishiyama S, Kawabata K, Kobayashi T, Fujioka D, Saito Y, Yano T, Watanabe Y, Ishihara H, Kugiyama K: Inhibition of secretory phospholipase A2 activity attenuates lipopolysaccharide-induced acute lung injury in a mouse model. Exp Lung Res. 2010, 36 (4): 191-200. 10.3109/01902140903288026.

  8. 8.

    Reynolds SD, Malkinson AM: Clara cell: Progenitor for the bronchiolar epithelium. Int J Biochem Cell Biol. 2010, 42 (1): 1-4. 10.1016/j.biocel.2009.09.002.

  9. 9.

    Levine CR, Gewolb IH, Allen K, Welch RW, Melby JM, Pollack S, Shaffer T, Pilon AL, Davis JM: The safety, pharmacokinetics, and anti-inflammatory effects of intratracheal recombinant human Clara cell protein in premature infants with respiratory distress syndrome. Pediatr Res. 2005, 58 (1): 15-21. 10.1203/01.PDR.0000156371.89952.35.

  10. 10.

    Shashikant BN, Miller TL, Welch RW, Pilon AL, Shaffer TH, Wolfson MR: Dose response to rhCC10-augmented surfactant therapy in a lamb model of infant respiratory distress syndrome: physiological, inflammatory, and kinetic profiles. J Appl Physiol. 2005, 99 (6): 2204-2211. 10.1152/japplphysiol.00246.2005.

  11. 11.

    Harrod KS, Jaramillo RJ: Pseudomonas aeruginosa and tumor necrosis factor-α attenuate clara cell secretory protein promoter function. Am J Respir Cell Mol Biol. 2002, 26 (2): 216-223.

  12. 12.

    Katavolos P, Ackerley CA, Clark ME, Bienzle D: Clara cell secretory protein increases phagocytic and decreases oxidative activity of neutrophils. Vet Immunol Immunopathol. 2011, 139 (1): 1-9. 10.1016/j.vetimm.2010.07.021.

  13. 13.

    Coppens JT, Van Winkle LS, Pinkerton K, Plopper CG: Distribution of Clara cell secretory protein expression in the tracheobronchial airways of rhesus monkeys. Am J Physiol Lung Cell Mol Physiol. 2007, 292 (5): L1155-1162. 10.1152/ajplung.00454.2006.

  14. 14.

    Levin SW, Butler JD, Schumacher UK, Wightman PD, Mukherjee AB: Uteroglobin inhibits phospholipase A2 activity. Life Sci. 1986, 38 (20): 1813-1819. 10.1016/0024-3205(86)90135-9.

  15. 15.

    Jorens PG, Sibille Y, Goulding NJ, van Overveld FJ, Herman AG, Bossaert L, De Backer WA, Lauwerys R, Flower RJ, Bernard A: Potential role of clara cell protein, an endogenous phospholipase A2 inhibitor, in acute lung injury. Eur Respir J. 1995, 8 (10): 1647-1653. 10.1183/09031936.95.08101647.

  16. 16.

    Yoshikawa S, Miyahara T, Reynolds SD, Stripp BR, Anghelescu M, Eyal FG, Parker JC: Clara cell secretory protein and phospholipase A2 activity modulate acute ventilator-induced lung injury in mice. J Appl Physiol. 2005, 98 (4): 1264-1271.

  17. 17.

    Gao S, Fan G, Hong Z, Yin X, Yang S, Wu Y: HPLC determination of polydatin in rat biological matrices: application to pharmacokinetic studies. J Pharm Biomed Anal. 2006, 41 (1): 240-245. 10.1016/j.jpba.2005.08.027.

  18. 18.

    Du J, Sun LN, Xing WW, Huang BK, Jia M, Wu JZ, Zhang H, Qin LP: Lipid-lowering effects of polydatin from Polygonum cuspidatum in hyperlipidemic hamsters. Phytomedicine. 2009, 16 (6-7): 652-658. 10.1016/j.phymed.2008.10.001.

  19. 19.

    Zhang LP, Yang CY, Wang YP, Cui F, Zhang Y: Protective effect of polydatin against ischemia/reperfusion injury in rat heart. Sheng Li Xue Bao. 2008, 60 (2): 161-168.

  20. 20.

    Zhao Q, Huang HX, Jin CH: Protective effect of polydatin against lipopolysaccharide-induced myocardial injury. Di Yi Jun Yi Da Xue Xue Bao. 2003, 23 (4): 364-366.

  21. 21.

    Cheng YF, Zhang HT, Sun LS, Guo SL, Ouyang S, Zhang Y, Xu J: Involvement of cell adhesion molecules in polydatin protection of brain tissues from ischemia-reperfusion injury. Brain Res. 2006, 1110 (1): 193-200. 10.1016/j.brainres.2006.06.065.

  22. 22.

    Xing WW, Wu JZ, Jia M, Du J, Zhang H, Qin LP: Effects of polydatin from Polygonum cuspidatum on lipid profile in hyperlipidemic rabbits. Biomed Pharmacother. 2009, 63 (7): 457-462. 10.1016/j.biopha.2008.06.035.

  23. 23.

    Sheng C, Yu YH, Zhao KS, Qin W, Wang CH: Hypotensive resuscitation combined with polydatin improve microcirculation and survival in a rabbit model of uncontrolled hemorrhagic shock in pregnancy. J Surg Res. 2011, 168 (1): 103-110. 10.1016/j.jss.2009.09.007.

  24. 24.

    Zhou S, Yang R, Teng Z, Zhang B, Hu Y, Yang Z, Huan M, Mei Q: Dose-dependent absorption and metabolism of trans-Polydatin in rats. J Agric Food Chem. 2009, 57 (11): 4572-4579. 10.1021/jf803948g.

  25. 25.

    Zhao KS, Jin C, Huang X, Liu J, Yan WS, Huang Q, Kan W: The mechanism of Polydatin in shock treatment. Clin Hemorheol Microcirc. 2003, 29 (3-4): 211-217.

  26. 26.

    Shu SY, Ling ZY, Wang XY, Lu ZY: Effect of polydatin on phospholipase A2 in lung tissues in rats with endotoxic shock. Chinese Journal of Traumatology(English edition). 2004, 7 (4): 239-243.

  27. 27.

    Michel O, Murdoch R, Bernard A: Inhaled LPS induces blood release of clara cell specific protein (CC16) in human beings. J Allergy Clin Immunol. 2005, 115 (6): 1143-1147. 10.1016/j.jaci.2005.01.067.

  28. 28.

    Arsalane K, Broeckaert F, Knoops B, Wiedig M, Toubeau G, Bernard A: Clara cell specific protein(CC16) expression after acute lung inflammtion induced by intratracheal lipopolysaccharide administration. Am J Respir Crit Care Med. 2000, 161: 1624-1630.

  29. 29.

    Ge XN, Chu HW, Minor MN, Case SR, Bosch DG, Martin RJ: Roflumilast increases Clara cell secretory protein in cigarette smoke-exposed mice. COPD. 2009, 6 (3): 185-191. 10.1080/15412550902905979.

  30. 30.

    Angert RM, Pilon AL, Chester D, Davis JM: CC10 reduces inflammation in meconium aspiration syndrome in newborn piglets. Pediatr Res. 2007, 62 (6): 684-688. 10.1203/PDR.0b013e31815a5632.

  31. 31.

    Chandra S, Davis JM, Drexler S, Kowalewska J, Chester D, Koo HC, Pollack S, Welch R, Pilon A, Levine CR: Safty and efficacy of intratracheal recombinant human clara cell protein in a newborn piglet model of acute lung injury. Pediatr Res. 2003, 54 (3): 509-515.

  32. 32.

    Berg T, Cassel TN, Schwarze PE, Nord M: Glucocorticoids regulate the CCSP and CYP2B1 promoters via C/EBPbeta and delta in lung cells. Biochem Biophys Res Commun. 2002, 293 (3): 907-912. 10.1016/S0006-291X(02)00319-4.

  33. 33.

    Ramsay PL, Luo Z, Magdaleno SM, Whitbourne SK, Cao X, Park MS, Welty SE, Yu-Lee LY, DeMayo FJ: Transcriptional regulation of CCSP by interferon-γ in vitro and in vivo. Am J Physiol Lung Cell Mol Physiol. 2003, 284 (1): L108-118.

  34. 34.

    Cowan MJ, Huang X, Yao XL, Shelhamer JH: Tumor necrosis factor alpha stimulation of human Clara cell secretory protein production by human airway epithelial cells. Ann N Y Acad Sci. 2000, 923: 193-201.

  35. 35.

    Yao XL, Ikezono T, Cowan M, Logun C, Angus CW, Shelhamer JH: Interferon-gamma stimulates human Clara cell secretory protein production by human airway epithelial cells. Am J Physiol. 1998, 274 (5 Pt 1): L864-869.

  36. 36.

    Yao XL, Levine SJ, Cowan MJ, Logun C, Shelhamer JH: Tumor necrosis factor-α stimulates human clara cell secretory protein production by human airway epithelial cells. Am J Respir Cell Mol Biol. 1998, 19 (4): 629-635.

  37. 37.

    Kim S, Shim JJ, Burgel PR, Ueki IF, Dao-Pick T, Tam DC, Nadel JA: IL-13 induced clara cell secretory protein expression in airway epithelium:role of EGFR signaling pathway. Am J Physiol Lung Cell Mol Physiol. 2002, 283 (1): L67-75.

  38. 38.

    Teisanu RM, Lagasse E, Whitesides JF, Stripp BR, Teisanu Roxana, Lagasse Eric, Whitesides John, Barry R, Stripp BR: Prospective isolation of bronchiolar stem cells based upon immunophenotypic and autofluorescence characteristics. Stem Cells. 2009, 27 (3): 612-622. 10.1634/stemcells.2008-0838.

Download references

Acknowledgements

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)

Author information

Affiliations

  1. Department of Anesthesiology, Children's Hospital of Chongqing Medical University, Zhongshan Er Road NO136, Yuzhong District, Chongqing, 40 0014, China

    • Shu Shiyu
    • , Ye Mao
    •  & Bo Lin

  2. Department of Cardiology, Second Affiliated Hospital of Chongqing Medical University, Linjiang Road NO74, Yuzhong District, Chongqing, 40 0010, China

    • Ling Zhiyu

  3. Immunological laboratory, Ministry of Education Key Laboratory of Child Development and Disorders, Zhongshan Er Road NO136, Yuzhong District, Chongqing, 40 0014, China

    • Wang Lijia

  4. Department of Health and Toxicology, Second Military Medical University of PLA, Xiangyin Road NO800, Shanghai, 20 0433, China

    • Zhang Tianbao

  5. Children Nutrition Research Center, Key Laboratory of Pediatrics in Chongqing, CSTC2009CA 5002, Zhongshan Er Road NO136, Yuzhong District, Chongqing, 40 0014, China

    • Chen Jie

  6. Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Zhongshan Er Road NO136, Yuzhong District, Chongqing, 40 0014, China

    • Li Tingyu

Authors

  1. Search for Shu Shiyu in:

  2. Search for Ling Zhiyu in:

  3. Search for Ye Mao in:

  4. Search for Bo Lin in:

  5. Search for Wang Lijia in:

  6. Search for Zhang Tianbao in:

  7. Search for Chen Jie in:

  8. Search for Li Tingyu in:

Corresponding author

Correspondence to Li Tingyu.

Additional information

Authors' contributions

SYS conceived the experiments and wrote the manuscript. ZYL determined the protein expression. MY determined the gene expression. LB did the animal model. LJW cultured the BEAS-2B cells. TBZ contributed to do the cell experiment. JC performed the immunohistochemical analyses and statistic analysis. TYL edited the draft and contributed significantly to experimental design. All authors have read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Authors’ original file for figure 3

Authors’ original file for figure 4

Authors’ original file for figure 5

Authors’ original file for figure 6

Authors’ original file for figure 7

Authors’ original file for figure 8

Authors’ original file for figure 9

Authors’ original file for figure 10

Authors’ original file for figure 11

Authors’ original file for figure 12

Rights and permissions

Reprints and Permissions

About this article

Keywords

  • Mean Arterial Pressure
  • Acute Lung Injury
  • Clara Cell
  • Endotoxic Shock
  • Sham Operation Group

BMC Molecular and Cell Biology

ISSN: 2661-8850

Contact us