Increased oxidative stress and disrupted small intestinal tight junctions in cigarette smoke-exposed rats

Introduction

Chronic obstructive pulmonary disease (COPD) is characterized by persistent airflow limitation, and is a major public health problem (1). By the year 2030, COPD is predicted to have become the seventh most common disease and the fourth leading cause of mortality worldwide (2). Cigarette smoking is the most common risk factor for developing COPD, and the disease prevalence in numerous countries is associated with the rate of smoking (3). COPD also has a proven association with persistent systemic inflammation, excessive oxidative stress and abnormal immune function (4). These numerous effects highlight its multidimensional nature; although COPD damage is primarily observed in the lungs, it is often accompanied by disruptions to cardiovascular, musculoskeletal, renal and intestinal function (5).

Small intestinal integrity is maintained by intercellular tight junctions (TJs) between luminal cells. TJs regulate solute and ion transport through the paracellular pathway (6), which is the dominant pathway for passive transepithelial solute flow in the small intestine (7). A number of compounds regulate TJs, including transmembrane proteins such as occludin and claudins, and peripheral membrane proteins such as zonula occludens (ZOs). Claudins are integral TJ proteins regulating the size selectivity of the barrier, occludin is considered to provide the primary intercellular seal between epithelial cells, and ZOs provide the critical connection between transmembrane TJ components and the intracellular actin cytoskeleton (8).

TJ protein expression is regulated by extracellular stimuli including oxidative stress responses and pro-inflammatory cytokines (9,10). Hypoxia-inducible factor 1 (HIF-1), a transcription factor regulating oxidative stress and apoptotic genes (11), is a notable modulator of TJ protein expression (12,13). HIF-1 is selectively stabilized and activated during local hypoxia, and coordinates the tissue’s adaptive response to hypoxia by facilitating oxygen supply, glucose transport and angiogenesis (14). Functionally, HIF-1 is a heterodimer comprising an inducible HIF-1α subunit and a constitutively expressed HIF-1β subunit. HIF-1α is upregulated in response to hypoxia and accounts for the disruption of the intestinal luminal structure (15).

Significantly, the respiratory and intestinal tracts have a similar luminal structure; the two organs have an extensive luminal surface area, selective epithelial barrier and overlying mucus-gel layer (16). The absorptive and barrier function of the intestinal epithelium is sensitive to tissue hypoxia and reduced perfusion, and similarly, tissue hypoxia is one of the most notable characteristics in COPD pathology (17). Clinical findings indicate a combination of disturbed intestinal integrity, intestinal hyperpermeability and enhanced enterocyte loss in COPD patients (18,19). However, the underlying molecular mechanisms of this small intestinal damage remain unknown.

In the present study, we exposed rats to cigarette smoke (CS) to induce COPD, which is a well-established model (20). Gene expression analysis of intestinal samples by reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to evaluate the effect of CS on oxidative stress and inflammation. The present study may provide an essential molecular mechanism for intestinal barrier dysfunction and hyperpermeability in patients with COPD.

Materials and methods

Ethics

Rats were used in strict accordance with the protocol approved by the Animal Care Committee of Tianjin Medical University, China.

Exposure of rats to cigarette smoke

Male Wistar rats weighing 180±20 g and aged 6 weeks were purchased from the Model Animal Center of the Radiological Medicine Research Institute, Chinese Academy of Medical Science (Tianjin, China). Rats were housed in standard laboratory cages (five per cage) and had free access to food and water. Rats were randomly divided into two groups (n=15 per group) matched by body weight; a CS-exposed group and an unexposed control group. As described previously (21), the CS group received whole-body exposure to the smoke of five unfiltered cigarettes (Daqianmen™, tar ≤15 mg, nicotine ≤1.1 mg and CO ≤13 mg) for 30 min twice daily (before 9 am and after 5 pm), every day for 14 weeks inside a 0.6 m3 custom plexiglass chamber (made in-house), which included five ventilation holes. Naïve animals underwent an identical protocol but without CS exposure. Smoke contamination between the study groups was prevented by using different chambers for each.

Total RNA isolation

Following treatment, rats were anesthetized and sacrificed. The abdominal cavity was opened, and the duodenum was excised, rinsed in ice-cold phosphate-buffered saline (pH 7.4; Sangon Biotech, Shanghai, China), frozen in liquid nitrogen and stored at −80°C until analysis. RNA was extracted from duodenum tissues using TRIzol reagent (Invitrogen, Carlsbad, CA, USA). Extract yield and quality were determined by measuring absorbance at 260 and 280 nm with the MaestroNano Micro-Volume spectrophotometer (Maestrogen, Inc., Las Vegas, NV, USA). The absorbance ratio at 260:280 was between 1.8 and 2.0. The RNA was subsequently reverse transcribed into complementary DNA (cDNA).

RT-qPCR

Messenger RNA (mRNA; 3 μg) was reverse transcribed with oligo (dT) primer for 1 h at 50°C using a TIANScript RT kit (Tiangen Biotech Co., Ltd, Beijing, China) according to the manufacturer’s instructions. The cDNA served as templates for RT-qPCR, which was performed using SYBR-Green PCR core reagents (Bio-Rad Laboratories, Hercules, CA, USA). Specific gene primers were designed using Primer-Quest SM software available at http://www.idtdna.com/Scitools/Applications/PrimerQuest/ (Integrated DNA Technologies, Inc., Coralville, IA, USA), then commercially produced (BGI Tech, Shenzhen, Guangdong, China; Table I). DNA amplifications were performed on a CFX96 real-time system (Bio-Rad Laboratories) under the following reaction conditions: an initial heating cycle of 95°C for 2 min; 40 cycles alternating between denaturation at 95°C for 25 sec and primer annealing at 60°C for 25 sec; and extension at 72°C for 20 sec. Melt curves clarified the identity of amplicons, and the housekeeping gene, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), served as an internal control. The relative mRNA expression of targeted genes was calculated by the comparative threshold cycle (CT) method normalized to GAPDH mRNA in the same sample. Briefly, specific ΔCt was calculated as follows: ΔCt= (Cttarget)-(CtGAPDH); relative expression was defined as: 2−ΔCt.

Table I DNA primer sequences for quantitative reverse transcription-quantitative polymerase chain reaction.

Table I

DNA primer sequences for quantitative reverse transcription-quantitative polymerase chain reaction.

Gene	Forward primer	Reverse primer
GAPDH	5′-TGGAGTCTACTGGCGTCTTC-3′	5′-TTCACACCCATCACAAACATG-3′
claudin-1	5′-TGTCCACCATTGGCATGAAG-3′	5′-GCCACTAATGTCGCCAGACC-3′
claudin-2	5′-ACAGCACTGGCATCACCCA-3′	5′-GCGAGGACATTGCACTGGAT-3′
claudin-4	5′-AAGGCCAAGGTCATGATCACAG-3′	5′-GAAGTCGCGGATGACGTTGT-3′
occludin	5′-CTACTCCTCCAACGGCAAAG-3′	5′-AGTCATCCACGGACAAGGTC-3′
zo-1	5′-ATTCAGTTCGCTCCCATGAC-3′	5′-GCTGTGGAGACTGTGTGGAA-3′
HIF-1α	5′-AAGAAACCGCCTATGACGTG-3′	5′-CCACCTCTTTTTGCAAGCAT-3′
bax	5′-CCAGGACGCATCCACCAAGAAGC-3′	5′-TGCCACACGGAAGAAGACCTCTCG-3′
bcl-2	5′-GGATGACTTCTCTCGTCGCTACCGT-3′	5′-CGAGTGAGGATGTGCATGAA-3′
SOD	5′-GCAGAAGGCAAGCGGTGAAC-3′	5′-TCACACCACAAGCCAAGCGG-3′
p22phox	5′-AAGTACCTGACCGCTGTGG-3′	5′-AGGTAGATCACACTGGCAATG-3′
nox2	5′-GGCTGTGAATGAGGGACTC-3′	5′-CCAGTGCTGACCCAAGAAG-3′
TNF-α	5′-CGTCGTAGCAAACCACCAAG-3′	5′-CACAGAGCAATGACTCCAAAG-3′
NF-κB	5′-AGCCCTATGCCTTTTCAACAT-3′	5′-CACTCCTGGGTCTGTGTTGTT-3′

[i] GAPDH, glyceraldehyde 3-phosphate dehydrogenase; zo-1, zonula occludens 1; HIF-1α, hypoxia-inducible factor 1α; SOD, superoxide dismutase; TNF-α, tumor necrosis factor α.

Statistical analysis

Results are presented as the means ± SEM. Statistical comparisons were made using the one-tailed Student’s t-test. P<0.05 was considered to indicate a statistically significant difference.

Results

Exposure to CS affects oxidative stress-related genes

Both patients with COPD and animals exposed to CS demonstrate oxidative stress and inflammation systemically (4,22). In this study, we exposed rats to CS and then evaluated the effects of CS exposure on the expression of genes that are associated with oxidative stress and inflammation in the small intestine of rats by RT-qPCR. There was a significant increase in the expression of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase subunits nox2 (P<0.05) and p22phox (P<0.01) in the CS group (Fig. 1A and B). However, the antioxidant enzyme super-oxide dismutase (SOD) was reduced in the CS group compared with the control group (P<0.01; Fig. 1C), indicating that CS exposure increases oxidative stress in the small intestine.

Figure 1 Oxidative stress-related gene expression in rat small intestine following cigarette smoke (CS) exposure. The expression of nox2 (A), p22phox (B) and superoxide dismutase (SOD) (C) was determined using reverse transcription-quantitative polymerase chain reaction on the small intestine of naïve rats (n=3) and CS-exposed rats (n=3). The mRNA levels were normalized to glyceraldehyde 3-phosphate dehydrogenase levels. Data are expressed as the means ± SEM. *P<0.05 and **P<0.01 compared with naïve rats.

To investigate the correlation between CS-associated oxidative stress and intestinal apoptosis, we then measured pro-apoptotic bax and anti-apoptotic bcl-2 gene expression. The bax mRNA expression was over five times greater in the CS group compared with the control group (P<0.01; Fig. 2A). In addition, bcl-2 expression was significantly reduced in the CS group (P<0.01; Fig. 2B). These data suggested that CS exposure induces apoptosis in intestinal cells.

Figure 2 Apoptosis-related gene expression in rat small intestine following cigarette smoke (CS) exposure. Bax (A) and bcl-2 (B) mRNA expression was analyzed using reverse transcription-quantitative polymerase chain reaction. The mRNA levels were normalized to glyceraldehyde 3-phosphate dehydrogenase levels. Data are expressed as the means ± SEM. **P<0.01 compared with naïve rats.

The transcription factor NF-κB was evaluated to assess small intestinal inflammation in the study groups. NF-κB expression was higher in the CS group compared with the control group, but this change was not significant (P=0.09; Fig. 3A). There was no significant difference in the expression of inflammatory cytokine tumor necrosis factor α (TNF-α), which is controlled by NF-κB (23), between the two groups (Fig. 3B). These data together suggested that CS exposure induces oxidative stress and apoptosis in the small intestine.

Figure 3 Inflammatory cytokine tumor necrosis factor (TNF)-α and nuclear transcription factor NF-κB expression in rat small intestine following cigarette smoke (CS) exposure. The mRNA expression of NF-κB (A) and TNF-α (B) in naïve (n=3) and CS-exposed rats (n=3) was determined using reverse transcription-quantitative polymerase chain reaction; no association between CS exposure and cytokine expression was observed. The mRNA levels were normalized to glyceraldehyde 3-phosphate dehydrogenase levels. Data are expressed as the means ± SEM.

Exposure to CS upregulates HIF-1α

HIF-1α is usually elevated during hypoxic stress, but it may also be induced by oxidative stress (24). The HIF-1α subunit is selectively stabilized and primarily determines HIF-1 activity (14). Compared with the control rats, HIF-1α expression was significantly increased in the CS rats (P<0.05; Fig. 4). These data suggested that CS exposure may induce oxidative stress by upregulating HIF-1 in the small intestine.

Figure 4 Small intestinal hypoxia-inducible factor (HIF)-1α expression in rats following cigarette smoke (CS) exposure. HIF-1α mRNA expression, analyzed using reverse transcription-quantitative polymerase chain reaction, increased following CS exposure. The mRNA level was normalized to the glyceraldehyde 3-phosphate dehydrogenase level. Data are expressed as the means ± SEM. *P<0.05 compared with naïve rats.

Exposure to CS alters expression of TJ protein genes

The activation of HIF-1 is associated with the disruption of TJs (25). To gain insight into the mechanism of increased intestinal permeability in COPD, we measured the expression of several TJ components: claudin-1, claudin-2, claudin-4, occludin and zo-1. Compared with the control group, the CS group demonstrated significantly reduced claudin-1 expression (P<0.01; Fig. 5A), indicating that CS exposure loosens the TJ of intestinal luminal cells (26). By contrast, elevated expression of claudin-2 (P<0.05), a leaky protein playing an opposing role to claudin-1 (27), was observed in the CS group compared with the control group (Fig. 5B). However, no significant changes in claudin-4, occludin and zo-1 expression were observed (Fig. 5C–E). These data suggest that CS exposure increases intestinal permeability through the dysregulation of TJ components.

Figure 5 Tight junction protein mRNA expression in rat small intestine following cigarette smoke (CS) exposure. The small intestinal mRNA expression of claudin-1 (A), claudin-2 (B), claudin-4 (C), occludin (D) and zonula occludens (zo)-1 (E) in naïve rats (n=3) and CS-exposed rats (n=3) was determined using reverse transcription-quantitative polymerase chain reaction. The mRNA levels were normalized to glyceraldehyde 3-phosphate dehydrogenase levels. Data are expressed as the means ± SEM. *P<0.05 and **P<0.01 compared with naïve rats.

Discussion

Patients with COPD exhibit disrupted intestinal integrity. To highlight the mechanisms underlying this disorder, we used a CS model, which revealed that CS exposure increases oxidative stress and induces apoptosis in the rat small intestine, while the inflammatory cytokine TNF-α levels remained unchanged. Our data suggested that the disrupted intestinal barrier in COPD may be associated with HIF-1α elevation, which causes dysregulation of TJ components.

Tissue hypoxia is a key player in a number of the extrapulmonary comorbidities occurring in COPD (17). This hypoxia is primarily driven by a ventilation/perfusion mismatch resulting from progressive airflow limitation and emphysematous destruction of the pulmonary capillary bed. The risk of alveolar hypoxia and subsequent hypoxemia increases as the disease progresses (1). Hypoxia caused by COPD greatly impacts the expression of oxygen-dependent genes, including HIF-1α. Aside from oxygen-dependent regulation, HIF-1α expression is also regulated by growth factors and free radicals. Studies reveal that nicotine exposure, a significant component of cigarettes, mimics hypoxic effects by increasing the generation of mitochondrial reactive oxidative species (ROS) and thus stimulates HIF-1α accumulation and activity (28). An oxidative stress response frequently follows smoke exposure, and potentially, hypoxic stimulation in the CS exposure model worsened the oxidative stress response in the small intestine, resulting in HIF-1α upregulation.

The roles of HIF-1α in the regulation of barrier function remain controversial. One study suggests that HIF-1α is a protective factor for intestinal barrier function, as demonstrated in experimental murine colitis (29). However, another study reveals that HIF-1α injures the barrier function and TJs (12). Prolonged intestinal HIF-1α exposure is associated with potential ischemia/reperfusion-induced gut mucosal injury, which contributes to gut barrier function loss, bacterial translocation, apoptosis, gut-derived inflammatory response and resulting villous injury (30). The adverse effects of HIF-1α are apparently mediated by intestinal bacteria or bacterial products (31). Hence, HIF-1α appears to be involved intestinal barrier regulation, but its role, whether protective or injurious, may depend on the exact physiological conditions. Reportedly, HIF-1α upregulation is coupled to a reduction in zo-1 protein concentration and dislocation of zo-1 from the TJ, which enables redistribution of other TJ proteins, including claudin-1 (13). HIF-1α suppression is correlated with attenuated intestinal barrier dysfunction and morphologic redistribution of TJ proteins zo-1, occludin and claudin-1, triggered by pro-inflammatory cytokines (32). Therefore, HIF-1α may cause small intestinal epithelial barrier damage and hyperpermeability through TJ protein regulation.

Only claudin-1 and claudin-2 were affected by CS exposure in the present study, suggesting that CS selectively affects different TJ components. This selective effect has been previously observed (33). In a side-stream smoking study, increased TJ protein expression and reduced inflammation were observed in the large intestine (34). The divergence between these studies may result from the different smoke simulation methods and variable effect on the different intestinal segments evaluated by the studies.

Increased small intestine apoptosis following CS exposure has also been observed by other groups (35). HIF-1α induces apoptosis through an overexpression of pro-apoptotic proteins at the transcriptional level (36), which bind and inhibit the anti-apoptotic protein bcl-2 (37). Bcl-2 expression is correlated with intestinal damage and TJ breakdown (38). However, it is unclear whether intestinal cell apoptosis is the primary event associated with CS or whether it is induced indirectly by HIF-1α. Cell apoptosis can be induced by oxidative stress, which may impair intestinal epithelial integrity and TJs. ROS-induced damage represents an essential mechanism contributing to the TJ barrier defect (9). The antioxidant enzyme SOD is the first line of tissue defense against ROS. SOD expression increased in the rat small intestine following CS exposure in the present study, in line with a previous study (39). This may indicate a decreased radical-scavenging ability of the intestine following smoke exposure, increasing gut susceptibility to oxidative damage. In addition, the NADPH oxidase subunits, nox2 and p22phox, are elevated in the CS intestine; NADPH oxidase is potentially a source of ROS in CS exposure. Notably, COPD development is associated with NADPH oxidase increase (40), and this same redox status may occur in the small intestine in patients with COPD. Future analysis of intestinal protein expression using western blotting or immunohistochemistry is required to confirm this hypothesis.

In conclusion, CS exposure elevates oxidative stress, apoptosis and TJ component dysregulation, potentially mediated by HIF-1α. These data provide new insight into the mechanisms behind cigarette smoke and associated intestinal mucosal disruption in COPD patients.

Acknowledgments

This study was supported by the Natural Science Foundation of Tianjin City (13JCYBJC22400 and 13JCYBJC40000) and the National Natural Science Foundation of China (81270144).

References