Snail1 is positively correlated with atrial fibrosis in patients with atrial fibrillation and rheumatic heart disease
- Authors:
- Published online on: August 31, 2017 https://doi.org/10.3892/etm.2017.5084
- Pages: 4231-4237
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Copyright: © Guo et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Atrial fibrillation (AF) is becoming more common in patients with cardiovascular diseases, including rheumatic heart disease (RHD), hypertension, coronary heart disease, congenital heart disease, cardiomyopathy and pericardial disease (1). Atrial fibrillation can severely affect human health; rapid ventricular rates may result in the development of fatal malignant arrhythmia, such as ventricular fibrillation (1). Another condition induced by AF is mural thrombus, which may lead to the development of major adverse cardiovascular events, including acute myocardial infarction and stroke (2). Previous studies have demonstrated that atrial structural remodeling occurs during the onset and development of atrial fibrillation, which leads to a dilated left atrium and a decline in left ventricular ejection fraction (3–7). However, preventing or improving myocardial fibrosis may significantly reduce the left atrial diameter (LAD) and improve cardiac function in patients with AF (4,5,8). Therefore, blocking atrial fibrosis may be a better way of preventing the development and deterioration of atrial fibrillation.
Atrial fibrosis is mediated by cardiac fibroblasts, which can be transferred from local static cardiac fibroblasts, epithelial cells and bone marrow stem cells under pathological conditions, such as ischemic injury, anoxic injury and the stimulation of TGF-β (2,9). Previous studies have demonstrated that epithelial and endothelial cells can be transformed into fibroblasts in a process known as the epithelial mesenchymal transition (EMT), which serves important roles in pulmonary fibrosis, renal fibrosis, cardiac hypertrophy and cardiac fibrosis (10–14). Snail1 is an important regulator and specific marker of the EMT and contributes to the formation of many tissues during embryonic development and to the acquisition of invasive properties during epithelial carcinoma (15). It was determined that Snail1 may be activated in the myocardium following myocardial infarction and that it moves from the endothelium to the mesenchymal cells of the coronary artery, reflecting the progression of the EMT (16). Therefore, it is hypothesized that the EMT may be one of the mechanisms involved in the occurrence and development of atrial fibrosis, and inhibiting the activity of Snail1 may attenuate the EMT in patients with atrial fibrillation and therefore improve the symptoms of atrial fibrosis. Wnt signaling serves an important role in organ fibrosis, which is also involved in renal fibrosis, lung fibrosis and liver fibrosis (17–19). However, it remains unclear whether Wnt signaling participates in the atrial fibrosis activated by EMT that occurs in AF. Therefore, the current study aimed to investigate the association between Snail1 and atrial fibrosis in patients with AF and RHD.
Materials and methods
Patients
Patients with RHD aged 30–60 years old planning to receive heart valve replacement surgery who were admitted to the Department of Cardiovascular Surgery, Renmin Hospital of Wuhan University (Wuhan, China) between June 2015 and April 2016 were recruited in the current study. Cardiac function was ranked between Class I and Class III using the New York Heart Association Functional Classification (1). Patients with coronary atherosclerotic heart disease, chronic pulmonary heart disease, infective endocarditis, hyperthyroidism, serious liver, kidney or lung dysfunction, or malignant tumor were excluded from the current study. Patients taking drugs that could attenuate ventricular remodeling, including angiotensin converting enzyme inhibitors, angiotensin-receptor blockers, β-receptor blockers and spironolactone were also excluded. Following an initial evaluation, 19 patients (10 males and 9 females) were enrolled in the current study. These patients were divided into two groups: An AF group (n=10) and a sinus rhythm (SR) group (n=9). The general clinical characteristics of the patients are presented in Table I. The present study was approved by the Ethics Committee of Renmin Hospital of Wuhan University (Wuhan, China) and samples were obtained following the regulations of Renmin Hospital of Wuhan University. All patients provided written informed consent prior to their inclusion in the current study.
Reagents
Primary antibodies against Snail1 (cat. no. 125918) were purchased from GeneTex, Inc. (Irvine, CA, USA). Primary antibodies against Wnt1 (ab85060), Wnt8a (ab130930), phosphorylated glycogen synthase kinase 3β (P-GSK3β; ab130937) and GAPDH (ab37168) were obtained from Abcam (Cambridge, UK). Primary antibodies against Wnt3a (bs1700R) and Wnt5a (bs1948R) were purchased from BIOSS (Beijing, China). The primary antibody against Wnt11 (sc50360) was purchased from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA). Antibodies against β-catenin (BA0426) and β-actin (BM0627) were obtained from Wuhan Boster Biological Technology, Ltd. (Wuhan, China). The antibody against GSK3β (22104-1-AP) was purchased from Wuhan Sanying Biotechnology (Wuhan, China). The bicinchoninic acid (BCA) protein assay kit was purchased from Beyotime Institute of Biotechnology (Haimen, China). TRIzol (252250AX) was obtained from Aidlab Biotechnologies Co., Ltd. (Beijing, China). M-MLV Reverse Transcriptase (RNase H; CO2010A) and ddH2O (DNase/RNase Free; C1D230A) were purchased from GeneCopoeia, Inc. (Rockville, MD, USA) and RNase Inhibitor (I21222) was obtained from TransGen Biotech, Inc. (Beijing, China).
Human myocardium sample collection
All patients underwent heart valve replacement surgery, during which time ~200 mg right atrium tissue was collected from each patient. Each sample was divided into two sections. One section was rapidly placed into a liquid nitrogen container and then placed in a refrigerator at −80°C; the other section was washed with saline solution and subsequently soaked in 4% paraformaldehyde solution under the room temperature for pathological analysis.
Hematoxylin and eosin (H&E) staining
H&E staining was used to detect morphological changes in atrial myocytes. Right atrium tissues were fixed in 4% paraformaldehyde solution at room temperature for at least 24 h and embedded in paraffin wax. Sections 4-µm thick were placed on clean, positively-charged microscope slides. Following drying, the slides were heated at 60°C. Following deparaffinization and rehydration, the slides were washed, stained with hematoxylin for 7 min, differentiated with 0.3% acid alcohol, rinsed in Scott's tap water substitute, stained with eosin for 2 min and then dehydrated, cleared and mounted. All the above experiments were performed at room temperature. A light microscope was used to visualize slides.
Masson's staining
Masson's staining was conducted to determine the collagen deposition of interstitial and perivascular in atrial myocardium. Following deparaffinization and rehydration, the slides were washed and re-fixed in Bouin's solution for 1 h at 56°C to improve staining quality. Slides were then stained with Weigert's iron hematoxylin for 5 min, stained in Biebrich scarlet-acid fuchsin solution for 8 min and then stained in phosphomolybdic acid solution for 5 min. Slides were subsequently stained with aniline blue solution and differentiated in 1% acetic acid, rapidly dehydrated, cleared in xylene and mounted using resinous mounting medium. All steps of Masson's staining were conducted at room temperature. A blue stain indicated the presence of collagen and a red stain indicated the presence of muscle and cytoplasm. High-magnification light micrographs were captured using light microscopy. Image-Pro Plus 6.0 (Media Cybernetics, Inc. Rockville, MD, USA) was used to determine the collagen volume fraction (CVF).
Immunohistochemistry
Immunohistochemistry was used to measure the deposition of Snail1 in myocardium tissues. Following deparaffinization and rehydration, EnVision™ two-step protocol, the tissue specimens were fixed in 4% formaldehyde solution at room temperature for at least 24 h, embedded in paraffin and sliced at 4 µm thickness. The paraffin was then removed. Bovine serum albumin (BSA) solution (3%; Beijing Solarbio Science and Technology Co., Ltd., Beijing, China) was added to each slide until tissues were covered with BSA solution, and incubated for 30 min at room temperature. Subsequently, the slides were washed to get rid of the blocking solution and the primary antibody against Snail1 (dilution, 1:50) was added for 50 min at room temperature. Following washing with phosphate-buffered saline, horseradish peroxidase-conjugated AffiniPure goat anti-rabbit antibody (cat. no. K5007; Dako; Agilent Technologies, Inc., Santa Clara, CA, USA) was added to the slides for 50 min at room temperature. 3,3′-diaminobenzidine was subsequently added as color reagent until the positive expression of brown-yellow appeared under the microscope (maximum of 10 min). Then hematoxylin was used as a counterstain for 3 min. Slides were then fixed with a neutral gum mount. All experiments in this part were performed at room temperature. A light microscope was used to observe the slides. Brown-yellow expression in myocardium tissue indicated positive expression of Snail1.
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)
The expression of Snail1 was measured using RT-qPCR. Total RNA was isolated from the right atrium tissue using TRIzol reagent. A First Chain Synthesis kit for cDNA (Fermentas; Thermo Fisher Scientific, Inc., Waltham, MA, USA) was used for reverse transcription, according to the manufacturer's protocol. SYBR-Green/Fluorescein qPCR Master mix (2X) (Fermentas; Thermo Fisher Scientific, Inc.) and Ex Taq™ (Takara Bio, Inc., Otsu, Japan) were used for PCR. qPCR was performed on an Illumina-Eco machine (Illumina, Inc., San Diego, CA, USA). The result was normalized against β-actin gene expression. The sequences of all primers used in the current study were as follows: Snail1, forward, 5′-GCACATCCGAAGCCACA-3′ and reverse, 5′-GAGAAGGTCCGAGCACA-3′; β-actin, forward, 5′-AGCGAGCATCCCCCAAAGTT-3′ and reverse, 5′-GGGCACGAAGGCTCATCATT-3′. The reaction conditions were as follows: 50°C for 2 min, 95°C for 10 min, 95°C for 30 sec, 60°C for 30 sec. RT-PCR experiments were performed with 1 g of total RNA, followed by 40 cycles of PCR amplification. The expression levels were quantified using changes in the fluorescence signal through the analysis of the Cq value and standard curve (20); the starting template was quantitatively analyzed with RUO ViiA™ 7 software (Thermo Fisher Scientific, Inc.).
Western blot analysis
Total protein was extracted from the right atrium tissue using radioimmunoprecipitation assay lysis buffer (cat. no. P0013B; Beyotime Institute of Biotechnology). The BCA Protein assay kit was used to determine protein concentration. Denatured protein was loaded and separated using 10% SDS-PAGE and then transferred to a nitrocellulose membrane. Following blocking with 5% non-fat milk for 60 min at room temperature, the membrane was incubated with primary antibodies overnight at 4°C. Primary antibodies were as follows: Snail1 (dilution, 1:3,000), Wnt1 (dilution, 1:1,000), Wnt3a (dilution, 1:500), Wnt5a (dilution, 1:500), Wnt8a (dilution, 1:1,000), Wnt11 (dilution, 1:500), GAPDH (dilution, 1:10,000), β-catenin (dilution, 1:200), GSK3β (dilution, 1:2,000), P-GSK3β (dilution, 1:800), β-actin (dilution, 1:200). The following day, the membrane was incubated with HRP-conjugated goat anti-rabbit (cat. no. 074–1506, KPL, Inc., Gaithersburg, MD, USA; dilution, 1:10,000) as secondary antibodies for 2 h at room temperature. The ChemiDoc Touch Imaging System (Bio-Rad Laboratories, Inc., Hercules, CA, USA) was used to detect the protein signals and analysis was conducted using Bandscan 4.3; BioMarin Pharmaceutical, Inc., San Rafearl, CA, USA).
Statistical analysis
Data are expressed as the mean ± standard deviation. Differences between the two groups were analyzed using an unpaired Student's t-test. Linear correlation was applied to analyze the relationship between levels of Snail1 mRNA and CVF by Pearson's correlation coefficient. The value of r represents the correlation between two variables; r>0.5 indicates a positive correlation. Differences between the sex and heart function of two groups were analyzed using Fisher's exact test. Differences between the age, LVEF and LAD of two groups were analyzed using an unpaired Student's t-test. SPSS 19.0 statistical software (IBM Corp., Armonk, NY, USA) was used to perform statistical analysis. P<0.05 was considered to indicate a statistically significant difference.
Results
Patients with AF and RHD exhibit an expanded LAD
All patients participating in the present study received preoperative routine testing, including a blood test, chest X-ray, electrocardiogram and echocardiography. General information about patients was collected and it was determined that there were no significant differences in sex, age, left ventricular ejection fraction and New York heart function classification between the SR and AF groups (Table I). However, compared with the SR group, the patients with AF exhibited significantly expanded LAD (P<0.05; Table I). This indicates that patients with AF and RHD have a larger LAD than patients with SR.
Patients with AF and RHD exhibit expansive atrial myocytes and accumulated collagen
To investigate the effect of AF on atrial structural remodeling, H&E and Masson staining were used to evaluate the extent of myocardial fibrosis (Fig. 1). H&E staining indicated that the size of the myocardial cells in the AF group was greater than those in the SR group (Fig. 1A). Myocardial fibrosis was evaluated by measuring the total amount of collagen in the interstitial spaces of the myocardial tissue and determining the CVF. Compared with the SR group, the AF group exhibited a disorder in the arrangement of interstitial collagen fibers (Fig. 1B). Furthermore, the CVF was significantly higher in the AF group compared with the SR group (P<0.05; Fig. 1C). These results indicate that patients with AF and RHD have expansive atrial myocytes and exhibit extensive collagen deposition in the atrial myocardium.
Elevated Snail1 expression in the atrial myocardium of patients with AF and RHD
To determine the location and expression of Snail1, deposition of Snail1 in the myocardial tissues was measured using immunohistochemistry. The expression of Snail1 mRNA and protein was measured using RT-qPCR and western blotting, respectively. Immunohistochemical staining was performed in tissue sections to determine the distribution of Snail1; the results indicated that Snail1 was primarily distributed in the vascular endothelial and interstitial cells and was almost undetectable in myocardial cells in the AF group. (Fig. 2A). Additionally, levels of Snail1 mRNA and protein in the atrial tissues of patients with AF were significantly higher than those of the SR group (P<0.05; Fig. 2B and C). These data demonstrate that levels of Snail1 are increased in the myocardium of patients with AF and indicate that Snail1 may be involved in the development of atrial fibrosis.
Snail1 is positively correlated with atrial fibrosis in patients with AF and RHD
To determine the association between Snail1 expression and atrial fibrosis, a correlation analysis was performed. A positive correlation was identified between levels of Snail1 mRNA and CVF (r=0.717; P<0.001; Fig. 3). This confirms that there is a positive association between Snail1 expression and atrial fibrosis in patients with AF and suggests that Snail1 may be developed as a novel biomarker to evaluate myocardial fibrosis for patients with AF and RHD in the future.
The Wnt signaling pathway may participate in the process of increased Snail1 expression and atrial fibrosis in patients with AF and RHD
Wnt signaling serves an important role in organ fibrosis, which is involved in renal, lung and liver fibrosis (17,18,21). To determine whether the activity of the Wnt signaling pathway increased Snail1 expression and atrial fibrosis in patients with AF, the expression of proteins involved in the Wnt signaling pathway was investigated (Fig. 4). It was determined by western blotting that, compared with the SR group, the expression of Wnt1, 3a and 8a, which are involved in the canonical Wnt signaling pathway, were significantly increased in the AF group (P<0.05; Fig. 4B). Furthermore, the levels of Wnt5a and Wnt11, which are involved in the noncanonical Wnt signaling pathway, were also significantly higher in the AF group compared with the SR group (P<0.05; Fig. 4B). It was also observed that the phosphorylation levels of GSK3β, as well as the levels of β-catenin, were significantly elevated in the AF group (P<0.05; Fig. 4C). These results indicate that the Wnt signaling pathway, which is associated with the development of EMT, may also contribute to increased Snail1 expression and the development of atrial fibrosis.
Discussion
In the present study, it was determined that the size of myocardial cells was more expansive and the degree of myocardial fibrosis was significantly increased in patients with AF. Additionally, levels of Snail1 mRNA and protein were increased in patients with AF and Snail1 was primarily deposited in vascular endothelial and interstitial cells; expression in Snail1 was low in myocardial cells. Correlation analysis determined that levels of Snail1 mRNA were positively correlated with the degree of atrial fibrosis in patients with AF and RHD. Finally, the expression of factors involved in the canonical (Wnt1, 3a and 8a) and noncanonical Wnt signaling pathways (Wnt5a and 11) were significantly increased in the AF group and the phosphorylation levels of GSK3β and β-catenin were also elevated in the AF group. These results indicate that increased Snail1 expression is positively associated with the degree of atrial fibrosis. Furthermore, they suggest that the Wnt signaling pathway, which is associated with the development of EMT, may also contribute to increased Snail1 expression and atrial fibrosis in patients with AF and RHD.
Atrial fibrosis is the primary process by which atrial structure remodeling occurs and serves a key role in the development and persistence of AF (3). Therefore, attenuating atrial fibrosis to inhibit atrial structure remodeling is crucial to prevent the onset and development of AF. Furthermore, atrial fibrosis is mediated by cardiac fibroblasts and epithelial cells, and endothelial cells can be transformed to fibroblasts during the EMT, which performs important roles in pulmonary fibrosis, renal fibrosis, cardiac hypertrophy and cardiac fibrosis (10–14). Therefore, inhibiting the EMT to attenuate cardiac fibrosis may be an important method of preventing the development of AF.
Snail1 is a member of the Snail family, which is a specific marker of the EMT and serves an important role in tissue fibrosis, including kidney and liver fibrosis (13,16,22–24). It was demonstrated that during liver fibrosis, Snail1 expression is upregulated and that it serves a key role in the progression of liver fibrosis by upregulating the biosynthesis of the extracellular matrix and promoting chronic inflammatory responses (24). Additionally, it was determined that the pattern of Snail1 expression is spatial and temporal and may increase following injuries that occur during fibrogenesis (16,25). In the present study, it was demonstrated that Snail1 expression was markedly increased in the myocardium and that Snail1 was primarily deposited in the vascular endothelial and interstitial cells. Furthermore, it was determined that Snail1 was positively correlated with the degree of atrial fibrosis in patients with AF and RHD. These results indicate that the EMT may serve an important role in the development of atrial fibrosis in patients with AF and RHD.
Additionally, Wnt signaling is one of the most important signaling pathways involved in tissue fibrosis and regulates the adherence and migration of cells (15). It has been demonstrated that Wnt/β-catenin signaling serves an important role in renal and pulmonary fibrosis (17,18). Furthermore, it has been determined that the EMT may be induced by Wnt signaling that is activated by cardiac injury (26). Therefore, the present study also measured changes in the levels of proteins involved in Wnt signaling. It was demonstrated that, compared with the SR group, levels of Wnt1, 3a and 8a involved in the canonical Wnt signaling pathway and levels of Wnt5a and Wnt11 involved in the noncanonical Wnt signaling pathway were significantly higher in the AF group compared with the SR group. Additionally, the phosphorylation level of GSK3β and level of β-catenin were significantly increased in the AF group. It was thus determined that the canonical and noncanonical Wnt signaling pathways were activated in the myocardium of patients with AF. Previous studies have demonstrated that the Snail1-induced EMT occurs, at least in part, due to a decrease in E-cadherin transcription that stimulates the development of epithelial phenotypic cells with adhesive and polarity properties. These cells then gradually transform into loose and activated mesenchymal cells and stimulate the development of tissue fibrosis (22,27). These results indicate that the Wnt signaling pathway is associated with the development of EMT and may participate in the process of increased Snail1 and atrial fibrosis in patients with AF and RHD.
In conclusion, the present study demonstrated that Snail1 may be involved in the development and maintenance of atrial fibrosis in patients with AF and RHD, and that Snail1 may be used as a novel biomarker to evaluate atrial fibrosis in patients with AF and RHD in the future. Furthermore, the Wnt signaling pathway associated with the development of EMT may increase Snail1 expression and atrial fibrosis in patients with AF and RHD. Novel drugs that inhibit the expression and/or function of Snail1, or block the Wnt signaling pathway may prevent atrial fibrosis in patients with AF and RHD. However the sample size of the current study was relatively small and further studies with a larger sample size or involving multiple centers are required to further elucidate this mechanism of action. Future in vitro or in vivo studies are also required to determine how the Wnt signaling pathway regulates Snail1 expression and induces the development of EMT.
Acknowledgements
The authors wish to thank Professors Zhiwei Wang and Jun Xia, who helped out with the sample collection and all doctors in the Department of Cardiology and the Cardiovascular Research Institute of Renmin Hospital of Wuhan University for their expert technical assistance and advice. The present study was supported by grants from the National Natural Science Foundation of China (no. 81170085) and the Fundamental Research Funds for the Central Universities (no. 2042016kf0074).
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