Original Research ARTICLE
CML/RAGE Signal Bridges a Common Pathogenesis Between Atherosclerosis and Non-alcoholic Fatty Liver
- 1Department of Cardiology, Affiliated Hospital of Jiangsu University, Zhenjiang, China
- 2Department of Burn Surgery, Affiliated Hospital of Jiangsu University, Zhenjiang, China
- 3Department of Internal Medicine, Affiliated Hospital of Wuxi Maternity and Child Health of Nanjing Medical University, Wuxi, China
- 4Department of Pathology, Affiliated Hospital of Jiangsu University, Zhenjiang, China
Non-alcoholic fatty liver disease (NAFLD) has become a common chronic disease in the world. NAFLD is not only a simple intrahepatic lesion, but also affects the occurrence of a variety of extrahepatic complications. In particular, cardiovascular complications are particularly serious, which is the main cause of death in patients with NAFLD. To study the relationship between NAFLD and AS may be a new way to improve the quality of life in patients with NAFLD. As we all known, inflammatory response plays an important role in the occurrence and development of NAFLD and AS. In this study, we found that the accumulation of Nε-carboxymethyllysine (CML) in the liver leads to hepatic steatosis. CML can induce the expression of interleukin (IL-1β), interleukin (IL-6), tumor necrosis factor (TNF-α), C-reactionprotein (CRP) by binding with advanced glycosylation end-product receptor (RAGE) and accelerate the development of AS. After silencing RAGE expression, the expression of pro-inflammatory cytokines was inhibited and liver and aorta pathological changes were relieved. In conclusion, CML/RAGE signal promotes the progression of non-alcoholic fatty liver disease and atherosclerosis. We hope to provide new ideas for the study of liver vascular dialogue in multi organ communication.
With economic development, improvement in living standards, the prevalence of a high-fat, high-calorie diet, the acceleration of life and the prevalence of a lifestyle of less movement and more sitting, the prevalence of non-alcoholic fatty liver disease (NAFLD) is increasing (1, 2). NAFLD refers to excessive fat deposition in the liver in the absence of ethanol and other clear causes. The main characteristics of this disease are accumulation and diffuse fatty degeneration of hepatocytes (3, 4). NAFLD is the most common chronic liver disease (4, 5), and NAFLD has become a worldwide public health problem that endangers human health. According to statistics, the global prevalence of NAFLD has reached 25.2% (6). NAFLD has no obvious symptoms in the early stage, and liver fat infiltration of 30% or more can be diagnosed by liver ultrasound (7–9). As NAFLD is difficult to diagnose and its prevalence is likely to be underestimated.
As early as 1950, researchers found that NAFLD is associated with Atherosclerosis (AS) (10). NAFLD and AS often share common pathogenic factors. Exploring its common pathogenic factors not only inhibits the occurrence of NAFLD, it may even protect NAFLD patients from AS (11, 12).
At present, the “second strike” hypothesis is widely accepted regarding the pathogenesis of NAFLD, which is mainly caused by excessive lipid accumulation in the liver and oxidative stress caused by lipid peroxidation (13). Lipid peroxidation induces inflammation in the liver and promotes the formation of advanced glycation end products (AGEs) (14–17). Once AGEs are formed, they are difficult to degrade and accumulate in the body with age. Nε-carboxymethyllysine (CML) is the most important active center of AGEs (18). By binding with its receptor for AGEs (RAGE), it destroys cell antioxidant defense and the production of ROS (19). CML activate the receptor RAGE to cause cell activation and increase the production of pro-inflammatory cytokines (such as IL-1β, IL-6, TNF-α, CRP), leading to the occurrence of various diseases (20–22). Our previous research found that CML/RAGE signaling plays an important role in the development of AS (23). CML-RAGE interaction can change the role of the endothelial barrier, increase the permeability of endothelial cells, and destroy the normal function of vascular endothelial cells (24). CML-RAGE also promotes smooth muscle cells to take up excessive cholesterol and induces the formation of vascular smooth muscle cell-derived foam cells (25). Eventually promote the formation and progression of AS.
Liver is an important metabolic center of AGEs in the body (26). Existing research shows that AGEs research has found that AGEs have a significant effect on liver cells, such as promoting the release of pro-inflammatory cytokines and participating in the formation of liver fibrosis. We hypothesized that CML/RAGE signaling may be a common risk factor for the development of NAFLD and AS.
In this study, we collected liver biopsies from atherosclerotic patients, and used an in vivo model to explored the role of CML/RAGE in the development of NAFLD and AS.
Liver biopsy specimens of 80 individuals undergoing liver biopsy were collected from the affiliated hospital of Jiangsu University (The clinical baseline data in Supplementary Table 1). Liver biopsies were fixed in formalin and embedded in paraffin. We divided the patients into 4 groups according to the degree of steatosis:control group (no steatosis or steatotic liver cells <5%) the low steatosis group (steatotic liver cells 5–33%); the moderate steatosis group (steatotic liver cells 33–66%); and the severe steatosis group (steatotic liver cells> 66%).
1. Age: 40–75 years;
2. Voluntarily undergo liver biopsy and sign the consent form.
1. Drinking history (daily alcohol intake: female <20 g/d, male <30 g/d);
2. Viral hepatitis, drug-induced liver disease, total parenteral nutrition, hepatolenticular degeneration, autoimmune liver disease and other specific diseases that can cause fatty liver;
3. Excluded drugs (amiodarone, tamoxifen, sodium valproate, glucocorticoid, methotrexate, etc.), total parenteral nutrition, inflammatory bowel disease, hypothyroidism, etc. Special conditions of fatty liver;
4. History of infection or tissue damage in the last 1 month;
5. A history of malignant tumors or autoimmune diseases; and a history of liver transplant surgery.
Six-week-old ApoE−/− mice on a C57BL/6J background were purchased fromurchased from Cavens (Changzhou, China), Animals are kept in the barrier system of Jiangsu University Laboratory Animal Research Center. All animal experiments were approved by Institutional Animal Care and Use Committee of Jiangsu University. 1012 DNAse-resistant particles of adeno-associated viral (AAV) vectors consisting of AAV-shscramble (as a control group), AAV-shRAGE (Han HengBiological Technology Co., Ltd. Shanghai China) solution was injected into mice via the tail vein. 3 weeks after AAV injection, the high-fat diet (HFD) was introduced. Inject CML (10 mg/kg/day) into the tail vein of mice. The mice were randomly divided into 5 groups: control group (normal diet); model group (high-fat diet); CML group (high-fat diet+CML 10 mg/kg/d), AAV-shscramble group (high-fat diet +CML 10 mg/kg/d+AAV-shscramble); AAV-shRAGE group (high-fat diet +CML 10 mg/kg/d+AAV-shRAGE). Observe the pathological changes of the liver and aorta at 4, 8, 16 weeks after CML injection. Blood samples were collected through the tail vein at 16 weeks. After the mice were euthanized, the abdominal cavity and chest cavity were opened, liver tissues were removed, and the liver wet weight was accurately weighed to calculate the liver index. The liver index was calculated as follows: liver index = wet liver weight (g)/body weight (g).
The levels of total cholesterol (TC), triglyceride (TG), low-density lipoprotein (LDL-C), high-density lipoprotein (HDL-C), alanine aminotransferase (ALT), aspartate aminotransferase (AST) were measured by automatic biochemical instrument.
Paraffin sections were dewaxed, rehydrated and boiled in citric acid buffer for 10 min for antigen repair. The sections were blocked with 5% goat serum at room temperature for 1 h. Human liver samples were incubated with CML antibody (Abcam, 1:200) and RAGE antibody (Abcam, 1:200). ApoE−/− mice liver and aorta samples were incubated with RAGE antibody (Abcam, 1:200) overnight at 4°C. Then, we used a rabbit and mouse HRP kit (Conway, China Century Biotechnology Co., Ltd.) sample was photographed under a microscope.
The aorta and liver tissue were fixed in 4% formaldehyde buffer and then embedded in paraffin. Paraffin embedded tissue was cut into 5 μm thick sections and stained with hematoxylin and eosin. The stained samples were photographed under a microscope.
Oil Red O Staining
Frozen sections of mice liver were fixed with 4% paraformaldehyde for 1 h and washed with isopropanol 3 times (15 s each time). Then, the slices were dyed in oil red O working solution (3 oil red O stock solution: 2 distilled solution) for 30 min and washed in isopropanol 3 times. The stained samples were photographed under a microscope.
Detection of Gene Expression by Real-time Quantitative PCR
Total RNA was extracted from the mice liver and aorta using TRIzol reagent (Invitrogen, Carlsbad, CA, USA). The RNA concentration was determined by measuring the optical density at 260 and 280 nm. Then, the RNA was reverse transcribed into cDNA. Real-time PCR was performed using primers for mice IL-1β, IL-6, TNF-α, CRP, and β-actin (synthesized by Sangon). The primer sequences are detailed in Supplementary Table 1. The RT-PCR reaction conditions were as follows: 94°C for 1 min, followed by 33 cycles at 94°C for 30 s, 63°C for 30 s, and 72°C for 1 min, and a final extension at 72°C for 7 min.
All data are expressed as mean ± SD.SPSS 25.0 was used for analysis. The multiple groups were compared using a one-way analysis of variance and between two groups by Student's t-test analysis. p < 0.05 was considered statistically significant.
CML Accumulation in Liver Tissue of Patients With Non-alcoholic Fatty Liver
We performed liver biopsies on 80 individuals in the affiliated hospital of Jiangsu University. The degree of fatty degeneration of the liver was divided into four groups according to H&E staining (Figure 1A). To investigate whether CML accumulates in the liver, we performed immunohistochemical staining. We observed no obvious CML staining in the liver tissue of the control group (Figures 1A,B). With steatosis of the liver, CML staining gradually increased. We detected the expression of the CML receptor RAGE by immunohistochemistry and found that RAGE was significantly expressed on the steatotic liver cell membrane (Figures 1A,C). We hypothesize that liver steatosis may be related to CML accumulation and CML may play a role in inducing liver inflammation by binding with RAGE.
Figure 1. CML accumulation in liver tissue of patients with non-alcoholic fatty liver (A). First row: Liver biopsy H&E (×200). Second and third row: immunohistochemistry shows the expression of CML (×200) and RAGE (×400) (B). Percentage of CML-positive immunohistochemical staining area (C). Percentage of RAGE-positive immunohistochemical staining area. The proportion of the positive area to the total liver area was calculated by ImageJ. All data are expressed as the means ± SEM. *P < 0.05, compared to control group.
CML Promotes High Fat-Induced Liver Steatosis and Intravascular Plaque Formation in ApoE-/- Mice
The pathological changes of liver and aorta of ApoE−/− mice were detected by H&E staining in 4 and 8 weeks (Figure 2). At the time of 4 weeks, the hepatocytes were arranged in a radial pattern, hepatocytes were uniform in size, the nucleus was centrally distributed, thickness of the vascular intima was uniform, and the endoplasm was neatly arranged in the control group. In the model group, hepatocytes showed balloon-like degeneration, hepatocytes were uneven in size, the nucleus shifted to one side, and the vascular endoplasmic arrangement was disordered, the thickness of intima and media was uneven. In the CML group, hepatocytes were larger in size, with obvious balloon-like degeneration of hepatocytes and the thickness of intima and media increased, and a large number of monocytes gathered (Figure 2A). At the time of 8 weeks (Figures 2B,C), the fatty degeneration of liver cells in mice was further aggravated, and foam cells and fibrous plaques can be seen under the vascular intima, which protrude into the lumen, and the basement membrane is destroyed. After CML intervention, the mice liver steatosis and severe changes in aortic plaque compared with the model group.
Figure 2. CML promotes high fat-induced liver steatosis and intravascular plaque formation in ApoE−/− mice (A,B). At the time of 4, 8 weeks, ApoE−/− mice liver (×200) and aorta H&E staining (×100) (C). Image J analyzes plaque area.*P < 0.05, compared to control group; #P < 0.05, compared to model group.
All ApoE−/− mice were euthanized after 16 weeks. By observing the general picture of mice liver (Figure 3A), we found that compared with the control group, the liver volume of the model group was significantly increased (P < 0.05), and the liver surface was greasy. Under CML stimulation, there was no significant change in liver volume (P > 0.05), but the liver color was pale, which we speculated may be related to lipid deposition. To prove this idea, we calculate the liver index (Figure 3B). We found that the liver indices of the mice under CML interventions significantly increased compared with the control group (P < 0.05), but there was no significant difference in body weights (P > 0.05) (Figure 3C). The formation of NAFLD is accompanied by disorders of lipid metabolism and liver damage. Therefore, we measured the levels of TC, TG, LDL-C, HDL-C, AST, and ALT in the serum (Figure 4). After CML intervention, the level of TC, TG, LDL-C, AST, and ALT were significantly higher (P < 0.05), But the level of HDL-C is obviously reduced compare with the control group (P < 0.05).
Figure 3. Effect of CML on liver lipid accumulation (A). Observation of overall liver morphology (B). Liver body mass indexin ApoE−/− mice (C). ApoE−/− mice body weight and wet liver weight. *P < 0.05 compared with control group; #P < 0.05 compared with model group.
Figure 4. Observe the effect of 16 weeks CML on related biochemical indexes of ApoE−/− mice (A). Total cholesterol (TC), Triglyceride (TG) (B). Low-density lipoprotein (LDL-C) and high-density lipoprotein (HDL-C) (C). Aspartate aminotransferase (AST) (D). Alanine aminotransferase (ALT) levels were measured using an automatic biochemical analyzer. All data are expressed as the means ± SEM. *P < 0.05, compared with control group; #P < 0.05, compared with model group.
H&E and Oil Red O staining were used to observe the liver pathological changes in the mice (Figures 5A,B). The control group showed normal structures in the liver, without obvious lipid droplet infiltration. After CML intervention, the liver tissue structure was unclear, and typical vacuole-like steatotic cells and red spherical lipid droplets formed. CML effectively induces the formation of NAFLD. Then observe the pathological changes of the aorta by H&E staining and Masson staining (Figures 5A,C). There was no obvious plaque formation in the control group. In the model group showed plaque protruding into the lumen. However, CML group had a significantly larger plaque area in the vascular lumen, a large amount of cholesterol crystals, a weak fiber cap, and poor plaque stability.
Figure 5. Pathological changes of liver and aorta after ApoE−/− mice at the time of 16 weeks (A). First row: H&E staining of ApoE−/− mice liver (×200). Second row: Oil Red O staining of ApoE−/− mice liver (×400). Third row: H&E staining of ApoE−/− mice aorta (×100). Fourth row: Masson staining of liver aorta in ApoE−/− mice (×100). (B). Total cholesterol content in ApoE−/− mice liver (C). Quantification of vascular plaque area by Image J. *P < 0.05, compared with control group; #P < 0.05, compared with model group.
CML Promotes the Expression of Pro-inflammatory Cytokines in the Liver and Blood Vessels of ApoE-/- Mice
To investigate whether the pathogenic role of CML in the liver and aorta is related to inflammation, we examined the expression of IL-1β, IL-6, TNF-α, CRP mRNA in the liver and aorta. We found that IL-1β, IL-6, TNF-α, CRP mRNA expression increased by 1.68, 2.0, 1.85, 2.51 times in liver tissues respectively compared with the control group (Figure 6), while IL-1β, IL-6,TNF-α CRP mRNA expression increased by 1.32, 1.87, 1.19,1.61 times in aorta (Figure 6).
Figure 6. CML promotes the expression of pro-inflammatory cytokines in liver and blood vessels of ApoE−/− mice (A–D) Detection of IL-1β, IL-6, TNF-α, CRP mRNA expression levels in liver and aorta by PCR. *P < 0.05, compared with control group; #P < 0.05, compared with model group.
CML Promotes the Expression of Pro-inflammatory Cytokines by RAGE
Inflammatory cell infiltration in liver and aorta were observed by H&E staining (Figure 7). There was no significant inflammatory cell infiltration in the control group. In the model group, infiltration of inflammatory cells in liver tissue and aortic plaques can be observed. However, after CML intervention, the inflammatory cell infiltration in the liver tissue and aortic plaques were significantly aggravated, focal necrosis of hepatocytes was observed. After silencing the expression of RAGE, the inflammatory cell infiltration in the liver tissue and aortic plaques were significantly reduced. To detect whether CML promotes the expression of pro-inflammatory cytokines by upregulating the expression of RAGE, we used CML combined with AAV treatment (AAV-shRAGE and AAV-shscramble). Immunohistochemistry and quantification showed that RAGE expression did not change significantly after the injection of AAV-shscramble. AAV-shRAGE significantly downregulated the expression of RAGE (Figures 8A,B,G,H). We measured the expression of IL-1β, IL-6, TNF-α, and CRP mRNA in the liver and aorta (Figures 8C–F). The results showed that the levels of IL-1β, IL-6, TNF-α, and CRP mRNA in liver and aorta were significantly lower in the AAV-shRAGE group compared with the CML group (P < 0.05). This may be related to silencing the expression of RAGE down-regulating the expression of pro-inflammatory cytokines.
Figure 7. CML increases the density of inflammatory cells infiltrating the plaque and liver (A) H&E staining of ApoE−/− mice liver (×200) (B) H&E staining of ApoE−/− mice aotra plaque (×200). The red arrow points to the location of inflammatory cell infiltration.
Figure 8. After AAV injection, the expression of RAGE in liver and aorta changed (A) and (B) Immunohistochemistry shows the expression of RAGE (×400). (C–F) Detection of IL-1β, IL-6, TNF-α, CRP mRNA expression levels in liver and aorta by PCR (G,H) Percentage of RAGE positive immunohistochemical staining area. The proportion of the positive area to the total Liver area was calculated by ImageJ. *P < 0.05, compared with normal control group; #P < 0.05, compared with model group;&P < 0.05, compared with CML group.
At present, there is a high prevalence of NAFLD in the world, which has attracted increasing attention. NAFLD includes a series of diseases, from simple fatty liver to non-alcoholic steatohepatitis (NASH), which may develop into liver cirrhosis or even liver cancer (27). Studies have shown that in the past 10 years, NAFLD has been associated with liver related incidence rate or mortality (28, 29). But most of NAFLD deaths are due to AS (30–33). In recent years, researchers have found that NAFLD may be the cause of AS, indicating that the relationship between NAFLD and AS is bidirectional or both diseases are caused by a common pathogenic link (34–37). Therefore, it is very important to find the common pathogenic factors between them.
Abnormal lipid metabolism is the basis for the occurrence of AS. Hyperlipidemia can directly cause endothelial cell dysfunction, increase the permeability of endothelial cells, and provide a basis for lipid deposition on the vascular inner membrane and platelet adhesion (38). Therefore, lipids Metabolic abnormalities are believed to be related to the acceleration of the progression of AS. As early as 1998, Professor ROSS proved that AS is a chronic persistent inflammatory disease (39). The development process of AS can be divided into lipid streak stage, fibrous plaque stage, atheroma stage, unstable plaque stage, plaque rupture and thrombosis stage. In the different development stages of AS, AS is always accompanied by inflammatory reactions (40). IL-1β, CRP, TNF-α, and IL-6 are commonly used indicators to assess the risk of cardiovascular events (41, 42). These pro-inflammatory cytokines are also closely related to the occurrence and prognosis of NAFLD disease (43, 44). Therefore, regulating lipids and inhibiting inflammation have become an important way to combat AS in recent years. Increased fatty liver inflammation is a sign of the progression of NAFLD, therefore, inhibiting inflammation damage is also an important way to prevent and treat NAFLD (45).
Studies have found that NAFLD is formed during the occurrence and development of AS and can promote the development of AS (46). The main mechanism may be that the formation of NAFLD causes the body to be in a chronic inflammatory state for a long time, promotes the release of pro-inflammatory cytokines, leads to damage to the endothelial cells of the vascular intima, and accelerates the formation of atherosclerosis (47–49). The blood lipid metabolism disorder of NAFLD patients is manifested by plasma hypertriglyceridemia, increased low-density lipoprotein and decreased high-density lipoprotein levels, which also contribute to the development of AS (50).
In our clinical study, we found that CML aggregation in liver tissue of NAFLD patients, with the progress of liver steatosis, the expression of CML significantly increased. Therefore, we hypothesized that CML participated in the development of NAFLD, to explore the relationship between CML and non-alcoholic fatty liver and atherosclerosis. We established an in vivo model of ApoE−/− mice and monitored the liver and vascular lesions at 4, 8, and 16 weeks respectively. It was found that the fatty degeneration of the liver and the change of the plaque in the aorta gradually increased with the change of time. Moreover, fatty degeneration of liver occurs earlier than atherosclerosis.
NAFLD is a disease characterized by dyslipidemia and impaired liver function (51). Hyperlipidemia is an important risk factor for fatty liver formation. 20–92% of patients with hyperlipidemia have fatty liver (52). NAFLD is not only the excessive deposition of liver fat, but also the damage of liver cell function. AST and ALT in serum were commonly used as indexes to measure the function of hepatocytes (53). After 16 weeks of experimental intervention, serum related biochemical indexes and morphological changes of liver were detected. We found that the serum TG, TC, LDL-C, ALT, AST levels increased and HDL-C levels decreased in the model group after 16 weeks of continuous high fat feeding. The model of mice NAFLD was established successfully, and obvious plaque formation was found in the vascular lumen. After CML stimulation, the lesions of mice non-alcoholic fatty liver were aggravated and the plaque was more unstable. This confirms our hypothesis that CML is the link of NAFLD and AS.
How CML mediates the pathogenesis of NAFLD and AS has attracted our attention. In clinical trials, we found that in the liver samples of NAFLD, RAGE staining was stronger and positively correlated with fatty liver degeneration. Studies have shown that RAGE is an important receptor for CML, which is difficult to clear after binding to its receptor and can activate multiple signal cascades, target genes that regulate the inflammatory response (54). Excessive inflammation is not only a sign of the progression of NAFLD to Non-alcoholic steatohepatitis (NASH) but also an important influencing factor of as progress (55–57). In vivo study, we found that after CML stimulation, significant infiltration of inflammatory cells and focal necrosis were observed in liver tissue. This may indicate that CML can promote the progression of NAFLD to NASH.
The expression levels of RAGE and pro-inflammatory cytokines IL-1β, IL-6, TNF-α, CRP in liver and aorta were significantly increased after CML stimulation. In this study, when RAGE was silenced, the expression level of pro-inflammatory cytokines was down regulated, which significantly alleviated the pathological changes of NAFLD and AS. This finding indicates that CML is responsible for the up-regulation of pro-inflammatory cytokines by up-regulating RAGE expression.
In this study, we confirmed that the activation of CML/RAGE signal leads to an imbalance in pro-inflammatory cytokine expression mediates the development of NAFLD and AS. Inhibition of CML/RAGE signal in liver can inhibit the occurrence of NAFLD and delay the progression of AS. It is hoped that our findings could provide a worthwhile intervention target for the treatment and prevention of AS in NAFLD.
Data Availability Statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
The animal study was reviewed and approved by Institutional Animal Care and Use Committee at Jiangsu University. Human studies conform to the principles outlined in the Declaration of Helsinki (1964) and was approved by the Ethical Committee of the Affiliated Hospital of Jiangsu University. All patients agreed and signed informed consent before enrollment.
QP designed experimental ideas, completed experiments, and analyzed data. ZW provided suggestions for experimental design. ZB and ZS assisted the analysis of experimental data. LZ and LJ assisted in collecting clinical data. LL assisted in preparing sections and assessing the degree of liver tissue lesion. CS, HC, and LW supervised the experiment and read and approved the final draft. QP completed the manuscript with the help of everyone. All authors are involved in experimental research.
This work was supported as follows: the National Natural Science Foundation of China (81770450, 81370408); the related Foundation of Jiangsu Province (WSN-044, LGY2018092, QNRC2016836); Postgraduate Research & Practice Innovation Program of Jiangsu Province (SJKY19_2585, KYCX20_2881); Zhenjiang Cardiovascular Clinical Research Center Project (SS2018008).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2020.583943/full#supplementary-material
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Keywords: atherosclerosis (AS), non-alcoholic fatty liver disease (NAFLD), Nε-carboxymethyllysine (CML), advanced glycosylation end-product receptor (RAGE), pro-inflammatory
Citation: Pang Q, Sun Z, Shao C, Cai H, Bao Z, Wang L, Li L, Jing L, Zhang L and Wang Z (2020) CML/RAGE Signal Bridges a Common Pathogenesis Between Atherosclerosis and Non-alcoholic Fatty Liver. Front. Med. 7:583943. doi: 10.3389/fmed.2020.583943
Received: 16 July 2020; Accepted: 07 October 2020;
Published: 06 November 2020.
Edited by:Chao Yan, Xuzhou Medical University, China
Reviewed by:Giuseppe Losurdo, University of Bari Medical School, Italy
Yuncheng Lv, Guilin Medical University, China
Copyright © 2020 Pang, Sun, Shao, Cai, Bao, Wang, Li, Jing, Zhang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Zhongqun Wang, firstname.lastname@example.org