Huijuan Yang1,2†
Hongqi Li3†Weidong Chen1Zhijie Mei4Yuan Yuan2,5Xiaoli Wang2,5Liang Chu6Yu Xu2,5Yan Sun2,5Dingru Li2,5Hongyu Gao2,5
Bin Zhan7
Huihui Li2,5*Xiaodi Yang2,5*- 1Department of Nephrology, First Affiliated Hospital of Bengbu Medical College, Bengbu, China
- 2Anhui Key Laboratory of Infection and Immunity of Bengbu Medical College, Bengbu, China
- 3Department of Gerontology, Anhui Provincial Hospital, First Affiliated Hospital of University of Science and Technology of China, Hefei, China
- 4Department of Urology, First Affiliated Hospital of Bengbu Medical College, Bengbu, China
- 5Basic Medical College of Bengbu Medical College, Bengbu, China
- 6Second Affiliated Hospital of Bengbu Medical College, Bengbu, China
- 7National School of Tropical Medicine, Baylor College of Medicine, Houston, TX, United States
Atherosclerosis is a chronic inflammation of the arterial vessel wall driven by lipid metabolism disorders. Although helminthic infection and their derivatives have been identified to attenuate the chronic inflammatory diseases, the immunomodulatory effect of recombinant Schistosoma japonicum cystatin (rSj-Cys) on metabolic diseases and atherosclerosis has not been reported. In this study, we investigated the therapeutic efficacy of rSj-Cys on atherosclerotic renal damage and explored the related immunological mechanism. The results demonstrated that treatment with rSj-Cys significantly reduced body weight gain, hyperlipidemia, and atherosclerosis induced by the high-fat diet in apoE–/– mice. The treatment of rSj-Cys also significantly improved kidney functions through promoting macrophage polarization from M1 to M2, therefore inhibiting M1 macrophage–induced inflammation. The possible mechanism underlying the regulatory effect of rSj-Cys on reducing atherosclerosis and atherosclerotic renal damage is that rSj-Cys stimulates regulatory T cell and M2 macrophage polarization that produce regulatory cytokines, such as interleukin 10 and transforming growth factor β. The therapeutic effect of rSj-Cys on atherosclerotic renal damage is possibly through inhibiting the activation of TLR2/Myd88 signaling pathway. The results in this study provide evidence for the first time that Schistosoma-derived cystatin could be developed as a therapeutic agent to treat lipid metabolism disorder and atherosclerosis that threats million lives around the world.
Introduction
Atherosclerosis is the chronic process of plaque buildup with deposition of fats, cholesterol, and other substances in and on artery walls, leading to the blood vessel hardened and narrowed and tissue ischemia (Li et al., 2015; Gistera and Hansson, 2017). Eventually, it causes a series of complications with life-threatening consequences, especially in the heart, brain, legs, arms, or kidneys. Atherosclerosis is the major cause of myocardial infarctions and cerebral strokes, as well as kidney failure (Geovanini and Libby, 2018). Since the hypothesis of lipid renal damage was put forward, studies have confirmed that renal damage and lipid metabolism disorders are interconnected and exacerbated by each other. Lipid metabolism disorder is the major cause of atherosclerosis and renal damage (Moorhead et al., 1982; Lu et al., 2019). The obesity, hypertension, and hyperlipidemia are the risk factors for atherosclerosis (van Rooy and Pretorius, 2014; Libby et al., 2019). The prevalence of atherosclerosis is increasing worldwide as a result of the economic development and the adoption of the Western lifestyle (Torres et al., 2015). At present, the pathogenesis of atherosclerosis is not fully understood. It is generally believed that abnormal lipid metabolism, chronic inflammation, oxidative stress, and immune disorder can lead to atherosclerosis (Förstermann et al., 2017; Kattoor et al., 2017; Raggi et al., 2018; Shah, 2019). More evidence demonstrated that atherosclerosis actually is a lipid-driven chronic inflammatory disorder within the arterial wall characterized by the chronic activation of macrophages. Both innate and adaptive immunoinflammatory mechanisms are involved (Taleb, 2016; Geovanini and Libby, 2018). When the arterial epithelia are activated by the oxidized fatty acids such as oxidized low-density lipoprotein (oxLDL), the chemokines and other adhesion molecules are released, leading to monocyte/lymphocyte recruitment and infiltration into the subendothelium (Tedgui and Mallat, 2006). The recruited inflammatory mononuclear phagocytes secreted inflammatory cytokines or matrix proteases that devastate the inflammation and tissue damage in the arterial walls (Binder et al., 2002; Tedgui and Mallat, 2006). The macrophages eventually become lipid-laden foam cells that accumulate in the plaque (Witztum and Steinberg, 1991). However, the immunoinflammatory response in atherosclerosis is modulated by the regulatory pathways in which the two anti-inflammatory cytokines, interleukin 10 (IL-10) and transforming growth factor β (TGF-β), play a critical role. IL-10 has potent anti-inflammatory properties on macrophages (Bogdan et al., 1991) and plays an active role in limiting the inflammatory response in the vessel wall (Tedgui and Mallat, 2001). TGF-β is a potent anti-inflammatory, immunosuppressive cytokine and plays a potential antiatherogenic role (Lutgens and Daemen, 2001). Disruption of TGF-β signaling in T cells exhibited markedly larger atherosclerotic lesions (Robertson et al., 2003).
Recent researches have demonstrated that helminthic and their derivatives modulate the host immune responses as a strategy to survive in the host. These immunomodulatory includes the induction of regulatory T cells (Tregs), anti-inflammatory cytokines, and alternately activated macrophages to reduce host immune response to the parasites to facilitate their survival in the host (Elliott and Weinstock, 2012; van der Vlugt et al., 2012; Wammes et al., 2014; Radovic et al., 2015). Based on this observation, the helminthic infection or helminth-derived products have been widely used to treat chronic inflammation–associated diseases including inflammatory bowel disease (Weinstock et al., 2005; Smith et al., 2007), asthma (Schwartz et al., 2018; Sun et al., 2019), and arthritis (Cheng et al., 2018). Because of the inflammatory property of atherosclerosis, some helminth-derived proteins have been successfully applied to alleviate atherosclerosis. Filarial nematode Acanthocheilonema viteae–secreted ES-82 was able to reduce lupus-associated accelerated atherosclerosis in a mouse model (Aprahamian et al., 2015). Schistosoma mansoni infection and its soluble egg antigens enabled to modulate macrophage inflammatory responses and protected against atherosclerosis in a mouse model (Wolfs et al., 2014). Infection of S. mansoni reduced 50% atherosclerotic lesions in the aortic arch associated with reduced cholesterol level in blood of mice (Doenhoff et al., 2002). Schistosoma japonicum–secreted cystatin (Sj-Cys) is a strong immunomodulatory protein to regulate macrophage activation and inhibit host inflammatory cytokines (Vray et al., 2002) and has been successfully used to treat murine collagen-induced arthritis (Liu et al., 2016), type 1 diabetes (Yan et al., 2020), trinitrobenzene sulfonic acid (TNBS)-induced experimental colitis (Wang et al., 2016), and bacterial sepsis (Li et al., 2017; Gao et al., 2020; Xie et al., 2021). Whether rSj-Cys has therapeutic effect on atherosclerosis and its complications has not yet been reported. In this study, we induced atherosclerosis in apoE–/– mice by feeding them with a high-fat diet (HFD) and observed the therapeutic efficacy of rSj-Cys in reducing atherosclerosis and atherosclerotic renal damage.
Materials and Methods
Ethics Statement
Experimental animals were purchased from the animal center of Bengbu Medical College. All animal experiment protocols were reviewed and approved by the Ethics Committee of Bengbu Medical College (approval no. LAEC-2014-039).
Production of rSj-Cys
DNA-encoding Sj-Cys (GenBank: FJ617450) was amplified from S. japonicum total cDNA and cloned into yeast expression vector pPIC9k. Recombinant Sj-Cys (rSj-Cys) with His-tag at C-terminus was expressed in Pichia pastoris GS115 using the method described previously (Xie et al., 2021). The contaminated endotoxin in the purified rSj-Cys was removed by using a ToxOutTM High Capacity Endotoxin Removal Kit (BioVision, Palo Alto, CA, United States) and confirmed by PierceTM LAL Chromogenic Endotoxin Quantitation Kit (Thermo Fisher Scientific Inc., Waltham, MA, United States). The concentration of rSj-Cys was measured by BCA Protein Quantitation Kit (Beyotime Biotechnology, Shanghai, China). The purity and molecular weight were measured by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE). The purified protein was stored at –80°C until use.
Induction of Atherosclerosis in Mice and Treatments
Male apoE–/– mice (with C57BL/6J background, specific pathogen free) with 7–8 weeks old were purchased from the Animal Center of Bengbu Medical College and housed in a temperature-controlled room with a 12-h light–dark cycle. All mice had ad libitum available for food and water. Total 12 apoE–/– mice were fed with HFD (D12108C: 20% fat, 1.25% cholesterol; Xietong Biotechnology, Nanjing, China) to induce atherosclerosis (Liu et al., 2017); six of them were intraperitoneally treated with 20 μg of rSj-Cys per mouse four times at the first week of HFD feeding and once a week for the following 11 weeks, whereas the other six mice received phosphate-buffered saline (PBS) only at the same regimen. For the control groups, 12 apoE–/– mice were fed with normal control diet (NCD) and divided into two groups; six NCD-mice were intraperitoneally injected with rSj-Cys, and the other six received PBS only at the same regimen as the treated groups. After 12 weeks, all mice were euthanized, and the sera, aortas, and kidneys were collected to evaluate the inflammatory cytokines and pathological changes by histochemical staining (Doenhoff et al., 2002).
Isolation and Stimulation of Murine Peritoneal Macrophages
Peritoneal exudate cells were collected from apoE–/– mice by flushing the peritoneal cavity with 5 mL ice-cold PBS containing 2% fetal bovine serum (FBS; Zhejiang Tianhang Biological Technology, Hangzhou, China). Cells were cultured on a six-well plate (4 × 106 cells/well in 2 mL) at 37°C, 5% CO2 in RPMI 1640 medium containing 10% FBS, 1% penicillin/streptomycin (Beyotime Biotechnology) for 6 h. Non-adherent cells were washed away with PBS, and adherent cells were collected as peritoneal macrophages. The collected peritoneal macrophage cells were stimulated with oxLDL (Yiyuan Biotechnologies, Guangzhou, China) at 50 μg/mL and treated with rSj-Cys (1 μg/mL), or cells without oxLDL were cultured with rSj-Cys or medium only as controls. After 24 h, the secretion of inflammatory cytokines in the culture supernatants were detected by enzyme-linked immunosorbent assay (ELISA) kits [tumor necrosis factor α (TNF-α), IL-6, IL-10 using corresponding kits from Dakewe Biotech, Beijing, China; inducible nitric oxide synthase (iNOS), Arg-1 detection kits from Elabscience Biotechnology, Wuhan, China; and TGF-β kit from ABclonal Biotechnology, Wuhan, China].
Blood Lipid Detection and Renal Function Assay
After the mice were fasted for 8 h, sera were isolated from blood samples of mice and stored at –80°C until use. The total cholesterol (TC) and triglyceride (TG), low-density lipoprotein cholesterol (LDL-c), high-density lipoprotein cholesterol (HDL-c), creatinine (Cr), and blood urea nitrogen (BUN) were measured by an automatic biochemical analyzer (Beckman Coulter, Brea, CA, United States).
Detection of Oxidative Stress in Kidney and Urine Protein
The levels of oxidative stress in kidney were quantified by measuring malondialdehyde (MDA) using the MDA activity assay kit; MDA is one of the final products of polyunsaturated fatty acid peroxidation. The free radicals cause overproduction of MDA; therefore, the level of MDA is used as a marker of oxidative stress and lipid peroxidation (Gaweł et al., 2004). Superoxide dismutase (SOD) activity was measured using an SOD activity assay kit (Beyotime Biotechnology). In brief, renal tissues were homogenized using a homogenizer (Jingxin Experimental Technology, Shanghai, China); the homogenate supernatant was collected by centrifuging at 12,000g for 15 min at 4°C, which was used for measuring MDA at an absorbance 530–540 nm and SOD at 560 nm. The levels of MDA and SOD were standardization to unit weight of total protein content.
On the last day of the 12th week of the experiment, the urine was collected by using metabolic cage and centrifuged at 4,000 revolutions/min for 15 min at 4°C to obtain urine supernatant. Coomassie brilliant blue assay kit (Jiancheng Bioengineering Institute, Nanjing, China) was used to quantify the levels of urine albumin.
Renal and Aortic Histological Analysis and Renal Immunohistochemical Staining
The kidney was collected from each mouse of different experimental groups and fixed with 4% paraformaldehyde. The renal tissue sections were stained with hematoxylin and eosin (HE) and neutral lipids and adipocytes stained with the oil red O staining solution (Servicebio Technology, Wuhan, China). All stained sections were examined at 200× magnification under a microscope (Nikon, Tokyo, Japan).
Heart tissues and the whole aorta were collected from each mouse of different experimental groups. The adipose tissue around the blood vessels was removed as much as possible. The aorta vessel was opened vertically and stained with the oil red O staining solution. The mouse hearts were dissected in order to obtain the aortic sinus stained with the oil red O. The aortic plaque lesion was observed and quantified.
To investigate the phenotypes of macrophages infiltrated in the kidneys, we performed immunohistochemical staining on paraffin sections of kidneys. Briefly, after being dewaxed and blocked with goat serum, the kidney tissue sections were incubated with rabbit anti-CD86 monoclonal antibody (1:300) and rabbit anti-CD206 polyclonal antibody (1:800) (Abcam, Cambridge, MA, United States) overnight at 4°C in a humidified box, followed by the horseradish peroxidase (HRP)–labeled anti-rabbit secondary antibody at room temperature for 50 min, and visualized with 3,3′-diaminobenzidine (ZSbio, Beijing, China). The nuclei were counterstained with DAPI. The sections were dehydrated and examined under microscope with 400 × magnification. Image Pro Plus 6.0 (IPP6.0) software was used for semiquantitative analysis, and the mean density was used to reflect the expression level of CD86 and CD206.
Hemodynamic Analysis
In brief, the experimental mice were anesthetized by inhalation of isoflurane, and the hemodynamic analysis was performed by a high-resolution ultrasound imaging system (Vevo 2100; VisualSonics, Canada). The peak velocity and mean gradient of ascending aorta were measured by color Doppler echocardiography. All measurements were performed for three times at the consecutive cardiac cycles.
Cytokine Profile in Sera and Renal Tissues
The levels of proinflammatory factor (TNF-α, IL-6, iNOS) and immunoregulatory factors (IL-10, TGF-β, Arg-1) were measured in sera of mice using corresponding ELISA kit as mentioned previously. The mRNA expression levels of these cytokines in the renal tissue were analyzed by quantitative reverse transcription–polymerase chain reaction (qRT-PCR) using primers listed in Table 1. Briefly, the total RNAs were isolated from the renal tissues using Trizol reagent (Ambion, Austin, TX, United States), and the cDNAs were synthesized from 2 μg of total RNA by using a reverse transcription kit (Thermo Fisher Scientific Inc.). Total 2 μL cDNA was used as the template in volume of 20 μL for qRT-PCR using the SYBR Green Super Mix Kit (Takara Bio Inc., Tokyo, Japan) and performed in a Roche LightCycler® 96 real-time PCR system (Roche Molecular Systems, Inc., United States). The relative mRNA expression levels of each cytokine in the renal tissue were measured with the comparative △Cq method using the formula 2–△△ Cq normalized to GAPDH.
Table 1. Primer sequences used for qRT-PCR analysis.
Detection of TLR2 and Myd88 in the Renal Tissue by Western Blot
The levels of TLR2 and Myd88 in the renal tissues were measured by Western blot with specific antibodies. Briefly, the total proteins were extracted from the renal tissues, and the concentration was measured by BCA Protein Quantitation Kit. Equal amounts of proteins were separated in 12% SDS-PAGE gel and transferred onto 0.45 μm polyvinylidene fluoride membranes (Macklin Biochemical Co., Shanghai, China). The membranes were blocked with 5% skimmed milk at room temperature for 2 h and then incubated with rabbit anti-TLR2 polyclonal antibody (1:1,500) (Abcam), or rabbit anti-Myd88 monoclonal antibody (1:1,000) (Affinity Biosciences, Cincinnati, OH, United States), or rabbit anti–β-actin polyclonal antibody (1:2,000) (Cell Signaling Technology, Danvers, MA, United States) overnight at 4°C followed by incubation with HRP-conjugated goat anti-rabbit immunoglobulin G (1:5,000) (Biosharp, Hefei, China). The recognized bands were semiquantitatively analyzed by Image Lab System. The results are expressed as ratios of TLR2 and Myd88 to β-actin control.
Flow Cytometry Analysis of CD3+CD4+CD25+FoxP3+ Tregs in the Splenocytes
The splenocytes were isolated from spleens of experimental mice and cultured in RPMI 1640 medium (Thermo Fisher Scientific Inc.). The cell surfaces were blocked with rat anti-mouse CD16/32 antibody for 15 min at 4°C and then incubated with anti-mouse CD3ε-Pecy7, anti-mouse CD4-FITC, and anti-mouse CD25-APC (Biolegend, United States) for 30 min at 4°C in the dark. After being washed and resuspended in 300 μL fixation buffer (Thermo Fisher Scientific Inc.) for 30 min at 4°C and then in 1 mL permeabilization buffer (Thermo Fisher Scientific Inc.) for 30 min at 4°C, the cells were stained with anti-mouse Foxp3-PE (Biolegend) for 30 min at 4°C in the dark. The isotype-matched immunoglobulins (Biolegend, London, United Kingdom) and fluorescence minus one were used as controls for non-specific staining as baseline. The cells were washed three times and resuspended in 400 μL of 2% paraformaldehyde and detected by DxP AthenaTM flow cytometer (CYTEK, United States). All the data were analyzed using FlowJo-V10 software (BD Biosciences, United States).
Statistical Analysis
All data are presented as the mean ± SEM (standard error of the mean), and the statistical analyses were performed using GraphPad Prism 5.0 software (GraphPad Inc., La Jolla, CA, United States). The same parameters in multigroup were compared by using one-way analysis of variance followed by the Student–Newman–Keuls test. p < 0.05 was regarded as statistically significant.
Results
Expression, Purification, and Identification of rSj-Cys
The Sj-Cys protein was successfully expressed as 12-kDa soluble recombinant protein (rSj-Cys) in P. pastoris GS115 under induction of 0.5% methanol. The rSj-Cys with His-tag expressed at the C-terminus was purified using immobilized metal ion affinity chromatography and verified using 12% SDS-PAGE analysis (Figure 1). The endotoxin level kept low (0.06 EU/mL) in the protein.
Figure 1. SDS-PAGE of rSj-Cys. Two micrograms of purified rSj-Cys was separated in 12% polyacrylamide gel.
rSj-Cys Treatment Reduces High-Fat Diet-Induced Body/Kidney Weight Gain in Mice
Four weeks after being treated with 20 μg of rSj-Cys, the body weight of each mouse fed with HFD started to reduce, and the body weight loss became more significant 11–12 weeks after treatment compared to the HFD mice without rSj-Cys treatment (p < 0.01) (Figure 2A). The kidney weight–body weight ratio of HFD-fed mice treated with rSj-Cys was significantly lower than those without rSj-Cys treatment (Figure 2B), indicating that treatment with rSj-Cys not only reduces the body weight gain in mice fed with FHD, but also even more significantly reduces kidney weight. rSj-Cys itself has no effect on the body weight in mice fed with NCD.
Figure 2. rSj-Cys treatment reduced HFD-induced body weight gain in mice. (A) The changes in body weight throughout the experimental period. (B) The changes in the percentage of kidney weight/body weight ratio. The results are shown as the mean ± SEM for each group (n = 6 per group). *P < 0.05, **P < 0.01, ***P < 0.001.
rSj-Cys Reduces the Development of Atherosclerosis and the Histological Damage in Kidney
We measured the development of atherosclerotic plaques on the entire aorta and aortic sinus and quantified the plaque area. The results showed that HFD feeding caused significant atherosclerotic lesions in both aorta and aortic sinus. Treatment with rSj-Cys significantly reduced the atherosclerotic plaques in both aorta and aortic sinus (Figures 3A–C). Kidney histochemical examination demonstrated that fat deposition was obvious in the glomerular structure of mice fed with HFD when stained with oil red O solution (Figure 3D). HE staining showed that the glomerular structure was damaged with inflammatory cell infiltration within renal interstitium in kidneys of mice fed with HFD for 12 weeks (Figure 3E). Treatment with rSj-Cys significantly reduced the fat deposition in kidney and glomerular damage caused by the HFD. There was no obvious oil red O–colored atherosclerotic lesions and renal tissue damage in groups of mice fed with NCD and NCD/rSj-Cys.
Figure 3. rSj-Cys reduced the development of atherosclerosis. (A) Representative oil red O staining of aorta. (B) Representative oil red O staining of the aortic sinus. (C) The plaque area quantified as a percentage of the whole area. (D) rSj-Cys treatment reduced glomerular fat deposition (×200, scale bar 50 μm). (E) Representative HE staining of the renal tissue sections (×200, scale bar 100 μm). The data are shown as the mean ± SEM for each group (n = 6 per group). ***P < 0.001.
rSj-Cys Treatment Alleviates Hemodynamic Disorder in Heart of Mice Fed With High-Fat Diet
The blood flow of the heart was checked by echocardiography in mice 12 weeks after the treatment. As shown in Figure 4A, the peak velocity and mean gradient of ascending aorta in HFD mice were significantly increased compared to the NCD group. rSj-Cys treatment significantly reversed the hemodynamic disturbances caused by HFD (Figure 4B). There was no significant change in the NCD group or group with NCD/rSj-Cys.
Figure 4. Treatment of rSj-Cys improved hemodynamic function. (A) Representative color Doppler ultrasound of the heart. (B) rSj-Cys improves the AV peak velocity and mean gradient of the ascending aorta. The data are shown as the mean ± SEM for each group (n = 6 per group). **P < 0.01, ***P < 0.001.
rSj-Cys Reduces Lipid Level and Improves Renal Function of Mice Fed With High-Fat Diet
As expected, the serum levels of TC, TG, and LDL-c were greatly increased, and the HDL-c level reduced in apoE–/– mice fed with HFD compared to the mice fed with NCD. After being treated with rSj-Cys, the levels of TC, TG, and LDL-c in sera were significantly reduced, and the levels of HDL-c were increased compared to the HFD-fed mice without rSj-Cys treatment (Figure 5A). Feeding with HFD for 12 weeks significantly increased the level of Cr and BUN in sera and the total protein in urine, indicating the renal function was impaired after being fed with HFD; however, treatment with rSj-Cys significantly reduced the levels of Cr and BUN in the sera and the protein level in the urine (Figures 5B,C), indicating that rSj-Cys can regulate lipid metabolism disorders and improve kidney harmed functions.
Figure 5. rSj-Cys reduced the serum lipid levels and improved renal function. (A) The changes of TC, TG, LDL-c, and HDL-c in sera. (B) rSj-Cys reduced the levels of Cr and BUN in sera. (C) rSj-Cys reduced the levels of urine protein. The data are shown as the mean ± SEM for each group (n = 6 per group). **P < 0.01, ***P < 0.001.
rSj-Cys Treatment Suppresses High-Fat Diet-Induced Peroxidation in the Kidney
MDA reflects the degree of lipid peroxidation and SOD as an antioxidant enzyme that protect cells from toxic oxygen metabolites. Feeding with HFD greatly increased the levels of MDA and reduced the level of SOD in kidneys of mice compared to the control mice fed with NCD; however, treatment with rSj-Cys significantly reduced the MDA level and increased SOD level in kidney tissue. There were no significant differences between the NCD group and the NCD treated with rSj-Cys group (Figure 6). The results indicate that treatment with rSj-Cys can reduce MDA levels and increase SOD levels in kidneys of mice fed with HFD, thereby protecting the kidney from lipid peroxidation–caused damage.
Figure 6. The changes of MDA and SOD in the renal tissue after the treatment of rSj-Cys. The data are shown as the mean ± SEM for each group (n = 6 per group). ***P < 0.001.
Treatment With rSj-Cys Reduces M1 Macrophages and Includes M2 Macrophages in Renal Tissue of Mice Fed With High-Fat Diet
As we know, macrophage and its polarization to different phenotypes play an important role in atherosclerotic inflammation and damages (Barrett, 2020). M1 or classically activated macrophages maintain local inflammatory responses, and M2 or alternatively activated macrophages have anti-inflammatory and tissue repair/recovery properties (Colin et al., 2014). We chose CD86 as the marker for M1 macrophages and CD206 as the marker for M2 macrophages. We also performed immunohistochemical staining on the kidney to observe the effect of rSj-Cys on inflammatory cell infiltration induced by HFD. The results showed that CD86+ M1macrophages in the kidney of the HFD-fed group were significantly increased, and the CD206+ M2 macrophages were significantly reduced compared with the NCD group (Figures 7A,B), indicating that feeding with HFD stimulates the M1 macrophage polarization and inflammation in kidney. Treatment with rSj-Cys significantly reduced the expression of CD86+ and increased the expression of CD206+ macrophages in renal tissue (Figures 7A,B), indicating that rSj-Cys stimulates the polarization of macrophages from M1 to M2 and thus reduces the HFD-induced inflammation. There were no significant differences between the NCD group and the NCD with rSj-Cys group on the expression of CD86+ and CD206+ macrophages in renal tissue.
Figure 7. (A) Representative immunohistochemistry staining of CD86+ and CD206+ expression in sections of the kidney from different groups of mice (×200, scale bar 50 μm). (B) rSj-Cys reduced the mean density of CD86+ and increased the mean density of CD206+. The results are shown as the mean ± SEM for each group (n = 6 per group). **P < 0.01, ***P < 0.001.
rSj-Cys Reduces the Oxidized Low-Density Lipoprotein-Induced Inflammatory Responses and Boosts Regulatory Response in Murine Peritoneal Macrophages in vitro
The oxLDL, a major risk factor for atherosclerosis, induces polarization of macrophages to the M1 phenotype and promotes inflammatory responses (Kaplan et al., 2018). In this study, we confirmed that oxLDL significantly stimulated the secretion of inflammatory cytokines TNF-α, IL-6, and iNOS in peritoneal macrophages of mice. In the presence of rSj-Cys (1 μg/mL), these oxLDL-stimulated inflammatory cytokines were significantly reduced; at the same time, secretion of immunomodulatory cytokines IL-10, TGF-β, and M2 macrophage marker Arg-1 in the culture supernatant was significantly increased compared to the cells without rSj-Cys treatment. The rSj-Cys alone had no effect on the peritoneal macrophages (Figure 8). The results indicate that rSj-Cys is able to inhibit oxLDL-stimulated inflammatory responses and increased regulatory cytokines secreted by peritoneal macrophages.
Figure 8. rSj-Cys down-regulated proinflammatory cytokines (TNF-α, IL-6) and iNOS and up-regulated immunomodulatory cytokines (IL-10, TGF-β) and Arg-1 from murine peritoneal macrophages stimulated by oxLDL. The levels of these cytokines/enzymes in the culture supernatants were detected by ELISA 24 h after incubation. The results are shown as the mean ± SEM for each group (n = 6 per group). ***P < 0.001.
rSj-Cys Inhibits Proinflammatory Cytokines and Induces Immunoregulatory Cytokines in Mice With Atherosclerosis
In order to explore the immune mechanism underlying the renal damage caused by HFD-induced atherosclerosis, we tested the levels of proinflammatory cytokines (TNF-α, IL-6) and immunoregulatory cytokines (IL-10, TGF-β) or M1-related iNOS and M2-related Arg-1 in the sera and measured their mRNA expression levels in the kidneys. Similar to the peritoneal macrophages stimulated by oxLDL in vitro, the mice fed with HFD significantly increased the expression levels of TNF-α, IL-6, and iNOS in the sera (Figure 9A) and the transcriptional levels of their mRNAs in renal tissues (Figure 9B) compared to mice fed with NCD and NCD with rSj-Cys. However, treatment with rSj-Cys significantly reduced the expression levels of these proinflammatory cytokines and iNOS, but increased the expression levels of regulatory cytokines IL-10 and TGF-β and M2-related Arg-1 in both protein levels in sera and mRNA levels in renal tissues. There were no significant differences of them in sera of mice or their mRNA in renal tissues between the NCD group and the NCD group with rSj-Cys (Figure 9B). The results indicate that treatment with rSj-Cys reduces HFD-induced atherosclerosis and aortic/renal damage possibly through stimulating the polarization of M1 macrophages to M2 macrophages, therefore reducing inflammation and boosting tissue repair and recovery.
Figure 9. rSj-Cys inhibited proinflammatory cytokines (TNF-α and IL-6) and iNOS and induced immunomodulatory cytokines (IL-10 and TGF-β) and Arg-1 in sera (A) and the similar mRNA expression pattern observed in renal tissues relative to the level of mice with NCD (B). The data are shown as the mean ± SE for each group (n = 6 per group). **P < 0.01, ***P < 0.001.
rSj-Cys Decreases the Expression of TLR2 and Myd88 in Atherosclerotic Kidney
Toll-like receptors (TLRs) are pattern recognition receptors expressed in a variety of immune cells. Myd88 is the adaptor protein of TLRs that acts as a bridge connecting downstream inflammation signals. To investigate whether rSj-Cys protects atherosclerotic renal damage by inhibiting the expression of TLR2 and Myd88, we detected the expression level of TLR2 and Myd88 proteins in the renal tissues (Figure 10A). The results showed that the expression of TLR2 and Myd88 was remarkably increased in the renal tissues of mice fed with HFD compared with the kidneys in NCD group and the NCD group with rSj-Cys. Treatment with rSj-Cys significantly inhibited their expression in the HFD group. There was no effect of the rSj-Cys itself on the expression of TLR2 and MyD88 in NCD mice (Figure 10B). The results indicate the inhibition of inflammation by rSj-Cys may act through inhibiting the TLR2 and Myd88 signal pathway.
Figure 10. rSj-Cys reduced the expression of TLR2, MyD88 in the kidneys of mice detected by Western blot (A). The β-actin was measured as control. The density ratios of TLR2/β-actin and MyD88/β-actin are shown on the right (B). The results are shown as the density mean ± SEM for each group (n = 6). ***P < 0.001.
The Effect of rSj-Cys Induces the Generation of Tregs in the Spleen
To explore whether rSj-Cys reduces the development of atherosclerosis by stimulating Treg, we detected the Treg-expressed CD3ε, CD4, and CD25 on the surface and the intracellular expression of Foxp3 in splenocytes (Figure 11A). The results showed that the rate of CD3ε+CD4+CD25+Foxp3+ Treg in the HFD group was significantly lower than that in the NCD group. Treatment with rSj-Cys significantly recovered and boosted the level of CD3ε+CD4+CD25+Foxp3+ Tregs. There were no statistical differences between group NCD and group NCD with rSj-Cys (Figure 11B). The results are consistent with the down-regulated proinflammatory cytokines and up-regulted anti-inflammatory cytokines IL-10 and TGF-β in sera and renal tissues measured previously. Our data indicate that the rSj-Cys–stimulated Treg is closely related to the attenuated atherosclerosis.
Figure 11. (A) Representative data from the FACS analysis of the CD3+CD4+CD25+Foxp3+ Tregs and the numbers in the upper right quadrants indicate the positive percentages of Tregs. (B) The corresponding bar graphs of the percentage of CD3+CD4+CD25+Foxp3+ Tregs. The results are shown as the mean ± SEM for each group (n = 6). ***P < 0.001.
Discussion
Apolipoprotein E knockout mice (apoE–/–) display poor lipoprotein clearance with subsequent accumulation of cholesterol, leading to atherosclerotic lesions under the feed of HFD (Zhang et al., 1994). In this study, we successfully developed the atherosclerotic lesions in the aorta and aortic sinus of apoE–/– mice after being fed with HFD for 12 weeks, showing the significant lipid deposition and plaque stained by oil red O (Figures 3A–C). The mice with induced atherosclerosis also showed significantly reduced heart function characterized by the increased peak velocity and mean gradient of the ascending aorta (Figure 4) and impaired kidney function with significantly increased levels of Cr and BUN in the sera and the total protein in urine (Figures 5B,C), indicating serious damage of cardiac and renal functions caused by atherosclerosis in the apoE–/– mice fed with HFD. Strikingly, the atherosclerotic lesions were reduced, and the functions of the heart and kidney improved significantly after being treated with rSj-Cys compared to mice without treatment, indicating that rSj-Cys possesses potential as a therapeutic agent for atherosclerosis.
Atherosclerosis is the progressive damage of arteries, which can be caused by various factors such as abnormal blood lipid metabolism and systemic chronic inflammation (Raggi et al., 2018; Shah, 2019). In this study, we demonstrated that the body weight, TC, TG, and low-density lipoprotein cholesterol (LDL-c) were significantly increased, whereas high-density lipoprotein cholesterol (HDL-c) decreased in apoE–/– mice fed with HFD, indicating the imbalanced lipid metabolism (Figure 5A). The diet with high cholesterol and saturated fatty acids can significantly build up body weight, elevate plasma cholesterol levels, and increase the risk of atherosclerosis (Manzini et al., 2019). After being treated with rSj-Cys for 4 weeks, body weight gain stopped in mice, and the mice started to lose weight afterward until the end of the experiment (12 weeks). It is the first time we observed that treatment with rSj-Cys significantly reduced the body weight of mice fed with HFD compared to the mice without rSj-Cys treatment (Figure 2). We also observed that the levels of blood lipids including TC, TG, and LDL-c were reduced, and HDL-c increased significantly after rSj-Cys treatment. The results indicate that rSj-Cys can significantly improve lipid metabolism in apoE–/– mice with HFD. It has long been noticed that helminthic infection was associated with the considerably lower prevalence of obesity (Okada et al., 2013). Mice infected with S. mansoni reduced body weight by improving insulin sensitivity and glucose intolerance (Hussaarts et al., 2015). S. japonicum infection improved lipid metabolism in mice fed with an HFD, possibly through a soluble worm egg protein called Sjp40 to inhibit host microRNA miRNA-802, resulting in the attenuation of lipogenesis (Ni et al., 2021). Our results are consistent with these observations and further support the negative correlation between helminthic infection or its derivatives and the incidence of obesity and lipid metabolism disorder (Wiria et al., 2012); however, it is still needed to further study how Sj-Cys improves the lipid metabolism and reduces the body weight.
As we have already known, atherosclerosis is a chronic inflammatory disease, and macrophages are the major inflammatory cells involved in the pathological development of atherosclerosis (De Paoli et al., 2014; Zhang et al., 2018). Some risk factors such as dyslipidemia, oxidized lipids, and cytokines can activate polarization of M1 macrophages that secrete proinflammatory cytokines such as TNF-α, IL-6, IL-1β, and iNOS, thereby creating inflammatory environment and promoting the development of atherosclerosis (Khallou-Laschet et al., 2010; Colin et al., 2014; Liu et al., 2014; Raggi et al., 2018). In order to evaluate whether rSj-Cys can alleviate the development of atherosclerosis by regulating the polarization and functions of macrophages, the peritoneal macrophages were isolated from mice and stimulated with oxidized LDL in the presence of rSj-Cys. We found that the macrophages were strongly stimulated by the oxidized LDL to release proinflammatory cytokines TNF-α, IL-6, and iNOS. IL-6 has been identified as a major cytokine that promotes atherosclerosis in apoE–/– mice (Fan et al., 2020). Incubation with rSj-Cys significantly suppressed the secretion of these proinflammatory cytokines stimulated by oxidized LDL and simultaneously up-regulated the secretion of IL-10, TGF-β, and Arg-1, the regulatory cytokine/chemokine mostly secreted by M2 macrophages (Figure 8). Our results confirmed oxidized lipid as a strong stimulator for inflammatory macrophages (M1) and the link between lipid oxidation and the macrophage polarization (Adamson and Leitinger, 2011; Xu et al., 2019). This link can be interrupted by rSj-Cys that induces the polarization of macrophages from M1 to M2 and stimulates the secretion of related regulatory cytokines to alleviate the inflammatory responses caused by lipid disorders. As we know, M2 macrophages possess antiatherosclerotic functions by producing high levels of anti-inflammatory cytokines IL-10 and TGF-β to rebuild the cytokine balance to counteract the inflammatory response maintained by M1 macrophages (Colin et al., 2014; Liu et al., 2014). The regulatory effects of rSj-Cys on programming monocytes/macrophages to an anti-inflammatory phenotype have been further confirmed by measuring the proinflammatory and anti-inflammatory cytokines in sera of treated mice. We found that rSj-Cys significantly reduced the levels of TNF-α, IL-6, and iNOS and increased the levels of IL-10, TGF-β, and Arg-1 in sera (Figure 9A). It may provide a novel and feasible approach for the treatment of atherosclerosis by promoting macrophage polarization from M1 to M2 phenotype.
Kidney is one of the major organs affected by atherosclerosis. The renal damage and function failure is the major consequence of atherosclerosis. Hyperlipidemia can lead to atherosclerosis and abnormal lipoprotein deposits in renal tissue damages glomerulus and endothelial cells and induces inflammation in the kidney (Ruan et al., 2009; Bobulescu, 2010). Patients with existing basic renal disease can increase the mortality by accelerating the process of atherosclerosis (Swaminathan and Shah, 2011; Shoji et al., 2012). In this study, we observed not only the significant increase of kidney weight but also the significant deposit of fat and the inflammatory cell infiltration in glomerular tissue of mice fed with HFD (Figures 3D,E). More specifically, we identified that CD86+ M1 macrophages (Figure 7) and M1 macrophage–produced IL-6, TNF-α, and iNOS mRNA expression (Figure 9B) were significantly increased in the kidneys of mice fed with HFD, indicating that M1 macrophages and their inflammatory activities are significantly activated in kidneys with atherosclerosis. These results indicate that renal tissue is dominated by inflammatory macrophages when atherosclerotic lesion occurs. In addition, oxidative stress has been shown to play an important role in the development of atherosclerosis (Jiang et al., 2011). Lipid peroxidation is the major risk factor for atherosclerosis, which induces M1 macrophage polarization and promotes inflammatory responses. In this study, we found that MDA, as a marker for oxidative stress, was significantly accumulated in kidneys of HFD-fed mice (Figure 6), further indicating the inflammatory status of kidney during atherosclerosis. The HFD-induced atherosclerosis and inflammation damaged the function of kidney reflected by the increased Cr and BUN levels in sera and increased protein content in urine (Figures 5B,C). Treatment with rSj-Cys not only significantly reduced the kidney weight at the rate even higher than body weight (Figure 2B) but also improved the kidney function associated with reduced fatty acid deposition and less inflammatory cell infiltration and recovered structure of glomerular tissue as well in mice fed with HFD (Figures 3D,E). We further identified that rSj-Cys was able to induce macrophage polarization from M1 (CD86+) to M2 (CD206+) in renal tissue associated with reduced proinflammatory cytokines (IL-6, TNF-α) and iNOS and increased regulatory or anti-inflammatory cytokines (IL-10, TGF-β) and Arg-1. All results suggest that the therapeutic effect of rSj-Cys on atherosclerotic renal damage takes place through inhibiting renal inflammation by promoting M1 to M2 macrophage polarization.
In recent years, more and more studies have identified that Treg plays a vital role in regulating the progression of atherosclerosis. Decreasing the number of CD4+CD25+Foxp3+ Tregs was related to the progression of atherosclerosis (Butcher et al., 2016; Tian et al., 2017, 2018; Ou et al., 2018). Therefore, increasing the numbers and improving the immune regulation function of Treg may serve as a basic immunotherapy for the treatment of atherosclerosis (Ou et al., 2018). CD4+CD25+Foxp3+ Treg exerts immunomodulatory effects by releasing anti-inflammatory cytokines IL-10 and TGF-β to inhibit the development of atherosclerosis possibly through promoting the conversion of M1 to M2 macrophages (Tiemessen et al., 2007; Lin et al., 2010). As a return, IL-10 and TGF-β also enhance the production and function of Tregs (Ji et al., 2017). In this study, we observed the significant induction of IL-10 and TGF-β in both local renal tissues and in sera of mice treated with rSj-Cys. Further investigation found that CD4+CD25+Foxp3+ Tregs were significantly decreased in HFD-induced atherosclerosis, and the treatment with rSj-Cys significantly stimulated the proliferation of Tregs in splenocytes (Figures 11A,B). The results are consistent with the findings by Chen et al. (2017) that infection of S. japonicum stimulated the differentiation of Tregs and our previous findings of the therapeutic effects of rSj-Cys on sepsis related to the increased levels of IL-10 and TGF-β (Li et al., 2017; Xie et al., 2021). Our results strongly suggest that rSj-Cys plays a role in inhibiting inflammation and prevention of atherosclerosis mainly through stimulating T regulatory response. The rSj-Cys itself had little effect on the cytokine profile, suggesting that rSj-Cys mainly exhibits immunomodulatory effects when inflammation occurs.
TLRs are expressed in a variety of immune cells such as monocytes/macrophages and dendritic cells, which can recognize pathogen-associated molecular pattern molecules. TLRs are key players in the pathogenesis of inflammatory diseases (Roshan et al., 2016). Many studies have shown that patients with atherosclerosis increased the expression of TLR2 in atherosclerotic aorta (Chen et al., 2016). The TLR-mediated cascade immune response requires the participation of Myd88 as an adaptor or bridge to connect downstream inflammatory signals, leading to the activation of nuclear transcription factor NF-κB to regulate the expression of inflammatory genes such as TNF-α, IL-1β, and IL-6 (Kawai and Akira, 2007; Gay et al., 2014; Li et al., 2020). TLR2/Myd88 signaling pathway plays an important role in the pathogenesis of atherosclerosis. Blocking the expression of TLR2 or Myd88 reduced the plaque size, lipid level, macrophage infiltration, and proinflammatory cytokine levels in apoE–/– mice (Björkbacka et al., 2004; Wang et al., 2013). In order to investigate whether rSj-Cys exerts antiatherosclerotic effects by inhibiting the TLR2/Myd88-dependent signaling pathway, we measured the expression of TLR2 and Myd88 in kidney tissue of apoE–/– mice. Our study found that the expression of TLR2 and Myd88 was increased in apoE–/– mice fed with HFD. Treatment with rSj-Cys significantly reduced the expression levels of TLR2 and Myd88 in the renal tissues of mice fed with HFD (Figures 10A,B), indicating that the anti-inflammatory effect of rSj-Cys may act through inhibiting the TLR2/Myd88 pathway. However, helminthic infections or their derivatives may exert their effect on antimetabolic diseases through other different mechanisms, such as activating the STAT6 signaling pathway, changing the intestinal microbiota (Yang et al., 2013; Crowe et al., 2020). Any other mechanism involved in the therapeutic effect of rSj-Cys on atherosclerosis and atherosclerotic renal damage needs to be further investigated. Because of the inhibitory activity of rSj-Cys on cathepsins (Vray et al., 2002), it cannot be excluded that rSj-Cys plays its role in lipid metabolism and atherosclerosis through inhibiting cathepsins related to lipid metabolism and atherosclerosis. The imbalance between cystatins and cathepsins has been identified to be involved in the development of atherosclerosis (Wu et al., 2018).
In this study, we revealed that inflammatory macrophages play an important role in the pathogenesis of atherosclerosis. Treatment with rSj-Cys significantly inhibited atherosclerosis and improved kidney functions through promoting macrophage polarization from M1 to M2, therefore inhibiting M1 macrophage–induced inflammation. The possible mechanism underlying the regulatory effect of rSj-Cys on reducing atherosclerosis and atherosclerotic renal damage is that rSj-Cys stimulates Tregs and M2 macrophage polarization to produce regulatory cytokines IL-10 and TGF-β, thereby inhibiting the production of proinflammatory cytokines through inhibiting the activation of TLR2/MyD88 signaling pathway. However, immune regulation of inflammation and atherosclerosis is a complicated process with different mechanisms, except for the macrophage polarization and Treg regulation. For example, more evidence demonstrated that neutrophils act as an important regulator in the atherosclerosis and cardiovascular inflammation (Silvestre-Roig et al., 2020). At the early stage, hypercholesterolemia and hyperglycemia stimulated the production of neutrophils in the bone marrow (Drechsler et al., 2010); the increased neutrophils secreted chemotactic proteins to recruit monocytes, thereby accelerating atherosclerosis and cardiovascular inflammation (Soehnlein et al., 2009). Neutrophils also play roles in accelerating all stages of atherosclerosis by fostering monocyte recruitment and macrophage activation and through cytotoxicity (Silvestre-Roig et al., 2020). It has been known that platelets are also involved in the development and manifestation of atherosclerosis by secreting chemokines including CXCL4 or platelet factor 4, CCL5, CXCL12 to recruit monocytes or neutrophils to promote local inflammatory processes at sites of vascular injury (Bakogiannis et al., 2019). Recent studies also showed that gut microbiota and their metabolites play roles in atherosclerosis (Duttaroy, 2021). Further investigation is needed to determine whether rSj-Cys has an effect on the modulation of neutrophil and platelet functions, or altering gut microbiota, in the process of atherosclerosis. The results in this study provide consolidate evidence that Schistosoma-derived cystatin exhibits anti-inflammation property and could be developed as a therapeutic agent to treat lipid metabolism disorder and atherosclerosis that threats million lives around the world.
Conclusion
This study identified that rSj-Cys stimulated Treg and M2 macrophages to secrete regulatory cytokines IL-10 and TGF-β that inhibit oxidized lipid-induced inflammation and atherosclerosis through inhibiting the TLR2/Myd88 pathway. Therefore, rSj-Cys can be used as a potential therapeutic agent for the prevention and treatment of atherosclerosis.
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding authors.
Ethics Statement
The animal study was reviewed and approved by Animal Care and Use Committee of Bengbu Medical College (approval no: LAEC-2014-039).
Author Contributions
XY, HuL, HY, and HoL conceived and designed the study. HY, HoL, ZM, YX, YS, DL, and HG performed the experiments. HY, HoL, WC, YY, XW, and LC analyzed the data. HY wrote the manuscript. BZ, XY, and HuL critically revised the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This study was supported by the Science Foundation of Anhui Province (2008085MH260 and gxyq2021188); the Cardiovascular Injury and Protection Foundation and Clinical Application Innovation Team (No. BYKC201906); Anhui Provincial Key Research and Development Project (202004j07020011); the construction projects key medical and health specialty in Anhui Province; the Program of Natural Science Foundation of the Anhui Higher Education Institutions (AHWJ2021a005, KJ2020A0554, KJ2020A0566, and KJ2020A0572); 512 Talents Development Project of Bengbu Medical College (by51201205 and by51201306); the Science Foundation of Bengbu Medical College (2020bypd007); the Postgraduate Scientific Research Innovation Program of Bengbu Medical College (Byycx20016), and the innovation and entrepreneurship training program for college students (Nos. 202010367006 and S202010367040).
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.
Publisher’s Note
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References
Adamson, S., and Leitinger, N. (2011). Phenotypic modulation of macrophages in response to plaque lipids. Curr. Opin. Lipidol. 22, 335–342. doi: 10.1097/MOL.0b013e32834a97e4
Aprahamian, T. R., Zhong, X., Amir, S., Binder, C. J., Chiang, L. K., Al-Riyami, L., et al. (2015). The immunomodulatory parasitic worm product ES-62 reduces lupus-associated accelerated atherosclerosis in a mouse model. Int. J. Parasitol. 45, 203–207. doi: 10.1016/j.ijpara.2014.12.006
Bakogiannis, C., Sachse, M., Stamatelopoulos, K., and Stellos, K. (2019). Platelet-derived chemokines in inflammation and atherosclerosis. Cytokine 122:154157. doi: 10.1016/j.cyto.2017.09.013
Barrett, T. J. (2020). Macrophages in atherosclerosis regression. Arterioscler. Thromb. Vasc. Biol. 40, 20–33. doi: 10.1161/ATVBAHA.119.312802
Binder, C. J., Chang, M. K., Shaw, P. X., Miller, Y. I., Hartvigsen, K., Dewan, A., et al. (2002). Innate and acquired immunity in atherogenesis. Nat. Med. 8, 1218–1226. doi: 10.1038/nm1102-1218
Björkbacka, H., Kunjathoor, V. V., Moore, K. J., Koehn, S., Ordija, C. M., Lee, M. A., et al. (2004). Reduced atherosclerosis in MyD88-null mice links elevated serum cholesterol levels to activation of innate immunity signaling pathways. Nat. Med. 10, 416–421. doi: 10.1038/nm1008
Bobulescu, I. A. (2010). Renal lipid metabolism and lipotoxicity. Curr. Opin. Nephrol. Hypertens 19, 393–402. doi: 10.1097/MNH.0b013e32833aa4ac
Bogdan, C., Vodovotz, Y., and Nathan, C. (1991). Macrophage deactivation by interleukin 10. J. Exp. Med. 174, 1549–1555. doi: 10.1084/jem.174.6.1549
Butcher, M. J., Filipowicz, A. R., Waseem, T. C., McGary, C. M., Crow, K. J., Magilnick, N., et al. (2016). Atherosclerosis-driven treg plasticity results in formation of a dysfunctional subset of plastic IFNγ+ Th1/Tregs. Circ. Res. 119, 1190–1203. doi: 10.1161/CIRCRESAHA.116.309764
Chen, L., He, B., Hou, W., and He, L. (2017). Cysteine protease inhibitor of Schistosoma japonicum - a parasite - derived negative immunoregulatory factor. Parasitol. Res. 116, 901–908. doi: 10.1007/s00436-016-5363-0
Chen, X., Cui, R., Li, R., Lin, H., Huang, Z., and Lin, L. (2016). Development of pristane induced mice model for lupus with atherosclerosis and analysis of TLR expression. Clin. Exp. Rheumatol. 34, 600–608.
Cheng, Y., Zhu, X., Wang, X., Zhuang, Q., Huyan, X., Sun, X., et al. (2018). Trichinella spiralis infection mitigates collagen-induced arthritis via programmed death 1-mediated immunomodulation. Front. Immunol. 9:1566. doi: 10.3389/fimmu.2018.01566
Colin, S., Chinetti-Gbaguidi, G., and Staels, B. (2014). Macrophage phenotypes in atherosclerosis. Immunol. Rev. 262, 153–166. doi: 10.1111/imr.12218
Crowe, J., Lumb, F. E., Doonan, J., Broussard, M., Tarafdar, A., Pineda, M. A., et al. (2020). The parasitic worm product ES-62 promotes health- and life-span in a high calorie diet-accelerated mouse model of ageing. PLoS Pathog. 16:e1008391. doi: 10.1371/journal.ppat.1008391
De Paoli, F., Staels, B., and Chinetti-Gbaguidi, G. (2014). Macrophage phenotypes and their modulation in atherosclerosis. Circ. J. 78, 1775–1781.
Doenhoff, M. J., Stanley, R. G., Griffiths, K., and Jackson, C. L. (2002). An anti-atherogenic effect of Schistosoma mansoni infections in mice associated with a parasite-induced lowering of blood total cholesterol. Parasitology 125(Pt 5), 415–421. doi: 10.1017/s0031182002002275
Drechsler, M., Megens, R. T., van Zandvoort, M., Weber, C., and Soehnlein, O. (2010). Hyperlipidemia-triggered neutrophilia promotes early atherosclerosis. Circulation 122, 1837–1845. doi: 10.1161/CIRCULATIONAHA.110.961714
Duttaroy, A. K. (2021). Role of gut microbiota and their metabolites on atherosclerosis, hypertension and human blood platelet function: a review. Nutrients 13:144. doi: 10.3390/nu13010144
Elliott, D. E., and Weinstock, J. V. (2012). Helminth-host immunological interactions: prevention and control of immune-mediated diseases. Ann. N. Y. Acad. Sci. 1247, 83–96. doi: 10.1111/j.1749-6632.2011.06292.x
Fan, Q., Liu, Y., Rao, J., Zhang, Z., Xiao, W., Zhu, T., et al. (2020). Anti-atherosclerosis effect of angong niuhuang pill via regulating Th17/treg immune balance and inhibiting chronic inflammatory on ApoE-/- mice model of early and mid-term atherosclerosis. Front. Pharmacol. 10:1584. doi: 10.3389/fphar.2019.01584
Förstermann, U., Xia, N., and Li, H. (2017). Roles of vascular oxidative stress and nitric oxide in the pathogenesis of atherosclerosis. Circ. Res. 120, 713–735. doi: 10.1161/CIRCRESAHA.116.309326
Gao, S., Li, H., Xie, H., Wu, S., Yuan, Y., Chu, L., et al. (2020). Therapeutic efficacy of Schistosoma japonicum cystatin on sepsis-induced cardiomyopathy in a mouse model. Parasit. Vectors 13:260. doi: 10.1186/s13071-020-04104-3
Gaweł, S., Wardas, M., Niedworok, E., and Wardas, P. (2004). Dialdehyd malonowy (MDA) jako wskaźnik procesów peroksydacji lipidów w organizmie [malondialdehyde (MDA) as a lipid peroxidation marker]. Wiad. Lek. 57, 453–455.
Gay, N. J., Symmons, M. F., Gangloff, M., and Bryant, C. E. (2014). Assembly and localization of toll-like receptor signalling complexes. Nat. Rev. Immunol. 14, 546–558. doi: 10.1038/nri3713
Geovanini, G. R., and Libby, P. (2018). Atherosclerosis and inflammation: overview and updates. Clin. Sci. 132, 1243–1252. doi: 10.1042/CS20180306
Gistera, A., and Hansson, G. K. (2017). The immunology of atherosclerosis. Nat. Rev. Nephrol. 13, 368–380. doi: 10.1038/nrneph.2017.51
Hussaarts, L., García-Tardón, N., van Beek, L., Heemskerk, M. M., Haeberlein, S., van der Zon, G. C., et al. (2015). Chronic helminth infection and helminth-derived egg antigens promote adipose tissue M2 macrophages and improve insulin sensitivity in obese mice. FASEB J. 29, 3027–3039. doi: 10.1096/fj.14-266239
Jiang, F., Qian, J., Chen, S., Zhang, W., and Liu, C. (2011). Ligustrazine improves atherosclerosis in rat via attenuation of oxidative stress. Pharm. Biol. 49, 856–863. doi: 10.3109/13880209.2010.551776
Ji, Q., Meng, K., Yu, K., Huang, S., Huang, Y., Min, X., et al. (2017). Exogenous interleukin 37 ameliorates atherosclerosis via inducing the Treg response in ApoE-deficient mice. Sci. Rep. 7:3310. doi: 10.1038/s41598-017-02987-4
Kaplan, M., Shur, A., and Tendler, Y. (2018). M1 macrophages but not M2 macrophages are characterized by upregulation of CRP expression via activation of NFκB: a possible role for Ox-LDL in macrophage polarization. Inflammation 41, 1477–1487. doi: 10.1007/s10753-018-0793-8
Kattoor, A. J., Pothineni, N. V. K., Palagiri, D., and Mehta, J. L. (2017). Oxidative stress in atherosclerosis. Curr. Atheroscler. Rep. 19:42. doi: 10.1007/s11883-017-0678-6
Kawai, T., and Akira, S. (2007). Signaling to NF-kappaB by toll-like receptors. Trends Mol. Med. 13, 460–469. doi: 10.1016/j.molmed.2007.09.002
Khallou-Laschet, J., Varthaman, A., Fornasa, G., Compain, C., Gaston, A. T., Clement, M., et al. (2010). Macrophage plasticity in experimental atherosclerosis. PLoS One 5:e8852. doi: 10.1371/journal.pone.0008852
Li, B., Xia, Y., and Hu, B. (2020). Infection and atherosclerosis: TLR-dependent pathways. Cell Mol. Life Sci. 77, 2751–2769. doi: 10.1007/s00018-020-03453-7
Li, D., Zhang, L., Dong, F., Liu, Y., Li, N., Li, H., et al. (2015). Metabonomic changes associated with atherosclerosis progression for LDLR(-/-) mice. J. Proteome Res. 14, 2237–2254. doi: 10.1021/acs.jproteome.5b00032
Li, H., Wang, S., Zhan, B., He, W., Chu, L., Qiu, D., et al. (2017). Therapeutic effect of Schistosoma japonicum cystatin on bacterial sepsis in mice. Parasit. Vectors 10:222. doi: 10.1186/s13071-017-2162-0
Libby, P., Buring, J. E., Badimon, L., Hansson, G. K., Deanfield, J., Bittencourt, M. S., et al. (2019). Atherosclerosis. Nat. Rev. Dis. Primers 5:56. doi: 10.1038/s41572-019-0106-z
Lin, J., Li, M., Wang, Z., He, S., Ma, X., and Li, D. (2010). The role of CD4+CD25+ regulatory T cells in macrophage-derived foam-cell formation. J. Lipid Res. 51, 1208–1217. doi: 10.1194/jlr.D000497
Liu, F., Cheng, W., Pappoe, F., Hu, X., Wen, H., Luo, Q., et al. (2016). Schistosoma japonicum cystatin attenuates murine collagen-induced arthritis. Parasitol. Res. 115, 3795–3806. doi: 10.1007/s00436-016-5140-0
Liu, M., Chen, X., Ma, J., Hassan, W., Wu, H., Ling, J., et al. (2017). β-Elemene attenuates atherosclerosis in apolipoprotein E-deficient mice via restoring NO levels and alleviating oxidative stress. Biomed. Pharmacother. 95, 1789–1798. doi: 10.1016/j.biopha.2017.08.092
Liu, Y. C., Zou, X. B., Chai, Y. F., and Yao, Y. M. (2014). Macrophage polarization in inflammatory diseases. Int. J. Biol. Sci. 10, 520–529. doi: 10.7150/ijbs.8879
Lu, H. S., Kukida, M., and Daugherty, A. (2019). Links lipoproteins to chronic kidney disease and atherosclerosis. Curr. Opin. Lipidol. 30, 410–411. doi: 10.1097/MOL.0000000000000625
Lutgens, E., and Daemen, M. J. (2001). Transforming growth factor-beta: a local or systemic mediator of plaque stability? Circ. Res. 89, 853–855.
Manzini, S., Busnelli, M., Parolini, C., Minoli, L., Ossoli, A., Brambilla, E., et al. (2019). Topiramate protects apoE-deficient mice from kidney damage without affecting plasma lipids. Pharmacol. Res. 141, 189–200. doi: 10.1016/j.phrs.2018.12.022
Moorhead, J. F., Chan, M. K., El-Nahas, M., and Varghese, Z. (1982). Lipid nephrotoxicity in chronic progressive glomerular and tubulo-interstitial disease. Lancet 2, 1309–1311. doi: 10.1016/s0140-6736(82)91513-6
Ni, Y., Xu, Z., Li, C., Zhu, Y., Liu, R., Zhang, F., et al. (2021). Therapeutic inhibition of miR-802 protects against obesity through AMPK-mediated regulation of hepatic lipid metabolism. Theranostics 11, 1079–1099. doi: 10.7150/thno.49354
Okada, H., Ikeda, T., Kajita, K., Mori, I., Hanamoto, T., Fujioka, K., et al. (2013). Effect of nematode Trichinella infection on glucose tolerance and status of macrophage in obese mice. Endocr. J. 60, 1241–1249. doi: 10.1507/endocrj.ej13-0312
Ou, H. X., Guo, B. B., Liu, Q., Li, Y. K., Yang, Z., Feng, W. J., et al. (2018). Regulatory T cells as a new therapeutic target for atherosclerosis. Acta Pharmacol. Sin. 39, 1249–1258. doi: 10.1038/aps.2017.140
Radovic, I., Gruden-Movsesijan, A., Ilic, N., Cvetkovic, J., Mojsilovic, S., Devic, M., et al. (2015). Immunomodulatory effects of Trichinella spiralis-derived excretory-secretory antigens. Immunol. Res. 61, 312–325. doi: 10.1007/s12026-015-8626-4
Raggi, P., Genest, J., Giles, J. T., Rayner, K. J., Dwivedi, G., Beanlands, R. S., et al. (2018). Role of inflammation in the pathogenesis of atherosclerosis and therapeutic interventions. Atherosclerosis 276, 98–108. doi: 10.1016/j.atherosclerosis.2018.07.014
Robertson, A. K., Rudling, M., Zhou, X., Gorelik, L., Flavell, R. A., and Hansson, G. K. (2003). Disruption of TGF-beta signaling in T cells accelerates atherosclerosis. J. Clin. Invest. 112, 1342–1350. doi: 10.1172/JCI18607
Roshan, M. H., Tambo, A., and Pace, N. P. (2016). The Role of TLR2, TLR4, and TLR9 in the pathogenesis of atherosclerosis. Int. J. Inflam. 2016:1532832. doi: 10.1155/2016/1532832
Ruan, X. Z., Varghese, Z., and Moorhead, J. F. (2009). An update on the lipid nephrotoxicity hypothesis. Nat. Rev. Nephrol. 5, 713–721. doi: 10.1038/nrneph.2009.184
Schwartz, C., Hams, E., and Fallon, P. G. (2018). Helminth modulation of lung inflammation. Trends Parasitol. 34, 388–403. doi: 10.1016/j.pt.2017.12.007
Shah, P. K. (2019). Inflammation, infection and atherosclerosis. Trends Cardiovasc. Med. 29, 468–472. doi: 10.1016/j.tcm.2019.01.004
Shoji, T., Abe, T., Matsuo, H., Egusa, G., Yamasaki, Y., Kashihara, N., et al. (2012). Committee of renal and peripheral arteries, japan atherosclerosis society. chronic kidney disease, dyslipidemia, and atherosclerosis. J. Atheroscler. Thromb. 19, 299–315. doi: 10.5551/jat.10454
Silvestre-Roig, C., Braster, Q., Ortega-Gomez, A., and Soehnlein, O. (2020). Neutrophils as regulators of cardiovascular inflammation. Nat. Rev. Cardiol. 17, 327–340. doi: 10.1038/s41569-019-0326-7
Smith, P., Mangan, N. E., Walsh, C. M., Fallon, R. E., McKenzie, A. N., van Rooijen, N., et al. (2007). Infection with a helminth parasite prevents experimental colitis via a macrophage-mediated mechanism. J. Immunol. 178, 4557–4566. doi: 10.4049/jimmunol.178.7.4557
Soehnlein, O., Lindbom, L., and Weber, C. (2009). Mechanisms underlying neutrophil-mediated monocyte recruitment. Blood 114, 4613–4623. doi: 10.1182/blood-2009-06-221630
Sun, S., Li, H., Yuan, Y., Wang, L., He, W., Xie, H., et al. (2019). Preventive and therapeutic effects of Trichinella spiralis adult extracts on allergic inflammation in an experimental asthma mouse model. Parasit. Vectors 12:326. doi: 10.1186/s13071-019-3561-1
Swaminathan, S., and Shah, S. V. (2011). Novel inflammatory mechanisms of accelerated atherosclerosis in kidney disease. Kidney Int. 80, 453–463. doi: 10.1038/ki.2011.178
Taleb, S. (2016). Inflammation in atherosclerosis. Arch. Cardiovasc. Dis. 109, 708–715. doi: 10.1016/j.acvd.2016.04.002
Tedgui, A., and Mallat, Z. (2001). Anti-inflammatory mechanisms in the vascular wall. Circ. Res. 88, 877–887. doi: 10.1161/hh0901.090440
Tedgui, A., and Mallat, Z. (2006). Cytokines in atherosclerosis: pathogenic and regulatory pathways. Physiol. Rev. 86, 515–581. doi: 10.1152/physrev.00024.2005
Tian, Y., Chen, T., Wu, Y., Yang, L., Wang, L., Fan, X., et al. (2017). Pioglitazone stabilizes atherosclerotic plaque by regulating the Th17/Treg balance in AMPK-dependent mechanisms. Cardiovasc. Diabetol. 16:140. doi: 10.1186/s12933-017-0623-6
Tian, Y., Liang, X., and Wu, Y. (2018). The alternation of autophagy/apoptosis in CD4+CD25+Foxp3+ Tregs on the developmental stages of atherosclerosis. Biomed. Pharmacother. 97, 1053–1060. doi: 10.1016/j.biopha.2017.11.013
Tiemessen, M. M., Jagger, A. L., Evans, H. G., van Herwijnen, M. J., John, S., and Taams, L. S. (2007). CD4+CD25+Foxp3+ regulatory T cells induce alternative activation of human monocytes/macrophages. Proc. Natl. Acad. Sci. U.S.A. 104, 19446–19451. doi: 10.1073/pnas.0706832104
Torres, N., Guevara-Cruz, M., Velázquez-Villegas, L. A., and Tovar, A. R. (2015). Nutrition and atherosclerosis. Arch. Med. Res. 46, 408–426. doi: 10.1016/j.arcmed.2015.05.010
van der Vlugt, L. E., Labuda, L. A., Ozir-Fazalalikhan, A., Lievers, E., Gloudemans, A. K., Liu, K. Y., et al. (2012). Schistosomes induce regulatory features in human and mouse CD1d(hi) B cells: inhibition of allergic inflammation by IL-10 and regulatory T cells. PLoS One 7:e30883. doi: 10.1371/journal.pone.0030883
van Rooy, M. J., and Pretorius, E. (2014). Obesity, hypertension and hypercholesterolemia as risk factors for atherosclerosis leading to ischemic events. Curr. Med. Chem. 21, 2121–2129. doi: 10.2174/0929867321666131227162950
Vray, B., Hartmann, S., and Hoebeke, J. (2002). Immunomodulatory properties of cystatins. Cell Mol. Life Sci. 59, 1503–1512. doi: 10.1007/s00018-002-8525-4
Wammes, L. J., Mpairwe, H., Elliott, A. M., and Yazdanbakhsh, M. (2014). Helminth therapy or elimination: epidemiological, immunological, and clinical considerations. Lancet Infect. Dis. 14, 1150–1162. doi: 10.1016/S1473-3099(14)70771-6
Wang, S., Xie, Y., Yang, X., Wang, X., Yan, K., Zhong, Z., et al. (2016). Therapeutic potential of recombinant cystatin from Schistosoma japonicum in TNBS-induced experimental colitis of mice. Parasit. Vectors 9:6. doi: 10.1186/s13071-015-1288-1
Wang, X. X., Lv, X. X., Wang, J. P., Yan, H. M., Wang, Z. Y., Liu, H. Z., et al. (2013). Blocking TLR2 activity diminishes and stabilizes advanced atherosclerotic lesions in apolipoprotein E-deficient mice. Acta Pharmacol. Sin. 34, 1025–1035. doi: 10.1038/aps.2013.75
Weinstock, J. V., Summers, R. W., and Elliott, D. E. (2005). Role of helminths in regulating mucosal inflammation. Springer Semin. Immunopathol. 27, 249–271. doi: 10.1007/s00281-005-0209-3
Wiria, A. E., Djuardi, Y., Supali, T., Sartono, E., and Yazdanbakhsh, M. (2012). Helminth infection in populations undergoing epidemiological transition: a friend or foe? Semin. Immunopathol. 34, 889–901. doi: 10.1007/s00281-012-0358-0
Witztum, J. L., and Steinberg, D. (1991). Role of oxidized low density lipoprotein in atherogenesis. J. Clin. Invest. 88, 1785–1792. doi: 10.1172/JCI115499
Wolfs, I. M., Stöger, J. L., Goossens, P., Pöttgens, C., Gijbels, M. J., Wijnands, E., et al. (2014). Reprogramming macrophages to an anti-inflammatory phenotype by helminth antigens reduces murine atherosclerosis. FASEB J. 28, 288–299. doi: 10.1096/fj.13-235911
Wu, H., Du, Q., Dai, Q., Ge, J., and Cheng, X. (2018). Cysteine protease cathepsins in atherosclerotic cardiovascular diseases. J. Atheroscler. Thromb. 25, 111–123. doi: 10.5551/jat.RV17016
Xie, H., Wu, L., Chen, X., Gao, S., Li, H., Yuan, Y., et al. (2021). Schistosoma japonicum cystatin alleviates sepsis through activating regulatory macrophages. Front. Cell Infect. Microbiol. 11:617461. doi: 10.3389/fcimb.2021.617461
Xu, H., Jiang, J., Chen, W., Li, W., and Chen, Z. (2019). Vascular macrophages in atherosclerosis. J. Immunol. Res. 2019:4354786. doi: 10.1155/2019/4354786
Yan, K., Wang, B., Zhou, H., Luo, Q., Shen, J., Xu, Y., et al. (2020). Amelioration of type 1 diabetes by recombinant fructose-1,6-bisphosphate aldolase and cystatin derived from Schistosoma japonicum in a murine model. Parasitol. Res. 119, 203–214. doi: 10.1007/s00436-019-06511-7
Yang, Z., Grinchuk, V., Smith, A., Qin, B., Bohl, J. A., Sun, R., et al. (2013). Parasitic nematode-induced modulation of body weight and associated metabolic dysfunction in mouse models of obesity. Infect. Immun. 81, 1905–1914. doi: 10.1128/IAI.00053-13
Zhang, B., Ma, Y., and Xiang, C. (2018). SIRT2 decreases atherosclerotic plaque formation in low-density lipoprotein receptor-deficient mice by modulating macrophage polarization. Biomed. Pharmacother. 97, 1238–1242. doi: 10.1016/j.biopha.2017.11.061
Keywords: cystatin, Schistosoma japonicum, atherosclerosis, renal, immunoregulation
Citation: Yang H, Li H, Chen W, Mei Z, Yuan Y, Wang X, Chu L, Xu Y, Sun Y, Li D, Gao H, Zhan B, Li H and Yang X (2021) Therapeutic Effect of Schistosoma japonicum Cystatin on Atherosclerotic Renal Damage. Front. Cell Dev. Biol. 9:760980. doi: 10.3389/fcell.2021.760980
Received: 19 August 2021; Accepted: 11 October 2021;
Published: 25 November 2021.
Edited by:
Qingfeng Zhang, Tongji University, ChinaCopyright © 2021 Yang, Li, Chen, Mei, Yuan, Wang, Chu, Xu, Sun, Li, Gao, Zhan, Li and Yang. 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: Huihui Li, dearlxh@bbmc.edu.cn; Xiaodi Yang, yxd_qf@bbmc.edu.cn
†These authors have contributed equally to this work