- Open Access
NLRP3 inflammasome activation from Kupffer cells is involved in liver fibrosis of Schistosoma japonicum-infected mice via NF-κB
Parasites & Vectors volume 12, Article number: 29 (2019)
NOD-like receptor protein 3 (NLRP3) inflammasome was reported as expressed in schistosomiasis-induced liver fibrosis (SSLF). We used an NLRP3 inflammasome inhibitor, MCC950, to investigate whether it inhibited liver fibrosis, and explored the preliminary molecular mechanism.
BALB/c mice were infected with 15 cercariae through the abdominal skin. They received intraperitoneal injections of MCC950 on the day of infection and at day 22 post-infection. We examined their SSLF phenotype and the effect on liver fibrosis, primary Kupffer cells (KCs), and HSCs. Human hepatic stellate cell lines (human LX-2 cells) were treated with soluble egg antigen (SEA) released from the eggs. We then determined the expression of NLRP3 inflammasome and liver fibrosis-associated markers, liver granuloma and ALT/AST.
NLRP3 inflammasome expression in the liver was significantly increased, and eosinophilic granuloma and collagen deposition were found around the eggs in mice infected for 56 days. Additionally, IL-1β, ALT/AST in plasma, and NF-κB in liver tissue and in KCs were all greatly significantly increased. The above-mentioned indicators were largely reduced in mice treated with MCC950 on the day of infection. In vitro, lipopolysaccharide (LPS)/SEA could induce LX-2 cells to express NLRP3 and fibrosis markers, and the SEA-treated group was reversed by MCC950. Furthermore, NLRP3 inflammasome and liver fibrosis-associated markers were both increased in the primary KCs and HSCs isolated from infected mice. However, this effect was not observed in the same cells from the mice treated with MCC950 on the day of infection. Contrary to the aforementioned results, MCC950 treatment at day 22 post-infection aggravated this process. Surprisingly, NLRP3 inflammasome was involved in liver fibrosis mostly from KCs.
MCC950 acts dually on SSLF pathology and fibrosis in infected mice. Although MCC950 treatment improved SSLF on the day of infection, it exacerbated the pathological effects at day 22 post-infection. These dual effects were mediated via NF-κB. Moreover, NLRP3 inflammasome mainly came from KCs. Our results suggest that blocking NLRP3 on the day of infection may prove to be a promising direction in preventing SSLF.
Schistosomiasis is a helminthic infectious disease and is prevalent in Asia, Africa and Latin America, where the susceptible population has reached 200 million people and spread to 74 countries and regions [1, 2]. Liver fibrosis is the main pathological feature of S. japonicum infection [1, 3]. The immune reaction and inflammatory response is caused by soluble egg antigen (SEA) released from schistosome eggs. Hepatic stellate cells (HSCs) activation is vital for liver fibrosis in schistosomiasis [3,4,5,6]. Kupffer cells (KCs), as immune cells, can quickly sense hepatic injury and produce inflammatory cytokines or chemokines such as interleukin 1β (IL-1β), tumor necrosis factor-α (TNF-α) or transforming growth factor-β (TGF-β) [7,8,9,10]. These factors could contribute to HSCs proliferation and activation, and then the extracellular matrix (ECM) synthesis, and could result in liver fibrosis . The multiple cytokines secreted by HSCs could recruit KCs and subsequently promote KCs to release more inflammatory mediators in turn, leading to the cell-cell interactions with one another [12, 13]. As an injury stimulating factor, SEA could initiate HSCs activation and transformation into myofibroblasts, which could ultimately develop into collagen and other ECM component deposition in the liver. This results in granulomas and hepatic fibrosis surrounding the eggs [14, 15].
NLRP3 inflammasome is a multi-protein complex and a natural component of the immune system. It usually participates in the pathogenesis of inflammatory responses with pro-cysteinyl aspartate specific proteinase (pro-caspase I) and pro-IL-1β, involved in human liver disease [16,17,18]. In particular, resident macrophages or KCs become activated and trigger an inflammatory response through common pathways of the NLRP3 inflammasome and IL-1β . Growing evidence has linked NLRP3 inflammasome-driven inflammation to tissue damage and liver fibrosis in conditions such as drug-induced liver injury, alcoholic steatohepatitis (ASH) and angiotensin II (Ang-II) [20, 21]. In fact, recent studies have found that NLRP3 inflammasome is present in liver fibrosis induced by S. japonicum infection [17, 22]. NLRP3 inflammasome is composed of NLRP3 protein, apoptosis associated speck-like protein (ASC) and pro-caspase I [19, 23]. NLRP3 serves as a backbone protein of the complex and ASC acts as a linker protein linking NLRP3 with pro-caspase I. The NLRP3 inflammasome can be recognized by extracellular pathogen-associated molecular patterns (PAMPs) and intracellular danger-associated molecular patterns (DAMPs), and it activates downstream signaling pathways by pattern recognition receptors (PRRs) on the cell surface [24,25,26]. Recently, studies have shown that a western diet can evoke NLRP3 inflammasome activation in liver fibrosis . NLRP3 inflammasome activation traditionally requires a dual signal. The first signal is mostly from TLR activation for inflammasome expression and the second signal comes from the inflammasome ligand for inflammasome activation . After the NLRP3 inflammasome forms, pro-caspase I could then be activated to caspase I. This, in turn, leads to pro-IL-lβ and pro-IL-18 to be cleaved and to enter their activated forms [23, 24]. These cytokines could activate KCs, which then mediate HSCs activation and promote liver fibrosis . Nuclear factor-κB (NF-κB), a transcription factor, regulates the formation of NLRP3 inflammasome [28, 30] and takes part in the progression of liver fibrosis . NF-κB could affect NLRP3 inflammasome in two ways. One way is through TLR induced NLRP3 inflammasome activation via NF-κB  and the other is through NF-κB elimination of damaged mitochondria via autophagy receptor p62, which eventually inhibits activation of NLRP3 inflammasome . In recent years, NF-κB has been shown to play a negative regulatory role in NLRP3 inflammasome via ubiquitin-modifying enzyme A20 [33, 34]. Together, these findings indicate that NLRP3 inflammasome and NF-κB are both implicated in liver fibrosis.
Currently, a large number of studies focus on NLRP3 inflammasome expression and its activation mechanisms [35, 36] but few have examined how NLRP3 inflammasome regulates liver fibrosis [7, 22]. Here, we aim to provide more data to deeply understand the effects of NLRP3 on the process of liver fibrosis in schistosomiasis. NLRP3 inflammasome is widely expressed in a variety of cells in the liver, including KCs, HSCs and hepatocytes . KCs  and HSCs  play a key role in liver fibrosis and are both often used to explore liver development. However, the question of which cells are responsible for NLRP3 inflammasome-mediated liver fibrosis remains unanswered.
The NLRP3 inflammasome inhibitor MCC950 (also known as CP-456,773), has been reported to counteract the LPS-induced increase of IL-1β and IL-6 in serum from an autoimmune encephalomyelitis (EAE) mouse model . As far as we know, liver fibrosis of S. japonicum is different from other liver fibrosis models because the host is affected by both the growth of the worm and the stimulation of the eggs. Therefore, MCC950 could block NLRP3 inflammasome at different time points, enabling us to observe hepatic granulomas and fibrosis caused by S. japonicum infection. The main purpose of this study was to use NLRP3 inflammasome inhibitor, MCC950, to block liver granuloma and fibrosis that resulted from S. japonicum in order to uncover the underlying molecular mechanism and potential treatments for schistosomiasis. To address these issues, we used mouse models to detect NLRP3 inflammasome and pro-fibrosis markers, as well as LX-2 cells, primary KCs and HSCs from mice.
Animals, S. japonicum infections and reagents
BALB/c mice (6–8 weeks-old, female, body weight 18–20 g) were purchased from Hubei Provincial Center for Disease Control and Prevention (Wuhan, China). All mice were bred in a specific pathogen-free (SPF) condition. Oncomelania hupensis snails were provided by Nanjing Institute of Schistosomiasis Prevention and Control (Nanjing, China). Mice were randomly divided into four groups, with six mice in each group. In the SJ group, after the mice were anesthetized, they were infected with 15 S. japonicum cercariae through the abdominal skin. In the M0 group, the mice were intraperitoneally (i.p.) injected with MCC950 (Sigma-Aldrich, St. Louis, USA, 10 mg/kg) starting from the day of infection, days 1 and 2, and then every 2 days until day 56 post-infection. In the M4 group, the mice were given i.p. injections of MCC950 (10 mg/kg) at day 22 post-infection, days 23 and 24, and every 2 days thereafter until day 56 post-infection. In the control group, the mice were injected with vehicle (0.9% NaCl) at the same time points.
Schistosoma japonicum SEA was prepared from purified eggs in the livers of S. japonicum-infected rabbits (1500 ± 100 cercariae/rabbit) and sterile filtered via a 0.22 μm filter (Millipore, Bedford, MA, USA), as previously described  with a minor modification. Briefly, eggs of S. japonicum were collected from infected rabbit livers. The rabbits were sacrificed, and liver tissues were separated. The rabbit livers were cut and ground into pieces. The eggs were collected through coarse screening, digesting, fine screening, cleaning and purifying. Eggs were transferred to a 0.9% NaCl solution, then homogenized for 20 min on ice, and received a freeze/thaw treatment at least three times. The SEA was centrifuged at 14,000× g for 20 min at 4 °C, and the supernatant was collected. A BCA protein assay kit was used to determine protein concentration (Beyotime, Shanghai, China). SEA (1 g/ml) was diluted with phosphate-buffered saline (PBS) for storage or diluted into working concentration with Dulbecco’s modified Eagle’s medium (DMEM) containing 2% fetal bovine serum (FBS) before use.
Sample preparation, liver and spleen indexes, and worm and egg burden examination in the livers
Mice were weighed once per week until the end of the experiment. At the end point, all mice were sacrificed and blood, livers, spleens and mesenteric tissues were collected to perform pathological and molecular biological analysis. The livers and spleens were weighed and 1–2 liver fragments (0.5 × 0.5 × 0.5 cm) were soaked in 4% paraformaldehyde (PFA). The remaining fragments were placed into tubes, flash frozen in liquid nitrogen, and stored at -80 °C. The mesenteric tissues were placed in ice-cold normal saline solution containing sodium heparin (1%).
The liver and spleen indexes were calculated according to liver/spleen weight versus body weight. Adult worms located in the mesenteric veins were recorded. To estimate the egg burden, 0.2 g of each liver was digested with 20 ml KOH (10%) for 3 h at 37 °C, and the numbers of eggs were counted under a microscope. Total eggs per gram (epg) in the liver were calculated using the following formula: epg = the number of eggs calculated × 5.
Analyses of liver fibrosis, liver function, pathology and immunohistochemical staining
The serum was obtained by centrifugation of mouse blood at 3500× rpm for 15 min at 4 °C to examine liver function and IL-1β. Alamine aminotransferase (ALT), aspartate aminotransferase (AST) and hepatic hydroxyproline (Hyp) content were tested using commercial kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China) according to the kit instructions.
The liver tissues were embedded in paraffin and sliced into 4 μm sections. Hematoxylin-eosin (HE) staining analyzed the area of granuloma. Masson staining analyzed the severity of collagen deposition. After HE and Masson stainings, 3 different fields under a microscope with 200× magnification were randomly selected from each sample for analysis. The area of the granulomas in HE-staining was quantified using the Mshot Image Analysis System (Micro-shot Technology, Guangzhou, China). In addition, the percentage of each slide area was positive for the blue in Masson staining, which was then analyzed using Image-Pro Plus 6.0 software (Media Cybernetics, Bethesda, MA, USA). The reagents in immunohistochemical staining are summarized in Table 1. Samples were both blocked with 3% hydrogen peroxide (H2O2) for endogenous peroxidase and 3% bovine serum albumin (BSA) for non-specific binding sites of the primary antibody. The samples were incubated with primary antibodies (Table 1), such as goat anti-NLRP3 (1:200), rabbit anti-Caspase-1 (1:200) and goat anti-IL-1β (1:100) overnight at 4 °C, and then washed 3 times in PBS. They were then incubated with rabbit anti-goat or goat anti-rabbit HRP-conjugated secondary antibodies (1:500; Earthox, CA, USA) (Table 1) at room temperature for 1 h, then washed 3 times in PBS. For the color reaction of HRP, streptavidin-peroxidase complex 3, 3-diaminobenzidine tetrahydroxychloride (DAB) was used as a substrate. Negative controls were not added to the primary antibody. A total of 3 fields per sample were examined. Positive immunostainings were quantified as integrated optical density (IOD) using the Image-Pro Plus6.0 software.
Separation of mouse primary KCs and HSCs
The main solutions were prepared according to the following formulas: Solution I: 0.05% Collagenase IV (Sigma-Aldrich); Solution II: 0.2% Collagenase IV + 0.2% Pronase E (Yuanye, Shanghai, China).
In selected experiments, we isolated and cultured KCs and HSCs from mice. The primary KCs and HSCs were separated by a collagenase perfusion method and a discontinuous density gradient centrifugation technique [40, 41]. In brief, the livers were perfused with PBS, then with two kinds of collagenase through the portal veins. The remaining liver tissues were cut into small pieces and suspended in PBS. After filtration through a 200-gauge mesh, the supernatant was separated from the collected cell suspension by centrifugation at 50× g for 3 min, then centrifuged at 500× g for 5 min to pellet the KCs and HSCs. The pellets were resuspended in PBS and then added to a 30/70% Percoll non-continuous density gradient separation liquid upper layer (Solarbio, Beijing, China) and centrifuged at 900× g for 15 min. The KCs and HSCs were collected from the interface of 30% and 70% Percoll, PBS and 30% Percoll, respectively. The two kinds of cells were both resuspended in mouse liver Kupffer cell and hepatic stellate cell medium (DMEM containing 10% heat-inactivated FBS, 1% glutamine and 1% penicillin-streptomycin) (Procell, Wuhan, China), respectively. They were centrifuged at 400× g for 5 min to remove the remaining Percoll solution in the cells.
Cell culture and in vitro treatment
The collected mouse primary cells were resuspended in mouse liver Kupffer cell and hepatic stellate cell complete medium, then plated in six-well plates coated with Poly-L-Lysine (Procell, Wuhan, China) and cultured in a humidified incubator at 37 °C with 5% CO2. The KCs were cultured 2–3 h for further purification. The medium was changed after 3 h and the following day. Cells were then obtained on the third day. KCs were examined for their staining with mouse epidermal growth factor-like module-containing mucin-like hormone receptor-like 1 (F4/80). HSCs were cultured 24 h for further purification. The medium was changed after 24 h and on the third day. Cells were then collected on the fourth day. HSCs were identified by their staining with α-smooth muscle actin (α-SMA). Immunofluorescence was used for staining cells. Both the purity and viability of the cells were greater than 90% (Trypan Blue exclusion).
LX-2 cells (human HSCs line) were acquired from the Cell Collection Center of Wuhan University (China). The cells were derived from normal human HSCs and had the property of immortalized proliferation. The cells were cultured in DMEM (Gibco-Invitrogen, Carlsbad, CA, USA) containing 10% heat-inactivated FBS (Gibco, Carlsbad, CA, USA) and 1% penicillin-streptomycin (Life Technologies, Leuven, Belgium) at 37 °C in an atmosphere with 5% CO2. The cultures were passaged with 0.05% trypsin-EDTA (Gibco) every one or two days, and studies were performed during the fourth to seventh passages in vitro. For all experiments, LX-2 cells (5 × 105 cells/well) were plated in six-well plates and cultured for 24 h. The cells were serum-starved for 12 h before treatment.
LX-2 cells were treated with SEA (10 μg/ml) at the appropriate time. In certain experiments, the cells were pre-treated for 4 h with NLRP3 inflammasome inhibitor, MCC950 (1 μM), to inhibit the corresponding target. Lipopolysaccharide (LPS) (100 ng/ml, Sigma-Aldrich) was used as a positive control. PBS was added as a vehicle control. The optimal expression of NLRP3 protein in our experiment followed SEA stimulation for 24 h and LPS stimulation for 2 h. Subsequent experiments were similar.
Immunofluorescence was performed on 2 μm sections of paraffin-embedded liver tissues, LX-2 cells, primary mouse KCs and HSCs seeded on six-well chamber slides. They were then fixed in 4% PFA, permeabilized with 0.15% Triton X-100, and blocked with 3% H2O2 and 3% BSA. Primary antibodies were used for immunofluorescence double staining (Table 1): goat anti-NLRP3 (1:200) with rabbit anti-F4/80 (1:100) or with mouse anti-α-SMA/ACTA2 antibody (1:200), and rabbit anti-NF-κB (1:200) and mouse anti-F4/80 (1:50) were incubated overnight at 4 °C. Then, the samples were washed 3 times in PBS. Fluorescein isothiocyanate (FITC) (green, 1:50, ProteinTech Group, Chicago, USA) labeled donkey anti-goat and goat anti-rabbit, or cyanine 3.18 (Cy3) (red, 1:50, Aspen, Wuhan, China) labeled goat anti-rabbit and goat anti-mouse secondary antibodies (Table 1) were used for 50 min at room temperature. The samples were washed 3 times in PBS again. Nuclei were stained with DAPI. Fluorescent images were taken using an inverted fluorescence microscope (MF53 Mercury, Guangzhou, China). The co-localization area percentage of NLRP3 vs F4/80 or α-SMA, and NF-κB vs F4/80 in specific target cells of liver tissues was analyzed, along with integrated optical density (IOD) for target protein in cells by Image-Pro Plus 6.0 software.
Total RNA was extracted from cells and liver tissues by Trizol (Invitrogen, Carlsbad, CA, USA) and quantified by a spectrophotometer. In total, 2 μg RNA was reverse-transcribed to cDNA via the PrimeScript RT reagent kit (Toyob, Osaka, Japan), and real-time PCR (RT-PCR) was carried out using SYBR green master mix (Toyob) on a MyiQTM2 (Bio-Rad, Hercules, CA, USA). PCR primers were designed by a primer blasting tool on the NCBI website; primer sequences are summarized in Table 2. The glyceraldehyde-3-phosphate dehydrogenase (GAPDH) housekeeping gene was used as a reference control. The relative changes in gene expression were calculated by the 2−ΔΔCT method.
Western blot and ELISA
Liver tissues and cells were lysed in RIPA Lysis buffer (Beyotime). Next, 40 μg of protein was loaded and boiled at 95 °C for 5 min, followed by fractionation using sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE). The protein was transferred to PVDF membranes and then blocked with 5% non-fat milk in tris-buffered saline with tween 20 (TBST) before immune detection with the following primary antibodies: NLRP3 (1:500, Abcam, Cambridge, UK), Caspase 1 (1:500, Novus Biologicals, Littleton, CO, USA), IL-1β (1:500, Bioss, Beijing, China), α-SMA/ACTA2 (1:1000, Abcam), Collagen I (1:1000, Abcam), NF-κB (1:1000, CST, Danvers, MA, USA) and GAPDH (1:1000, CST). These antibodies were incubated overnight at 4 °C and HRP-conjugated secondary antibodies (1:5000, Aspen) were incubated for 1 h at room temperature. The protein was then labeled with enhanced chemiluminescent substrate (ECL, Millipore), and the band densities were detected by ImageJ software v.1.44 using the GAPDH band for standardization. All primary antibodies were rabbit anti-mouse IgG antibodies. All secondary antibodies were goat anti-rabbit IgG antibodies.
The serum was harvested and the IL-1β level was measured with a mouse IL-1β enzyme linked immunosorbent assay (ELISA) kit (eBioscience, San Diego, USA) according to kit instructions.
Data were shown as the means ± standard error of mean (SEM). They were analyzed by SPSS 17.0 or GraphPad Prism 5.0 software. Student’s t-test was performed to determine differences between two groups. One-way ANOVA was used to evaluate all other differences among multiple groups. P < 0.05 indicated statistical significance.
Pro-fibrotic markers depended on NLRP3 protein activation in LX-2 cells induced by SEA in vitro
Liver fibrosis was caused by schistosome eggs located in the portal system of the liver and was accompanied by inflammatory responses. SEA was released from schistosome eggs, which led to schistosomiasis-induced liver fibrosis (SSLF) . LX-2 cells were used to study liver fibrosis because they are spontaneously immortalized in low serum conditions . NLRP3 is a major proinflammatory “danger” receptor  and we wished to determine whether it was responsible for liver fibrosis. To directly address the role of NLRP3 during the development of SSLF, we first investigated whether SEA was sufficient to drive NLRP3 and pro-fibrotic markers (α-SMA and Collagen I) to increase in vitro. When we stimulated the LX-2 cells with SEA/LPS in vitro (Fig. 1a), we discovered that mRNA (NLRP3: F(3,8) = 42.15, P < 0.0001; α-SMA: F(3,8) = 59.83, P < 0.0001; Collagen I: F(3,8) = 17.44, P = 0.0002) and protein (NLRP3: F(3,8) = 39.38, α-SMA: F(3,8) = 37.08, Collagen I: F(3,8) = 26.61; all P < 0.0001) expressions of NLRP3, α-SMA and Collagen I were upregulated (Fig. 1b). Moreover, mRNA expression of NLRP3 exhibited a dose-dependent response in LX-2 cells that were treated with LPS after 1 h (F(2,6) = 43.55, P = 0.0003), 2 h (F(2,6) = 56.48, P = 0.0001) and 4 h (F(2,6) = 39.53, P = 0.0004; Fig. 1c). The results suggest that NLRP3 protein and pro-fibrotic markers were upregulated in HSCs stimulated by SEA in vitro.
To verify that α-SMA and Collagen I production relied on the activation of NLRP3 inflammasome, we inhibited NLRP3 expression with MCC950. The mRNA (F(3,8) = 42.15, P < 0.0001) and protein (F(3,8) = 39.38, P < 0.0001) expressions of NLRP3 in the MCC950-treated cells were lower than those in the MCC950-untreated cells (Fig. 1b). As shown in Fig. 1d, similar results were obtained using immunofluorescence double staining. NLRP3 protein expression was upregulated in the LX-2 cells treated with SEA/LPS, and the SEA-treated group effect was reversed by MCC950 (F(3,8) = 30.93, P < 0.0001; Fig. 1d). In addition, to determine the maximum expression of NLRP3 for the experiment, the optimal concentration and time of LPS, SEA and MCC950 was measured by RT-PCR. Experimental data indicated that the optimal concentration and time for LPS, SEA and MCC950 was 100 ng/ml and 2 h, 10 μg/ml and 24 h, and 1 μM and 4 h, respectively (Fig. 1c). In our experiments, LX-2 cells were treated with the above optimal concentration and time of LPS, SEA and MCC950. The results showed that the activation of NLRP3 led to an increase in α-SMA and Collagen I production, and this could be reduced by MCC950 in SEA-treated group (Fig. 1). This suggests that SEA induced α-SMA and Collagen I production is dependent on the expression of NLRP3 protein in LX-2 cells.
ECM deposition depended on NLRP3 inflammasome activation in the liver of S. japonicum-infected mice in vivo
To further elucidate the role of NLRP3 inflammasome in the process of SSLF, we performed a mouse model using S. japonicum. BALB/c mice were infected with 15 cercariae through the abdominal skin for 56 days (Fig. 2a). The infected mice exhibited increased mRNA (NLRP3: F(3,20) = 104.6, Caspase I: F(3,20) = 91.18, IL-1β: F(3,20) = 132.9, α-SMA: F(3,20) = 167.4, Collagen I: F(3,20) = 245.4; all P < 0.0001) and protein (NLRP3: F(3,20) = 51.83, Caspase I: F(3,20) = 143.9, IL-1β: F(3,20) = 203.5, α-SMA: F(3,20) = 81.15, Collagen I: F(3,20) = 19.12; all P < 0.0001) expressions of NLRP3 inflammasome (Fig. 2b, c) and liver fibrosis markers (α-SMA and Collagen I) (Fig. 2d). In general, NLRP3 inflammasome was more broadly detected in close proximity to areas containing egg granulomas (Fig. 2c). IL-1β in serum could also be detected by ELISA (Fig. 2e). Collectively, these results suggest that NLRP3 inflammasome formation in the liver and liver fibrosis were the result of egg deposition and that the inflammasome contributed to the pathogenesis of schistosomiasis.
To further study the relationship between NLRP3 inflammasome and liver fibrosis during S. japonicum infection, we infected BALB/c mice in a similar way, but infected mice then received i.p. injections of MCC950 or vehicle, on the day of infection (M0 group) or at day 22 post-infection (M4 group) (experimental design summarized in Fig. 2a). Livers of the infected mice with SSLF exhibited substantial increases in NLRP3 inflammasome and ECM deposition (Fig. 2b-f). MCC950 injections in the M0 group reduced mRNA and protein expressions when compared with vehicle-treated infected mice (SJ group). However, MCC950 injections in the M4 group aggravated NLRP3 inflammasome and ECM deposition (Fig. 2b-f). As seen in Fig. 2f, the percentage of the fibrosis area showed a larger positive area for collagen staining in the liver of infected mice (SJ group) compared to control mice. This was smaller in the M0 group but larger in the M4 group (F(3,20) = 91.12, P < 0.0001). Hyp content in the liver was indirectly measured for deposition of tissue collagen. These data showed Hyp content was increased in the liver of S. japonicum-infected mice, and this was counteracted by MCC950 in the M0 group but increased by MCC950 in the M4 group (F(3,20) = 64.2, P < 0.0001; Fig. 2g). These results demonstrate that ECM deposition was synchronized with the expression of NLRP3 inflammasome. We speculate that ECM deposition depended on NLRP3 inflammasome expression.
MCC950 altered conventional markers indicating pathological changes in mice infected with S. japonicum
The infected mice exhibited typical clinical symptoms, including anemia, hepatosplenomegaly, liver granuloma and fibrosis, and ascites . To observe the conventional influences of MCC950 on liver disease caused by S. japonicum, all mice were first weighed and then sacrificed. The gross morphology of the liver and spleen, liver and spleen indexes and liver function were evaluated and analyzed. Normal livers displayed a bright red color, whereas the liver of the infected mice appeared a dark red and had many small white granulomatous nodules on the surface. Compared with the SJ group, the liver surface of the MCC950-treated (M0 group) mice had fewer white nodules, whereas livers from mice in the M4 group had more obvious white spots and the liver itself was a darker red (Fig. 3a). Liver and spleen indexes of SJ mice showed an increase over control mice (Fig. 3b). MCC950 treatment (M0 group) reversed this increase, whereas MCC950 treatment (M4 group) greatly increased the liver and spleen indexes over the SJ group (liver index: F(3,20) = 33.22, spleen index: F(3,20) = 156.6; both P < 0.0001). The spleen was enlarged at 56 days after infection, but there were no statistically significant differences among these three groups (SJ, M0 and M4 groups) (P > 0.05, Fig. 3b). Plasma ALT and AST increased substantially at 56 days in mice infected with S. japonicum compared to control mice (ALT: F(3,20) = 32.47, AST: F(3,20) = 59.97; both P < 0.0001; Fig. 3c). The liver function (ALT and AST) in serum was higher in the M4 group when compared to the SJ group. However, administration of MCC950 (M0 group) could not have abrogated the increase in ALT and AST on the day of infection in SSLF mice (Fig. 3c). Liver granulomas are a typical pathological hallmark of schistosomiasis. To evaluate the influences of MCC950 on S. japonicum egg-induced liver granuloma, HE-staining of liver sections was used. Control livers showed normal cellular organization of uninfected hepatic lobules, with the typical actinomorphous distribution of hepatic cords around central veins and little collagen around periportal areas (Fig. 3d). Infected livers showed a markedly altered histological structure. At 56 days post-infection, inflammatory granulomatous lesions were seen in the liver tissue around schistosome eggs, and the amount of collagen fibers were remarkably increased, with most being found around granulomas. MCC950 treatment markedly reduced the area of granulomas in the M0 group. Nevertheless, compared with SJ group, the area of liver granulomas from the M4 group was significantly larger (F(3,20) = 98.74, P < 0.0001; Fig. 3d). In addition, body weight showed a sharp drop in infected mice (SJ, M0 and M4 groups) from the 35th to 42nd day, followed by more gradual weight loss, while control mice showed a steady gain in body weight until the 56th day (Fig. 3e). There were no statistically significant differences in body weight among SJ, M0 and M4 groups at the 56th day (P > 0.05), but a higher weight gain rate was observed at the 7th day in the M0 group (F(3,20) = 4.678, P = 0.0124) and a lower weight was observed at the 35th day in the M4 group (F(3,20) = 5.153, P = 0.0084) when compared to control mice (Fig. 3e). Thus, the liver surface of mice in the MCC950 treatment group (M0 group) was improved. Additionally, liver and spleen indexes, egg-induced liver granuloma and liver function were significantly reduced in the M0 group. In contrast, these indicators in the M4 group showed a more obvious increase than in the SJ group (Fig. 3).
Egg burden and pairing of adult worms were similar in MCC950-treated and untreated mice infected with S. japonicum
The pathological differences in the liver of mice infected with S. japonicum depended on the time of MCC950 administration. The liver pathology of mice infected with S. japonicum was reduced by MCC950 administered on the day of infection, whereas it exacerbated the pathology when MCC950 was administered at day 22 post-infection. The SEA released by S. japonicum eggs resulted in a granulomatous formation, suggesting that egg load in the liver determines the severity of liver pathology. We evaluated the egg burden (Fig. 4a) and the number, proportion and percentage of female and male adult worms (Fig. 4b, c) in the mesenteric veins from MCC950-treated and untreated mice infected with S. japonicum. Results showed that the number of male and total S. japonicum was dramatically lower in the M4 group compared to infected mice that did not receive this treatment. Interestingly, liver egg burden (F(3,20) = 0.7777, P = 0.4771), number of females (F(3,20) = 0.7777, P = 0.4771), and proportion (F(3,20) = 0.614, P = 0.5542) and percentage (female: F(3,20) = 1.057, P = 0.372; male: F(3,20) = 1.057, P = 0.372) of female and male S. japonicum were all similar among infected mice (Fig. 4). This result implies that MCC950 treatment does not affect the egg burden in the liver and the differential effect of MCC950 on hepatic injury was mainly caused by administration time.
MCC950 altered pro-fibrotic markers in primary HSCs derived from S. japonicum-infected mice
The pro-fibrotic markers play a major role in liver fibrosis of schistosomiasis [3, 6]. To further explore whether MCC950 affected pro-fibrotic markers, we separated primary HSCs from the livers of S. japonicum-infected mice. As illustrated in Fig. 5, the expressions of pro-fibrotic markers’ (α-SMA and Collagen I) mRNA (α-SMA: F(3,8) = 58.15, Collagen I: F(3,8) = 34.06; both P < 0.0001) and protein (α-SMA: F(3,8) = 40.62, Collagen I: F(3,8) = 55.27; both P < 0.0001) were dramatically increased in the SJ group when compared to the control group. This was reduced by MCC950 in the M0 group but increased in the M4 group when compared to the SJ group using RT-PCR (Fig. 5a) and western blotting (Fig. 5b).
NLRP3 inflammasome expression in KCs was more involved in liver fibrosis than in HSCs in mice infected with S. japonicum
In our experiments we observed that MCC950 can reduce NLRP3 expression in both LX-2 cells and primary HSCs. NLRP3 inflammasome was widely expressed in KCs and HSCs. These two kinds of cells both play an essential role in liver fibrosis. To better demonstrate which kind of cells originated from NLRP3 inflammasome implicated in hepatic fibrosis (particularly in KCs or HSCs in mice infected with S. japonicum), we examined the co-localization of NLRP3 with the KCs marker F4/80 or with the HSCs marker α-SMA in liver tissues. As shown in Fig. 6a, the co-localization area percentage of NLRP3 with F4/80 (F(3,20) = 118.8, P < 0.0001), or with α-SMA (F(3,20) = 49.9, P < 0.0001) in target cells was significantly increased surrounding liver granulomas in the infected mice when compared to control mice. Additionally, these measures were decreased in the M0 group but enhanced in the M4 group. However, there was no statistically significant difference in the expression of NLRP3 protein between primary KCs and HSCs within the same group from the SJ (t(4) = 0.7622, P = 0.4884), M0 (t(4) = 1.038, P = 0.3578) and M4 (t(4) = 0.3865, P = 0.7188) groups.
To further survey the effects of NLRP3 inflammasome expression in KCs and HSCs, cells were successfully separated from the livers at the indicated time (Fig. 6b). NLRP3 with F4/80 in KCs or with α-SMA in HSCs were labelled by immunofluorescence double staining (Fig. 6c), and NLRP3, Caspase 1 and IL-1β were all detected in KCs and HSCs by RT-PCR and western blotting (Fig. 6d, e). The above results showed an enhancement in the mRNA and protein levels of NLRP3, Caspase1 and IL-1β in primary KCs (NLRP3 mRNA: F(3,8) = 92.16, NLRP3 protein: F(3,8) = 146, Caspase1 mRNA: F(3,8) = 292.1, Caspase1 protein: F(3,8) = 62.16, IL-1β mRNA: F(3,8) = 67.27, IL-1β protein: F(3,8) = 192.8; all P < 0.0001) and HSCs (NLRP3 mRNA: F(3,8) = 108.8, NLRP3 protein: F(3,8) = 118, Caspase1 mRNA: F(3,8) = 44.15, Caspase1 protein: F(3,8) = 83.8, IL-1β mRNA: F(3,8) = 63.65, IL-1β protein: F(3,8) = 55.3; all P < 0.0001) from the SJ group in comparison to control mice. NLRP3 inflammasome was downregulated in the M0 group but was markedly upregulated in the M4 group when compared to the SJ group. The mRNA of NLRP3 inflammasome expression was higher in KCs than in HSCs for SJ (NLRP3: t(4) = 4.787, P = 0.0087; Caspase1: t(4) = 4.229, P = 0.0134; IL-1β: t(4) = 3.487, P = 0.0252), M0 (NLRP3: t(4) = 5.181, P = 0.0066; Caspase1: t(4) = 5.427, P = 0.0056; IL-1β: t(4) = 4.776, P = 0.0088) and M4 (NLRP3: t(4) = 4.787, P = 0.0087; Caspase1: t(4) = 3.053, P = 0.0379; IL-1β: t(4) = 6.218, P = 0.0034) groups (Fig. 6e). The NLRP3 inflammasome protein expression was also higher in KCs than in HSCs for the M4 group (NLRP3: t(4) = 4.410, P = 0.0116; Caspase1: t(4) = 4.490, P = 0.0109; IL-1β: t(4) = 10.02, P = 0.0006) (Fig. 6c, d). The protein expression of IL-1β was higher in KCs than in HSCs for the SJ (t(4) = 5.967, P = 0.004) and M0 (t(4) = 3.307, P = 0.0297) groups, as well as for the M4 (t(4) = 10.02, P = 0.0006) group (Fig. 6d). Taken together, the present study raises the possibility that NLRP3 inflammasome is activated and formed in both primary KCs and HSCs in S. japonicum-infected mice. Nonetheless, KCs as immune cells were more sensitive to NLRP3 inflammasome expression than HSCs.
NF-κB was involved in NLRP3 inflammasome-induced liver fibrosis in mice infected with S. japonicum
NF-κB is primarily composed of p50 and p65 subunits. NF-κB is part of a key signal transduction pathway and is generally used to study infection, inflammation and fibrosis through p65 subunit nuclear transfer . To further elucidate the mechanism by which infection with S. japonicum induces NLRP3-dependent liver fibrosis, we examined the role of NF-κB in this process. We attempted to detect the NF-κB p65 subunit protein in the liver tissues from all mice. As expected, the NF-κB p65 protein was significantly increased in the SJ group compared to control mice. By contrast, the NF-κB p65 protein showed a decreased presence in the M0 group but strong expression in the M4 group relative to the SJ group (F(3,20) = 30.92, P < 0.0001; Fig. 7a). As NLRP3 inflammasome participation in liver fibrosis triggered by S. japonicum is principally derived from KCs, we analyzed the co-localization of NF-κB and the KCs marker F4/80 in liver tissues. The expression of NF-κB protein in KCs was significantly increased in mice infected with S. japonicum. Interestingly, the NF-κB p65 protein in KCs was decreased when MCC950 was applied on the day of infection, but was displayed an opposite trend when MCC950 was given at day 22 post-infection (F(3,20) = 45.62, P < 0.0001; Fig. 7b). To further understand the expression of NF-κB protein in KCs, the NF-κB p65 protein was examined in primary KCs by western blotting. We found that the expression of NF-κB p65 protein in primary KCs was similar to that found in liver tissues (F(3,20) = 30.04, P = 0.0001; Fig. 7c). Collectively, NF-κB p65 expression is responsible for the effects of MCC950 on liver fibrosis. We speculate that NF-κB might be downstream of NLRP3 inflammasome, which then participates in NLRP3 inflammasome-induced liver fibrosis in mice infected with S. japonicum.
Chronic inflammation and inflammasome activation are crucial factors in the pathogenesis of liver fibrosis [16, 18]. To date, the NLRP3 inflammasome is reported to be one of the most-studied inflammasomes with respect to its role in antivirus responses , antifungal responses  and various human diseases [46, 47]. From the present study, it is reasonable to conclude that ECM deposition depended on NLRP3 inflammasome expression in mice infected with S. japonicum via NF-κB. We therefore propose that there are four main issues to be addressed. The first issue involves whether NLRP3 inflammasome can be activated in S. japonicum-infected mice and expressed in LX-2 cells evoked by SEA from S. japonicum eggs. The second problem relates to how MCC950 can alter NLRP3 inflammasome and liver fibrosis of S. japonicum differently depending on the time of MCC950 administration. The third issue deals with how the NLRP3 inflammasome is principally involved in liver fibrosis of S. japonicum derived from KCs. Finally, we tentatively put forward that NF-κB is a key point for NLRP3 inflammasome induced ECM deposition.
We confirm that NLRP3 inflammasome was expressed in liver fibrosis of mice infected with S. japonicum. NLRP3 inflammasome expression was investigated in liver tissues and in primary KCs and HSCs isolated from S. japonicum-infected mice. Our results largely support those of Tang and colleagues [17, 22]; however, NLRP3 protein was only detected in the LX-2 cells induced by SEA. Nevertheless, SEA alone was unable to induce other components of the NLRP3 inflammasome in the LX-2 cells. Similar data was gathered in bone marrow-derived DCs (BMDCs) treated with SEA alone . However, contradictory results have been reported that NLRP3 inflammasome is expressed in LX-2 cells induced by LPS , mouse primary HSCs induced by SEA from S. japonicum eggs , and BMDCs induced by SEA from S. mansoni eggs following TLR-stimulation . NLRP3 inflammasome expression is usually regulated by activated TLR . LPS, acting as a ligand for TLR4, could induce a small amount of NLRP3 inflammasome expression . We speculate that SEA is a multi-component complex with different effects on different cells. LX-2 cells derived from humans may be less vulnerable to SEA induced NLRP3 inflammasome activation.
The results reported here indicate that NLRP3 inflammasome activation plays an essential function in SSLF. NLRP3 inflammasome and ECM deposition were decreased by MCC950 in the M0 group, whereas they were increased by MCC950 in the M4 group in vivo. Parallel experiments showed NLRP3 inflammasome and pro-fibrotic markers had a weak expression in LX-2 cells co-treated with SEA and MCC950, as well as in primary KCs and HSCs from the M0 group. However, these markers showed a strong expression in the above-mentioned primary cells from the M4 group. Using MCC950 and NLRP3 siRNA, NLRP3 inflammasome and liver fibrosis can be reduced in nonalcoholic steatohepatitis (NASH) and S. japonicum mice, respectively [22, 50]. Using MCC950, similar findings were also obtained in other disease model including diabetic encephalopathy, hemorrhagic brain damage and lupus nephritis [51,52,53]. NLRP3 protein was not affected while Caspase I and IL-1β were both reduced when MCC950 was used in LPS and ATP co-induced mouse bone marrow derived macrophages (BMDM) . Currently, MCC950 has dual effects on the NLRP3. One view is that MCC950 only affects NLRP3 inflammsome activation. The other view is that MCC950 not only affects NLRP3 inflammsome activation, but also affects the NLRP3. This difference may be related to different treatment methods. NLRP3 was reduced by MCC950 in our experiments, which may be attributed to blocking the upstream signal of NLRP3, like NEK7 [54, 55]. At present, MCC950 is used in the Ang-II induced cardiac fibrosis mouse model, and a reduction in fibrosis is also observed . Several researchers pointed out that NLRP3 inflammsome deficiency has a protective effect against carbon tetrachloride (CCl4) or thioacetamide (TAA)-induced liver fibrosis, and that it reduces mortality and liver injury after acetaminophen administration [57, 58]. The development of liver fibrosis induced by CCl4 and TAA was apparently delayed in mice lacking NLRP3 or ASC, and the upregulation of Collagen I and TGF-β induced by MSU could not be observed in ASC-/- HSCs . Likewise, it has been reported that NLRP3 inflammasome activation was required for fibrosis development in NLRP3 knockout and mutant mice [18, 59]. Similar results were found in liver fibrosis after bile duct ligation (BDL) or Ang-II infusion . We believe that hepatic fibrosis induced by S. japonicum is due to the presence of the eggs . To understand whether NLRP3 inflammasome activation induced ECM deposition in a S. japonicum mouse model, we sought to block NLRP3 expression. We thought it was better to block NLRP3 inflammasome at two time points. One time point was at the beginning of S. japonicum infection and the second was prior to S. japonicum egg production. We found that ECM deposition was differently affected depending on the time of MCC950 administration. ECM deposition was alleviated when MCC950 was administered at the beginning of infection but was augmented when MCC950 was administered before S. japonicum egg production. We propose that the decrease in ECM deposition at the first time point was due to MCC950 inhibiting inflammation. The results were similar to other disease models, including NASH , BDL and Ang-II . Our results are again consistent with the results obtained by Tang and colleagues, who used NLRP3 siRNA technology in the same mouse model . The expression of kidney fibrosis markers, MCC950 administration on the seventh day, was similar to the non-administered group in adenine-enriched diet-induced kidney fibrosis . This result is possibly due to inflammation-driven fibrosis. We hypothesize that MCC950 administration led to an increase in ECM deposition at the later time point and that this was too late to block inflammation and hence promoted liver fibrosis. Liver inflammation and fibrosis have an interacting relationship in that inflammation is the initiator of liver fibrosis, and liver fibrosis is the ultimate outcome of excessive inflammation [12, 61]. When S. japonicum-infected mice were administered MCC950 before egg production, it was the equivalent to suppressing the excessive inflammatory response in the liver. Undoubtedly, liver fibrosis in the M4 group should be exacerbated. The results in the present study suggest that during the period of S. japonicum infection, inflammasome activation is accompanied with fibrogenic changes in the liver.
Our results show that NLRP3 inflammasome in KCs and HSCs are both implicated in the progression of liver fibrosis in mice infected with S. japonicum. Interestingly, NLRP3 inflammasome derived from KCs is larger than in HSCs. Using immunofluorescence double staining, we identified that the co-localization area percentage of NLRP3 with F4/80, or with α-SMA in target cells was increased in liver tissues and in primary KCs and HSCs from the SJ group in comparison to control mice. This could be suppressed by MCC950 in the M0 group but reinforced by MCC950 in the M4 group. We confirmed this in primary KCs and HSCs via RT-PCR and western blot. Additionally, there is substantial evidence that NLRP3 inflammasome activation and formation is present in KCs and HSCs. By comparing the expression of the NLRP3 inflammasome in the above two kinds of cells, we found that the NLRP3 inflammasome expression in KCs was generally higher than in HSCs. KCs and HSCs are pivotal for chronic inflammation and fibrogenesis [4, 12, 37, 61]. The effect of macrophages and HSCs on liver fibrosis depends on their activation state [37, 62]. The NLRP3 inflammasome has been reported to amplify chronic liver inflammation and activate HSCs . NLRP3 inflammasome was expressed not only in HSCs [21, 57] but also in KCs [50, 63]. In vitro and in vivo experiments showed cholesterol crystals  or LPS  could induce KCs to release IL-1β, and this process can be inhibited by MCC950 . Currently, toxicological profiling of metal oxide nanoparticles (TMO) has a similar effect in KCs . These results support the view that activation of NLRP3 inflammasome contributes to liver fibrosis of S. japonicum infected mice in both KCs and HSCs. Our study showed that NLRP3 inflammasome activation mostly comes from KCs. We recognize that there are some limitations in our study, in that we did not examine other mouse strains, the activity and numbers of S. japonicum cercariae, and other time points of S. japonicum infection.
We have demonstrated that NF-κB is involved in NLRP3 inflammasome induced liver fibrosis of S. japonicum-infected mice. Our results indicate that NF-κB expression is increased in liver tissues and in KCs of the SJ group compared to the control group, and this was suppressed by MCC950 in the M0 group but enhanced by MCC950 in the M4 group. NF-κB, as a transcription factor, regulates liver inflammation and takes part in the development of liver fibrosis . The traditional view is that NF-κB is upstream to the NLRP3 inflammasome [28, 30], but in our study we found that NF-κB was regulated by NLRP3 inflammasome. The expression of NF-κB was blocked by NLRP3 inhibitor MCC950 and NLRP3 gene knockout, in the model of inflammatory hyperalgesia and chronic unpredictable mild stress (CUMS) induced depression, respectively [64, 65]. It was also reduced following NLRP3 knocked down in the early stage of Staphylococcus aureus infection by siRNA in human monocytic cell line THP-1 . The latest papers report that attenuating the degradation of NF-κB inhibitor (IκB) could decrease collagen synthesis following silencing of NLRP3 in lung fibrosis . These studies demonstrate that NF-κB and NLRP3 inflammasome have an upstream and downstream relationship with each other.
In addition, liver function (ALT/AST) and liver granuloma induced by the eggs were both altered by MCC950, but different time points of administration led to different results. AST recovery level was not as good as ALT in the M0 group, which may result in statistical differences between the N and M0 groups. ALT is mainly distributed in the liver and is expressed in the cytoplasm of hepatocytes, while AST is mainly distributed in the myocardium, followed by the liver, and is expressed in the mitochondria . Therefore, AST is not as sensitive to ALT when the liver is affected. ALT/AST was reduced by MCC950 administration for 56 days in methionine/choline deficiency (MCD) diet induced non-alcoholic fatty liver disease (NAFLD) mice . Our previous administration results are similar to these results. MCC950 could also reduce the number of worms. Male worms are more numerous than female worms, but single males are more susceptible than females to MCC950, which are less likely to survive in MCC950 administration. The numbers of male worms were reduced more obviously owing to significant sex differentiation in the M4 group, but the mechanism needs to be further elucidated. To our knowledge, we are the first to use MCC950 in the liver fibrosis mouse model caused by S. japonicum. We tentatively propose that the relationship between MCC950 and liver fibrosis is triggered by S. japonicum eggs (Fig. 8).
So far, our conclusion is that the NLRP3 inflammasome mainly participates in the inflammatory response in the acute phase of S. japonicum infection and induces immune cells KCs to produce a large number of cytokines such as IL-1β , IL-6 , IL-17 , IL-18  and TGF-β . These massively released cytokines alter the immune microenvironment of the liver and evoke cascading signal responses through the cytokine receptors itself on the surface of the cell membrane . These induce the resting hepatic stellate cells to activate and to convert into myofibroblasts, eventually forming ECM deposition and leading to liver fibrosis [4, 6]. Moreover, there is no evidence that NLRP3 inflammasome is directly involved in the process of liver fibrosis.
In summary, we have demonstrated that the NLRP3 inflammasome takes part in the process of S. japonicum induced liver fibrosis via NF-κB signaling. The results indicate that the activation of NLRP3 inflammasome is both in KCs and HSCs, with a more robust effect in KCs. We surmise that the activation of NLRP3 inflammasome in KCs may be followed by the production of cytokines, for instance IL-1β. This then activates HSCs accompanied by NLRP3 inflammasome activation, and then results in ECM deposition and liver fibrosis. The data provide new arguments about the development of liver fibrosis following S. japonicum infection. We have also identified novel molecular targets that could have the potential to be developed into preventative measures for SSLF. In the future, we may further explore whether there are other signaling pathways involved in NLRP3 inflammasome induced liver fibrosis following S. japonicum infection.
Apoptosis-associated speck-like protein containing a caspase recruitment domain
Bile duct ligation
Bone marrow-derived DCs
Mouse bone marrow derived macrophages
Bovine serum albumin
Caspase recruitment domain-containing protein 8
- Caspase 1:
Cysteinyl aspartate specific proteinase
Cytokine release inhibitory drug 3
Chronic unpredictable mild stress
Streptavidin-peroxidase complex 3, 3-diaminobenzidine tetrahydroxychloride
Danger-associated molecular patterns
Dulbecco’s modified Eagle’s medium
Enhanced chemiluminescent substrate
Enzyme linked immunosorbent assay
Eggs per gram
Mouse epidermal growth factor-like module-containing mucin-like hormone receptor-like 1
Fetal bovine serum
- H2O2 :
Hepatic stellate cells
Integrated optical density
Inhibitor of NF-κB
Non-alcoholic fatty liver disease
Nod-like receptor protein-3
Nucleotide-binding oligomerization domain (NOD) leucine-rich repeat containing receptors
Pathogen-associated molecular patterns
Pattern recognition receptors
Dodecyl sulphate polyacrylamide gel electrophoresis
Soluble egg antigen
Standard error of mean
Schistosomiasis-induced liver fibrosis
Tris-buffered saline with tween 20
Transforming growth factor-β
Toxicological profiling of metal oxide nanoparticles
Tumor necrosis factor-α
α-smooth muscle actin
Chuah C, Jones MK, Burke ML, McManus DP, Gobert GN. Cellular and chemokine-mediated regulation in schistosome-induced hepatic pathology. Trends Parasitol. 2014;30:141–50.
Colley DG, Bustinduy AL, Secor WE, King CH. Human schistosomiasis. Lancet. 2014;383:2253–64.
Anthony BJ, Ramm GA, McManus DP. Role of resident liver cells in the pathogenesis of schistosomiasis. Trends Parasitol. 2012;28:572–9.
Higashi T, Friedman SL, Hoshida Y. Hepatic stellate cells as key target in liver fibrosis. Adv Drug Deliv Rev. 2017;121:27–42.
Puche JE, Saiman Y, Friedman SL. Hepatic stellate cells and liver fibrosis. Compar Physiol. 2013;3:1473–92.
Carson JP, Ramm GA, Robinson MW, McManus DP, Gobert GN. Schistosome-induced fibrotic disease: the role of hepatic stellate cells. Trends Parasitol. 2018;34:524–40.
Wree A, McGeough MD, Inzaugarat ME, Eguchi A, Schuster S, Johnson CD, et al. NLRP3 inflammasome driven liver injury and fibrosis: roles of IL-17 and TNF in mice. Hepatology. 2017. https://doi.org/10.1002/hep.29523.
Seki E, De Minicis S, Osterreicher CH, Kluwe J, Osawa Y, Brenner DA, et al. TLR4 enhances TGF-β signaling and hepatic fibrosis. Nat Med. 2007;13:1324–32.
Sasaki R, Devhare PB, Steele R, Ray R, Ray RB. Hepatitis C virus-induced CCL5 secretion from macrophages activates hepatic stellate cells. Hepatology. 2017;66:746–57.
Krenkel O, Tacke F. Liver macrophages in tissue homeostasis and disease. Nat Rev Immunol. 2017;17:306–21.
Bieghs V, Trautwein C. The innate immune response during liver inflammation and metabolic disease. Trends Immunol. 2013;34:446–52.
Koyama Y, Brenner DA. Liver inflammation and fibrosis. J Clin Invest. 2017;127:55–64.
Czaja AJ. Hepatic inflammation and progressive liver fibrosis in chronic liver disease. World J Gastroenterol. 2014;20:2515–32.
Burke ML, Jones MK, Gobert GN, Li YS, Ellis MK, McManus DP. Immunopathogenesis of human schistosomiasis. Parasite Immunol. 2009;31:163–76.
Hirata M, Fukuma T. Cytokine regulation in experimentally-induced Schistosoma japonicum egg granuloma formation. Parasitol Int. 2003;52:341–9.
Alegre F, Pelegrin P, Feldstein AE. Inflammasomes in liver fibrosis. Semin Liver Dis. 2017;37:119–27.
Meng N, Xia M, Lu YQ, Wang M, Boini KM, Li PL, et al. Activation of NLRP3 inflammasomes in mouse hepatic stellate cells during Schistosoma infection. Oncotarget. 2016;7:39316–31.
Wree A, Eguchi A, McGeough MD, Pena CA, Johnson CD, Canbay A, et al. NLRP3 inflammasome activation results in hepatocyte pyroptosis, liver inflammation, and fibrosis in mice. Hepatology. 2014;59:898–910.
Latz E, Xiao TS, Stutz A. Activation and regulation of the inflammasomes. Nat Rev Immunol. 2013;13:397–411.
Nagy LE. The role of innate immunity in alcoholic liver disease. Alcohol Res. 2015;37:237–50.
Ning ZW, Luo XY, Wang GZ, Li Y, Pan MX, Yang RQ, et al. MicroRNA-21 mediates angiotensin II-induced liver fibrosis by activating NLRP3 inflammasome/IL-1β axis via targeting Smad7 and Spry1. Antioxid Redox Signal. 2017;27:1–20.
Lu YQ, Zhong S, Meng N, Fan YP, Tang WX. NLRP3 inflammasome activation results in liver inflammation and fibrosis in mice infected with Schistosoma japonicum in a Syk-dependent manner. Sci Rep. 2017;7:8120.
Jo EK, Kim JK, Shin DM, Sasakawa C. Molecular mechanisms regulating NLRP3 inflammasome activation. Cell Mol Immunol. 2016;13:148–59.
He Y, Hara H, Núñez G. Mechanism and regulation of NLRP3 inflammasome activation. Trends Biochem Sci. 2016;41:1012–21.
Yu SY, Tang L, Zhao GJ, Zhou SH. Statin protects the heart against ischemia-reperfusion injury via inhibition of the NLRP3 inflammasome. Int J Cardiol. 2017;229:23–4.
Liston A, Masters SL. Homeostasis-altering molecular processes as mechanisms of inflammasome activation. Nat Rev Immunol. 2017;17:208–14.
Christ A, Gunther P, Lauterbach MAR, Duewell P, Biswas D, Pelka K, et al. Western diet triggers NLRP3-dependent innate immune reprogramming. Cell. 2018;172:162–75 e14.
Szabo G, Csak T. Inflammasomes in liver diseases. J Hepatol. 2012;57:642–54.
Petrasek J, Bala S, Csak T, Lippai D, Kodys K, Menashy V, et al. IL-1 receptor antagonist ameliorates inflammasome-dependent alcoholic steatohepatitis in mice. J Clin Invest. 2012;122:3476–89.
Zhong Z, Umemura A, Sanchez-Lopez E, Liang S, Shalapour S, Wong J, et al. NF-κB restricts inflammasome activation via elimination of damaged mitochondria. Cell. 2016;164:896–910.
Luedde T, Schwabe RF. NF-κB in the liver - linking injury, fibrosis and hepatocellular carcinoma. Nat Rev Gastroenterol Hepatol. 2011;8:108–18.
Yu X, Lan P, Hou X, Han Q, Lu N, Li T, et al. HBV inhibits LPS-induced NLRP3 inflammasome activation and IL-1β production via suppressing the NF-κB pathway and ROS production. J Hepatol. 2017;66:693–702.
Afonina IS, Zhong Z, Karin M, Beyaert R. Limiting inflammation-the negative regulation of NF-κB and the NLRP3 inflammasome. Nat Immunol. 2017;18:861–9.
Duong BH, Onizawa M, Oses-Prieto JA, Advincula R, Burlingame A, Malynn BA, et al. A20 restricts ubiquitination of pro-interleukin-1β protein complexes and suppresses NLRP3 inflammasome activity. Immunity. 2015;42:55–67.
Lee HM, Yuk JM, Kim KH, Jang J, Kang G, Park JB, et al. Mycobacterium abscessus activates the NLRP3 inflammasome via Dectin-1-Syk and p62/SQSTM1. Immunol Cell Biol. 2012;90:601–10.
Mao L, Zhang L, Li H, Chen W, Wang H, Wu S, et al. Pathogenic fungus Microsporum canis activates the NLRP3 inflammasome. Infect Immun. 2014;82:882–92.
Barron L, Wynn TA. Macrophage activation governs schistosomiasis-induced inflammation and fibrosis. Eur J Immunol. 2011;41:2509–14.
Coll RC, Robertson AA, Chae JJ, Higgins SC, Munoz-Planillo R, Inserra MC, et al. A small-molecule inhibitor of the NLRP3 inflammasome for the treatment of inflammatory diseases. Nat Med. 2015;21:248–55.
Zhu Y, Hua W, Xu M, He W, Wang X, Dai Y, et al. A novel immunodiagnostic assay to detect serum antibody response against selected soluble egg antigen fractions from Schistosoma japonicum. PLoS One. 2012;7:e44032.
Aparicio-Vergara M, Tencerova M, Morgantini C, Barreby E, Aouadi M. Isolation of Kupffer cells and hepatocytes from a single mouse liver. Methods Mol Biol. 2017;1639:161–71.
Weiskirchen S, Tag CG, Sauer-Lehnen S, Tacke F, Weiskirchen R. Isolation and culture of primary murine hepatic stellate cells. Methods Mol Biol. 2017;1627:165–91.
Xu L, Hui AY, Albanis E, Arthur MJ, O'Byrne SM, Blaner WS, et al. Human hepatic stellate cell lines, LX-1 and LX-2: new tools for analysis of hepatic fibrosis. Gut. 2005;54:142–51.
Dostert C, Pétrilli V, Van Bruggen R, Steele C, Mossman BT, Tschopp J. Innate immune activation through Nalp3 inflammasome sensing of asbestos and silica. Science. 2008;320:674–7.
Gasparini C, Feldmann M. NF-κB as a target for modulating inflammatory responses. Curr Pharm Des. 2012;18:5735–45.
He Z, Chen J, Zhu X, An S, Dong X, Yu J, et al. The NLRP3 inflammasome activation mediates Zika virus associated inflammation. J Infect Dis. 2018;217:1942–51.
Vakrakou AG, Boiu S, Ziakas PD, Xingi E, Boleti H, Manoussakis MN. Systemic activation of NLRP3 inflammasome in patients with severe primary Sjogren’s syndrome fueled by inflammagenic DNA accumulations. J Autoimmun. 2018;91:23–33.
Lee HM, Kim JJ, Kim HJ, Shong M, Ku BJ, Jo EK. Upregulated NLRP3 inflammasome activation in patients with type 2 diabetes. Diabetes. 2013;62:194–204.
Ritter M, Gross O, Kays S, Ruland J, Nimmerjahn F, Saijo S, et al. Schistosoma mansoni triggers Dectin-2, which activates the Nlrp3 inflammasome and alters adaptive immune responses. Proc Natl Acad Sci USA. 2010;107:20459–64.
Jiang S, Zhang Y, Zheng JH, Li X, Yao YL, Wu YL, et al. Potentiation of hepatic stellate cell activation by extracellular ATP is dependent on P2X7R-mediated NLRP3 inflammasome activation. Pharmacol Res. 2017;117:82–93.
Mridha AR, Wree A, Robertson AAB, Yeh MM, Johnson CD, Van Rooyen DM, et al. NLRP3 inflammasome blockade reduces liver inflammation and fibrosis in experimental NASH in mice. J Hepatol. 2017;66:1037–46.
Zhai Y, Meng X, Ye T, Xie W, Sun G, Sun X. Inhibiting the NLRP3 inflammasome activation with MCC950 ameliorates diabetic encephalopathy in db/db mice. Molecules. 2018;23:522.
Ren H, Kong Y, Liu Z, Zang D, Yang X, Wood K, et al. Selective NLRP3 (pyrin domain-containing protein 3) inflammasome inhibitor reduces brain injury after intracerebral hemorrhage. Stroke. 2018;49:184–92.
Fu R, Guo C, Wang S, Huang Y, Jin O, Hu H, et al. Podocyte activation of NLRP3 inflammasomes contributes to the development of proteinuria in lupus nephritis. Arthritis Rheumatol. 2017;69:1636–46.
Xu J, Lu L, Li L. NEK7: a novel promising therapy target for NLRP3-related inflammatory diseases. Acta Biochim Biophys Sin. 2016;48:966–8.
Schmid-Burgk JL, Chauhan D, Schmidt T, Ebert TS, Reinhardt J, Endl E, et al. A genome-wide CRISPR (clustered regularly interspaced short palindromic repeats) screen identifies NEK7 as an essential component of NLRP3 inflammasome activation. J Biol Chem. 2016;291:103–9.
Gan W, Ren J, Li T, Lv S, Li C, Liu Z, et al. The SGK1 inhibitor EMD638683, prevents Angiotensin II-induced cardiac inflammation and fibrosis by blocking NLRP3 inflammasome activation. Biochim Biophys Acta. 2018;1864:1–10.
Watanabe A, Sohail MA, Gomes DA, Hashmi A, Nagata J, Sutterwala FS, et al. Inflammasome-mediated regulation of hepatic stellate cells. Am J Physiol Gastrointest Liver Physiol. 2009;296:G1248–57.
Imaeda AB, Watanabe A, Sohail MA, Mahmood S, Mohamadnejad M, Sutterwala FS, et al. Acetaminophen-induced hepatotoxicity in mice is dependent on Tlr9 and the Nalp3 inflammasome. J Clin Invest. 2009;119:305–14.
Wree A, McGeough MD, Pena CA, Schlattjan M, Li H, Inzaugarat ME, et al. NLRP3 inflammasome activation is required for fibrosis development in NAFLD. J Mol Med (Berl). 2014;92:1069–82.
Ludwig-Portugall I, Bartok E, Dhana E, Evers BD, Primiano MJ, Hall JP, et al. An NLRP3-specific inflammasome inhibitor attenuates crystal-induced kidney fibrosis in mice. Kidney Int. 2016;90:525–39.
Mack M. Inflammation and fibrosis. Matrix Biol. 2018;68–69:106–21.
Tsuchida T, Friedman SL. Mechanisms of hepatic stellate cell activation. Nat Rev Gastroenterol Hepatol. 2017;14:397–411.
Mirshafiee V, Sun B, Chang CH, Liao YP, Jiang W, Jiang J, et al. Toxicological profiling of metal oxide nanoparticles in liver context reveals pyroptosis in Kupffer cells and macrophages versus apoptosis in hepatocytes. ACS Nano. 2018;12:3836–52.
Dolunay A, Senol SP, Temiz-Resitoglu M, Guden DS, Sari AN, Sahan-Firat S, et al. Inhibition of NLRP3 inflammasome prevents LPS-induced inflammatory hyperalgesia in mice: contribution of NF-κB, Caspase-1/11, ASC, NOX, and NOS isoforms. Inflammation. 2017;40:366–86.
Su WJ, Zhang Y, Chen Y, Gong H, Lian YJ, Peng W, et al. NLRP3 gene knockout blocks NF-κB and MAPK signaling pathway in CUMS-induced depression mouse model. Behav Brain Res. 2017;322:1–8.
Kinoshita T, Imamura R, Kushiyama H, Suda T. NLRP3 mediates NF-κB activation and cytokine induction in microbially induced and sterile inflammation. PLoS One. 2015;10:e0119179.
Kuang J, Xie M, Wei X. The NALP3 inflammasome is required for collagen synthesis via the NF-κB pathway. Int J Mol Med. 2018;41:2279–87.
Amacher DE. Serum transaminase elevations as indicators of hepatic injury following the administration of drugs. Regul Toxicol Pharmacol. 1998;27:119–30.
Lorenz G, Darisipudi MN, Anders HJ. Canonical and non-canonical effects of the NLRP3 inflammasome in kidney inflammation and fibrosis. Nephrol Dial Transplant. 2014;29:41–8.
Iannitti RG, Napolioni V, Oikonomou V, De Luca A, Galosi C, Pariano M, et al. IL-1 receptor antagonist ameliorates inflammasome-dependent inflammation in murine and human cystic fibrosis. Nat Commun. 2016;7:10791.
The authors would like to thank Zhi-Gang Fan and Ji-Sheng Hu for technical assistance.
This work was financially supported by the Fundamental Research Funds for the Central Universities, HUST (grant no. 2014QN033). The funders had no role in study design, data collection, analysis and interpretation, or the decision to write the manuscript for publication.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article.
Ethics approval and consent to participate
The animal experiments were performed in accordance with the guidelines of the Chinese Council on Animal Care, and were approved by the Ethics Committee of Animal Experimentation of Tongji Medical College (Wuhan, China).
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Zhang, W., Fang, Z. & Liu, W. NLRP3 inflammasome activation from Kupffer cells is involved in liver fibrosis of Schistosoma japonicum-infected mice via NF-κB. Parasites Vectors 12, 29 (2019) doi:10.1186/s13071-018-3223-8
- NLRP3 inflammasome
- Liver fibrosis
- Schistosoma japonicum
- Kupffer cells