Complement Component C3: A Novel Biomarker Participating in the Pathogenesis of Non-alcoholic Fatty Liver Disease

Non-alcoholic fatty liver disease (NAFLD) is currently the most common cause of chronic liver disorder worldwide. The pathological spectrum of NAFLD ranges from simple steatosis to non-alcoholic steatohepatitis (NASH) that induces progressive liver cirrhosis and eventually hepatocellular carcinoma (HCC). However, the molecular mechanisms driving the transformation of NASH are obscure. There is a compelling need for understanding the pathogenic mechanisms of NASH, and thereby providing new insight into mechanism-based therapy. Currently, several studies reported that complement system, an innate immune system, played an important role in the pathogenesis of NAFLD, which was also proved by our recent study. Complement component 3 (C3), a protein of the innate immune system, plays a hub role in the complement system. Herein, we present a review on the role and molecular mechanism of C3 in NASH as well as its implication in NASH diagnosis and treatment.


INTRODUCTION
Non-alcoholic fatty liver disease (NAFLD) has become a very common liver disease worldwide. The disease spectrum includes non-alcoholic fatty liver (NAFL), non-alcoholic steatohepatitis(NASH), nutritional fibrosis and hepatocellular carcinoma Cancer (HCC). Epidemiological investigations show that the prevalence of NAFLD is 25-30% in western countries (1). With the change of diet structure and lifestyle, the prevalence of NAFLD is 17-46% in China (2). Notably, the prevalence of NAFLD in young children is currently increasing year by year, and the high prevalence rate is alarming (3). Among NAFLD patients, the prevalence of NASH is about 20% (4). However, the diagnosis of NASH relies on liver biopsy and the non-invasive diagnostic methods are limited. To date, there's no Food and Drug Administration (FDA)-approved drug for NAFLD and NASH treatment. Therefore, there is an unmet clinical need for the diagnosis, prevention and treatment of NAFLD and NASH. In recent years, innate immunity is thought to play an important role in the development of NAFLD. Therefore, we summarized previous studies and provided a holistic framework concerning the relationship between complement and NAFLD.

THE OVERVIEW OF COMPLEMENTS SYSTEM
In the early stage of NAFLD, bacterial endotoxin, free fatty acid (FFA), cholesterol and many other substances in the body can activate the complement system through danger associated molecular patterns (DAMPs) or pathogen associated molecular pattern (PAMPs) (5,6). Complement system, which is considered as an important innate immunity (7)(8)(9)(10), has been confirmed to be cascade-activated through the following three pathways: classical, lectin and alternative, all of which converge in the formation of fraction C3. Briefly, in the activated complement signaling pathway, complement component C3 is cleaved into C3a and C3b through C3 converting enzyme, in which C3b binds with C3 converting enzyme complex to form C4bC2aC3b complex in classical pathway and lectin pathway and C3bBbC3b complex in alternative pathway. Both complexes are converting enzymes of complement molecule C5, and then further activate the downstream molecules of Complement system to form membrane attack complex (MAC/C5b-9). Furthermore, the classical activation pathway mainly involves the binding of antigen with immunoglobulin (IgM or IgG) or C-reactive protein. In the lectin pathway, Complement activation is triggered by the interaction complex carbohydrate residues with the surface of pathogens to circulating mannose binding lectins (MBL) or ficolins. The alternative pathway is activated by the direct combination of hydrolyzed C3b and bacterial membrane surface (Figure 1).

COMPLEMENT C3 AND NAFLD
Currently, the role of Complement system in NAFLD disorders has been extensively investigated in clinical epidemiological studies (11). Serum complement C3 levels are positively associated with the severity of NAFLD. A Turkish case-control study involving 46 NAFLD patients demonstrated that the level of Complement component C3 was significantly higher in peripheral blood of NAFLD patients than that of healthy control group and chronic hepatitis B control group (12). Moreover, a Dutch cross-sectional study involving 523 middle-aged and elderly patients with NAFLD found that the level of C3a, the active product of complement C3, was closely related to liver fat content (13). Consistently, two large sample epidemiological studies recruited thousands of cases in China showed that the level of serum complement C3 was an independent risk factor for the diagnosis of NAFLD and related to the prevalence and the severity of NAFLD (14,15). Apart from the serum, the deposition of C3 is also identified in the liver tissue of NAFLD patients accompanied with the deposition of MAC-C9 (16). The deposition of C3 was proved to be mainly Abbreviations: NAFLD, Non-alcoholic fatty liver disease; NASH, Non-alcoholic steatohepatitis; HCC, hepatocellular carcinoma; C3, Complement component 3; NAFL, non-alcoholic fatty liver; FDA, Food and Drug Administration; FFA, free fatty acid; DAMPs, danger associated molecular patterns; PAMPs, pathogen associated molecular patterns; MAC, membrane attack complex; MBL, mannosebinding lectin; IL, interleukin; KCs, Kupffer cells; NLR, neutrophil to lymphocyte ratio; NAS, NAFLD activity score. located around the hepatocytes with macrovesicular steatosis. Subsequently, clinicopathological examination confirmed that a large number of hepatic parenchymal cells were apoptotic in the liver tissue with complement C3 activation. Complement C3 activation could lead to a large number of neutrophils infiltration and abnormal increase of IL-8 and IL-6 expression in liver tissue, while C9 deposition could lead to increased IL-1β expression in liver cells. Additionally, in other patients with NAFLD, there was a close correlation between serum C3 level and NAFLD. For example, Pan et al. demonstrated that C3 was the only highly predictive factor in diagnosing NAFLD from 648 recruited patients with chronic kidney disease by Logistic regression analysis (17). Ursini et al. recruited 164 patients with rheumatoid arthritis, of which 25% (41/164) were complicated with NAFLD. Further logistic regression analysis also confirmed the high correlation between C3 and NAFLD analysis (18). Most importantly, Himoto et al. found that the increased serum C3 levels are closely related to the abnormal metabolism of the body including obesity, insulin resistance, and/or hepatic steatosis in those patients with chronic hepatitis C, which had nothing to do with chronic HCV infection (19). Collectively, the complement system is closely related to NAFLD. It is speculated that the complement system is largely activated to regulate the immune inflammatory response in the pathogenesis of NAFLD, which directly participates in the occurrence, development and prognosis of NAFLD.

THE PATHOGENIC C3 ACTIVATION IN NAFLD PROGRESSION
NAFLD severity was closely associated with accumulation of activation products of C3 around steatotic hepatocytes. However, the underlying mechanism by which complement C3 in NAFLD remained elusive. Hepatocytes are confirmed to be the predominant origin of complement components including C3 protein. Because C3 is the key molecule in the pathway of complement system activation (7), several hypotheses are proposed that C3 plays an important role in lipid metabolism in the pathogenesis of NAFLD (Figure 2): Firstly, C3 is mainly synthesized by hepatocytes and identified to appear in lipoprotein particles such as high density lipoprotein and chylomicron (20,21). When complement C3 gene was knocked out in mice, serum triglyceride levels increased 58% higher compared with wild-type mice, and the increased lipoprotein profile is mainly low-density lipoprotein and very low-density lipoprotein (21), indicating a potential role of C3 in lipid metabolism regulation (22). Secondly, Complement system directly regulates the oxidative stress in hepatocytes with excessive fat accumulation. It is well-known that multiple-hit hypothesis has been widely accepted in the pathogenesis of NAFLD. The first hit is closely linked with insulin resistance under fat accumulation. With the response of hepatocytes to oxidative stress, a large number of inflammatory cytokines are secreted in the liver, which further cause the second hit in hepatocytes (23). Complement component C3, as a major player in innate immune response, might be activated by the first hit and forming the second hit in NAFLD pathogenesis (24). Thirdly, the phenomenon of apoptosis is a typical pathological feature in the liver with NAFL and NASH. Due to the accumulated fat droplets in hepatocytes, a variety of apoptotic cascade pathways are activated including caspases 3 and 7 or cleavage of cytokeratin 18, resulting in a large number of hepatocytes apoptosis. Complement system was found to be quickly activated by the apoptotic hepatocyte debris. Furthermore, the activated Complement system immediately recognized and cleaned the apoptotic pathological liver cells, thus maintaining the homostasis in liver (25). Thus, elevation of serum complement C3 might act as a protective response in NAFLD mediated by apoptosis. Finally, Complement activation is indicated to be involved of novel molecular mechanism in the pathogenesis of NAFLD. Acylation-stimulating protein (ASP), a C3 derivative involved in adipocyte lipid metabolism by stimulating triglyceride synthesis, was reported to be increased in NAFLD patients (26). A vicious cycle has been further confirmed in the pathogenesis of NAFLD. ASP can promote the fat accumulation in liver cells to exacerbates hepatic steatosis. On the other hand, the fatty liver promotes the activation of complement system to increase ASP synthesis (12). In brief, there is a potential balance in the pathogenesis of NAFLD between complement system activation and hepatocyte lipid metabolism signaling, which maintains the stability of liver internal environment. Once the balance is broken, the process of hepatocyte lipid metabolism will enter a vicious circle, which exacerbates irreversibly hepatic steatosis as a consequence.

C3a/C3aR ACTIVATION AND METABOLIC FUNCTION
Recently, increased evidence showed that C3a can change the storage, transportation and utilization of glycolipids in adipocytes and directly affect adipogenesis, glucose uptake and lipolysis in the pathogenesis of NAFLD. Oral administration of selective C3aR antagonist for 8 weeks can significantly improve the typical symptoms of metabolic syndrome in dietinduced obese rats, including weight loss, visceral fat reduction, glucose and insulin intolerance improvement, adipose tissue inflammation relief, blood lipid concentration dropping, etc. The above research results innovatively provide two novel mechanisms of C3a involved in energy metabolism on theoretical and experimental basis, that is, C3a can not only promote the uptake of fatty acids and glucose by adipocytes, but also inhibit fat burn-off by inhibiting cAMP synthesis and lipolysis in adipocytes (27). These studies fully elucidate the important correlation between complement C3a/C3aR signaling pathway and energetic metabolism, and further reveal the molecular mechanism of abnormal immune response aggravating obesity and metabolic dysfunction. More importantly, antagonists targeting C3a/C3aR signaling pathway is considered as a novel strategy for the treatment of metabolic dysfunction, including NAFLD. Consistently, our recent result also found that C3a/C3aR signal pathway was closely related to the development of NASH-fibrosis. In C3aR −/− mice model, we also demonstrated that C3aR depletion significantly reduced the progression of NASH related liver fibrosis (28).Studies have confirmed that C3a is an important derivative produced by C3 cleavage when complement system is activated. C3a has significant biological characteristics of anaphylactic toxin and is an important proinflammatory molecule in the body. It can directly trigger mast cells degranulation, inflammatory reaction, chemotaxis effect, granulocyte activation as well increasing vascular permeability, promoting smooth muscle contraction and clearing away the immune complexes, etc (29). In other words, C3a plays an important role in the pathogenesis of a variety of clinical diseases, including organ ischemia-reperfusion injury, sepsis and metabolic inflammation (27,(30)(31)(32)(33)(34)(35)(36)(37). Structurally, C3a is composed of 77-aa polypeptide containing three to four helical regions. A series of irregular amino acid residues is also proved in the C-terminal of C3a protein, which is flexible in spatial conformation. There is evidence that these flexible C-terminal residues are necessary to stabilize the conformation on binding C3aR by the upstream a helix (38)(39)(40). It has been demonstrated that C3a exerts its biological effect mainly by binding to its receptor C3aR, which belongs to G protein-coupled receptor containing seven trans-membrane regions. C3a/C3aR interaction is generally regulated by G protein-coupled receptor kinasemediated receptor phosphorylation (41). In the past, it has been considered that C3aR is the only specific receptor of C3a. It shares close homology with C5a specific receptors C5aR1 and C5aR2. However, recent studies have showed that the interaction of C3a/C3aR seems to be more complex than expected. For example, C3aR has been found to be able to couple with heterotrimeric G proteins depending on different cell types (42)(43)(44). In human granulocytes, C5a can inhibit the activity of C3aR. Ruan et al. confirmed that C3a can form a complex with CpG oligonucleotides to improve the release of IFN-a in monocytes (45). Neuropeptide TLQP-21 (a cleaved fragment of VGL propeptide) was found to specifically binds on C3aR and fully activate the biological function of C3aR in mice, which completely comply with the conformational change of ligand/receptor interaction (46,47). Additionally, recent studies have demonstrated that C3a can bind to the receptor of advanced glycation end products (RAGE) with very high affinity, but this high affinity interaction cannot be explained by a simple ligand upon receptor binding (45,48).

C3a/C3aR AXIS AND IMMUNE RESPONSE IN NAFLD
Kupffer Cells/Macrophages and C3a/C3aR Axis in NAFLD Liver is the largest reservoir of macrophages in the body, and macrophages in liver play a key role in the pathogenesis of NAFLD (23,49,50). According to different origin, macrophages in liver can be divided into two types, one is Kupffer cells fixed in liver, the other is monocytes/macrophages derived from bone marrow. They mainly play the role of innate immunity such as phagocytosis and secretion of inflammatory cytokines. At the early stage of NAFLD, Kupffer/macrophage cells are the first defense lines against the accumulation of excessive lipid metabolites in the liver. Firstly, steatotic hepatocytes disturb hepatic sinusoidal perfusion because of the "gap occupying" effect and Kupffer cells are subsequently attracted by neutrophils to the sinusoidal gap to participate inflammation. Secondly, free fatty acids (FFA) excessively interact with the FFA specific receptors on Kupffer/macrophage cells surface to regulate inflammatory response. Thirdly, Kupffer/macrophage cells mistakenly attribute the abnormal hepatocytes full of excessive lipid accumulation to the harmful substances and immediately phagocytize and destroy them, which further aggravate hepatocyte damage (51). Under the above conditions, these overactivated Kupffer/macrophage cells secrete a large number of inflammatory cytokines (such as TNFα, IL-6, IL-1β) as well as inflammatory chemokines (such as CCL2, CCL3, CCL5, CXCL16, CX3CL1,). In addition, Kupffer cells also recruit a large number of bone marrow-derived monocytes/macrophages into the liver to expand the inflammatory response and accelerate the liver from simple steatosis to NASH (52). CCL2/CCR2 interaction is proved to be the first signal pathway in Kupffer/macrophage recruiting monocytes from bone marrow (53). Afterwards, some other chemokines signal pathways are also confirmed through Kuppfer cells mechanisms such as CXCL10/CXCR3, CCL5/CCR1, and CCL1/CCR8 (11). In recent years, a number of research groups have got the highly consistent results by various ways to delete macrophages in NAFLD mice model (54)(55)(56). Namely, knocking-out monocytes/macrophages can reduce significantly the severity of liver steatosis and inflammation and further delay the process of NAFLD. However, so far, there is no systematic and in-depth study on the specific molecular mechanism of regulating macrophage activation in the whole pathogenesis of NAFLD.
As mentioned above, hepatocytes are the main origin to synthesize C3a molecules, and C3aR is predominantly located in the cell membrane of monocytes/macrophages. In the chronic phase of liver inflammation, C3a/C3aR signaling activity is showed more significant in monocytes/macrophages than that of neutrophils (57,58). Under this condition, C3a can activate the signal pathway of peripheral blood monocytes with the co-stimulation of TLR-4, and further induce the secretion of various proinflammatory factors such as IL-1 β, TNF-α, IL-6 and PGE2 (59)(60)(61)(62)(63). This view is supported by evidence that liver steatosis have modest pathology reductions in C3aR1 −/− mice models (57). Therefore, we speculate that the C3a/C3aR interaction may be a novel signaling pathway by activating macrophages to regulate the occurrence and development of NAFLD. In the early stage of NAFLD, a large amount of fat accumulates in hepatocytes, resulting in the broken balance between complement system activation and hepatocyte lipid metabolism. Subsequently, Complement cascades enter into an overactivated state and excessive amount of C3 molecular is cleaved to release C3a. Through the specific interaction of C3a/C3aR, Kupffer/macrophages cells in the liver are directly activated to secrete inflammatory chemokines to recruit monocytes from peripheral blood into the liver, which further expand the inflammatory response in the steatotic liver (24) (Figure 2).

Hepatic Stellate Cell and C3a/C3aR Axis in NAFLD
Under normal physiological conditions, component C3 is mainly expressed in hepatic parenchymal cells. However, recent evidence has demonstrated that C3 is also slightly expressed in other type cells such as bone marrow cells, lymphocytes, fibroblasts and endothelial like cells (64). Activated hepatic stellate cells, as the initiating factor of hepatic fibrogenesis, have obvious characteristics of fibroblasts. Up to now, there are relatively few reports about complement C3 directly involved in the activation of hepatic stellate cells (HSCs) about NAFLD. A recent study showed that activated hepatic stellate cells could promote the hepatocarcinogenesis through C3 signaling pathway by inhibiting the proliferation of CD4 + and CD8 + cells, promoting the exhausting anti-tumor T lymphocytes as well as improving the differentiation of bone marrow-derived suppressor cells (MDSC) (65). Consistently, our recent results demonstrated that C3a/C3aR signaling pathway was activated in the mouse model of nutritional fibrosis. The related mechanism is being further explored in C3aR −/− mice (28). However, Component cascade activated C5 molecular is found to be a key factor that contributes to hepatic fibrosisgenesis by enhancing the migration ability of hepatic stellate cells. Furthermore, the C5a/C5aR axis was shown to directly mediate inflammatory, chemotactic and anaphylatoxic properties in innate and adaptive immunity as well as to modulate activation and migration of HSCs (66).

T Cell and C3a/C3aR Axis in NAFLD
It has been confirmed that T cells play an important regulatory role in the pathogenesis of NAFLD. The balance has a directly effect in the pathogenesis of NAFLD between Th1-secreted proinflammatory cytokines and Th2-secreted anti-inflammatory cytokines (67). The number of CD4 + helper T cell 17 (Th17) subsets was significantly higher than that of regulatory T cells (Treg) in the pathogenesis of NAFLD (68)(69)(70)(71)(72). With the development from simple steatosis to NASH, the number of Th17 cells in liver and peripheral blood increased continuously in a clinical epidemiological study of 104 human subjects (including 30 patients with NASH, 31 patients with simple steatosis and 43 healthy controls), resulting in a significant increase in Th17/resting T regulatory cell ratio (70). There is no doubt that C3a molecule directly participates in T cells proliferation and differentiation as well as regulates the biological function, but the mechanism is complex (73,74). It is still controversial whether C3aR is widely expressed in T cells (75). When C3aR gene was knocked-out as a target, the number of T cells was significantly reduced in C3aR −/− mice model (73,76). Further studies confirmed that increasing the intracellular expression of C3a in T cells can significantly prolong their survival (77,78). TCR stimulation can significantly up-regulate the expression of C3aR mRNA in T cells (79). Therefore, it is speculated that C3a further regulates T cells proliferation, differentiation and biological functions through a potential autocrine way. Recent studies have shown that C3a can promote T cell proliferation, enhance T cell reaction and prolong inflammatory response by inhibiting Treg production (73,76). After adoptive transfer of C3aR −/− T cells into wild-type animals, the immunological function of Treg was seriously changed (76). In addition, there is evidence that C3aR activation in antigen-presenting cells (APCs) can inhibit Th2 polarization and further block IL-4 secretion (80). Under the synergistic effect of C5aR1 signaling pathway, C3aR can suppress the production of TGF -β1 by dendritic cells, reduce the stimulation of Treg differentiation, and then eliminate the inhibitory response to Th1 (76).

Neutrophil and C3a/C3aR Axis in NAFLD
Neutrophil infiltration is usually observed in the liver of NAFLD patients, and the severity of infiltration is closely related to disease progression (81,82). The excessive fat accumulation overloads the normal metabolic capacity of hepatocytes. Subsequently, the abnormal metabolic injury results in neutrophils to be overactivated and recruited to the steatosic liver. After administration the neutrophil-specific antibody 1A8 into mice, hepatic lipid accumulation and inflammation were significantly attenuated in HFD diet induced NAFLD models, which further slowed down the progress of NASH (83). Currently, neutrophil to lymphocyte ratio (NLR) has been clinically used as an effective biomarker to predict the severity of NAFLD (84)(85)(86). Accumulating evidence shows that NLR is positively correlated with NAFLD activity score (NAS) and an independent predictor of NAFLD prognosis. The higher the NLR value, the higher the severity of the disease, and the worse the prognosis of NAFLD. In the study of 101 NASH patients, the NLR value was significantly higher than that of controls without NAFLD (mean 2.5 vs. 1.6, P < 0.001) (87). In the stage of NASH related fibrosis, the NLR value in advanced fibrosis stage (f3-4) was significantly higher than that of patients with early fibrosis stage (f1-2) (median: 2.9 and 1.8, P < 0.001) (87). So far, it has been controversial for C3a/C3aR interaction in neutrophils because the pure neutrophils was isolated difficultly over a long period in the past, which resulted in the doubt that C3a induced neutrophil activation may be contaminated by non-neutrophils (88). At present, C3aR is definitely identified to express with high level on the surface of neutrophils. Curiously, although C3a/C3aR interaction can activate downstream ERK1/2/Akt signaling pathway, C3a alone does not play chemotactic function as well as stimulate neutrophil degranulation. Recent study suggested that the signaling produced by C3a stimulation of neutrophils was found to be dependent under the synergistic effect of C5aR2 (89). Another study demonstrated that C3a directly prevents neutrophils migration from bone marrow to peripheral circulation by antagonizing neutrophils migration factors (such as G-CSF) (72). Altogether, the specific mechanism of C3a/C3aR in neutrophils in the pathogenesis of NAFLD needs to further explore in the coming future.

C3a AS A BIOMARKER FOR NON-INVASIVE NASH DIAGNOSIS
Although NASH is increasingly prevalent, it's hard to be diagnosed. Yet liver biopsy is recognized as the gold standard, but it is limited by its sampling bias, poor acceptability, and severe complications. Therefore, non-invasive methods are urgently needed to avoid biopsy for diagnosing NAFLD. Currently, some serum biomarkers have been widely accepted for the diagnosis of NASH such as the circulating serum levels of CK-18, the single nucleotide polymorphisms located in PNPLA3 as well as the non-coding RNAs, etc. (90). Especially, the most recent efforts concentrating on "omics" approaches (lipidomics, proteomics, and metabolomics) using high-throughput technologies have shown promising results to identify novel biomarkers of NAFLD, NASH, and advanced fibrosis (91). However, those diagnostic accuracy need to be further improved by combining other different approaches.
Complement system activation has been demonstrated in liver biopsies from patients with NAFLD compared to healthy controls. It has been confirmed that complement C3 levels increased in patients with NASH, but not in those with viral liver disease. More recently, circulating C3 levels have been demonstrated to predict the presence of NAFLD in a large cohort from general population independently of the most plausible confounders such as the presence of metabolic syndrome and obesity. In addition, some similar evidence was also confirmed in the other disease combined with NAFLD. Ursini et al. provide an important evidence for the potential role of complement C3 as a surrogate biomarker of NAFLD in a large cohort of Rheumatoid arthritis (RA) patients at the best cut-off value of 1.23 g/l for complement C3 with a sensitivity of 76% and a specificity of 64% (18). Pan et al. demonstrated the predictive role of complement C3 as a candidate biomarker for diagnosing NAFLD in chronic kidney disease (CKD) patients at the best cutoff value of 993.5 mg/L for complement C3 with a sensitivity of 63.9% and a specificity of 70.1% (17). Therefore, serum C3 may be fully used as a non-invasive diagnostic marker in the coming clinical diagnosis of NASH.

THE POTENTIAL BENEFIT FROM ANTAGONIZING C3aR IN NASH THERAPY
With the increasing incidence of global NAFLD, more and more strategies are explored to prevent effectively NASH in medical treatment nowadays. It is of great significance to find the specific signal pathway leading to the occurrence of NAFLD. Intriguingly, C3aR was indicated to be a remarkable gene closely related to obesity and potential insulin resistance in the mice model intercrossed among different strains by integrated genomic analysis (92). On this base, it is speculated to be a very promising treatment through targeting C3a/C3aR in the pathogenesis of NAFLD. So far, researchers have designed a variety of small molecule antagonists for C3a/C3aR signaling pathway and verified their pharmacological effects. For example, a series of diaminoisoindoline compounds can play a significant role as C3a antagonist at the micromolar level (93). A new oral selective antagonist of C3a receptor, discovered by heterocyclic hinge control conformation, can significantly block the recruitment and activation of macrophages and neutrophils and then play the role of inhibiting the expression of inflammatory mediators (94). Also known is FLTChaAR (IC50 240 nM, Ca2+, macrophages), a significant hexapeptide C3a antagonist, which provide an important reference for the coming antagonist design (95). As C3aR antagonist obtained through high-throughput screening, Sb290157 is thought as the most promising drug for the treatment of metabolic syndrome including NAFLD in the clinical future (88,96). In the obese rat models fed by high carbohydrate and saturated fat diet, SB 290157 can attenuate the inflammatory response by mainly controlling macrophages into adipose or liver tissue (97), which significantly reduce the obesity and body weight by effectively improving liver metabolism (27). Subsequently, it was further confirmed that the IC50s of sb290157 were 27.7 nm in RBL-C3aR cells and 28 nm human neutrophils, respectively. Most importantly, sb290157 is found to acts selectively on C3aR not C5aR or other six chemotactic G protein coupled receptors, which indicates very potential effect in the clinical application (96).
Recent evidence has elucidated C3 as a potent lipogenic hormone in the pathogenesis of NAFLD according to preclinical and translational evidence. Theoretically, initial discussions primarily relied on considerations of C3 deficiency which often leads to a broader range of susceptibilities to infections. As a matter of factor, it can be effectively avoided by developing therapies targeting C3a/C3aR, which participates in inflammatory responses such as anti COVID-19 and anti-HCC treatment (97)(98)(99)(100)(101)(102). Complement C3 activation may interfere with NAFLD with at least two distinct mechanisms by enhancing adipose tissue inflammation via the local engagement of C3a and C5a receptors as well as by providing the substrate for the conversion of C3a into ASP that may exerts its effects systemically (103). Regretfully, no clinical registered trial is found to target C3a or C3aR in NASH therapy so far. Our previous studies have shown that C3a/C3aR participates in the pathogenesis of NASH even fibrosis by regulating various signaling pathways and mentioned the protective function in the C3aR −/− mice model (28). Therefore, in-depth investigations and awareness of the roles of C3a/C3aR in NASH are urgently needed that will lead to a further expansion of potential indications for complement treatments in the future.
Traditionally, C3a/C3aR signaling axis plays a proinflammatory role in the pathogenesis of NAFLD. However, recent studies have found that in the early stage of NAFLD, C3a plays an anti-inflammatory role by preventing neutrophils from accumulating in liver tissue (58). In fact, whether C3a is pro-inflammatory or anti-inflammatory is not mutually exclusive in the pathogenesis of NAFLD, but depends on the balance between pro-inflammatory and anti-inflammatory effects of C3a, which determines the final outcome of the disease (Figure 3). For example, C3a plays a pro-inflammatory role in the NASH stage of NAFLD by activating Kupffer cells under the effect of neutrophil elastase. If neutrophils were deleted at that time, the activation of Kupffer cells was significantly delayed (104). Therefore, the dual role of C3a/C3aR signaling axis should be considered for the rational designing therapeutic strategies targeting C3a/C3aR in the effective treatment of NAFLD.

CONCLUSION
Complement system is one of the most important innate immune barriers in the body, among which complement C3 is the critical component in complement cascade activation. Clinically, increased epidemiological evidence has shown that C3 is closely related to the pathogenesis of NAFLD. Serum fatty acids, adipose tissue-derived cytokines and gut derived endotoxin can take part in complement activation. After complement activation, C3 interacts with different types of liver innate immune cells, and ultimately participates in the pathogenesis of NAFLD. C3a is an important derivative from C3 when complement cascades are activated. Accumulating studies indicate that C3a plays an important role in the pathogenesis of NAFLD by interacting with its receptor C3aR. Targeted inhibition of C3aR activation is a potential strategy for the prevention and treatment of NAFLD. Although SB 290157 is an effective and selective C3aR antagonist in some experimental animal models, the preclinical and clinical evidence of SB 290157 needs to be explored to prevent dietary obesity, metabolic dysfunction and NAFLD in the coming future.

AUTHOR CONTRIBUTIONS
JH and XZ were involved in study design and drafted the paper. XZ supervised and reviewed the paper. All authors contributed to the article and approved the submitted version.

FUNDING
The project was supported by a grant from National Natural Science Foundation of China (No. 81970512).