TWEAK and LTβ Signaling during Chronic Liver Disease

Abstract

Chronic liver diseases (CLD) such as hepatitis B and C virus infection, alcoholic liver disease, and non-alcoholic steatohepatitis are associated with hepatocellular necrosis, continual inflammation, and hepatic fibrosis. The induced microenvironment triggers the activation of liver-resident progenitor cells (LPCs) while hepatocyte replication is inhibited. In the early injury stages, LPCs regenerate the liver by proliferation, migration to sites of injury, and differentiation into functional biliary epithelial cells or hepatocytes. However, when this process becomes dysregulated, wound healing can progress to pathological fibrosis, cirrhosis, and eventually hepatocellular carcinoma. The other key mediators in the pathogenesis of progressive CLD are fibrosis-driving, activated hepatic stellate cells (HSCs) that usually proliferate in very close spatial association with LPCs. Recent studies from our group and others have suggested the potential for cytokine and chemokine cross-talk between LPCs and HSCs, which is mainly driven by the tumor necrosis factor (TNF) family members, TNF-like weak inducer of apoptosis (TWEAK) and lymphotoxin-β, potentially dictating the pathological outcomes of chronic liver injury.

Introduction

The liver possesses an extraordinary ability to orchestrate hepatocyte-mediated regeneration from acute injuries such as tissue resection or hepatic necrosis. However, hepatocyte proliferation is impaired or ablated by severe and chronic injury, dictating the need for an alternative liver regeneration pathway. Through a complex network of chemical and cellular mediators, the liver regenerates via the activation of a progenitor cell compartment, which retains proliferative and restorative capacity under severe injury conditions. Early chronic liver disease is typified by hepatocellular necrosis, hepatic inflammation, and release of immunomodulatory molecules by resident and recruited inflammatory cells, and dying hepatocytes, which activate the regenerative and fibrogenic wound healing responses.

The regenerative response consists of the “ductular reaction” (DR), in which bile ductules and liver progenitor cells (LPCs) proliferate from the Canals of Hering, the interface between the hepatocyte canaliculi and the biliary tree (1), resulting in biliary hyperplasia and the appearance of intermediate hepatocytes (2). Recent lineage-labeling studies have demonstrated that LPCs arise from a population of Sox9-expressing ductal cells that are activated to proliferate and differentiate into hepatocytes under certain chronic liver injury conditions (3, 4). This expansion is initiated and maintained by inflammatory cell-derived stimuli such as tumor necrosis factor (TNF) (5, 6) and interferon (IFN)-γ (7). Importantly, IFNγ has been shown to promote LPC expansion and inhibit proliferation of hepatocytes in concert with TNF stimulation (7). Additionally, transforming growth factor (TGF)-β suppresses liver epithelial cell proliferation. However, LPCs are significantly less sensitive to TGFβ-mediated growth inhibition during chronic liver injury and in vitro (8). In addition to stimuli from inflammatory cells, dying hepatocytes release hedgehog ligand (9), which has recently been shown to signal via the canonical Smoothened-dependent signaling cascade in primary cilium-positive LPCs, promoting their proliferation (10). Thus, the consequence of chronic hepatocyte injury and the subsequent inflammatory response is a liver microenvironment, which supports LPC expansion, while disabling hepatocyte-mediated regeneration.

LPC expansion occurs almost synchronously with fibrogenic wound healing, which is primarily driven by the action of hepatic stellate cells (HSCs). During chronic liver disease, quiescent HSCs are “activated” by inflammatory cytokines and begin to express α-smooth muscle actin (αSMA), signifying their transition to a myofibroblastic phenotype (11). Following this transition, activated HSCs drive fibrosis by depositing extracellular matrix (ECM) proteins, which assists to control LPC proliferation and differentiation. Accumulation of ECM is supported by the expression of tissue inhibitor of metalloproteinase (TIMP) proteins that inhibit matrix metalloproteases (MMPs), which function to degrade ECM proteins (12). Activated HSCs further reinforce regenerative and repair responses by expressing chemotactic factors such as intercellular adhesion molecule 1 (ICAM-1) and regulated upon activation, normal T-cell expressed, and secreted (RANTES), which attract additional inflammatory and progenitor cells to the site of injury (13). If the hepatic insult is resolved, LPCs mature to replace the lost epithelial cell types, hepatocytes, and/or cholangiocytes, depending on the underlying pathology. At the same time fibrosis recedes restoring structural and functional integrity of the liver. However, if injury persists, the regenerative and wound healing processes spiral out of control and become pathological. Chronic stimulation of HSCs results in fibrosis from excessive matrix deposition. With further impaired regeneration, this may progress to cirrhosis and liver failure. Furthermore, the prolonged stimulation of LPCs by pro-proliferative/survival cytokines from inflammatory cells generates a niche favoring the accumulation of genetic and epigenetic alterations, which can lead to the malignant transformation of LPCs and ultimately the formation of hepatocellular carcinoma (HCC).

A combination of association studies in patients and pathway manipulation experiments in rodents implicate LPCs as key regulatory cells in progressive chronic liver injury. LPCs are observed in many diseases with a predisposition to HCC, including chronic hepatitis B (HBV) and C virus (HCV) infection (14, 15), non-alcoholic fatty liver disease (16), alcoholic liver disease, and genetic hemochromatosis (14). Importantly, the numbers of LPCs increase as liver fibrosis progresses to cirrhosis, regardless of the underlying liver pathology (14, 17). Since LPCs proliferate at various stages of human liver tumorigenesis, ranging from preneoplastic lesions (18) to well-developed HCCs (19–21), they have been suggested as causative players during tumor development and maintenance. Supporting evidence comes from murine intervention studies where selective inhibition of c-kit⁺ LPCs by imatinib mesylate resulted in reduced tumor formation (6). These studies suggest that LPCs either represent direct cellular precursors of HCC or they crucially influence disease development by regulating other contributing cells such as fibrosis-driving HSCs. Either way they represent ideal chemotherapeutic targets for HCC prevention strategies in chronic liver injury.

The processes of inflammation, fibrosis, and LPC induction are tightly regulated and occur in close spatial association (Figure 1), suggesting the potential for cellular communication (Figure 2). Cross-talk between the hepatic wound healing and regenerative responses occurs via several factors including ECM proteins, growth factors, and cytokines, particularly of the TNF superfamily. In this review, we will discuss the role of two TNF superfamily members, lymphotoxin-β (LTβ), and TNF-like weak inducer of apoptosis (TWEAK), in regulating liver regeneration and wound healing.

Figure 1.

The intrahepatic wound healing and regenerative niche in CDE-induced chronic liver injury in mice. Confocal microscopy of 2-week CDE-injured mouse liver shows the close association of PanCK⁺ liver progenitor cells with both αSMA⁺ activated hepatic stellate cells and CD45⁺ inflammatory cells. The spatial proximity of all three cell types suggests the potential for cellular cross-talk and co-regulation of the inflammatory, fibrogenic, and progenitor cell responses. Nuclei are stained with DAPI (blue). Scale bars represent 50 μm.

Figure 2.

Co-regulation of hepatic wound healing and regenerative responses via TWEAK- and LTβ-mediated cellular cross-talk. In chronic liver injury liver progenitor cell (LPC) proliferation is induced via macrophage/natural killer (NK) cell-produced TWEAK activation of the NFκB pathway. Interaction between LPCs and activated hepatic stellate cells (HSCs)/myofibroblasts via Notch pathway and other potential mediators may drive LPC differentiation to cholangiocytes. LPCs and ductular reaction cells produce chemokines, such as CCL2 (red) and CX₃CL1 (orange), which promote chemotaxis of inflammatory/myofibroblastic cells. Interactions between lymphotoxin-β (LTβ) expressed on LPCs and the LTβ receptor (LTβR) on activated HSCs triggers NFκB-driven expression of chemotaxis-associated factors ICAM-1 (blue) and RANTES (green) by HSCs, which may play a role in mediating recruitment of LPCs, HSCs, and leukocytes for wound healing, fibrogenesis and regeneration during chronic liver injury (13, 22–27).

TWEAK/FN14 Signaling

TWEAK/FN14 signaling induces LPC proliferation via NFκB activation

TWEAK ligand was first identified as a novel cell-associated and secreted factor with TNF family homology, which induced cytotoxicity in the human adenocarcinoma cell line HT29 in combination with IFNϒ treatment (28). TWEAK interacts with target cells via its receptor, fibroblast growth factor-inducible 14 (Fn14) (29), which is highly homologous in mouse and human tissues, and is upregulated in HCC lines and tissues (30). Biologically, TWEAK has been shown to regulate numerous cellular processes including proliferation, differentiation, migration, and cell survival and has also been described as a pro-angiogenic and pro-inflammatory factor (31). In chronic liver injury and repair, the principal function of TWEAK appears to initiate ductal proliferation and LPC expansion via activation of NFκB signaling. Ductal hyperplasia is observed in livers of mice overexpressing TWEAK under the control of the liver-specific α1-antitrypsin promoter, demonstrating the ability of TWEAK signaling, in isolation, to initiate ductal expansion (32). Conversely, ductal cell expansion is mitigated after pharmacological blocking of TWEAK signaling as well as in Fn14-knockout mice subjected to either 3,5-diethoxycarbonyl-1,4-dihydrocollidine (DDC) or choline-deficient, ethionine-supplemented (CDE)-induced chronic liver injury (22, 32). Furthermore, macrophages and natural killer cells have been shown to be the primary producers of TWEAK ligand in chronic liver injury, providing an important link between the inflammatory response and TWEAK-mediated ductal expansion (33). In the CDE model, TWEAK-producing macrophages have been observed in close association with expanding ductal cells (33), suggesting a mechanism whereby focal points of inflammatory cells signal via the TWEAK/Fn14 pathway to promote LPC expansion. Accordingly, transplantation of bone marrow-derived macrophages into normal liver stimulates a TWEAK-dependent response in LPCs and biliary cells, demonstrating a primary role of macrophage-generated TWEAK in initiating the DR (23). Previous studies indicate that this effect is mediated via TWEAK-induced activation of NFκB signaling (22).

The NFκB family comprises five monomers, which interact via N-terminal Rel homology domain (RHD) polypeptides. These monomers, RelA, RelB, cRel, p50, and p52, interact to form an active NFκB homo- or heterodimer and translocate to the nucleus to activate transcription of genes involved in numerous biological processes including, but not limited to, inflammation, proliferation, and cell survival (34). Regulation of nuclear localization occurs by sequestering of NFκB dimers through binding with inhibitory proteins (IκBs). Inhibition is released through phosphorylation and subsequent proteolytic degradation of IκB. Phosphorylation of IκB is initiated by binding of extracellular mediators to their receptors, which lead to activation of IκB-kinase (IKK) via NFκB essential modulator (NEMO)-dependent (canonical) or independent (non-canonical) mechanisms (35). NFκB plays a vital role in all aspects of chronic liver diseases (CLD), acting as a transducer of cytokine-mediated signals promoting inflammation and fibrosis (36), particularly in the survival and activation of HSCs (37, 38). NFκB signaling is activated upon TNF treatment of LPCs, promoting its mitogenic effects (39), and also regulates IL-6/TNF-mediated upregulation of LTβ in LPCs (40, 41).

TWEAK has been shown to activate NFκB via canonical (42) and non-canonical mechanisms (43). Accordingly, strong cytoplasmic and nuclear NFκB is observed in proliferating pan cytokeratin-expressing cholangiocytes and LPCs following recombinant TWEAK administration in CDE-injured mice (22). In vitro studies in the LPC lines BMOL and BMOL-TAT demonstrated dose-dependent proliferation following TWEAK stimulation. Mitogenesis was inhibited by transfection with siRNA targeting the NFκB p50 subunit, confirming the pro-proliferative effect of TWEAK in LPCs is NFκB-dependent (22). The ability of TWEAK to promote proliferation and self-renewal of LPCs appears to be vital in allowing LPCs to survive and thrive in the chronic liver injury setting. Interestingly, this modulation also affects the dynamics of hepatic fibrosis and inflammation.

TWEAK as a regulator of fibrogenesis

Assessing the cellular players involved in TWEAK signaling provides unique insights into its versatile role in establishing a niche conducive to wound healing, regeneration as well as carcinogenesis. In addition to stimulating ductal/LPC expansion, one of the therapeutically interesting consequences of altering TWEAK signaling in chronic liver injury is the co-modulation of liver fibrosis. Experiments utilizing TWEAK pathway knockout mice and exogenous TWEAK stimulation/inhibition have shown a positive correlation between LPC proliferation and the fibrogenic response to chronic liver injury. Collagen deposition and the expression of TIMPs are reduced in Fn14-knockout mice on the CDE diet (22). Similarly, a recent study of TWEAK modulation in CCl₄-stimulated fibrosis with partial hepatectomy (PHx)-induced hepatocyte deficit has shown that pharmacological TWEAK inhibition decreases collagen deposition during LPC expansion following PHx (44).

Given that the main function of TWEAK signaling appears to be in activating LPC proliferation, how might the TWEAK pathway regulate the fibrotic response of the liver? One possibility that is yet to be investigated is that TWEAK could act directly on fibrosis-driving HSCs. Supportive evidence for this possible scenario is provided by results showing that at least a subset of freshly isolated, activated HSCs express the receptor Fn14 and are therefore potentially TWEAK-responsive in CDE-induced liver injury (22). Another intriguing possibility is that modulating TWEAK/Fn14 signaling could influence the potency of the fibrogenic and inflammatory responses by modulating ductal/LPC cross-talk with leukocytes and/or HSCs. In the next section of this review, we will explore the mechanisms by which TWEAK signaling might regulate the inflammatory and fibrogenic responses through its effects on the LPC compartment.

TWEAK regulation of hepatic inflammation

Through its effects on LPC numbers, TWEAK/Fn14 signaling could affect the dynamics of inflammation in chronic liver injury via LPC-mediated recruitment of inflammatory cells. Fn14-deficient mice fed a CDE diet display a delayed response of CD45⁺ (general inflammatory) and F4/80⁺ (macrophage) leukocytes. Conversely, stimulation of LPC proliferation and the DR with recombinant TWEAK injections results in an increase in CD45⁺ cells (22), suggesting that the amplitude of the DR might have an impact on the level of inflammatory cell recruitment. Given that LPCs express chemokine (C–C motif) ligand 2 (CCL2), also referred to as monocyte chemotactic protein-1 (MCP-1), and chemokine (C-X3-C motif) ligand 1 (CX₃CL1), and have a demonstrated ability to attract CD11b⁺ macrophages isolated from normal and CDE-injured livers in vitro (33), the dynamics of the DR may play a role in regulating the inflammatory response. Since inflammatory cells, particularly the macrophage compartment, support the establishment of fibrosis in chronic liver injury by affecting HSC activation (45), influences on inflammatory cell recruitment may also affect the dynamics of liver fibrosis initiation and injury progression. Consequently, targeting the TWEAK/Fn14 pathway may be an effective way to alter the wound healing response by influencing the dynamics of LPC/inflammatory cell/HSC cross-talk.

LPC/HSC Cross-Talk via LTβ Signaling

In an effort to understand the opposing roles of LPCs and HSCs in controlling regeneration and wound healing versus fibrogenesis progression and carcinogenesis, pathways involved in LPC/HSC cross-talk are currently under investigation. As we have discussed, modulating the LPC response via TWEAK signaling affects the dynamics of liver fibrosis mediated by HSCs. Additionally, Boulter et al. demonstrated regulation of LPC differentiation by activated HSCs through expression of the Notch ligand Jagged 1 and Notch-dependent biliary specification in adjacent LPCs (24). Conversely, expression of MCP-1 by cholangiocytes within hyperplastic or mature bile ducts was shown to drive HSC/myofibroblast chemotaxis in chronic cholestatic liver disease (25). These studies demonstrate the clear interactions of LPCs and HSCs during progressive chronic liver injury. Thus, interventions targeting pathways modulating LPC/HSC interactions might be of therapeutic benefit in patients with chronic liver disease. One such novel target is the TNF family member LTβ, which was recently discovered as a key regulator of LPC/HSC cross-talk, facilitated by NFκB-dependent downstream signaling (13).

LTβ is a type II transmembrane protein that signals as a cell surface-anchored heterotrimer with LTα (i.e., LTα2:β1 or predominantly LTα1:β2) (46). LTβ levels are increased in various animal chronic liver injury models including bile duct ligation (47) and CDE-induced injury (48, 49) and its expression correlates with the severity of fibrosis in chronic HCV infection in humans (50). It has been demonstrated on the surface of cells of the lymphocytic lineage, including activated B and T cells as well as natural killer cells (51) but interestingly also on small portal hepatocytes and proliferating LPCs during chronic liver injury (50). In our CDE injury model, these LTβ⁺ LPCs are observed in close proximity to activated HSCs, which express the LTβ receptor (LTβR). In vitro studies revealed that upon receptor binding, LTβ initiates a NFκB-dependent signaling cascade in HSCs that results in expression of chemotaxis-associated mediators ICAM-1 and RANTES, which in turn recruit RANTES receptor (C–C chemokine receptor type 5, CCR5)-positive LPCs (13). Hence this paracrine cytokine/chemokine cross-talk has the capacity to facilitate LPC and HSC migration through the liver parenchyma to sites of injury in addition to promoting wound healing by recruitment of new leukocytes, LPCs and HSCs. The LTβ signaling pathway also plays a role in fibrogenesis, since chronically injured LTβR knockout mice show reduced numbers of αSMA⁺ HSCs and decreased collagen deposition as evidenced by reduced Sirius Red staining (13). Concurrently, numbers of A6⁺ and muscle pyruvate kinase 2 (M₂PK)⁺ LPCs are reduced (48), which once again suggests the co-regulation of the fibrogenic and the progenitor cell response in chronic liver injury. The significance of the LTβ pathway in liver disease and hepatocarcinogenesis was highlighted by Haybaeck et al. who analyzed tg1223 mice, which overexpress lymphotoxin in the liver, and showed that sustained expression leads to chronic hepatitis and eventually to HCC. To confirm results, LTβ overexpression was neutralized by pharmacological blocking of LTβR, which drastically reduced liver injury and prevented HCC formation (19). Hence, suppression of this pathway might be beneficial in liver diseases with a chronic overexpression of cytokines that signal through LTβR, including LTα and LTβ or LTβ-related inducible ligand competing for glycoprotein D binding to herpes virus entry mediator on T cells (LIGHT), such as seen in chronic HBV or HCV infection.

Therapeutic Potential and Future Directions

In the Western world, chronic liver injury is ever increasing in prevalence. A variety of etiologies including chronic HBV/HCV infection, and non-alcoholic fatty liver disease can cause fibrosis and, subsequently, cirrhosis and HCC. The World Health Organization ranks CLD as the ninth commonest global cause of death with end organ failure as a result of cirrhosis and HCC, accounting for half the mortality each (52). Most HCC cases arise in the setting of established cirrhosis, with a median survival of 6–16 months, if untreated (53). At present, a range of primary treatment options including antiviral therapy and weight reduction strategies are variably effective in these conditions. Unfortunately, a significant number of patients still progress to end-stage liver disease and many require orthotopic liver transplantation. However, limited availability of donor organs and religious and/or economic reasons may restrict access to transplantation surgery. Prolonged waiting times for donor organs often result in disease progression and death of patients with initially treatable disease. Thus, the development of new therapeutic strategies for the prevention or treatment of hepatic fibrosis and its sequelae of cirrhosis and HCC are urgently required.

The carcinogenic and fibrogenic processes are amenable to manipulation by agents, which interfere with these processes, however to date approaches have been limited, and new targeted therapies such as tyrosine kinase inhibitors have not significantly improved survival (54, 55). Identification of new cellular targets for preventative therapies that minimize fibrosis or carcinogenesis represent the future for advancement of therapy, and knowledge of cross-talk and signaling pathways such as those defined here are critical for such advancement. The key will be balancing beneficial effects on reduced fibrosis and carcinogenesis against detrimental effects consequential to impaired replacement of healthy hepatocytes or cholangiocytes, as can be seen following IFN-based therapies for chronic viral hepatitis (56).

Summary

The liver responds to chronic injury by initiating an inflammatory response, which enables the dual action of resolving injury, through the activation of fibrosis, and regeneration of injured tissue comprising the activation and differentiation of LPCs. These processes are inextricably linked and act in concert to reinforce and progress the chronic injury response until such a time that injury abates. Since these processes are linked, affecting the biology of one necessarily affects the dynamics of the whole system. As we have discussed in this review, TWEAK/Fn14 signaling plays a primary role in regulating LPC expansion and in doing so, affects both the inflammatory and wound healing responses of the liver through cellular cross-talk. Through interactions between LPCs and the immune system, TWEAK modulation of LPC numbers may act to enhance the inflammatory response at the site of regeneration, reinforcing LPC expansion. Likewise, LPC interactions with HSCs via LTβ signaling may also promote recruitment of leukocytes to the site of injury, amplifying the fibrogenic response of the liver. Accordingly, TWEAK signaling may be an important “valve” with which we might modulate the landscape of chronic liver injury. Therefore, we propose that therapies targeting TWEAK signaling in chronic liver injury may be useful for reducing the severity of fibrosis through its dual action on the inflammatory and HSC compartments via LPCs. In doing so, it may be possible to diminish progression to cirrhosis and liver failure, as well as limiting the pro-tumorigenic environment existing in the regenerative niche supporting LPCs.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.