Zhanghao Li1†
Xiaoxin Wen2†Nanxi Li1Chuanxin Zhong1Li Chen3
Feng Zhang3
Ge Zhang1
Aiping Lyu1,4*
Jin Liu1,4*- 1Law Sau Fai Institute for Advancing Translational Medicine in Bone and Joint Diseases (TMBJ), School of Chinese Medicine, Hong Kong Baptist University (HKBU), Hong Kong, Hong Kong SAR, China
- 2Department of Anatomy, Jinzhou Medical University, Jinzhou, China
- 3Jiangsu Key Laboratory for Pharmacology and Safety Evaluation of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China
- 4Guangdong-Hong Kong-Macau Joint Lab on Chinese Medicine and Immune Disease Research, Guangzhou, China
Both the liver and bone are important secretory organs in the endocrine system. By secreting organ factors (hepatokines), the liver regulates the activity of other organs. Similarly, bone-derived factors, osteokines, are created during bone metabolism and act in an endocrine manner. Generally, the dysregulation of hepatokines is frequently accompanied by changes in bone mass, and osteokines can also disrupt liver metabolism. The crosstalk between the liver and bone, particularly the function and mechanism of hepatokines and osteokines, has increasingly gained notoriety as a topic of interest in recent years. Here, based on preclinical and clinical evidence, we summarize the potential roles of hepatokines and osteokines in liver-bone interaction, discuss the current shortcomings and contradictions, and make recommendations for future research.
1 Introduction
Multiple factors could lead to liver diseases with visible extrahepatic complications, influencing disease progression and therapy efficacy. Reduced bone mineral density (BMD) caused by both decreased physiological bone turnover and limited osteosynthesis processes is one of the most common extrahepatic complications found in adults suffering from end-stage liver disease (1). In addition, most patients suffering from liver disease also have multiple risk factors for osteodystrophy, including protein-calorie malnutrition and vitamin D deficiency (2). Hepatic osteodystrophy (HOD), a term for bone loss and fractures caused by liver disease (3), occurs in up to 50% of patients undergoing chronic liver disease (CLD) (4). Typical liver-derived hormone fibroblast growth factor 21 (FGF21) could inhibit osteoblast activity and increase bone resorption (5). In terms of hepcidin, the other hepatokine, its deficiency led to the reduction of bone formation. Thus, it is undoubted that abnormal liver disease and bone metabolism are closely related.
Apart from the key component of motor system, bone has been recognized as an endocrine organ that regulates energy metabolism (6). For instance, osteocytes and osteoblasts secreted FGF23 is positively correlated with liver fat content (7). Furthermore, osteoblasts-expressed osteocalcin (OCN) has also been reported to increase insulin secretion and sensitivity (8). The secreted bone factor LCN2 conditional knockout mice in osteoblasts showed increased blood glucose levels and body fat (9). Other bone-derived factors, such as calcitonin and sclerostin (SOST), are also closely linked to liver metabolism. Calcitonin knockout mice were protected against high-fat diet (HFD)-induced obesity. After receiving SOST-neutralizing antibody, mice were also resistant to diet-induced insulin resistance, indicating the possible role of osteokines in regulating liver metabolism. However, liver abnormalities are frequently underestimated as a side effect of medication for treating bone diseases rather than direct harm caused by the abnormal bone metabolism characterized by excessive bone resorption and/or constrained bone formation (10). Emerging evidence has advocated that liver and bone are mutually regulated through liver-bone crosstalk, a constant interorgan communications mediated by the hepatic and osteal endocrine factors. The physiological liver-bone crosstalk is important for liver and bone health while the pathological liver-bone crosstalk could substantially contribute to the development of bone-related comorbidities in liver diseases, i.e., HOD. In this review, we focused on research progress regarding the roles of hepatokine and osteokine in liver-bone crosstalk and their contributions to liver disease associated with abnormal bone metabolism or abnormal liver glucose and lipid metabolism of bone disease, respectively. We thoroughly analyzed direct evidence from basic studies and indirect evidence from clinical studies. Besides, some seemingly contradictory findings in basic and clinical studies were also summarized and discussed.
2 Hepatokines: From liver to bone
2.1 Fibroblast growth factor 21
Fibroblast growth factor 21 (FGF21) is a member of the FGF subfamily produced primarily in the liver. Its major function is to regulate the energy metabolism of carbohydrates and lipids in the body through endocrine and other mechanisms (5, 11–13). The deficiency of FGF21 facilitates the development of steatosis, inflammation, hepatocyte damage, and fibrosis in the liver (14, 15). Supplementation of FGF21 or its analogists could be conductive to alleviating the development of nonalcoholic steatohepatitis (NASH) (16). However, studies have shown that FGF21 makes deleterious effects on bone mass (17, 18). Compared with the wild-type controls, the transgenic mice with overexpressed FGF21 had a striking decrease in trabecular bone mass. Meanwhile, FGF21-knockout mice developed a high-bone-mass phenotype (19). Reduction of FGF21 levels in serum and liver was capable of preventing osteoclastogenesis and bone loss via tail vein injection of agomir-miR-100-5p, which could combine with 3’ UTR of FGF21 (17). Due to the obviously negative correlation between FGF21 and bone mass, the mechanism of FGF21 in regulating bone homeostasis has aroused researchers’ interest. Wei et al. confirmed that overexpressed circulating FGF21 stimulated lipogenesis of bone marrow precursors, inhibited osteoblast activity, and increased osteoclast activity by enhancing peroxisome proliferator-activated receptor γ (PPARγ) activity in bone marrow mesenchymal stem cells (19). Wang et al. identified that the pro-osteoclastogenic activity of FGF21 was related to insulin-like growth factor binding protein 1 (IGFBP1). In the transgenic mice with overexpression of FGF21, IGFBP1 secretion was indirectly induced, and IGFBP1 bound to osteoclast precursor integrin β1, enhancing the receptor activator of nuclear factor κB ligand (RANKL)-stimulated extracellular regulated protein kinases phosphorylation and NASH nuclear factor of activated T cells 1 activation, ultimately promoting osteoclast differentiation and resulting in decreased BMD (18).
However, different from the clear and overwhelming evidence in animal research, there is little clinical research, and the research results remain controversial. Overweight subjects with type 2 diabetes experienced increased bone resorption marker C-telopeptide of type I collagen after administration of a long-acting FGF21 analog PF-05231023, as well as the lower circulating levels of IGF1 and various markers of bone formation, including OCN, P1NP, and bone-specific alkaline phosphatase (46). Elevated FGF21 levels in individuals with HIV-1 infection are strongly associated with increased bone resorption, making it a potential biomarker for disrupted bone homeostasis and indicators of metabolic derangement (47). However, in younger adults between 22-39 years old and older adults between 60-71 years old, the relationship between FGF21 and IGFBP1 appears to differ from the previous studies (18). According to Lee et al., there was a negative relationship between BMD at the spine and the circulating FGF21, while no association was found between BMD at the hip or spine and IGFBP1 (48). In middle-aged and elderly European men (between the ages of 40 and 79 years), there was a negative correlation between serum IGFBP1 concentrations and calcaneal BMD (49). Moreover, it remains to validate whether the FGF21-IGFBP1-RANKL pathway is involved in age-related bone loss in human. In contrast, another study revealed a significantly positive correlation between plasma FGF21 levels and total BMD in healthy women (50). In Chinese Han postmenopausal women, Hu et al. discovered that serum FGF21 concentrations were positively associated with lumbar spine BMD, but not with bone turnover markers or with fragility fracture (51). In a clinical trial of obese children and adolescents, there was no correlation between FGF21 levels and antero-posterior vertebral L2-4 BMD z-score values (52). As a result, it is unclear whether the inner linkage between FGF21 and IGFBP1 still exists in the clinical aspect. Different populations, such as age groups, should be included and considered as interfering factors. Moreover, further clinical research is needed to fully understand the role of FGF21 and bone loss in physiological and pathological conditions, particularly whether the association is limited to a specific pathological condition, such as HOD.
2.2 Bone morphogenetic protein 9
Even though the precise distribution varies slightly between species (53), in general, bone morphogenetic protein 9 (BMP9) is considered to be mainly expressed in the liver of adult individuals as a circulating factor produced by hepatic stellate cells (54). In managing liver sinusoidal endothelial cells fenestration and guarding against perivascular hepatic fibrosis, it is a crucial paracrine regulator of liver homeostasis (55, 56). In nonalcoholic fatty liver disease (NAFLD) patients and animal models, BMP9 levels were lower in the liver and serum. BMP9-knockout mice also exhibit hepatosteatosis because of down-regulated PPARα expression and reduced fatty acid oxidation (20). In addition, BMP9-knockout mice featured alveolar bone with reduced volume, decreased mineral density, and trabecular thickness (57). As the strong inducer of osteocyte differentiation in the BMP family, BMP9 is a crucial regulator of skeletal homeostasis (54, 58). In osteoporotic rats with femora fractures, global overexpression of BMP9 by adenovirus (Ad) mediated callus formation and increased bone mass and strength to great extent via promoting osteoblastic differentiation (59). Similarly, Zhou et al. proved that overexpression of BMP9 led to not only elevated BMP9 levels in the liver and serum but also suppressed bone resorption activity, improved cortical and trabecular volumetric BMD, and ameliorated bone strength in an ovariectomy mouse model (21, 60). BMP9 increased bone mass in aged mice by preventing osteoblast senescence and stimulating osteoblast differentiation, improved bone biomechanical properties, and ameliorated the bone microenvironment (61). Aside from directly influencing bone resorption and bone formation, BMP9 upregulated the endogenous expression of RUNX3 in mesenchymal stem cells (62), which are undifferentiated stem cells with the potential to differentiate into multiple lineages, including osteoblasts (63). The in vivo liver-specific BMP9 knockout model should be established to investigate the role of BMP9 in liver-bone crosstalk. Besides, more clinical research should be performed to determine whether BMP9 derived from liver non-parenchymal cells is linked to bone disease. Considering the pro-anabolic and anti-resorptive effect of BMP9 on bone, manipulating BMP9 could be a potential therapeutic strategy for bone loss associated with liver disease.
2.3 Vitamin D
Vitamin D (VitD) plays an active role in immune function, protein synthesis, cardiovascular function, and musculoskeletal regulation. In the healthy liver, VitD is hydroxylated by VitD 25-hydroxylase (CYP2R1) and sterol 27-hydroxylase (CYP27A1). The expression of both enzymes decreased in fibrotic and cirrhotic livers (64, 65). VitD binding protein, which is synthesized by the liver and acts in binding and transporting VitD, is shown to be low-expressed in sepsis-induced liver injury (66). Thus, the metabolism and transportation of VitD are impaired in advanced liver disease (67, 68). VitD is also key to bone mineral homeostasis. When VitD levels decrease below normal limits, parathyroid hormone increases bone resorption to satisfy the body’s demands for calcium, increasing bone turnover with an added risk of bone fracture (22). An observational study verified that VitD deficiency was closely related to HOD, which is a metabolic bone disease often associated with chronic liver disease and is marked by the bone loss (69). Compared to patients with Child-Pugh grades A and B cirrhosis, lumbar BMD and VitD active metabolites were extremely lower, whereas the bone resorption marker β-CTX was higher, in patients with grade C cirrhosis (70), suggesting that cirrhosis is a risk factor for osteoporosis and VitD level could be an important marker for evaluating HOD. At present, there is no direct study to demonstrate that liver regulation VitD in chronic liver disease is involved in hepatic bone disease, and further confirmation is necessary. Calcium and/or VitD supplementation may be of importance in reducing HOD, but its safety and efficacy must also be taken into consideration to prevent the hypercalcemia, hypercalciuria, and hyperphosphatemia that can be brought on by prolonged vitamin D supplementation.
2.4 Fetuins
Both fetuins-A and fetuins-B are important hepatokines in human metabolism regulation (71). Fetuins-A, also known as Alpha-2-HS-glycoprotein, is mainly expressed, and secreted by the liver and adipose tissue (72). The upward fetuin-A serum level is correlated with high liver fat content (25, 26). As a mineral carrier protein and the inhibitor of pathological soft tissue calcification, it is also enriched in bone (27). Heterotopic ossification (HO) is the abnormal formation of bone in extraskeletal sites. Therapy with recombinant fetuin-A prevents injury-induced and BMP4-dependent HO and associated bone loss through increasing the expression of programmed cell death protein 1 reducing macrophage infiltration and inhibiting hyperinflammation (72). Several studies have suggested that fetuin-A was intimately associated with BMD (27, 73, 74). A single dose of bovine fetuin-A could reduce the visible osteolytic lesions and eroded bone surface in mice subjected to particle-induced osteolysis (27). However, in a large sample of community-dwelling older adults, fetuin-A was positively associated with areal BMD in a small degree, and there was no evidence of an association between fetuin-A and the risk of clinical fracture (75). The liver-specific fetuins-A overexpression mice may be an interesting model in further investigation. Like fetuin-A, fetuin-B is also a liver-derived plasma protein. It is increased in patients with type 2 diabetes and impairs insulin sensitivity in myotubes and hepatocytes (76, 77). A 4-year prospective study in China showed serum level of fetuin-B is associated with osteoporosis (78). Nevertheless, research on the role of fetuin-B in bone metabolism remains limited, both in vivo and in vitro. Further research is required to determine the relationship between fetuin-B and bone mass.
2.5 Hepcidin
Hepcidin, a key regulator of iron metabolism, is primarily synthesized in hepatocytes and has emerged as a new marker of fibrosis and cirrhosis (79). Patients with CLD usually had lower serum levels of hepcidin (80). Overexpression of hepcidin increased adiponectin expression in hepatocytes and hepcidin treatment inhibited hepatic stellate cells activation, thus alleviating liver fibrosis (28). Interestingly, in a recent study, the relationship between hepcidin and bone loss has been revealed. Hepcidin-/- mice as iron overload models, showed the phenotype of reduced bone formation and enhanced bone resorption, which could be caused by the increased reactive oxygen species and resultant sclerostin (SOST) and RANKL/OPG expression alteration (81). Guo et al. created TgHamp1-Alb mice that specifically express hepcidin in liver hepatocytes by hybridization of LSL-Hamp1 (TgHamp1) mice with albumin (Alb) promoter-driven Cre (Alb-Cre). At 3 months old, TgHamp1-Alb mice displayed the reduced trabecular volume/total volume, trabecular number, and trabecular thickness (29). Min et al. pointed out that the increased hepcidin levels were closely related to reduced 25‐hydroxyvitamin D in chronic kidney disease (CKD), further causing CKD-related bone fracture (82). Clinical research on hepcidin in bone loss is still lacking. The development of in vivo models for hepatocytes hepcidin knockout or overexpression is fundamental to determining whether liver-derived hepcidin affects bone loss.
2.6 Lecithin-cholesterol acyltransferase
As a liver-derived enzyme (83), the lecithin cholesterol acyltransferase gene (LCAT) plays an important role in lipoprotein metabolism (84). Low LCAT activity may be the cause of the lipoprotein changes in parenchymal liver disease (85, 86). The loss of LCAT in progressive liver injury caused worse liver fibrosis and HOD, and markedly exacerbated the bone loss phenotype. Tail vein rAAV8-LCAT or recombinant LCAT (rLCAT) injection significantly increased bone mass and inhibited osteoclastogenesis in HOD mice (83, 87). At present, the mechanistic understanding of LCAT on bone metabolism are limited to the regulation of cholesterol metabolism in osteoblasts and osteoclasts. rLCAT dramatically lowered the intracellular cholesterol in primary osteoclasts isolated from mice and disrupted estrogen-related receptor alpha transcription, thereby inhibiting osteoclast differentiation. Cholesterol treatment prevented osteoblast differentiation by decreasing the mRNA levels of osteoblast marker genes, but rLCAT treatment could restore osteoblast differentiation and reduce intracellular cholesterol. However, the target of LCAT needs to be further defined (87). Moreover, there is still a lack of clinical evidence linking LCAT to bone loss. In this case, further research is needed to ascertain the precise mechanism by which LCAT maintains bone homeostasis, whether and to what extent LCAT-mediated bone metabolism depends on cholesterol metabolism, and whether LCAT having the potential to serve as a marker of bone loss associated with liver disease. The findings of hepatokines are summarised in Table 1.
Table 1 Hepatokines involved in bone regulation.
3 Osteokines: From bone to liver
3.1 Fibroblast growth factor 23
Fibroblast growth factor 23 (FGF23) is a bone-derived hormone secreted by osteocytes and osteoblasts binding to FGF receptor-Klotho complexes (88). It interferes with osteoblast differentiation and matrix mineralization and increases renal phosphate excretion (32, 89). As an important marker of CKD, rising FGF23 levels indicated appropriate compensation to maintain a neutral phosphorus balance in renal dysfunction (90). High levels of serum FGF23 are associated with hypophosphataemia-related rickets (91), as well as the autosomal dominant hypophosphataemic rickets (ADHR), which is characterized by mutations of two FGF23 cleavage sites Arg179 and Ser180 and is frequently accompanied by markedly elevated serum ALP, which may reflect underlying liver abnormalities (92). Massive elevations in circulating FGF23 contribute to the elevation of liver inflammation, whereas the normal mouse liver itself possesses very low levels of FGF23 mRNA and protein (33, 93). FGF23 could stimulate calcineurin signaling by activating FGF receptor isoform 4 in cultured hepatocytes, which increased the expression and secretion of inflammatory cytokines (94). Besides, it also directly regulated liver fetuin-A expression. When FGF23 increased up to 400-600 pg/mL, fetuin-A increased progressively and declined at higher FGF23 concentrations (95), which may act in a bidirectional manner to control fetuin-A’s involvement in hepatic glucose homeostasis. In Chinese diabetes mellitus type 2 patients, both high FGF23 and low VitD levels had an independent relationship with NAFLD (96). Furthermore, a community-based cohort also revealed that FGF23 in serum was positively related to MAFLD and liver fat content (7). Although FGF23 is involved in the regulation of bone-liver axis, it has received less attention in liver diseases than in kidney disease. In addition, there are not enough reliable in vivo experimental and clinical data to consolidate the role of FGF23 in liver pathology. Thus, it would be valuable to exam the glucose lipid metabolism and inflammatory microenvironment in liver of bone-specific FGF23 knockout mice and validate the association between FGF23 and various liver diseases in clinical study.
3.2 Osteocalcin
Osteocalcin, also known as bone γ-carboxyglutamate protein (Bglap), is the most abundant osteoblast-specific non-collagenous protein that is expressed by osteoblasts (97). As a determinant of bone formation, the osteocalcin-deficient mouse is characterized by increased cortical thickness and trabecular bone mass (98). Besides its known role in bone health, osteocalcin may influence glucose homeostasis (99). Several studies have demonstrated a protective effect of osteocalcin against NAFLD (35, 36). In wild-type mice fed a western diet, osteocalcin increased the secretion and sensitivity of insulin (8, 100), reduced hepatic sterol regulatory element-binding protein-1 (101), triglyceride accumulation, malondialdehyde as well as the ratio of oxidized to reduced glutathione (102). Osteocalcin robustly reduced the expression of proinflammatory and profibrotic genes in liver of Ldlr-/- mice fed with a high-fat, high-cholesterol diet for 12 weeks to induce metabolic syndrome and NASH (103). In old laying hens with fatty liver hemorrhagic syndrome, osteocalcin restricted the metabolic disorder, oxidative stress, and related pathological damage (104). In addition, a putative receptor of osteocalcin, GPRC6A, was found in the liver. With the construction of liver-specific GPRC6A knockout mice, Zhang et al. demonstrated that intraperitoneal injection of osteocalcin significantly protected wild-type mice from obesity and NAFLD, but not liver-specific GPRC6A knockout mice, suggesting that GPRC6A mediated the ability of osteocalcin to inhibit lipid synthesis and promote lipolysis (35). A murine circulating pentadecapeptide derived from pre-osteocalcin, binding to GPRC6A, could also alleviate the symptoms of NAFLD by inhibiting lipid absorption and insulin resistance (36). Consistent with the results from preclinical studies, osteocalcin was also found to negatively correlate with NAFLD in several clinical studies. In men with NAFLD or postmenopausal women, the large N-mid fragment of osteocalcin was negatively related to the probable presence of significant fibrosis or probable NASH (105). In a South Korean study involving 7,067 women, osteocalcin was also linked to insulin resistance. The serum osteocalcin level was found to be an independent risk factor for NAFLD (106). Further prospective clinical and in-depth animal studies are required to understand the relationship and underlying mechanisms of osteocalcin and liver disease progression. Moreover, the development of osteocalcin-specific receptor-targeted binding peptides in the liver will also be conducive to the treatment of glucose and lipid metabolism disorders.
3.3 Calcitonin
Calcitonin inhibits calcium efflux from bone rapidly lowers circulating calcium levels (107), and suppresses bone resorption through its corresponding receptor, the calcitonin receptor (CTR) (108). Calcitonin deficiency has been implicated in the pathogenesis of accelerated bone loss. Clinically, calcitonin has been adopted for conditions of accelerated bone turnover for several years, including Paget’s disease and osteoporosis (109). Compared with wild-type old age mice, calcitonin knockout mice, lost weight and had significantly lower levels of liver fat, adipocyte droplets, and lipids after HFD induction, and were protected against HFD-induced insulin resistance. The in vitro study verified that physiological concentrations of calcitonin promoted lipid accumulation, and suppressed adiponectin release in 3T3-L1 cells (110). However, in obese HFD-fed rats, although rat calcitonin (rCT) treatment made no effect, the combination of dual amylin and calcitonin receptor agonists (DACRAs) KBP-088, rat amylin (rAMY) significantly ameliorated rat glucose tolerance (111). The administration of DACRA combined with liraglutide for obese rats generated a significant effect on appetite suppression and body weight loss (112). The role of calcitonin in the liver and systemic glucose metabolism, as well as insulin resistance, appears to be conflicting. Moreover, it is still unknown whether calcitonin is used clinically to prevent bone calcium loss and whether it causes unexpected insulin resistance or improves insulin sensitivity. Therefore, more clinical data are required to observe the application of calcitonin. Furthermore, calcitonin and its splicing products could also be synthesized by hepatocytes, and the liver also possessed related receptors in non-parenchymal cells (113). Besides, the regulatory effect of calcitonin in liver on systemic metabolism is still insufficient.
3.4 Sclerostin
Sclerostin (SOST), which is mostly expressed in osteocytes, suppresses bone formation via the inhibition of the Wnt-low-density-lipoprotein receptor-related protein (LRP) 5/6 signaling pathway on osteoblasts (41). At present, the anti-SOST monoclonal antibody is used to treat severe osteoporosis (114–116). The bone volume in Sost-/- mice experienced a marked increase, along with decreased accumulation of adipose tissue and increased insulin sensitivity. After administration of SOST-neutralizing antibody, mice were resistant to obesogenic diet-induced disturbances in metabolism. After treatment with recombinant sclerostin, Bmp4, Bmpr1a and Smad1/5/9 phosphorylation levels were increased in cultured primary adipocytes. Wnt3a treatment produced the opposite effect. Thus, sclerostin favors adipogenesis and adipose hypertrophy via the suppression of Wnt signaling (117). In a cross-sectional observational study, elevated SOST levels in alcoholics are linked to abnormal liver function, fat deposition, and elevated BMI (118). Serum SOST levels were also significantly higher in patients with cirrhosis (119), besides, it could reflect altered bone microarchitecture in those patients (120). However, another study showed that circulating SOST levels were significantly lower in NAFLD subjects compared with normal controls, which may mainly reflect reduced SOST secretion from bone tissues (121). Whether circulating SOST can be taken as a surrogate marker of bone metabolic status in patients with liver injury is uncertain, and the exact mechanism is still unknown. Furthermore, whether anti-SOST monoclonal antibodies can delay liver damage while treating severe osteoporosis is worth investigating.
3.5 Lipocalin 2
Lipocalin 2 (LCN2), which is also termed 24p3 or neutrophil gelatinase-associated lipocalin, was one of the adipokines (122). As a secreted bone factor, LCN2 positively affected osteogenesis in vivo and osteogenic differentiation of MC3T3-E1 (44). Mice who had LCN2 in their osteoblasts conditionally knocked out showed increased blood glucose levels and body fat. It was discovered that the appetite was directly suppressed by the melanocortin receptor 4 (MC4R) in the paraventricular and ventromedial neurons of the hypothalamus, which was bound by osteoblasts-derived LCN2. Additionally, wild-type mice receiving LCN2 continuously were featured with enhanced glucose metabolism and increased energy expenditure while reducing food intake, fat mass, and body weight (9). The expression of the chemokine receptor CXCR2 was also increased by lipocalin-2, thereby activating the mitogen-activated protein (MAP) kinase and extracellular regulated protein kinases 1/2 and producing proinflammatory chemokines, and aggravating steatohepatitis (45). LCN2 can also act as a key mediator of HSC activation in leptin-deficient obesity via α-SMA/MMP9/STAT3 signaling and accelerated NASH (123). In clinical research, higher blood level of LCN2 was linked to obesity, insulin resistance, and dyslipidemia in people with type 2 diabetes (124, 125). In patients with alcoholic hepatitis (AH), hepatic LCN2 expression and serum LCN2 levels both dramatically increased and were connected with disease severity and portal hypertension (45, 126, 127) LCN2 levels in the blood are a biomarker for metabolic diseases as a result and are expected to be a new therapeutic target to control appetite and obesity (8). Further investigation is needed in both experimental and clinical studies.
3.6 Transforming growth factor β
In healthy subjects, transforming growth factor β (TGF-β) is by far the most abundant cytokine in bone (42), which is secreted in its latent form by osteoblasts and osteoclasts. Upon secretion, the latent TGF-β is incorporated into the bone matrix (128). During bone resorption or fracture, osteoclasts activate TGF-β in their resorption lacuna via proteolytic and acidic hydrolysis (65), and it is also considered to be the major factor regulating liver carcinogenesis and accelerating liver fibrosis (43). In terms of activation of TGF-β, it promotes liver fibrosis by activating HSCs, which can be prevented by stabilizing extracellular matrix-deposited TGF-β in its inactive form by interacting with αv integrins (129, 130). In hepatocellular carcinoma (HCC), TGF-β plays a dual role, acting as a tumor-suppressor at early stages but contributing to tumor progression at late stages. Inhibition of TGF-β pathway may constitute an effective option for HCC treatment. However, the one-sided inhibition of TGF-β could have negative effects. Thus, it is mandatory to identify relevant biomarkers in TGF-β signaling with HCC (131). Furthermore, the increased bone resorption in liver disease may promote the release of TGF-β, and whether it may further aggravate the progression of liver disease needs further study. The findings of osteokines are summarised in Table 2.
Table 2 Osteokines involved in liver regulation.
4 Discussion
Increased bone fragility and decreased bone mass are common in patients with chronic liver disease. Abnormal liver metabolism is also related to the disruption of bone homeostasis. In recent years, some advancements have been made in liver-bone crosstalk. However, most of the mechanisms and clinical studies remain insufficient, and existing research has some contradictions. In this review, the role of hepatokines in bone homeostasis and osteokines in bone-liver crosstalk in preclinical and clinical research was discussed Figure 1.
Figure 1 The current research status of related hepatokines and osteokines. BMP9, bone morphogenetic protein 9; FGF21, fibroblast growth factor 21; FGF23, fibroblast growth factor 23; HSCs, hepatic stellate cells; LCN2, lipocalin 2; LCAT, lecithin cholesterol acyltransferase; SOST, sclerostin; TGF-β, transforming growth factor β; VitD, vitamin D.
The crucial roles of hepatokines FGF21 and BMP9 in controlling bone homeostasis, and osteokines calcitonin and SOST in regulating liver metabolism, are all elegantly demonstrated by transgenic animal studies and direct clinical investigations. Thus, these hepatokines and osteokines warrant further clinical translation as therapeutic targets or diagnostic markers for HOD or liver abnormalities in bone diseases. Although basic studies have revealed the potential contributions of hepatokines fetuins, hepcidin, and LCAT, and osteokine FGF23 to liver-bone crosstalk, the clinical significance still need to be verified in further studies. As for TGF-β, a widely distributed factor with dual regulatory effect on liver and bone, it is still worth exploring whether the massive release of bone-derived TGF-β causes additional burden on the liver directly or indirectly.
Other secretory components may be involved in the dialogue between the liver and bone in addition to hepatokines and osteokines. Currently, small extracellular vesicles derived from bone marrow mesenchymal stem cells exhibited the ability to promote bone and liver regeneration, and control immune responses (132). Exosome studies in liver-bone crosstalk are still lacking. Moreover, the release of inflammatory factors linked to bone disease can also cause damage to the liver microenvironment. These are worth exploring in future studies. Furthermore, multiple organ interactions, such as the liver-gut axis to the bone, and the bone-brain axis to the liver, may play an important role that cannot be overlooked. Some scattered clues are already observed. The Trimethylamine-N-Oxide, which is related to liver-associated bile acid metabolism and gut microbiota (133), could protect against BMD reduction (134). Besides, the gut-derived hormone FGF19 that belongs to the subfamily of FGF21 (135), could inhibit hepatic bile acid synthesis (136) and protect against obesity-induced bone loss (137). It might be a potential therapeutic target for the effects of obesity on skeletal muscle (138). The complicated relationship among the liver, gut, and bone may be better understood through research on those factors.
In addition, when it comes to clinical applications, several issues remain to be addressed. It is still difficult to differentiate the hepatic abnormalities between drug-related side effect and comorbid condition with aberrant bone metabolism. On the other hand, some biomarkers of bone metabolism, such as ALP, could be upregulated during liver injury, therefore, are not reliable in patients with hepatobiliary illnesses. Thus, it is desirable to develop reliable biomarkers for reflecting the pathological liver-bone crosstalk in the future.
With the growing recognition of the dynamic crosstalk between liver and bone and its contribution to pathological bone loss and liver abnormalities, we should not neglect the harmful signals from liver to bone when treating bone diseases or bone-related comorbidities in liver diseases, i.e., HOD, and vice versa. Thus, preserving the physiological liver-bone crosstalk could be a promising strategy for improving liver and bone health, while interfering the pathological liver-bone crosstalk could be an alternative strategy for combating HODs. Importantly, the benefits and risks of targeting those hepatic or osteal factors involved in liver-bone crosstalk are currently ambiguous, which required to be evaluated by in-depth mechanistic studies and large-scale clinical trials in future.
Author contributions
The construction of the main framework: ZL, JL. Collection of references: ZL, XW, NL, CZ, LC, FZ. References organization: ZL, XW. Literature analysis: ZL, XW, NL, JL. Manuscripts preparation: ZL, XW, JL. Manuscript revision: JL, GZ, AL. Funding: JL, AL. All authors approved the final version of the manuscript.
Funding
This work was financially supported by the Theme-based Research Scheme (T12-201/20-R) and General Research Fund (12136616 and 12103519) of Research Grants Council of Hong Kong SAR, The 2020 Guangdong Provincial Science and Technology Innovation Strategy Special Fund (Guangdong-Hong Kong-Macau Joint Lab, No: 2020B1212030006), Interdisciplinary Research Clusters Matching Scheme of Hong Kong Baptist University (RC-IRCs/17-18/02).
Acknowledgments
The graphical abstract was produced by BioRender (www.biorender.com).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: liver, bone, hepatokine, osteokine, endocrine
Citation: Li Z, Wen X, Li N, Zhong C, Chen L, Zhang F, Zhang G, Lyu A and Liu J (2023) The roles of hepatokine and osteokine in liver-bone crosstalk: Advance in basic and clinical aspects. Front. Endocrinol. 14:1149233. doi: 10.3389/fendo.2023.1149233
Received: 21 January 2023; Accepted: 22 March 2023;
Published: 06 April 2023.
Edited by:
Bingdong Sui, Air Force Medical University, ChinaReviewed by:
Siqi Ying, Air Force Medical University, ChinaCheng-Hu Hu, Northwestern Polytechnical University, China
Shengfeng Bai, Fourth Military Medical University, China
Copyright © 2023 Li, Wen, Li, Zhong, Chen, Zhang, Zhang, Lyu and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jin Liu, bGl1amluQGhrYnUuZWR1Lmhr; Aiping Lyu, YWlwaW5nbHVAaGtidS5lZHUuaGs=
†These authors have contributed equally to this work