Oxygen is a critical signaling molecule that regulates the metabolic activities of the liver.1, 2 Dysregulation of the normal oxygen gradient in the liver can induce liver steatosis and inflammation.2 Decreased cellular oxygen affects gene expression through the transcription factor, hypoxia-inducible factor (HIF). During normal cellular oxygen levels, HIFα subunits are rapidly degraded by the ubiquitin proteasome system in which Von Hippel-Lindau (VHL) tumor suppressor protein is the critical E3 ubiquitin ligase required for HIF degradation.3-8 HIF-1α and HIF-2α regulate the expression of genes critical for adaptation to low oxygen levels. Targeted disruption of Vhl in the liver increased HIF-1α and HIF-2α expression, and this mouse model has demonstrated that HIFs are critical in erythropoiesis, iron metabolism, hepatic lipid homeostasis, glucose metabolism, and tumor formation in the liver.9-14 Because overexpression of HIF through disruption of Vhl has many robust pleiotropic effects, it is difficult to assess which are the direct responses of the liver after hypoxia. Furthermore, finding direct mediators of HIF signaling in the liver, which contribute to the phenotype, has been difficult. To overcome this problem, we describe a liver-specific temporal disruption of Vhl using a cre-ERT2 system, which activates a liver-specific cre recombinase expression in the presence of the estrogen analog, tamoxifen. Acute disruption of Vhl resulted in a robust accumulation of lipids in the liver and an increase in liver inflammation and fibrosis. Using a compound double deletion of Vhl and Hif-1α or Hif-2α, liver steatosis, inflammation, and fibrosis were mediated in a HIF-2α–dependent manner. To assess direct signaling pathways activated by HIF, global gene expression analysis was performed in the livers of mice with a temporal disruption of Vhl for 24 hours or 2 weeks. Gene expression profiles demonstrated that HIF rapidly regulates a large battery of genes important for fatty acid synthesis, uptake, and β-oxidation. Moreover, several proinflammatory mediators and profibrogenic genes were rapidly activated after Vhl deletion. These data demonstrate that liver injury resulting from hypoxia is a primary response mediated by HIF-2α.
Oxygen dynamics in the liver is a central signaling mediator controlling hepatic homeostasis, and dysregulation of cellular oxygen is associated with liver injury. Moreover, the transcription factor relaying changes in cellular oxygen levels, hypoxia-inducible factor (HIF), is critical in liver metabolism, and sustained increase in HIF signaling can lead to spontaneous steatosis, inflammation, and liver tumorigenesis. However, the direct responses and genetic networks regulated by HIFs in the liver are unclear. To help define the HIF signal-transduction pathway, an animal model of HIF overexpression was generated and characterized. In this model, overexpression was achieved by Von Hippel-Lindau (Vhl) disruption in a liver-specific temporal fashion. Acute disruption of Vhl induced hepatic lipid accumulation in an HIF-2α–dependent manner. In addition, HIF-2α activation rapidly increased liver inflammation and fibrosis, demonstrating that steatosis and inflammation are primary responses of the liver to hypoxia. To identify downstream effectors, a global microarray expression analysis was performed using livers lacking Vhl for 24 hours and 2 weeks, revealing a time-dependent effect of HIF on gene expression. Increase in genes involved in fatty acid synthesis were followed by an increase in fatty acid uptake-associated genes, and an inhibition of fatty acid β-oxidation. A rapid increase in proinflammatory cytokines and fibrogenic gene expression was also observed. In vivo chromatin immunoprecipitation assays revealed novel direct targets of HIF signaling that may contribute to hypoxia-mediated steatosis and inflammation. Conclusion: These data suggest that HIF-2α is a critical mediator in the progression from clinically manageable steatosis to more severe steatohepatitis and liver cancer, and may be a potential therapeutic target. (HEPATOLOGY 2011;)
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Materials and Methods
The mouse angiopoietin-like 3 (Angptl3)-promoter luciferase was previously described.15 Mouse transglutaminase 2 (Tgm2)-reporter plasmid was constructed by cloning the upstream regions into pGL3-basic vector (Promega, Madison, WI), using primers listed in Supporting Table 1. These luciferase reporters were transfected into Hepa-1 cells, and luciferase assays were performed as previously described.16
Animals and Diets.
VhlF/F, VhlF/FHif-1αF/F, and VhlF/FHif-2αF/F were previously described.16 For temporal hepatocyte-specific disruption, VhlF/F, VhlF/FHif-1αF/F, and VhlF/FHif-2αF/F mice were crossed with mice harboring the Cre-ERT2 recombinase under control of the albumin promoter, SA-Cre-ERT2.17 The mice are a mixed Sv129 and C57BL/6 background, and wild-type littermate control mice were used as a comparison for each experiment. Mice were used between the ages of 6 and 8 weeks for all experiments. For activation of the SA-Cre-ERT2 recombinase for short-term experiments (i.e., 1 and 3 days), mice were treated with 1 dose of tamoxifen (2 mg/mouse in corn oil) by intraperitoneal (IP) injection and killed 24 hours or 3 days after tamoxifen treatment. For the 7-day and 2-week experiments, mice were fed tamoxifen in the diet for 2 days, then replaced with regular chow and killed at 7 days or 2 weeks after initial tamoxifen administration. For the alcohol treatment, mice were treated with tamoxifen by IP injection on 2 consecutive days, then were fed, ad libitum, a 4% alcohol-containing liquid diet (Lieber-DeCarli Diet; Dyets, Inc., Bethlehem, PA) and killed 2 weeks after alcohol administration. Mice were housed in temperature- and light-controlled rooms and were given water and pelleted chow ad libitum. All animal studies were carried out in accordance with guidelines and approved by the National Cancer Institute and University of Michigan Animal Care and Use Committee.
RNA was extracted from tissues, reverse transcribed, and quantitative real-time reverse-transcriptase polymerase chain reaction (qRT-PCR) was performed using primer sequences listed in Supporting Table 1.
Western Blot Analysis.
Liver whole-cell or nuclear extracts were prepared. Membranes were incubated with antibodies against HIF-1α, HIF-2α (Novus Biologicals, Littleton, CO), ANGPTL3 (Santa Cruz Biotechnology, Inc., Santa Cruz, CA), and smooth muscle actin (SMA) (Sigma, St. Louis, MO), phophorylated, and total acetyl-CoA carboxylase (ACC) (Cell Signaling Technology, Beverly, MA) signals obtained were normalized to GAPDH (Santa Cruz) for whole cell extract and histone H1 (Santa Cruz), pregnane X receptor (PXR), and hepatic nuclear factor 4 (HNF-4α) (Abcam, Cambridge, MA) for nuclear extracts.
cDNA Microarray Analysis.
Liver cDNAs were hybridized to an Agilent 44 K mouse 60-peptide oligomer microarray (Agilent Technologies, Santa Clara, CA). Data were processed and analyzed by a Genespring GX software package (Agilent Technologies).
Hematoxylin and eosin (H&E) and Masson's trichrome staining were performed on formalin fixed paraffin embedded sections. Oil red O staining was performed on frozen liver sections or adherent hepatoma-derived Hepa-1 cells. For quantification of oil red O in Hepa-1 cells, isopropanol was added to the cells after staining. Absorbance was measured at 510 nm in the isopropanol extracts, and values were normalized to protein content.
Triglyceride and Cholesterol Analysis.
Hepatic lipids were extracted using a 2:1 chloroform-methanol solution. Liver and serum triglycerides were measured using the Serum Triglyceride and Cholesterol Determination Kit, according to the manufacturer's recommendation (Wako, Richmond, VA).
Livers were cross-linked in 1% formaldehyde in 1× phosphate-buffered saline at 37°C for 20 minutes. ChIP assays were performed for HIF-2α as previously described.16 Primers for qRT-PCR ChIP are available upon request. The primers for Tgm2 ChIP are listed in Supporting Table 1.
Results are expressed as mean ± standard deviation (SD). P values were calculated by independent t test. P < 0.05 was considered significant.
Generation of a Mouse Model Containing a Temporal Hepatocyte-specific Disruption of Vhl.
VhlF/F mice were crossed with SA-Cre-ERT2 transgenic mice to generate a temporal and conditional disruption of Vhl (VhlF/F;AlbERcre). The tamoxifen-inducible Cre provides an advantage of assessing immediate downstream pathways controlled by VHL and eliminates the confounding developmental effects of Vhl deletion. To confirm the inducibility and hepatocyte-specific disruption, VhlF/F and VhlF/F;AlbERcre mice were treated with one dose of vehicle or tamoxifen, and livers and extrahepatic tissues were isolated 24 hours post-treatment. VhlF/F and VhlF/F;AlbERcre mice treated with vehicle did not demonstrate a decrease in Vhl gene expression, whereas tamoxifen treatment dramatically decreased Vhl gene expression in the VhlF/F;AlbERcre but not the VhlF/F mice (Fig. 1A). Moreover, the decrease was specific for the liver; no other tissues assessed demonstrated a tamoxifen-dependent decrease in Vhl expression (Supporting Fig. 1). Western blot analysis of nuclear extracts demonstrated an increase in HIF-1α and HIF-2α expression (Fig. 1B). Consistent with HIFα subunit expression, an increase in pyruvate dehydrogenase kinase 1 (Pdk1) and erythropoietin (Epo), two well-characterized HIF-1α and HIF-2α target genes, were observed (Fig. 1C). In mice that contained a conditional disruption of Vhl, increased liver and spleen weights were noted at 6-8 weeks of age.9, 11 Therefore, to assess whether these were early events after loss of VHL, liver and spleen weights were measured in mice in which Vhl was disrupted for 14 days. A significant increase in liver and spleen weights was observed (Fig. 1D-F). Together, these data demonstrate that tamoxifen-inducible Vhl disruption is an optimal system to assess primary responses, which are critical in hypoxia-induced liver injury.
HIF-2α Increases Inflammation and Lipid Accumulation in the Liver.
Conditional inactivation of Vhl in hepatocytes results in liver inflammation and hepatic steatosis.9, 11, 14 However, it is not clear whether inflammation and lipid accumulation are early events after disruption of Vhl or are results of the developmental or chronic effects from loss of Vhl. To address these questions, livers were analyzed after disruption of Vhl for 2 weeks; a robust increase in liver inflammation was observed by H&E staining and qRT-PCR analysis of two proinflammatory mediators: interleukin-1β (Il-1β) and Il-6 (Fig. 2A-C). The increase in Il-6 and Il-1β gene expression was evident as early as 3 days after tamoxifen treatment (Fig. 2D). Overt inflammation, as observed by H&E staining, was evident at 7 days after tamoxifen treatment (Supporting Fig. 2A). To assess the influence of HIF-dependent pathways on inflammatory gene expression in the liver, mice with a double disruption of Vhl and Hif-1α or Hif-2α were generated. The double disruption of Vhl and Hif-2α (VhlF/FHif2aF/F;AlbERcre+tamoxifen) ameliorated the increase in Il-6 and Il-1β, compared to littermate controls (VhlF/FHif2aF/F+tamoxifen) (Fig. 2E). In contrast, a significant increase in Il-6 and Il-1β gene expression was observed in mice with a double disruption of Vhl and Hif-1α, compared to littermate controls (Supporting Fig. 2B). Furthermore, 2 weeks after the loss of Vhl, a dramatic increase in liver lipid accumulation was observed by oil red O staining (Fig. 3A,B). The increase in lipid accumulation could be observed as early as 24 hours after Vhl disruption (Fig. 3C,D). The compound disruption of Vhl and Hif-1α or Hif-2α demonstrated that the increase in lipid accumulation was caused by HIF-2α, but not HIF-1α (Fig. 3E,F). Consistent with oil red O staining, hepatic triglycerides and cholesterol increased after disruption of Vhl for 2 weeks (Fig. 3G). Together, these data demonstrate that HIF-2α is a direct regulator of liver inflammation and lipid accumulation in the liver.
HIF-Regulated Genetic Program in the Liver.
To understand the critical genes regulated after Vhl disruption, gene expression profiles of VhlF/F and VhlF/F;AlbERcre were assessed in livers isolated 24 hours or 2 weeks after Vhl disruption. In total, 3597 significantly regulated changes were identified after 2 weeks of Vhl deletion, whereas 470 genes were identified 24 hours after Vhl disruption (Fig. 4A; the full gene list with an average change of 1.5-fold is in Supporting Tables 2 and 3). The data suggested that a rapid increase in genes critical for lipid synthesis was followed by an increase in genes important for fatty acid uptake. Consistent with the microarray data, an increase was observed in the expression of fatty acid synthase (Fasn) and sterol regulatory element binding factor-1C (Srebp-1c) at 3 days after Vhl disruption. Interestingly, at 14 days after Vhl disruption, a significant repression of Fasn and Srebp-1c was observed (Fig. 4B), whereas a rapid repression of Cd36 gene expression was observed after 3 days of Vhl disruption, followed by a dramatic increase in gene expression 14 days after the loss of Vhl (Fig. 4B). In addition, a significant decrease was observed in genes critical in fatty acid β-oxidation, and a decrease in carnitine palmitoyltransferase 1A (Cpt1a), carnitine palmitoyltransferase 2 (Cpt2), acyl-CoA oxidase 1 (Acox), and peroxisome proliferator-activated receptor alpha (Pparα) were observed after 2 weeks of Vhl disruption; Pparα expression did not reach statistical significance (Fig. 4C). Interestingly, the expression of PPARα protein was significantly decreased 2 weeks after Vhl disruption, suggesting enhanced degradation (Fig. 4D). Expression of two other important nuclear receptors, PXR and HNF-4α, was unchanged. The decrease in β-oxidation genes was not observed at 3 days after Vhl disruption, but was dependent on HIF-2α expression (Supporting Fig. 3). These data suggest that HIF-2α regulates fatty acid synthesis, uptake, and β-oxidation in a time-dependent manner.
HIF-2α Is a Novel Regulator of Angptl3.
SREBP-1c, FASN, CD36, and PPARα have critical roles of in fatty acid homeostasis in the liver; however, their gene-expression patterns suggest that these genes may not be direct targets for HIF-2α in the liver. Interestingly, angiopoietin-like 3 (Angptl3) demonstrated rapid, sustained increase after Vhl disruption (Fig. 5A). ANGPTL3 is specifically expressed in the liver and is a direct regulator of lipid homeostasis.18-20 Mutations in Angptl3 in mice or humans are associated with low serum lipid levels, whereas overexpression of ANGPTL3 increases circulating lipid levels.18, 20 In mice with a double disruption of Vhl and Hif-2α, it was demonstrated that the induction of Angptl3 was the result of HIF-2α increase (Supporting Fig. 4). Gene-expression data correlated to an increase in protein expression, as tamoxifen-treated VhlF/F;AlbERcre mice demonstrated an increase in liver ANGPTL3 protein expression, compared to tamoxifen-treated VhlF/F mice (Fig. 5B). Because mouse models that overexpress ANGPTL3 demonstrated an increase in serum lipid levels,20 serum triglycerides were assessed in mice 2 weeks after the loss of Vhl. VhlF/F;AlbERcre mice treated with tamoxifen had elevated serum triglycerides, compared to similarly treated VhlF/F mice (Fig. 5C). In addition, liver-derived Hepa-1 cells, which overexpress ANGPTL3, demonstrated a dose-dependent increase in oil red O accumulation, suggesting that ANGPTL3 may play a critical role in HIF-mediated lipid accumulation (Fig. 5D). To assess whether ANGPTL3 could be a novel direct target of HIF-2α, Angptl3-promoter luciferase assays were performed. A 1.7-kilobase (kb) Angptl3 proximal promoter luciferase construct was transfected into Hepa-1 cells. Hypoxia (1% O2) induced luciferase expression (Fig. 5E), and cotransfection with a mammalian expression plasmid for HIF-1α moderately increased luciferase expression, whereas cotransfection with HIF-2α expression plasmid strongly increased luciferase expression. The HIF-1α and HIF-2α increase in luciferase expression was further potentiated in cells incubated in 1% O2 (Fig. 5E). Deletion analysis showed that the HIF-responsive site on the Angptl3 promoter was within the first 100 bp (base pairs) of the proximal promoter; however, no consensus HIF response element (HRE) was found in this site (Fig. 5F). Furthermore, in vivo ChIP assays failed to demonstrate HIF-2α binding to the promoter (data not shown). Together, these data suggest that Angptl3 is a rapid HIF-2α responsive gene through a yet-unknown mechanism.
HIF-2α Regulates Liver Fibrogenesis.
A dramatic induction of genes important in liver fibrosis were observed in the gene-expression profiling data. Increases in several fibrogenic genes were confirmed in VhlF/F;AlbERcre mice treated with tamoxifen, compared to littermate control mice (Fig. 6A). A specific increase in lysyl oxidase-like 1 (LOXL1), lysyl oxidase-like 2 (LOXL2), prolyl 4-hydroxylase alpha 1 (P4HA1), prolyl 4-hydroxylase alpha 2 (P4HA2), procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2 (PLOD2), and transglutaminase 2 (TGM2) was observed. These genes are critical for the formation and stabilization of collagen.21-26 In addition, smooth muscle actin (SMA), a marker of stellate cell activation and fibrosis, was significantly increased in VhlF/F;AlbERcre mice treated with tamoxifen, compared to littermate control mice, as assessed by qRT-PCR and western blot analysis (Fig. 6A,B). To confirm an increase in fibrosis, Masson's trichrome staining was performed (Fig. 6C,D). Livers isolated from VhlF/F;AlbERcre mice 14 days after tamoxifen treatment demonstrated a moderate increase in focal areas of fibrosis, compared to similarly treated VhlF/F mice (Fig. 6C). Moreover, VhlF/F and VhlF/F;AlbERcre mice were treated with tamoxifen, then put on liquid diet consisting of 4% ethanol for 2 weeks. Mice are resistant to alcohol-induced fibrosis, as chronic treatment with alcohol (i.e., over 3 months) typically results in no marked liver fibrogenesis in mice.27 However, in mice with a disruption of liver Vhl, alcohol treatment caused marked fibrosis, compared with littermate controls treated with alcohol (Fig. 6D). The double disruption of Vhl and Hif-2α (VhlF/FHif2aF/F;AlbERcre+tamoxifen) ameliorated the increase in SMA, whereas a significant increase in SMA expression was observed in mice with a double disruption of Vhl and Hif-1α (VhlF/FHif1aF/F;AlbERcre+ tamoxifen) (Fig. 7A). Similarly, the increase in fibrosis observed in Vhl-disrupted mice on an alcohol diet was completely lost in the Vhl and Hif-2α double knockout, but not the Vhl and Hif-1α double knockout (Fig. 7B). Consistent with the role of HIF-2α in exacerbating fibrosis, fibrogenic gene-expression levels were not increased in the Vhl and Hif-2α knockout, as compared to mice with a Vhl disruption (Fig. 7C). Together, these data demonstrate that HIF-2α is a critical transcription factor in exacerbating fibrosis in the liver.
HIF-2α Directly Regulates Several Profibrogenic Genes.
To assess whether HIF-2α could directly regulate fibrogenic genes in the liver, ChIP assays were performed using cross-linked liver DNA isolated from tamoxifen-treated VhlF/F and VhlF/F;AlbERcre mice, with the average shearing size of 1.5 kb. Primers were designed to the center of the proximal promoter to assess HIF-2α occupancy. This method provides an assessment of HIF-2α occupancy at promoters without defining the precise HIF response element. With this method, it was shown that HIF-2α was enriched at the promoters of several fibrogenic genes in VhlF/F;AlbERcre mice, compared with control littermates (Fig. 8A). To assess whether the low-resolution ChIP assays, indeed, did identify direct targets, TGM2 expression was further assessed. An increase in TGM2 protein expression was observed in VhlF/F;AlbERcre mice, compared to control littermates, after 2 weeks of Vhl disruption (Fig. 8B). Next, a Tgm2 proximal promoter luciferase construct was cotransfected into liver-derived Hepa-1 cells with a mammalian expression plasmid for HIF-1α, HIF-2α, or empty vector. HIF-2α specifically induced luciferase expression, whereas HIF-1α had no effect, compared with empty vector transfected control (Fig. 8C), and mutating the two putative HREs ablated HIF-2α activity (Fig. 8D). Using primers flanking the HREs and sheared cross-linked liver DNA (shearing size, 300 bp) from tamoxifen-treated VhlF/F and VhlF/F;AlbERcre mice demonstrated increased HIF-2α binding to the Tgm2 promoter in livers isolated from VhlF/F;AlbERcre mice, compared to VhlF/F mice (Fig. 8E). These data demonstrate that HIF-2α can directly regulate fibrogenic genes.
One-third of adults in the United States are diagnosed with fatty liver disease, mostly attributed to obesity or alcohol consumption. Approximately 10% will proceed to develop steatohepatitis and associated comorbidities (e.g., fibrosis, cirrhosis, and liver cancer).28 Currently, the mechanisms for the increased progression are not known. However, according to the two-hit hypothesis, the initial insult is the fat accumulation within the liver, with the second insult being increased oxidative stress and inflammation, and both are critical for steatohepatitis.29 The current study demonstrates that mice with a temporal hepatic disruption of Vhl have spontaneous fatty liver and liver inflammation that will progress to focal fibrosis and hepatomegaly in a HIF-2α–dependent manner. This demonstrates that hypoxia and HIF-2α play a critical role in both insults needed for the progression of fatty liver disease, as suggested by the two-hit hypothesis.
Gene-expression profiling demonstrated that several genes important in fatty acid synthesis, uptake, and β-oxidation are significantly altered after the loss of VHL. Fasn and Srebp-1c were repressed in mice with a conditional disruption of Vhl; therefore, fatty acid synthesis was not thought to be involved in increased lipid accumulation in the liver after Vhl disruption.14 However, the present data suggest that at early times points, lipid synthesis may contribute to steatosis, as both Fasn and Srebp-1c are significantly increased after acute disruption, then are significantly repressed after long-term Vhl deficiency. To assess whether, indeed, at early time points after HIF activation that fatty acid synthesis was increased, ACC activity was measured. However, both phosphorylated and total ACC were significantly repressed at 3 days after tamoxifen treatment in the VhlF/F;AlbERcre mice, compared with VhlF/F mice, making the data difficult to interpret (Supporting Fig. 5). However, 14 days after tamoxifen treatment, no change in phosphorylated or total ACC was observed in the VhlF/F;AlbERcre mice, compared with VhlF/F mice, suggesting that β-oxidation may be a critical driver in fat accumulation at later time points. In addition, the gene-expression analysis demonstrates a significant modulation of several nuclear receptor target genes (e.g., liver X receptor, farnesoid X receptor, and PPARγ). However, changes were not found in the expression of these nuclear receptors by qRT-PCR or microarray analysis, suggesting that nuclear receptors are not direct transcriptional targets of HIF. Interestingly, in mice with the conditional Vhl deletion, adipose differentiation-related protein (ADFP) was significantly induced and thought to be critical in the liver steatotic phenotype.14 However, in the VhlF/F;AlbERcre mice after tamoxifen treatment, no increase in ADFP was observed at any time point assessed (data not shown), suggesting that the increase in ADFP is a late secondary response or because of developmental defects after conditional Vhl disruption. These data highlight the importance of temporal gene disruption of Vhl to identify direct mediators of response.
One important mediator of lipid homeostasis, ANGPTL3, an endogenous lipoprotein lipase (LPL) inhibitor,30-32 was identified as an HIF-responsive gene. ANGPTL3 is important in regulating serum triglycerides levels.20 In tamoxifen-treated VhlF/F;AlbERcre mice, the increase of ANGPTL3 correlated to an increase in serum triglycerides, and ANGPTL3 directly increased lipid accumulation in Hepa-1 cells, as assessed by oil red O staining. Currently, it is not known whether the increase in lipid accumulation is through the LPL inhibitor function of ANGPTL3, but is a clear point of emphasis for future studies. Angptl3 gene expression and promoter activity were rapidly induced by HIF-2α. However, no HREs were identified in the promoter, suggesting that its activation is HIF-2α-mediated through an indirect mechanism. The HIF-responsive region was localized to a 100-bp region directly proximal to the transcription initiation site, and HIF-2α regulation of this sequence is being further assessed.
During the preparation of this article, others published similar findings in a temporally deleted, liver-specific VHL mouse model, in which disruption of Vhl was induced by tail vein injection of adenovirus encoding cre recombinase (ad-Cre).33 Five days after an injection of ad-Cre, mice demonstrated dramatic steatosis and a decrease in PPARα signaling, thus establishing, as does the present study, that HIF signaling has a primary role in liver lipid homeostasis. Furthermore, the present study demonstrates that these are immediate, rapid responses of HIF-2α signaling. Interestingly, after ad-Cre injection, mice demonstrated rapid death in an HIF-dependent manner, where the median survival was 6 days.34 The increase in survival in the VhlF/F;AlbERcre mice after tamoxifen administration allowed further assessment of the livers, revealing increased progression of steatosis to inflammation. Thus, VhlF/F;AlbERcre mice may be a valuable model of spontaneous steatohepatitis for use in preclinical drug development.
Although the direct effectors that increase inflammation are not known, it is possible that HIF-2α can directly activate inflammatory mediators in the liver. Indeed, it was shown that Il-6 is a direct HIF-2α target gene in macrophages.34 However, our data clearly show that HIF-2α can bind to the promoters of several profibrogenic genes, consistent with data demonstrating that hypoxia can activate fibrogenesis in hepatocytes and stellate cells.35-37 Hepatic stellate cells initiate the fibrotic process. In the liver, quiescent stellate cells are critical in the storage of vitamin A. During liver injury, stellate cells become activated, proliferate, and express a fibrogenic gene program.38 After Vhl disruption, a robust activation of stellate cells is observed in the liver resulting from high activation of collagen gene expression and an increase in SMA, both markers of stellate cell activation. The initiating factor in the activation of stellate cells after Vhl loss is thought to be the result of a sustained increase in lipid accumulation and inflammatory genes. In addition, the increase in fibrosis mediated by HIF-2α may be caused by collagen matrix stabilization. P4HA1, P4HA2, and PLOD2 are required for hydroxylation of lysyl and prolyl residues on collagen.23, 26 The resultant hydroxylysyl and hydroxyproline groups are critical for the stability and synthesis of collagen matrixes. Loxl1 and loxl2 gene expression were also increased in the livers of tamoxifen-treated VhlF/F;AlbERcre mice, and their respective promoters were occupied by HIF-2α. Lysyl oxidase activity is critical in the formation of insoluble collagen fibers, and HIF-1α has been shown to increase renal fibrosis through a lysyl oxidase-mediated mechanism.21, 22 Moreover, TGM2, a multifunction enzyme that covalently cross-links collagen matrices, has been shown to be critical in inducing apoptosis by inactivation of SP1 and c-met in injured livers after alcohol administration.24, 25 HIF-2α can directly regulate the promoter of Tgm2 in a distinct manner, as observed with HIF-1α.39 It is not clear whether Tgm2 is the key enzyme that regulates fibrosis, because Tgm2-null mice are not protected in the carbon tetrachloride and the thioacetamide-induced fibrosis models.40 However, it is likely that the cumulative increase in several profibrogenic genes are needed to increase liver fibrosis, and HIF-2α may be the critical transcription factor to integrate these signals.
The present study demonstrates that activation of HIF-2α in the liver regulates liver homeostasis and disease progression and establishes that steatosis, inflammation, and fibrosis are direct responses initiated by the liver after HIF-2α activation. In addition, the present work provides a novel animal model to study the precise molecular and genetic changes required for the progression of fatty liver disease to steatohepatitis. Together, these findings may lead to novel therapies for liver injury.