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Department of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, LA
Address reprint requests to: Tong Wu, M.D., Ph.D., Department of Pathology and Laboratory Medicine, Tulane University School of Medicine, 1430 Tulane Ave., SL-79, New Orleans, LA 70112. E-mail: email@example.com; fax: 504-988-7862.
Potential conflict of interest: Nothing to report.
MicroRNA-122 (miR-122), a pivotal liver-specific miRNA, has been implicated in several liver diseases including hepatocellular carcinoma (HCC) and hepatitis C and B viral infection. This study aimed to explore epigenetic regulation of miR-122 in human HCC cells and to examine the effect of hepatitis C virus (HCV) and hepatitis B virus (HBV). We performed microRNA microarray analysis and identified miR-122 as the most up-regulated miRNA (6-fold) in human HCC cells treated with 5′aza-2′deoxycytidine (5-Aza-CdR, DNA methylation inhibitor) and 4-phenylbutyric acid (PBA, histone deacetylation inhibitor). Real-time polymerase chain reaction (PCR) analysis verified significant up-regulation of miR-122 by 5′aza and PBA in HCC cells, and to a lesser extent in primary hepatocytes. Peroxisome proliferator activated receptor-gamma (PPARγ) and retinoid X receptor alpha (RXRα) complex was found to be associated with the DR1 and DR2 consensus site in the miR-122 gene promoter which enhanced miR-122 gene transcription. 5-Aza-CdR and PBA treatment increased the association of PPARγ/RXRα, but decreased the association of its corepressors (N-CoR and SMRT), with the miR-122 DR1 and DR2 motifs. The aforementioned DNA-protein complex also contains SUV39H1, an H3K9 histone methyl transferase, which down-regulates miR-122 expression. Conclusions: These findings establish a novel role of the PPARγ binding complex for epigenetic regulation of miR-122 in human HCC cells. Moreover, we show that hepatitis B virus X protein binds PPARγ and inhibits the transcription of miR-122, whereas hepatitis C viral particles exhibited no significant effect; these findings provide mechanistic insight into reduction of miR-122 in patients with HBV but not with HCV infection. (Hepatology 2013;58:1681–1692)
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silencing mediator of retinoid and thyroid hormone receptors
Hepatocellular carcinoma (HCC) is the most common primary malignant tumor of the liver and the third most common cause of cancer-related death worldwide. Major risk factors for HCC include infection of hepatitis C virus (HCV) and hepatitis B virus (HBV) and alcoholic and nonalcoholic fatty liver diseases. The global burden of HCC is expected to increase in the next decades, with HCV infection responsible for the rising incidence of HCC in the United States and HBV infection as the leading cause of HCC globally. Most of the HCC risk factors are known to cause epigenetic changes such as DNA methylation and histone modification, although the precise gene targets and the underlying mechanisms remain incompletely defined.
MicroRNAs (miRNAs) have emerged as important regulators of gene expression in both normal and disease states.[3, 4] Recent evidence suggests deregulation of miRNAs in hepatocarcinogenesis and tumor progression.[5, 6] In this context, it is noticeable that epigenetic modification is being recognized as a key mechanism for regulation of miRNA expression, although it remains largely unknown whether miRNAs in the liver are epigenetically regulated.
MiR-122 is the most highly expressed miRNA in the liver and is implicated in several important aspects of liver pathobiology, including hepatocarcinogenesis, HCV replication, lipid metabolism, and iron homeostasis.[9-13] MiR-122 is known to bind the 5′-untranslated region (UTR) of the HCV genome and stimulate the translation of HCV RNA; accordingly, inhibition of miR-122 decreases HCV viral load in cultured cells and in a chimpanzee model of HCV infection. The level of miR-122 is decreased in patients with HBV infection, although the mechanism for HBV-mediated reduction of miR-122 is not known. Deletion of miR-122 in mice has been shown to cause hepatosteatosis, liver inflammation and fibrosis, and ultimately HCC.[16, 17] Several liver-enriched transcription factors (LETFs) are known to regulate miR-122 expression[18, 19]; however, little is known about epigenetic regulation of miR-122 expression in the liver. Additionally, while recent studies have documented the effect of miR-122 in the liver, it remains unknown how miR-122 expression is regulated in HCC cells and in liver diseases.
Peroxisome proliferator-activated receptor-gamma (PPARγ) is a ligand-activated transcription factor that belongs to the nuclear hormone receptor superfamily. PPARγ forms a heterodimer with retinoid X receptor-alpha (RXRα) and binds to the DNA response element consisting of a direct repeat of two hexanucleotides spaced by one or two nucleotides (DR1 or DR2 motif, respectively).[22, 23] In the absence of ligands, PPARγ/RXRα associate with corepressors such as the nuclear receptor corepressor protein (NCoR) and the silencing mediator of retinoid and thyroid hormone receptors (SMRT); this nuclear receptor corepressor complex modify the chromatin environment through recruitment of histone deacetylase (HDAC) or histone methyltransferase (HMT), thereby down-regulating transcriptional activity.[24, 25] In the presence of PPARγ ligands, the corepressors become dissociated from PPARγ/RXRα, thus enabling gene transcription.
In the present study we performed miRNA microarray analysis and our data showed that miR-122 is one of the most up-regulated miRNA in HCC cells treated with the epigenetic drugs (5′aza-2′deoxycytidine [5-Aza-CdR] and 4-phenylbutyric acid [PBA]). Given that the promoter region of miR-122 contains DR1 and DR2 motifs, we postulated that the PPARγ/RXRα complex might be implicated in epigenetic regulation of miR-122 during hepatocarcinogenesis. Indeed, our experimental results demonstrate that PPARγ/RXRα associate with the DR1 and DR2 motifs of the miR-122 promoter to regulate miR-122 expression in HCC cells and the effect is dependent on two PPARγ corepressors, N-CoR and SMRT, and a key HMT, SUV39H1. Moreover, our data show that hepatitis B virus X protein (HBX) binds PPARγ and inhibits the transcription of miR-122 gene, which provides mechanistic explanation for the intriguing differential regulation of miR-122 by hepatitis B and C viruses.
Materials and Methods
Cell Culture and Reagents
Cells were maintained at 37°C and 5% CO2. Human HCC cell lines (HepG2, Huh7, and Hep3B cells) were obtained from the American Type Culture Collection (Rockville, MD). HepG2 and Hep3B cells were cultured in minimum essential medium (MEM) and Huh7 cells in Dulbecco's modified Eagle's medium (DMEM) containing 10% fetal bovine serum (FBS; Gibco) and antibiotic, respectively. Huh7.5 cells line was obtained from the laboratory of Charlie Rice (Rockefeller University, New York) and were cultured in DMEM with 10% FBS and antibiotics. Primary human hepatocyte cultures were purchased from Lonza (Walkersville, MD) and cultured in collagen I-coated plates (BD Bioscience, Bedford, MA) with hepatocyte basal medium supplemented with HCM SingleQuots growth factors (Lonza, Walkersville, MD). HepG2.2.15 cells were maintained in DMEM containing 10% FBS as described. The differentiated HepaRG cells were purchased from Invitrogen (Carlsbad, CA) and maintained in William's medium E with GlutaMax-1, supplemented with General Purpose Working Medium (Invitrogen). The immortalized untransformed human neonatal liver NeHepLxHT cells were purchased from the American Type Culture Collection and cultured as described. The 5-Aza-CdR, PBA, Chaetocin, and 9-cis retinoic acid were obtained from Sigma-Aldrich (St. Louis, MO). Pharmacological PPARγ ligands (rosiglitazone, troglitazone, ciglitazone, 15-keto prostaglandin E2, 15-deoxy-12, 14-prostaglandin J2) were purchased from Cayman Chemical (Ann Arbor, MI). Antibodies against di-methyl and tri-methyl histone H3K9, PPARγ (ChIP grade), SMRT, and acetyl histone were obtained from Abcam (Cambridge, MA). Anti-N-CoR antibody was purchased from Millipore (Billerica, MA). Anti-C/EBPα, anti-Akt, anti-PTEN, anti-mTOR, anti-phospho-mTOR, anti-Smad3, anti-Smad 4, and anti-SAPK/JNK were obtained from Cell Signaling (Beverly, MA). All other antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA).
HCV Infection and Detection
HCV virus infection was performed as described.[29, 30] Huh7.5 cells were transfected with 20 μg of in vitro transcribed full-length HCV JFH1-GFP RNA by an electroporation method. After 72 hours, the lysates and supernatant were collected by scraping and freeze-thaw cycle in dry-ice and infectious virus was clarified by centrifugation at 3,400 rpm for 5 minutes. Huh7.5 cells were plated on 6-well plates and the infectious culture medium containing HCV viral particles or control spent medium were added. After 96 hours postinfection, the HCV-infected green fluorescent protein (GFP)-positive cells were detected by fluorescence microscopy and quantitative real-time reverse-transcription polymerase chain reaction (RT-PCR) as described[29, 30] (the forward primer sequence is 5′-TCTTCACGCAGAAAGCGTCTA-3′; the reverse primer sequence is 5′-CGGTTCCGCAGACCACTATG-3′; the probe sequence is 5-'TGAGTGTCGTGCAGCCTCCAGGA-3′, labeled at the 5′ end with FAM [6-carboxyfluorescein] fluorophore reporter molecule and at the 3′ end with TAMRA [6-carboxytetramethylrhodamine)] quencher molecule).
HBV Infection and Detection
The HepG2.2.15 cell line was used for production of HBV particles. HBV inoculum was prepared from freshly collected supernatants of HepG2.2.15 cells by ultracentrifugation in Beckman rotor at 40,000 rpm for 1 hour at 4°C. The pellet was resuspended in Williams E medium. HepaRG cells were incubated with concentrated infectious source diluted 2-fold in culture medium supplemented with 4% PEG 8000 for 20 hours at 37°C. At the end of the incubation the cells were washed three times with the culture medium and maintained for 7 days (the medium was exchanged every 2 days). For detection of HBV DNA, the cells and supernatants were collected and DNA was extracted and purified with Qiagen DNeasy kit. The purified total DNA was used as template for quantitative RT-PCR. RT-PCR was performed using SYBR green PCR kit (Qiagen). Primers for amplification of the HBV DNA were 5′-ATCTTCTTGTTGGTTCTTCT-3′ (forward) and 5′-CTGAAAGCCAAACAGTGG-3′ (reverse). For detection of HBX, total RNA isolated using Trizol reagent (Invitrogen) was reverse-transcribed with Superscript II RT reagent kit (Invitrogen), followed by quantitative RT-PCR. Primers for amplification of the HBX messenger RNA (mRNA) were 5′-TCTCAGCAATGTCAACGAC-3′ (forward) and 5-TTTATGCCTACAGCCTCCT-3′ (reverse), and for the glyceraldehyde phosphate dehydrogenase (GAPDH) mRNA were 5′-TTGCCATCAATGACCCCTTCA-3′ (forward) and 5′-GCCCCACTTGATTTTGGA-3′ (reverse).
Epigenetically Regulated miRNAs in Human HCC Cells
To identify epigenetically regulated miRNAs in HCC, we performed miRNA microarray in human HCC cells (HepG2) treated with the DNA methylation inhibitor (5-Aza-CdR) and the histone deacetylase inhibitor (PBA). The microarray data were analyzed using hierarchical clustering of the log2 value and displayed in a heatmap (Fig. 1A). Out of 837 human miRNAs that were analyzed, 43 miRNAs were differentially expressed in 5-Aza-CdR- and PBA-treated cells compared to control vehicle-treated cells (at the level of P < 0.01). The up-regulated miRNAs include miR-122, miR-30e, miR-3922-5p, miR-125-5p, and miR-224; the down-regulated miRNAs include miR-654-3p, miR-4481, miR-133a, and miR-133b. Among these, miR-122 was identified as the most up-regulated miRNA (6.6-fold, Fig. 1B).
Given that miR-122 is the dominant hepatocyte-specific miRNA (accounting for ∼70% of the liver's total miRNAs)[8, 31] and its expression is decreased during hepatocarcinogenesis,[16, 32] we elected to focus on epigenetic regulation of miR-122. As determined by qRT-PCR analysis, 5-Aza-CdR/PBA treatment increased the levels of mature miR-122 in two HCC cell lines, HepG2 and Huh7, by 11.6- and 4.2-fold, respectively (Fig. 1C). 5-Aza-CdR- and PBA-treated HepG2 and Huh7 cells also showed significantly higher expression of pri-miR-122 level (6.3- and 5-fold increase, respectively) (Fig. 1D), suggesting that epigenetic up-regulation of miR-122 occurs predominantly at the transcriptional level. We observed that primary human hepatocytes express much higher basal levels of miR-122 compared to HCC cell lines (HepG2, Huh7, and Hep3B) (Fig. 1E). However, in primary human hepatocytes miR-122 expression was up-regulated to a lesser extent by 5-Aza-CdR/PBA (1.8-fold, Fig. 1F). These results suggest that the expression of miR-122 in HCC cells is epigenetically suppressed to a greater extent than in primary hepatocytes.
5-Aza-CdR and PBA Induce PPARγ/RXRα Binding to DR1 and DR2 Motifs of MiR-122 Gene Promoter
The promoter region of miR-122 gene contains specific binding sites for the liver-enriched transcription factors (LETFs), such as hepatocyte nuclear factors-4α (HNF-4α) and CCAAT/enhancer-binding proteins (C/EBPs), which regulate miR-122 gene transcription.[18, 19] To determine whether 5-Aza-CdR/PBA induce miR-122 expression through induction of these LETFs, we examined the protein levels of HNF-4α, C/EBPα, and related signaling molecules. As shown in Supporting Fig. S1, the levels of these molecules were not significantly altered by 5-Aza-CdR and PBA treatment. We observed that the level of E-cadherin expression is increased in HepG2 cells treated with 5-Aza-CdR and PBA; this finding is consistent with the notion that E-cadherin expression is frequently suppressed by epigenetic mechanisms such as promoter hypermethylation in HCC.
Given that the promoter region of miR-122 contains DR1 and DR2 motifs that are recognized by several members of the nuclear hormone receptor superfamily including PPARγ, we performed DNA pulldown assay using biotinylated DR1 or DR2 oligonucleotides corresponding to the miR-122 promoter. As shown in Fig. 2A, PPARγ and RXRα bound to miR-122 DR1 and DR2 motifs and the association was significantly enhanced by 5-Aza-CdR and PBA. In contrast, PPARα did not bind to either DR1 or DR2 consensus site. Transient transfection with a PPARγ expression vector further enhanced 5-Aza-CdR/PBA-induced PPARγ binding to miR-122 DR1 and DR2 motifs (Fig. 2B). To further determine PPARγ association with miR-122 promoter DNA, we performed a chromatin immunoprecipitation (ChIP) assay using three specific primer sets corresponding to the three DR1 and DR2 regions in the miR-122 gene promoter. As shown in Fig. 2C, 5-Aza-CdR/PBA treatment significantly enhanced PPARγ binding to the DR1 and DR2 regions of the miR-122 promoter. To analyze for miR-122 gene promoter transcription activity, we generated a luciferase reporter construct containing the DR1 and DR2 regions of the miR-122 promoter and our data showed that 5-Aza-CdR/PBA treatment significantly increased miR-122 gene promoter luciferase reporter activity (Fig. 2D). Therefore, 5-Aza-CdR and PBA treatment induces PPARγ/RXRα complex association with the DR1 and DR2 element and this mechanism is implicated in 5-Aza-CdR/PBA-induced miR-122 expression.
As the activity of PPARγ/RXRα is influenced by specific ligands, we next examined the effect of PPARγ and RXRα ligands on miR-122 expression. For these experiments, HepG2 cells were treated with the PPARγ agonists, 15-deoxy-prostaglandin J2 (15d-PGJ2, 10 μM) or 15-keto-prostaglandin E2 (15-keto-PGE2, 10 μM), and the RXRα agonist, 9-cis-retinoic acid (9-cis RA, 10 μM). As shown in Fig. 2E, the expression of miR-122 was increased by these three agonists and the effects were further augmented when PPARγ protein was overexpressed. Treatment with additional PPARγ agonists (rosiglitazone, troglitazone, ciglitazone) also increased the expression of miR-122 in PPARγ overexpressed HepG2 cells (Fig. 2F). To evaluate the effects of PPARγ on miR-122 expression in nonmalignant hepatocytes, NeHepLxHT cells (immortalized untransformed neonatal hepatocytes) were transfected with PPARγ small interfering RNA (siRNA) or expression vector. As shown Fig. 2G, knockdown of PPARγ decreased miR-122 expression, whereas overexpression of PPARγ increased it. These results demonstrate that miR-122 expression is positively regulated by PPARγ and RXRα in cells of hepatocyte origin.
5-Aza-CdR and PBA Induce N-CoR and SMRT Dissociation From PPARγ and DR1/DR2 Complex
Given that N-CoR and SMRT are corepressors of PPARγ, we performed a DNA pulldown assay to determine their association with the miR-122 DR1 and DR2 motifs. Our data showed that 5-Aza-CdR and PBA treatment decreased the binding of N-CoR and SMRT to DR1 and DR2 oligonucleotides (Fig. 3A). Accordingly, coimmunoprecipitation assay showed that 5-Aza-CdR and PBA treatment led to dissociation of N-CoR and SMRT from PPARγ (Fig. 3B), although the protein levels of N-CoR and SMRT were not altered. These findings suggest that dissociation of N-CoR and SMRT from PPARγ and DR1/DR2 complex contribute to 5-Aza-CdR/PBA-induced miR-122 expression.
Role of SUV39H1 and Histone Modification in MiR-122 Expression
Epigenetic regulation of gene expression is known to involve DNA methylation and histone modifications (acetylation and/or methylation). As miR-122 gene promoter contains no CpG island, we performed further experiments to determine whether histone modification might be involved in miR-122 regulation. As shown in Fig. 3C, 5-Aza-CdR/PBA treatment decreased the level of SUV39H1, a H3K9 histone methyl transferase (HMT), in both HepG2 and Huh7 cells. Consistent with this, the association of SUV39H1 with miR-122 DR1 and DR2 motifs was also reduced after 5-Aza-CdR/PBA treatment (Fig. 3D). Thus, SUV39H1 is a negative regulator for miR-122 gene expression; this assertion is consistent with the well-documented repression of gene transcription by SUV39H1 and its enzymatic products (H3K9 dimethyl and trimethyl).[35, 36] To further determine the role of SUV39H1 in miR-122 expression, we assessed miR-122 levels in cells transfected with SUV39H1 targeting siRNAs. As shown in Fig. 3E, knockdown of SUV39H1 by two different siRNAs enhanced miR-122 expression by 5.3- and 4.3-fold, respectively. Similarly, inhibition of SUV39H1 by its pharmacological inhibitor, chaetocin, increased miR-122 expression in both HepG2 and Huh7 cells (Fig. 3F). These findings are consistent with the observation that the levels of H3K9 dimethyl and trimethyl were decreased in human primary hepatocytes compared to HCC cells (Supporting Fig. S2). Furthermore, ChIP assay revealed that histone acetylation around DR1 and DR2 regions of the miR-122 promoter was increased in cells treated with 5-Aza-CdR and PBA (Fig. 3G). Taken together, these results suggest a role of SUV39H1-mediated histone H3K9 methylation and histone acetylation in regulation of miR-122 expression.
HCV Does Not Influence MiR-122 Expression
HCV and HBV infection are major epigenetic factors associated with HCC. MiR-122 has been shown to bind 5′-UTR of HCV RNA leading to HCV accumulation. To investigate whether HCV infection might influence miR-122 expression, we used Huh7.5 cells (which are optimal for HCV infection). In this system, more than 80% of the Huh7.5 cells become infected 96 hours after addition of HCV (clone JFH1-GFP), as visualized by GFP fluorescence; successful infection was also verified by qRT-PCR analysis for HCV RNA (Fig. 4A). As shown in Fig. 4B, the levels of miR-122 expression were not significantly different between HCV-infected and control cells. Likewise, HCV infection did not significantly alter miR-122 promoter luciferase reporter activity (Fig. 4C). Thus, HCV infection does not significantly influence miR-122 expression.
HBV Down-Regulates MiR-122 Expression
The expression of miR-122 is known to be down-regulated in patients with HBV infection. To investigate the relationship between miR-122 expression and HBV, we used HepG2.2.15 cells, which are derived from HepG2 cells and characterized by having stable HBV expression and replication in culture systems. As shown in Fig. 5A, successful HBV replication was confirmed by the presence of HBV DNA in HepG2.2.15 cells but not in HepG2 cells, whereas the expression of miR-122 was markedly down-regulated in HepG2.2.15 cells compared to HepG2 cells. Additionally, we performed HBV infection experiments by using supernatants of HepG2.2.15 cells in the presence of 4% polyethylene glycol (PEG). As shown in Fig. 5B,C, HBV-infected HepaRG and primary human hepatocytes showed significantly decreased miR-122 compared to uninfected cells (optimal infection efficiency was confirmed by detecting HBV DNA and HBX mRNA in infected cells). These results suggest that HBV infection down-regulates the expression of miR-122.
Effect of HBX on MiR-122 Expression
Given that HBX plays a pivotal role in HBV-mediated hepatocarcinogenesis and that HBX is known to modulate transcription machinery by way of protein-protein interaction, we investigated the potential effect of HBX on miR-122 expression in our system. As shown in Fig. 6A, transfection of HBX decreased miR-122 expression in HepG2 and Huh7 cells as well as in primary human hepatocytes. Accordingly, transfection of HBX also reduced miR-122 promoter luciferase reporter activity (Fig. 6B). On the other hand, siRNA knockdown of HBX in HepG2.2.15 cells significantly increased the expression of miR-122 (Fig. 6C). These results suggest that HBX protein is able to down-regulate miR-122 expression. Coimmunoprecipitation assay showed that HBX bound to PPARγ (Fig. 6D), which is consistent with the previous report that HBX binds to the DNA binding domain of PPARγ and suppresses PPARγ-mediated transactivation. These observations suggest that HBX protein negatively regulates miR-122 expression through binding and inhibiting PPARγ. The role of PPARγ for suppression of miR-122 gene transcription is further corroborated by the observation that overexpression of PPARγ prevented HBX-induced reduction of miR-122 mature and pri-miRNA levels (Fig. 6E,F). Taken together, these results provide a mechanistic explanation for the reduction of miR-122 in HBV-infected patients as recently reported by Wang et al.
The present study discloses a novel epigenetic regulatory mechanism for miR-122 expression in HCC cells, which involves PPARγ/RXRα binding to DR1 and DR2 motifs of the miR-122 promoter. Our findings suggest that this process is influenced by the PPARγ corepressors (N-CoR and SMRT) and by the histone methyl transferase (SUV39H1). We observe that PPARγ and RXRα bind to DR1 and DR2 motifs of the miR-122 promoter and their association is significantly increased in HCC cells treated with 5-Aza-CdR and PBA. The association is specific for PPARγ isoform, as PPARα did not bind to DR1 and DR2 motifs. Consistent with these findings, we observed that treatment with the PPARγ and RXRα agonists increased the expression of miR-122 in HCC cells. Additionally, overexpression and knockdown studies showed that PPARγ also regulated the expression of miR-122 in nonmalignant hepatocytes. These findings suggest that PPARγ and RXRα are positive regulators for miR-122 expression. On the other hand, we observed that 5-Aza-CdR and PBA treatment reduced the interaction of N-CoR/SMRT with PPARγ/RXRα and with DR1 and DR2 elements in the miR-122 promoter, suggesting that the PPARγ corepressors, N-CoR and SMRT, are negative regulators for miR-122 expression. In addition, we found that 5-Aza-CdR and PBA treatment inhibited the expression of SUV39H1 (an H3K9 methyltransferase that catalyzes the formation of H3K9 dimethyl and trimethyl, leading to suppression of gene transcription) and decreased SUV39H1 binding to the DR1 and DR2 regions of the miR-122 promoter. The role of SUV39H1 for miR-122 suppression is further supported by the observation that knockdown or inhibition of SUV39H1 enhanced miR-122 expression in HCC cells. The latter finding is also corroborated by the observation that human primary hepatocytes contain lower levels of H3K9 dimethyl and trimethyl compared to HCC cells. Thus, SUV39H1 is another negative regulator for miR-122 expression in HCC cells. Collectively, our findings suggest that PPARγ- and RXRα-mediated miR-122 expression is suppressed by N-CoR/SMRT/SUV39H1 in HCC cells (Fig. 7). It is plausible that reduction of SUV391 by 5-Aza-CdR and PBA may lead to dissociation of N-CoR/SMRT/SUV391 from the PPARγ/RXRα and DR1/DR2 binding complex, thus allowing transcription of the miR-122 gene. Furthermore, we observed that 5-Aza-CdR and PBA treatment also increased histone acetylation around miR-122 promoter regions. Therefore, epigenetic regulation of miR-122 in HCC cells is a complicated process that involves the PPARγ/RXRα/N-CoR/SMRT/SUV39H1/DR1/DR2 binding complex, histone acetylation, and histone H3K9 methylation.
Previous studies have shown that miR-122 expression is associated with the level of essential LETFs, including HNF4α and C/EBPα.[11, 18, 19] However, HNF4α and C/EBPα do not appear to be implicated in epigenetic silencing of miR-122 in HCC cells, as their levels were not significantly altered by 5-Aza-CdR and PBA treatment in our system. It is worth mentioning that C/EBPα is epigenetically silenced in several extrahepatic cancers including lung cancer and acute myelogenous leukemia[40, 41] and HNF4α is decreased due to epigenetic silencing of transcription factor 2 (TCF2) in ovarian cancer. Thus, susceptibility to epigenetic modifications may depend on specific tissue context and different tumor types.
HCV and HBV are major epigenetic environmental factors that are closely associated with HCC development. In this study, we investigated the mechanism for differential regulation of miR-122 by HCV and HBV. It is well known that miR-122 is essential for HCV RNA accumulation by binding to the 5′-UTR of the viral genome. Previous reports have shown that miR-122 stimulates HCV viral protein translation and binds HCV RNA in association with Agonaute 2 (Ago2) protein, thereby slowing decay of the viral RNA in infected cells. Silencing of miR-122 with a locked nucleic acid (LNA)-modified oligonucleotide leads to suppression of HCV viremia and improvement of HCV-induced liver pathology in chronic HCV-infected chimpanzees model. However, whether HCV is able to regulate miR-122 expression was not known prior to the current study. In our study, we did not observe significant changes in miR-122 expression and promoter activity in Huh7.5 cells infected with HCV particles. Thus, HCV infection does not appear to significantly influence the level of miR-122, despite that miR-122 positively regulates HCV replication and stability. Our findings are also consistent with the previous report showing no correlation between HCV RNA and miR-122 levels in liver biopsies from patients with chronic hepatitis C.
In contrast to HCV infection, miR-122 was significantly down-regulated in patients with HBV infection. miR-122 is known to down-regulate cyclin G1 and interrupt cyclin G1 interaction with p53, thus abrogating p53-mediated inhibition of HBV replication. However, the mechanism for HBV-mediated down-regulation of miR-122 was not known prior to the current study. In this study, we employed three HBV infection systems (stable HBV expression in HepG2.2.15 cells, transient HBV infection in HepaRG cells, and transient HBV infection in primary human hepatocytes); all of these systems showed that HBV infection down-regulated miR-122 expression. Our data indicate that HBX overexpression significantly decreases miR-122 gene promoter activity and down-regulates miR-122 expression, whereas siRNA knockdown of HBX enhances miR-122 expression. A previous study reports that HBX binds PPARγ and thus blocks nuclear localization and suppresses PPARγ-mediated transactivation. In our system, we also observed that HBX directly interacted with PPARγ, although we did not observe nuclear translocation of PPARγ by HBX, as PPARγ is localized in the nucleus and HBX is localized in both cytoplasm and nucleus in HepG2 cells (Supporting Fig. S3). Our findings provide novel evidence for HBX-mediated inhibition of miR-122 transcription by PPARγ.
In summary, this study provides the first evidence for epigenetic regulation of miR-122, a pivotal liver-specific miRNA, by PPARγ/RXRα complex through interaction with the corepressors and H3K9 histone methyltransferase (SUV39H1) in HCC cells. Our data also provide important mechanistic insight into differential regulation of miR-122 by HBV and HCV.
The authors thank Dr. Partha K. Chandra and Dr. Sidhartha Hazari for technical support on HCV infection and detection.