Oxidative stress induces the activation of liver fibrogenic cells (myofibroblasts), thus promoting the expression of fibrosis-related genes, leading to hepatic fibrogenesis. MicroRNAs (miRNAs) are a new class of small RNAs ~18–25 nucleotides in length involved in post-transcriptional regulation of gene expression. Wound-healing and remodeling processes in liver fibrosis have been associated with changes in hepatic miRNA expression. However, the role of miR-706 in liver fibrogenesis is currently unknown. In the present study, we show that miR-706 is abundantly expressed in hepatocytes. Moreover, oxidative stress leads to a significant downregulation of miR-706, and the further reintroduction of miR-706 inhibits oxidative stress-induced expression of fibrosis-related markers such as α-SMA. Subsequent studies revealed that miR-706 directly inhibits PKCα and TAOK1 expression via binding to the 3′-untranslated region, preventing epithelial mesenchymal transition. In vivo studies showed that intravenous injection of miR-706 agomir successfully increases hepatic miR-706 and decreases α-SMA, PKCα, and TAOK1 protein levels in livers of carbon tetrachloride (CCl4)-treated mice. In summary, this study reveals a protective role for miR-706 by blocking the oxidative stress-induced activation of PKCα/TAOK1. Our results further identify a major implication for miR-706 in preventing hepatic fibrogenesis and suggest that miR-706 may be a suitable molecular target for anti-fibrosis therapy.
Chronic liver insults, such as viral hepatitis, metabolic or toxic diseases, autoimmune diseases, and non-alcoholic steatohepatitis, lead to the excessive deposition of extracellular matrix (ECM) and to the destruction of hepatic cells’ structure and function, resulting in the development of liver fibrosis1,2. The process of liver fibrosis inevitably leads to cirrhosis, pathologically characterized by changes in septa formation and nodules of surviving hepatocytes surrounded with scar tissue. Epidemiological data indicates that cirrhosis kills millions of people worldwide2; it is the fourth most common cause of adult death in central Europe and fourteenth in the world3.
Due to the lack of effective treatments, liver cirrhosis has become a major health problem. It is necessary to find alternative effective therapeutic strategies that prevent the progression of hepatic fibrosis.
The activation and proliferation of fibroblasts plays a crucial role in hepatic fibrogenesis. Hepatic stellate cells (HSCs) are the major source of activated fibroblasts4,5. Moreover, recent studies have shown that activated HSCs, portal fibroblasts, and myofibroblasts of bone-marrow origin have fibrogenic properties6,7. Further, several in vitro and in vivo studies have suggested that hepatocytes may assume a fibroblast-like morphology and thus undergo epithelial–mesenchymal transition (EMT)8,9,10. Although clear evidence on hepatocyte EMT in diseased livers is still missing, Zeisberg and colleagues showed that TGF-β treatment induces hepatocyte EMT in vitro. Furthermore, microRNAs (miRNAs) are important regulators of EMT through the targeting of different components of signaling pathways. For example, miR-21 activates EMT via the PTEN/AKT pathway11 and downregulation of miR-101 promotes hepatocyte EMT12,13.
miRNAs are endogenous small non-coding RNAs that regulate gene expression by binding to the 3′ untranslated region (3′UTR) of the target mRNA14,15. miRNAs play fundamental physiological roles in a variety of biological processes, including cell proliferation, differentiation, metabolism, immune response, and apoptosis16. However, dysregulation of miRNA has been associated with liver diseases, such as hepatic fibrosis, fatty liver disease, viral hepatitis, and hepatocellular carcinoma (HCC)17,18,19. Whereas miR-214 and miR-34c levels are upregulated, miR-122 and miR-29b levels are downregulated during the progression of fibrogenesis20,21,22,23. However, the role of miR-706 in liver fibrosis is currently unknown. Interestingly, miR-706 has been related to fatty-acid-regulated insulin resistance in mouse myoblasts24, and to vesicular stomatitis virus-induced apoptosis by reducing the activation of caspase-3 and caspase-925. In this study, the levels of miR-706 were found to be significantly downregulated in CCl4-induced fibrotic livers. We further investigated the molecular mechanisms of miR-706 in liver fibrosis using bioinformatics indicating that PKCα and TAOK1 might be targeted genes regulated by miR-706.
PKCα plays a crucial role in signal transduction in different organs and tissues26. Interestingly, PKCα is activated in cells and tissues undergoing increased oxidative stress-induced disorders27 such as ischemic cerebrovascular disease, hematopoietic malignancy, and specifically in chronic liver disease, where PKCα has been shown to promote hepatic fibrogenesis28. TAOK1, another potential miR-706-targeted gene, is a MAP kinase kinase kinase (MAP3K) that activates the p38 MAPK29,30,31 cascade exacerbating liver fibrosis via overexpression of α-SMA29,30,31,32.
In the current study, oxidative-stress-induced hepatocyte EMT was detected in vivo using CCl4-induced fibrotic liver and in vitro using hydrogen peroxide in culture. Here, we show that miR-706 is a novel fibrosis-related liver microRNA, which is hepatocyte specific and nuclear rich, and is downregulated during hepatic fibrogenesis. Our results reveal that miR-706 prevents murine liver fibrosis by attenuating hepatocyte EMT. Furthermore, we characterized in vivo the therapeutic potential of miR-706 in hepatic fibrogenesis by using miR-706 agomir injections and in vitro by the overexpression of miR-706 in hepatocyte cell lines. In addition, we demonstrated that PKCα and TAOK1 are direct targets of miR-706 in hepatocytes responsible for EMT during liver fibrosis.
miR-706 is downregulated in fibrotic livers
To identify miRNAs involved in hepatic fibrogenesis, we applied a widely-used model of periportal fibrosis using CCl4 treatment, characterized by the excessive deposition of ECM, the reconstruction of hepatic lobules and loss of liver function (Supporting Fig. 1A–C). The expression of miRNAs expression in fibrotic liver tissue was analyzed using TLDA, and differentially expressed miRNAs were filtered by the RVM t test. A total of 15 miRNAs were significantly downregulated (P < 0.05), while 12 miRNAs were significantly upregulated in 4-week CCl4-induced fibrotic livers (Fig. 1A). Consistent with previous studies22,23, the miR-29 and miR-122 families associated with gene encoding for ECM protein and collagen in fibrotic livers were downregulated in our analysis. Interestingly, we observed that miR-706, a miRNA not yet reported in any liver disorder, was dramatically downregulated in CCl4-induced fibrotic livers. Our results were further validated by the levels of mRNA transcripts for miR-706 using qPCR (Fig. 1B). Moreover, miR-706 progressively decreased throughout the 8-week period of CCl4 treatment (Fig. 1C).
miR-706 is abundant in normal hepatocytes and downregulated in fibrotic hepatocytes
Previous studies have shown that hepatocytes and HSCs are the main intrinsic cell sources which contribute to the development of liver fibrosis4,5,8. To further clarify the biological roles of miR-706 in hepatic fibrosis, we performed in situ hybridization (ISH). Here, we aimed to detect the levels and the location of miR-706 in both CCl4-induced fibrotic livers and olive-oil control livers. We found that miR-706 expression levels in hepatocytes of fibrotic livers was dramatically lower than that of control livers. However, little expression of miR-706 was detected in nonparenchymal cells in both fibrotic and in control livers. Additionally, ISH using scrambled RNA did not produce any signal (Fig. 2A). Interestingly, miR-706 expression was scarce in human fibrotic liver and bile duct ligation (BDL)-induced fibrotic liver (Supporting Fig. 2A,C). Furthermore, the transcript levels of miR-706 confirmed its expression in isolated hepatocytes from normal control livers, whereas miR-706 expression was significantly decreased in isolated hepatocytes from fibrotic livers. Noticeably, the transcript levels of miR-706 were significantly lower in isolated HSCs from both control and fibrotic livers (Fig. 2B, Supporting Fig. 2B). Similarly, miR-706 was substantially expressed in immortalized mouse and human hepatocyte AML12 and L02 cell lines, but barely detectable in the human stellate cell line LX2 (Fig. 2C). These results indicated that miR-706 was abundant in normal hepatocytes but not in HSCs.
Oxidative stress-induced hepatocyte EMT is associated with decreased levels of miR-706
In the liver, CCl4 is metabolized by the cytochrome p450 isoenzyme 2E1, generating reactive oxygen species (ROS), which increase ECM deposition and induce the development of hepatic fibrosis33. In the current study, we detected increased levels of ROS characterized by 3′-nitrotyrosine-positive hepatocytes in fibrotic livers, compared to control livers (Fig. 3A). Additionally, hepatocytes gained the expression of mesenchymal markers such as α-SMA; however, some α-SMA-positive cells were also positive for desmin, very likely indicating that hepatocyte in partly contributed to the source of pro-fibrogenic fibroblasts (Fig. 3B). These results were further confirmed by the mRNA and protein expression of α-SMA detected in hepatocytes isolated from CCl4-treated livers but not from control livers (Fig. 3C). To ensure the lack of cross-contamination, we stained cells used in Fig. 3C with HNF-4, a hepatocyte (HCs) marker, which was not detected in HSCs from either control or CCl4-treated livers (Supplemental Figure 2B). Similarly, desmin, an HSCs marker, was not detected in HCs from either control or CCl4-treated livers (Supplemental Figure 2B). These data suggested that hepatocytes undergo EMT during liver fibrogenesis.
In order to determine the mechanisms of ROS-induced hepatocyte EMT, we administered 300 μM H2O2 to L02 cells for 2 days and collected cells from 6 to 48 h thereafter. The addition of H2O2 markedly decreased the levels of miR-706 in L02 cells in a time-dependent manner (Fig. 3D) and induced a fibroblast-like phenotype characterized by increased α-SMA expression and decreased albumin expression as assessed by immunofluorescence (Fig. 3E). To further confirm our results, we analyzed protein expression by Western blot. The overexpression of α-SMA and downregulation of albumin protein levels and increased α-SMA/albumin ratio (Fig. 3F) indicated a shift towards a mesenchymal phenotype. Consistent with our results in the human L02 cell line, H2O2 stimulation induced EMT in the AML12 murine hepatocyte cell line and primary hepatocytes, a mechanism associated with the downregulation of miR-706 (Supporting Fig. 3).
miR-706 inhibits oxidative stress-induced PKCα and TAOK1 signaling cascade
Since our results showed that H2O2 induced EMT and that this phenomenon was associated with decreased levels of miR-706, we used miR-706 mimics. The reintroduction of miR-706 significantly inhibited the ROS-induced EMT (Fig. 4A), further indicating that miR-706 downregulation may facilitate oxidative stress-induced hepatocyte mesenchymal transition. Similar findings were also reproducible using the murine AML12 cell line (Supporting Fig. 4A).
Next, we investigated the molecular mechanisms by which miR-706 attenuates hepatic fibrogenesis. Increase in ROS activates PKCα, a well-known promoter of hepatic fibrogenesis via phosphorylation of MAPK, including ERK and JNK33,34,35. As shown in Fig. 4B, increased PKCα protein levels were detected in 2-week CCl4-induced fibrotic livers, associated with higher phosphorylation of ERK and JNK. TAOK1 is a MAP3K that activates p38 MAPK and MEK3/631. Thus, we next validated that increase in TAOK1 protein levels correlated with higher phosphorylation of p38 MAPK and MEK3 in 2-week CCl4-induced fibrotic livers, (Fig. 4B). Interestingly, our bioinformatic analysis predicted that PKCα and TAOK1 were potentially regulated by miR-706 (Fig. 4C), and the putative miR-706 binding sites in the 3′-untranslated region (UTR) of PKCα and TAOK1 were predicted, as shown in Fig. 4D. Moreover, dual-luciferase reporter analysis indicated that co-expression of miR-706 significantly inhibited firefly luciferase expression with wild-type but not using the mutant 3′UTR of PKCα or TAOK1 (Fig. 4D). In vitro studies further confirmed that treatment with H2O2 resulted in increased PKCα and TAOK1 expression in L02 hepatocytes (Fig. 4E), and that the knockdown of PKCα and TAOK1 attenuated H2O2-induced α-SMA expression (Fig. 4F). The restoration of miR-706 attenuated H2O2-induced PKCα and TAOK1 protein levels, consequently inhibiting the increase in α-SMA (Fig. 4A). Consistently, miR-706 inhibition significantly increased the expression of PKCα and TAOK1 levels (Supporting Fig. 4B). All together, these results suggest that miR-706 may directly suppress PKCα and TAOK1 translation by binding to the 3′UTR and thus attenuate the oxidative stress-induced hepatocyte EMT.
Restoration of miR-706 expression alleviates hepatic fibrogenesis in vivo
We next investigated whether reintroduction of miR-706 could attenuate CCl4-induced hepatic fibrosis in vivo. After 4 weeks of CCl4 treatment, mice were injected intravenously either with control agomir or miR-706 agomir once per week for a period of 2 weeks. Injection of miR-706 agomir increased miR-706 levels in liver tissue (Fig. 5A). Quantitative analysis revealed that miR-706 significantly decreased hydroxyproline content compared to control agomir (Fig. 5B), and greatly attenuated the severity of liver fibrosis, as demonstrated by α-SMA, Col1a1, Sirius red staining (Fig. 5C,D). Moreover, Western blot analysis indicated that treatment with miR-706 agomir markedly inhibited α-SMA, Col1a1, PKCα, and TAOK1 expression in livers of CCl4-treated mice compared with those injected with control agomir (Fig. 5F). These data indicated that miR-706 may attenuate liver fibrosis progression to some extent. Furthermore, treatment with miR-706 agomir significantly reduced the mRNA levels of α-SMA, Col1a1, Prkca, and Taok1 in the livers of CCl4-treated mice (Fig. 5E). Furthermore, the injection of miR-706 antagomir promoted liver fibrosis characterized by increased α-SMA and Col1 expression, associated with high PKCα and TAOK1 expression (Supporting Fig. 5). All together, these results indicated that miR-706 may attenuate hepatic fibrogenesis in vivo via downregulation of PKCα and TAOK1 expression.
miR-706 has little effect on oxidative stress-induced apoptosis in hepatocytes
Previous studies have described oxidative stress-induced apoptosis of L02 cells36. In the current study, decreased cell viability was detected by H2O2 treatment from 6 h to 48 h (Fig. 6A), however, a certain proportion of cells still survived. These results suggest that surviving cells might undergo EMT. Then we investigated the effects of miR-706 on hepatocyte apoptosis. We found that miR-706 had little effect on H2O2-induced decreased hepatocyte cell viability and pro-apoptotic genes Bax, Bak1, Bbc3, and Bad (Fig. 6B,C). In our in vivo study, we found that CCl4 treatment induced increased expression of the pro-apoptotic genes Bax, Bak1, Bbc3, and Bad. Among them, Bax and Bad can be inhibited by adding miR-706 agomir. However, miR-706 agomir did not prevent the increase in expression of Bak1 and Bbc3 induced by CCl4 treatment (Fig. 6D). Furthermore, CCl4 treatment induced increased cleaved Caspase-3 expression, which was not alleviated by miR-706 agomir injection (Fig. 6E). These results indicate that miR-706 may inhibit some pro-apoptotic genes during liver fibrosis, but have no direct effect on overall hepatocyte apoptosis. Further mechanisms need to be investigated in future studies.
The progression of liver fibrosis leads to irreversible cirrhosis, end-stage hepatocellular carcinoma and, ultimately, to liver failure. Whereas liver fibrosis is an asymptomatic disorder, the progression from fibrosis to liver cirrhosis considerably increases the risk of mortality and morbidity37. Thus, for the prevention of hepatic fibrogenesis, it is essential to find an effective treatment. Activated fibroblasts are characterized by their contractile capacity, the deposition of ECM and subsequently the production of hepatic fibrosis38. HSCs are regarded as the main source of fibroblasts4. Moreover, profibrogenic fibroblasts can also originate from portal fibroblasts, bone marrow stem cells and hepatocytes undergoing EMT6,7,8. Recent reports have shown that hepatocyte EMT contributes to the development of liver cirrhosis in CCl4-treated rats10. In our study, we detected that hepatocytes acquire typical markers of profibrogenic fibroblasts not only in CCl4-induced fibrosis, but also in a H2O2-treated hepatocyte cell line. Hepatocytes undergoing EMT lose the expression of hepatocyte markers such as albumin but gain mesenchymal marker (α-SMA). Some reports indicated that the activation of EMT can be enhanced by the MAPK pathway, regulated by PKCα41,44. In the present study, increased PKCα and phosphorylation of MAPK JNK and ERK were characteristic of CCl4-treated fibrotic livers, indicating that PKCα signal cascade promotes hepatic fibrogenesis.
Oxidative stress is a key factor in the activation of PKCα. In experiments using long-term administration of CCl4, increased oxidative stress causes the oxidation of diacylglycerol (DAG), an agonist of PKCα, and the translocation of PKCα from the cytosol to the membrane where it becomes active41,42,43,44. In the present study, it increased the expression of 3′-nitrotyrosine, an indicator of ROS, which was also detected in fibrotic liver tissue.
MiRNAs play a crucial role in the regulation of gene expression during hepatic fibrogenesis. In fact, miR-21 promotes hepatic fibrosis via the PTEN/AKT pathway44 and miR-33a activates HSCs through the PI3K/AKT pathway21. Moreover, miR-122 is the most abundant and liver-specific miRNA in the adult human liver, where its overexpression represses collagen production and HSCs activation22. The miR-29 family is clearly involved in liver fibrosis, since the downregulation of miR-29 contributes to the HSCs activation through the NF-κB pathway23,46,47. Consequently, the aberrant expression of miRNAs may lead to hepatic fibrogenesis through different mechanisms. In contrast to previous studies, we provided new evidence for the functional role of miR-706 in both murine and human liver fibrosis. Our miRNA microarray analysis indicated that miR-706 was significantly decreased in fibrotic liver. These results were further validated by RT-PCR. By ISH, we determined that the expression of miR-706 was located in the nuclei of normal hepatocytes. Interestingly, the expression of miR-706 was barely detectable in fibrotic liver and non-parenchymal cells. Altogether, these results indicated that miR-706 is a hepatocyte-specific and nucleus-rich miRNA. Concomitant with our data, miR-706 was reported as a nuclear-enriched miRNA48. Since no data were available on the function of human miR-706, we next sought to locate the expression of miR-706 in human hepatocytes. MiR-706 expression was detected by ISH in human liver adjacent to carcinoma tissue. Additionally, we confirmed our results using the human hepatocyte cell line L02, the murine hepatocyte cell line AML12, and the human hepatic stellate cell line LX-2. We found decreased miR-706 expression in H2O2-treated L02 and AML12 cells, further confirming that miR-706 is hepatocyte specific and suggesting that its downregulation can lead to increased oxidative stress. However, the definite molecular mechanism by which miR-706 regulates liver fibrosis has yet to be investigated.
Interestingly, bioinformatics analysis predicted PKCα and TAOK1 as targets of miR-706. Indeed, both PKCα and TAOK1 are important mediators of the MAPK signaling cascade. Thus, we constructed pMIR-report plasmids which encode a firefly luciferase transcript with either a wild-type or a mutant 3′-UTR of human PKCα and TAOK1. We then assessed their respective dual luciferase reporter activities after co-transfection with miR-706 mimics or negative control in 293-T cells. From these experiments, we conclude that miR-706 can directly downregulate the expression of PKCα and TAOK1.
The MAPK signaling pathway and the process of EMT are major contributors to hepatic fibrogenesis. In the current study, increased levels of PKCα and TAOK1 were observed in CCl4-induced fibrotic livers associated with increased phosphorylation of JNK, ERK, p38, and MEK3, important mediators of the MAPK pathway. Similarly, increased PKCα and TAOK1 was detected in H2O2-treated hepatocytes. To further determine the regulation of PKCα and TAOK1 in hepatic EMT, suppression of PKCα and TAOK1 by siRNA inhibited H2O2-induced α-SMA expression in the human hepatocyte cell line L02.
To further confirm that dysregulation of miR-706 promotes fibroblast-like transformation of hepatocytes, we treated hepatocytes with miR-706 mimics. Interestingly, the overexpression of miR-706 reduced the H2O2-induced expression of PKCα and TAOK1, consequently blocking α-SMA expression. Concomitantly, miR-706 inhibition promoted H2O2-induced expression of PKCα and TAOK1. These findings implied that miR-706 reduces hepatic fibrosis by targeting PKCα and TAOK1-dependent regulation of the MAPK cascade.
To further investigate the in vivo effects of miR-706 on hepatic fibrogenesis, the reintroduction of miR-706 was established after 4 weeks of CCl4 treatment. The restoration of miR-706 dramatically reduced the amount of α-SMA associated with lower levels of PKCα and TAOK1. These results indicated that miR-706 may attenuate the progression of liver fibrogenesis, particularly at early time-points. Furthermore, the inhibition of miR-706 using antagomir aggravated hepatic fibrosis. Altogether, these results revealed that the remission of liver fibrosis can be attributed to the anti-fibrotic role of miR-706 via reversing EMT in hepatocytes. Therefore, the regulation of miR-706 expression may be a potentially useful therapeutic approach for attenuating the progression of liver fibrosis.
Materials and Methods
Animal models of liver fibrosis
C57BL/6 male mice were purchased from Beijing Vital River Laboratory Animal Technology Co., Ltd. (Beijing, China), bred in our facility, and used as controls or CCl4-treated groups. Only eight-week-old mice were used in this study. To induce liver fibrosis, mice were intraperitoneally injected with CCl4 (1:9 in olive oil) at a dose of 0.1 mL/kg body weight, twice weekly. Control animals were injected exclusively with olive oil. Animals were sacrificed under anesthesia at 2, 4, 6 and 8 weeks after CCl4 treatment. Part of the liver tissue was fixed using 10% buffered formalin overnight before embedding in paraffin or snapped frozen in liquid nitrogen and stored at −80 °C. Part of the liver tissue was stored in RNAlater solution or kept at −80 °C for western blot analysis. Serum was collected and analyzed for alanine aminotransferase (ALT) activity. All animal experiments were conducted in accordance with the Guide for the Care and Use of Laboratory Animals and approved by the Animal Experimentation Ethics Committee of the Capital Medical University.
RNA was isolated from liver tissue using Trizol (Invitrogen, USA) and processed using a miRNA microarray according to the manufacturer’s protocol. TaqMan Low Density Array (TLDA, Invitrogen, USA) on 7900HT Fast Real-Time PCR system (ABI, USA) was applied and the random variance model (RVM) t test was used to filter the differently expressed miRNAs. After significant and false discovery rate (FDR) analysis, differentially expressed miRNAs were selected according to their P value thresholds49.
Reintroduction of miR-706 in the liver
CCl4-treated mice were randomly divided into four groups after 4 weeks; miR-706 agomir negative control, miR-706 agomir, miR-706 antagomir negative control and miR-706 antagomir. All mice from all groups received tail vein injections of miRNA agomir/antagomir or their respective controls at a dose of 2 nmol for 2 weeks, once per week. miRNA agomir/antagomir and their respective controls were purchased from Biolino (Beijing, China). The agomir sequences are shown in Table 1.
Histological and immunohistochemical analyses
Formalin-fixed liver tissues were embedded in paraffin and cut into 4-μm sections. Sections were dewaxed in xylene and rehydrated in a series of descending percentages of ethanol. Liver specimens were incubated with primary antibody against α-SMA (Sigma-Aldrich), Col1 (Abcam), 3′-nitrotyrosine (Life). An UltraSensitiveTM S-P kit (MXB, China) and DAB kit (Zhongshanjinqiao, China) were used. For histopathological examination, H&E, Masson’s trichrome, and Sirius Red staining were used to assess the extent of fibrosis.
Cells were grown on chamber slides and fixed with 4% paraformaldehyde in PBS for 10 min then permeabilized with 0.3% Triton X-100 in PBS for 10 min. Frozen tissues were cut into 4-μm sections, fixed in acetone for 10 min at −20 °C, then dried in air for 1 h. After treatment with blocking solution (1% donkey serum in PBS) for 1 h at room temperature, slides were incubated with rabbit anti-albumin (Proteintech) antibody (1:100) or rabbit anti-E-cadherin (Cell Signaling technology) antibody (1:100) and mouse anti-α-SMA (Sigma-Aldrich) antibody (1:2000) overnight at 4 °C, followed by donkey anti-fluorescein isothiocyanate-labeled anti-mouse IgG (1:200) and Cy3-labeled donkey anti-rabbit IgG (1:200) antibodies for 30 min at room temperature. Nuclear counterstain was performed by 4′,6-diamidino-2-phenylindole (DAPI, Invitrogen). Tissue sections were analyzed by fluorescence microscopy.
Western blot analysis
Protein from frozen liver tissue (30 mg) or from cells was homogenized and then centrifuged at 12,000 rpm for 15 min, then separated in a 10% sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis (PAGE) and transferred to polyvinylidene fluoride (PVDF) membranes (Merck Millipore, Billerica, MA, USA) using a transblot system (Bio-Rad; Hercules, CA, USA). The membranes were blocked with 5% non-fat milk in TBS-T for 1 h at room temperature and then incubated with specific antibodies against PKCα, TAOK1, 3′-Nitrotyrosine, cleaved Caspase-3, α-SMA, Col1a1, total MEK3, pMEK3 (S189), p38 MAPK, p-p38 MAP Kinase (Thr180/Tyr182), JNK, p-JNK, ERK, p-ERK, β–actin and GAPDH. After washing, the PVDF membranes were incubated with horseradish peroxidase-conjugated secondary antibodies. Protein bands were visualized by chemiluminescence (Bio-Rad). The intensity of each band was quantified by densitometric analysis.
Dual luciferase reporter assay system
The potential miR-706 binding targets were predicted using TargetScan (www.targetscan.org) and miRBase (microRNA.sanger.ac.uk) databases. The sequence of segments with wild-type or mutant seed regions of PKCα and TAOK1 were synthesized and cloned into psiCHECKTM-2 Vectors (Promega, Madison, WI) between NotI and XhoI restriction sites. The synthesized oligos are shown in Table 1. All constructs were verified by sequencing. The 293-T cells (1 × 104 cells/well) transiently transfected with miR-706 (50 nM) or miR-control (50 nM) were seeded in 96-well plates. psiCHECKTM-2 Vectors (50 ng/well) were co-transfected using lipofectamine 2000 (Invitrogen). Cells were harvested 48 h post-transfection and luciferase activities were analyzed by the dual-luciferase reporter assay system (Promega, Madison, WI).
miR-706 mimic and scrambled oligonucleotides were purchased from Oligobio (China) and transfected into L-02 and AML12 cell lines (ATCC, Manassas, VA) using Lipofectamine 2000 reagent (Invitrogen, USA) according to the manufacturer’s instructions. siRNA oligonucleotides (Oligobio, China) were used to target the PKCα and TAOK1 transcripts (Table 1). After 8 h of transfection, cells were treated with 300 μM H2O2 for 1 h and 24 h harvested for mRNA analysis of bax, bad, bak, and bbc3, or for 48 h and harvested for protein analysis of α-SMA, PKCα, and TAOK1.
Total RNA was isolated from cells or liver tissues stored in RNAlater solution (Ambion, USA), using Trizol (Invitrogen) and treated with DNase I (Invitrogen) according to the manufacturers’ protocols. Quantitative real-time PCR of miR-706, α-SMA, col1a1, taok1, prkca, bax, bad, bak, and bbc3 was performed using SYBR Green Master mix on a 7500 system (Applied Biosystems, Foster City, CA). Standardization was performed using U6 primers for miR-706, and GAPDH for the other primers, and evaluated using the comparative CT Method (2−ΔΔCT). Semi-quantitative RT-PCR of HNF-4 and desmin were performed using hot start Taq Master Mix (Biolab, UK) according to manufacturer’s instructions. The primers are shown in Table 1.
In situ hybridization
For in situ hybridization (ISH), 10% buffered formalin-fixed liver tissues were embedded in paraffin and sliced into 4 μm sections, then deparaffinized in xylene, rehydrated in degraded ethanol, and finally in distilled water. The ISH was performed according to the manufacturer’s protocol (Boster, China). Briefly, tissue sections were treated with 3% H2O2 at room temperature for 10 min, pre-hybridised in the Exiqon hybridization buffer at 38 °C for 4 h, then hybridised with 20 μL miR-706 probe at 38 °C overnight, washed with 2 × SSC, 0.5 × SSC, and 0.2 × SSC buffers for 10 min at 38 °C, respectively. Following the blocking step in the blocked Exiqon at 37 °C for 30 min, sections were treated with alkaline phosphatase-conjugated mouse anti-digoxigenin (diluted 1:200 in 0.5 M TBS) at 37 °C for 60 min, and then treated with developing reagent for 30 min. For human tissue, commercially available adult human liver tissue adjacent to areas of HCC and fibrotic liver tissue arrays were obtained from Shanghai Zhuoli Biotechnology Co., Ltd (Zhuoli Biotechnology Co, Shanghai, China) with the approval of the ethics committee of Capital Medical University. Tissue arrays contained 20 points of a 1.5 mm diameter disk of formalin-fixed, paraffin-embedded tissues representing 8 cases of liver tissue adjacent to areas of HCC and 12 cases of fibrotic liver from individuals aged 25–75 years.
Isolation of mouse hepatocytes and HSCs
Hepatic cells were isolated using a well-known protocol50,51. Briefly, mice were anesthetized with pentobarbital sodium (40 mg/kg) intraperitoneally. After the use of a calcium and magnesium-free Hanks’ balanced salt solution containing 0.5 mM EDTA (Invitrogen), livers were perfused in situ through the portal vein with Dulbecco’s modified Eagle’s media (DMEM; Invitrogen) containing collagenase (Sigma), until the liver became soft. Then the liver was removed and gently shaken in DMEM containing collagenase at 37 °C for 10 min. The homogenate was filtered and centrifuged at 50 g for 1 min, the pellet washed three times with DMEM in order to harvest hepatocytes, and the supernatant was removed and placed into a new 15-mL centrifuge, using a density-gradient-based separation for culture of HSCs.
Determination of Liver Hydroxyproline Content
Briefly, wet liver samples (100 mg) stored at −80 °C were homogenized in 1 mL 6 mol/L HCl and incubated for 5 h at 95 °C, then the amount of hydroxyproline was assessed according to the procedure outlined in the Hydroxyproline Testing Kit (A030-2, Jiancheng, Nanjing, China). The optical density of the reaction product was read at 550 nm using a spectrophotometer and expressed as μg/mg wet tissue.
Viability detection by CCK8
L02 cells were treated with H2O2 (300 μM) for 6 to 48 h, and then 10 μL CCK8 (Dojindo, Kumamoto, Japan) was added to the cells, and the viability of the cells was measured at 490 nm using an ELISA reader (BioTek, Winooski, VT, USA) according to the manufacturer’s instructions.
Data are shown as mean ± standard error (SEM), and were obtained in at least three independent experiments. Student’s t test was used to analyze the differences between the two groups. ANOVA was performed when more than two experimental groups were used.
How to cite this article: Yin, R. et al. miR-706 inhibits the oxidative stress-induced activation of PKCα/TAOK1 in liver fibrogenesis. Sci. Rep. 6, 37509; doi: 10.1038/srep37509 (2016).
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This work was supported by National Natural Science Foundation of China Award number 81470864 and Program of Beijing Municipal Commission of Education, Award number KM201510025002.
The authors declare no competing financial interests.
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Yin, R., Guo, D., Zhang, S. et al. miR-706 inhibits the oxidative stress-induced activation of PKCα/TAOK1 in liver fibrogenesis. Sci Rep 6, 37509 (2016). https://doi.org/10.1038/srep37509
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