Research Article | Open Access
Weitao Ji, Hongyun Shi, Hailin Shen, Jing Kong, Jiayi Song, Hongyan Bian, Xinrui Lv, "Mechanism of KLF4 Protection against Acute Liver Injury via Inhibition of Apelin Signaling", Oxidative Medicine and Cellular Longevity, vol. 2019, Article ID 6140360, 10 pages, 2019. https://doi.org/10.1155/2019/6140360
Mechanism of KLF4 Protection against Acute Liver Injury via Inhibition of Apelin Signaling
Krüppel-like factor 4 (KLF4) is a key transcription factor that regulates genes involved in the proliferation or differentiation in different tissues. Apelin plays roles in cardiovascular functions, metabolic disease, and homeostatic disorder. However, the biological function of apelin in liver disease is still ongoing. In this study, we investigated the mechanism of KLF4-mediated protection against acute liver injury via the inhibition of the apelin signaling pathway. Mice were intraperitoneally injected with carbon tetrachloride (CCl4; 0.2 mL dissolved in 100 mL olive oil, 10 mL/kg) to establish an acute liver injury model. A KLF4 expression plasmid was injected through the tail vein 48 h before CCl4 treatment. In cultured LX-2 cells, pAd-KLF4 or siRNA KLF4 was overexpressed or knockdown, and the mRNA and protein levels of apelin were determined. The results showed that the apelin serum level in the CCl4-injected group was higher than that of control group, and the expression of apelin in the liver tissues was elevated while KLF4 expression was decreased in the CCl4-injected group compared to the KLF4-plasmid-injected group. HE staining revealed serious hepatocellular steatosis in the CCl4-injected mice, and KLF4 alleviated this steatosis in the mice injected with KLF4 plasmid. In vitro experiments showed that tumor necrosis factor-alpha (TNF-α) could downregulate the transcription and translation levels of apelin in LX-2 cells and also upregulate KLF4 mRNA and protein expression. RT-PCR and Western blotting showed that the overexpression of KLF4 markedly decreased basal apelin expression, but knockdown of KLF4 restored apelin expression in TNF-α-treated LX-2 cells. These in vivo and in vitro experiments suggest that KLF4 plays a key role in inhibiting hepatocellular steatosis in acute liver injury, and that its mechanism might be the inhibition of the apelin signaling pathway.
The liver is a crucial organ with metabolic and detoxification functions. Acute liver injury can arise from multiple factors, including viral infection, trauma, or chemical reagents, such as alcohol, drugs, and toxic substance [1, 2]. Serious or continuous liver injury leads to liver fibrosis, cirrhosis, and even the development of hepatocellular carcinoma cells (HCC) [3, 4]. Although the pathogenic factors and mechanisms of acute liver injury have been widely reported, the true nature of liver injury is still far from being well understood.
Krüppel-like factor 4 (KLF4) is a multifunctional, zinc-finger transcription factor that regulates genes involved in the cell cycle, proliferation, differentiation, apoptosis, and responses to external stress. Intriguingly, it is not only a tumor suppressor but also an oncogene in different tumor tissues where it regulates the expression of various genes [5, 6]. Studies have confirmed that KLF4 can regulate pathological processes such as liver fibrosis and HCC formation , and a recent study reported that KLF4 promoted HepG2 cell scattering induced by hepatocyte growth factor . The expression of KLF4 at both the protein and mRNA levels is drastically reduced in HCC tissues and all human HCC cell lines when compared with normal human liver tissues and hepatocyte lines [9, 10]. Additionally, KLF4 can reduce migration and invasion by HCC cells via the upregulation of tissue inhibitor of metalloproteinase (TIMP)-1 and TIMP-2 . However, the function of KLF4 in acute liver injury remains unclear.
It has been demonstrated that apelin plays important and varied roles in the physiology and pathophysiology of many organs, including the regulation of blood pressure, cardiac contraction, angiogenesis, metabolic balance, cell proliferation, apoptosis, and inflammation [12–16]. One study reported that the expression of apelin increases sharply in the liver tissues of cirrhotic human and rats when compared with that of control groups . In addition, circulating levels of apelin markedly increase in human and rats with cirrhosis . The expression of apelin is also enhanced under hypoxic or proinflammatory conditions in human hepatic stellate cells (HSCs), and it promotes liver fibrosis or cirrhosis progression [19, 20]. Apelin expression is upregulated in a murine HCC tumor model and in clinical specimens [21, 22]. However, the mechanism of the upregulation of apelin expression in liver disease was still under investigation. In the present study, we aimed to investigate the function and mechanism of KLF4 in protection against liver injury via the inhibition of apelin signaling.
2. Materials and Methods
2.1. Animal Experiments
C57BL/6 mice (SPF, male, 6 to 8 weeks old, 22–24 g) were purchased from the Institutional Animal Care and Use Committee of Charles River (Beijing, China, License number: SCXK 2012-0001). The mice were bred and housed in a specific pathogen-free environment at the Key Laboratory of Receptors-Mediated Gene Regulation and Drug Discovery of School of Basic Medicine, Henan University, and all procedures performed in studies involving animals were carried out in accordance with The Code of Ethics of the World Medical Association (Declaration of Helsinki) and the ethical standards of Animal Research Ethics Committee of Henan University. The mice were intraperitoneally injected with a mixture of carbon tetrachloride (0.2 mL CCl4 dissolved in 100 mL of olive oil) at a dose of 10 mL/kg body weight. The mice of the normal control group received an intraperitoneal injection of the same volume of olive oil as the CCl4 group. The mice were sacrificed at 24 h after the CCl4 injection. The KLF4 plasmid (10 mg/kg) was biosynthesized by Invitrogen and was injected into tail veins 48 h before CCl4 exposure, and the GFP plasmid vector was injected into the tail veins of the animals in the control group at the same time.
2.2. Cell Culture and Treatment
LX-2 cells were purchased from Meixuan Biological Science and Technology Ltd. (Shanghai, China). Cells were seeded in 60 mm plates and grown to confluence for 24 h in high-glucose Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal calf serum (FBS) in a humidified atmosphere containing 5% CO2 at 37 °C. Thereafter, cells were switched to serum-free DMEM for 24 h and then treated with TNF-α (10 ng/mL; Sigma-Aldrich) for the indicated times.
2.3. Hematoxylin-Eosin (HE) Staining
Liver tissues of mice were fixed in 10% neutral buffered formalin at room temperature (RT) for 24 h and then embedded in paraffin and sectioned to a thickness of approximately 5 μm. Sections were stained with HE following standard procedures and examined by light microscopy.
2.4. Serum Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) Level Measurement
Blood from mice was collected in a common tube from the angular vein when all the mice were sacrificed. Samples were left to stand for 4–6 h at RT and then centrifuged at 3000 g for 5 min. The serum was collected, and ALT and AST levels were determined by the Reitman Frankel method using commercially available assay kits (Jiancheng Bioengineering Institute, Nanjing, China).
Mouse liver tissues were fixed with 10% neutral buffered formalin at RT for 24 h and then embedded in paraffin and sectioned to a thickness of approximately 5 μm. Sections were immunostained using a standard protocol. The immunostaining of sections was performed with anti-apelin, anti-KLF4, and anti-cyclin D1 antibodies (1 : 100 dilution), and sections were also counterstained with haematoxylin. Staining intensities were determined by measurement of the integrated optical density following examination by light microscopy and by using Image-Pro Morphometric System software in a double-blind manner.
2.6. RNA Preparation and Quantitative Reverse Transcription-PCR (qRT-PCR)
Total RNA was isolated using TRIzol® reagent (Invitrogen) according to the manufacturer’s instructions. RNA concentrations and purity were determined by measuring the 260/280 nm absorbance ratio. GAPDH (glyceraldehyde-3-phosphate dehydrogenase) gene primers were used as an internal control for RNA template normalization. Quantitative PCR was performed using a Platinum SYBR Green qPCR Super Mix UDG Kit (Invitrogen and the following primers were: apelin (mouse) 5 TCTTGGCTCTTCCCTCTTTTCA 3 (sense) and 5 GTGCTGGAATCCACTGGAGAA 3 (antisense), KLF4 (mouse) 5 CAGCTGGCAAGCGCTACA 3 (sense) and 5 CCTTTCTCCTGATTATCCATTC 3 (antisense), cyclin D1 (mouse) 5 GCGTACCCTGACACCAATCTC 3 (sense) and 5 CTCCTCTTCGCACTTCTGCTC 3 (antisense), TNF-α (mouse) 5 AACGGGGAAGCAACTTAGCA 3 and 5 ACCACAGGGCAAAGGAGATT 3, GAPDH (mouse) 5 TGTGAACGGATTTGGCCGTA 3 (sense) and 5 ACTGTGCCGTTGAATTTGCC 3 (antisense), apelin (human) 5 GCTCTGGCTCTCCTTGACC 3 (sense) and 5 CCATTCCTTGACCCTCTGG 3 (antisense), KLF4 (human) 5 CGGACATCAACGACGTGAG 3 (sense) and 5 GACGCCTTCAGCACGAACT 3 (antisense), and GAPDH (human) 5 GGAGCGAGATCCCTCCAAAAT 3 (sense) and 5 GGCTGTTGTCATACTTCTCATGG 3 (antisense). The relative expression level was calculated using the following equation:
2.7. Western Blotting
Crude proteins were extracted from liver tissues of mice or LX-2 cells as described previously , resolved by SDS/PAGE, and then transferred to a PVDF membrane (Millipore). Membranes were blocked with 5% () nonfat dried skimmed milk powder in TTBS buffer (100 mM Tris/HCl, pH 7.5, 150 mM NaCl, and 0.5% Tween 20) for 2 h at 37°C and then incubated overnight at 4°C with the following primary antibodies: 1 : 300 dilution rabbit anti-apelin (GeneTex), 1 : 500 dilution rabbit anti-KLF4 (Abcam), 1 : 2500 dilution rabbit anti-cyclin D1 (Abcam), and anti-β-actin and rabbit anti-IgG (Santa Cruz Biotechnology). After incubation with the appropriate secondary antibody, the immunoreactive signals of antibody-antigens were visualized using a Chemiluminescence Plus Western Blot Analysis kit (Santa Cruz Biotechnology).
2.8. Immunofluorescence Staining
LX-2 cells were fixed in 4% paraformaldehyde and permeabilized with 0.1% Triton X-100 and then incubated with anti-apelin or anti-KLF4 antibody and further stained with FITC-conjugated secondary antibody. Staining with 4,6-diamidino-2-phenylindole (DAPI) was used to visualize nuclear localization. Each section was examined under an inverted fluorescence microscope (Leica).
2.9. Adenovirus Infection
PAd-KLF4 was kindly provided by Dr. Wen Jin-Kun (The Key Laboratory of Neural and Vascular Biology, China Administration of Education, Hebei Medical University). The adenovirus was amplified by infecting A293 cells, and culture supernatant with a titer of was used to infect LX-2 cells. After adenovirus delivery, KLF4 were detected using RT-PCR and Western blot analysis.
2.10. SiRNA Transfection
Small-interfering RNA (siRNA) targeting human KLF4 (si-KLF4) and a nonspecific siRNA (si-NS) were purchased from Santa Cruz Biotechnology. Transfection was performed using Lipofectamine™ reagent (Invitrogen) following the manufacturer’s instructions. At 24 h following transfection, LX-2 cells were incubated with or without TNF-α (10 ng/mL). Cells were then harvested and used for RT-PCR and Western blotting assays.
2.11. Statistical Analyses
Data are presented as from three or more independent experiments. Statistical analyses were performed using the Student’s -test or one-way ANOVA depending on the number of groups compared. Differences were considered significant at .
3.1. Differential Expression of Apelin and KLF4 in CCl4-Induced Acute Liver Injury in Mice
The murine acute liver injury model was established by single intraperitoneal injections of CCl4. HE staining showed that lobular structure of liver tissue from mice treated only with olive oil treatment was clear and that the hepatic cells were arranged in neat rows (Figure 1(a)). In contrast, hepatocellular steatosis was present around the central veins of hepatic lobules in CCl4-treated mice. Alanine aminotransferase (ALT) and aspartate transaminase (AST) levels in serum were significantly elevated after intraperitoneal injection of CCl4 (Figures 1(b) and 1(c)). Immunohistochemical staining indicated that the expression of apelin protein increased, while KLF4 protein expression decreased, in the hepatocytes of mice treated with CCl4 (Figure 1(d)). Protein levels of apelin and cyclin D1 (a cell cycle marker protein) and TNF-α mRNA and protein levels were upregulated, while KLF4 mRNA and protein levels were downregulated after CCl4 injection (Figures 1(e)–1(i)). These results indicate that apelin and KLF4 involved the hepatic stestosis in CCl4-induced acute liver injury.
3.2. KLF4 Protects Mice against CCl4-Induced Acute Liver Injury by Inhibiting Apelin Signaling
To evaluate whether KLF4 plays a protective role in CCl4-induced acute liver injury in mice, the KLF4 plasmid was injected into the tail vein 48 h prior to CCl4 treatment and the mice were sacrificed after 24 h of CCl4 treatment. The mice that received the KLF4 plasmid treatment exhibited less hepatic necrosis than those that had only been exposed CCl4 and the control GFP plasmid (Figure 2(a)). In addition, serum ALT and AST levels were significantly lower in the KLF4 plasmid-treated animals (Figures 2(b) and 2(c)). These results demonstrate that KLF4 can decrease hepatic necrosis and protect mice against CCl4-induced acute liver injury. Furthermore, RT-PCR and Western blotting analysis also revealed that mRNA and protein levels were substantially higher in the liver tissues of KLF4-overexpressing mice than in the null plasmid mice after CCl4 treatment (Figures 2(e) and 2(g)). These results confirmed that a KLF4 overexpression liver model had been successfully established in mice. Simultaneously, the results demonstrated lower expression of apelin in the KLF4-overexpressing mice than in the null plasmid mice after CCl4 treatment (Figures 2(d) and 2(g)). These results suggest that KLF4 can decrease apelin expression and so protect mice against CCl4-induced acute liver injury. Additionally, paraplastic hepatocytes are one of the main causes of liver fibrosis, and RT-PCR and Western blotting analyses showed that cyclin D1 expression levels were apparently lower in the KLF4-overexpressing mice than in those treated with the null plasmid prior to CCl4 administration (Figures 2(f) and 2(g)). Finally, immunohistochemical staining showed that the expression of apelin, KLF4, and cyclin D1 in different groups was concordant with the RT-PCR and Western blotting results (Figures 3(a)–3(d)).
3.3. TNF-α Decreases Apelin mRNA and Protein Levels, but Increases KLF4 Expression in LX-2 Cells
LX-2 cells, which are a type of HSC, and activated HSC play an important role in both acute liver injury and fibrosis. RT-PCR and Western blotting methods were used to evaluate the expression levels of apelin and KLF4 in LX-2 cells after TNF-α-stimulation. Both apelin mRNA and protein levels decreased in a time-dependent manner when LX-2 cells were treated with 10 ng/mL TNF-α. Moreover, TNF-α also dose-dependently decreased apelin mRNA and protein levels (Figures 4(a)–4(d)). Immunofluorescence staining showed that apelin was localized in the cytoplasm of LX-2 cells and that stimulation by TNF-α for 24 h decreased apelin basal expression (Figure 4(e)). In contrast, TNF-α treatment of LX-2 cells increased both KLF4 mRNA and protein levels in a time- and dose-dependent manner (Figures 4(a)–4(d)). Immunofluorescence staining showed an increase in the levels of KLF4, which was mainly localized to the nucleus (Figure 4(f)). These results demonstrated that TNF-α downregulated apelin gene expression, but upregulated KLF4 expression in vitro.
3.4. KLF4 Protects Hepatocytes by Inhibiting Apelin Signaling In Vitro
To further verify the importance of KLF4 in regulating apelin expression, LX-2 cells were infected with pAd-KLF4 or transfected with si-KLF4 to overexpress or knock down endogenous KLF4 expression, respectively. RT-PCR and Western blotting showed that the overexpression of KLF4 markedly decreased basal apelin expression at both transcription and translation levels (Figures 5(a)–5(d)). Conversely, knockdown of KLF4 recovered the decrease in apelin expression induced by TNF-α, whereas si-NS had no impact on apelin expression. These results suggest that KLF4 can negatively regulate apelin expression in LX-2 cells via TNF-α.
Previous studies had confirmed that the pathogenesis of acute liver injury involved a series of different of cell signaling pathways [24–27]. However, the nature of acute liver injury still remains mainly unelucidated. The present study clearly demonstrates, for the first time, that KLF4 can protect against liver injury by inhibiting apelin signaling in CCl4-induced acute liver injury model. Apelin is highly expressed in the lung, heart, mammary gland, brain, kidney, testicular, and ovarian tissues [28, 29], but exhibits lower expression levels in normal liver . Principe et al. reported that apelin expression increases sharply in the hepatic tissue of cirrhotic rats compared to that of controls . Furthermore, the circulating levels of apelin are markedly increased in rats with cirrhosis. Other studies have reported that apelin can promote Fas-induced liver injury via activation of JNK cell signaling, and it has been demonstrated that liver apoptosis and injury is significantly alleviated in APJ-/- mice compared with wild-type animals . Our results demonstrate that apelin expression exhibits a sharp rise upon CCl4-induced acute liver injury in mice (Figures 1(d), 1(e), and 1(i)). Additionally, some studies have reported that serum levels of apelin were increased in some liver diseases, such as nonalcoholic fatty liver disease and cirrhosis [32, 33]. The results presented here further indicate that apelin participates in hepatic stestosis in CCl4-induced acute liver injury.
These results also demonstrate that KLF4 mRNA and protein levels are downregulated following CCl4-induced acute liver injury in mice. KLF4, a gut-enriched GKLF and zinc-finger transcription factor, regulates a multitude of processes in cell growth and development, proliferation and differentiation, inflammation, and apoptosis, and is even both a tumor suppressor and oncogene. A recent study reported that the expression of KLF4 declines dramatically in activated rat HSCs in the liver tissues of cirrhotic patients . To determine whether KLF4 protects against CCl4-induced acute liver injury, a plasmid containing KLF4 was injected via tail veins 48 h prior to CCl4 treatment. Histological examination showed that the mice pretreated with the KLF4 plasmid exhibited less hepatic necrosis in their liver tissue (Figure 2(a)) and significantly decreased serum ALT and AST levels (Figures 2(b) and 2(c)). Furthermore, KLF4 mRNA and protein levels were substantially higher in the liver tissues of KLF4 plasmid-treated mice than those of their null plasmid-treated counterparts. These results confirm that a murine hepatic KLF4 overexpression model had been successfully established. Previous studies have shown that the expression of KLF4 is lower in HCC tissues or cell lines than in normal liver tissues or cells [35, 36], and that KLF4 can inhibit HCC cell proliferation and metastasis . Hyperplasia of hepatocytes is one of the main causes of liver fibrosis, which is consistent with our observations that the expression level of cyclin D1 is apparently lower in CCl4-treated KLF4-overexpressing mice than in those pretreated with the null plasmid. Furthermore, a study showed that the knockdown of KLF4 can significantly enhance apoptosis in the liver cell line BNCL.2 , indicating that KLF4 can protect against liver injury by suppressing hepatocyte growth, metastasis, and apoptosis.
Our results also show that, following CCl4 treatment, the expression and serum levels of apelin in the KLF4-overexpressing mice are lower than in those pretreated with the null plasmid. These results in part demonstrate that KLF4 can decrease hepatic necrosis and protect against liver tissue injury by decreasing apelin expression. A recent study showed that KLF4 can inhibit HCC cell growth and metastasis by the downregulation of Micro-135a-5p by TGF-β1 . It has been reported that KLF4 negatively regulates the epithelial-mesenchymal transition (EMT) of gastrointestinal cancers through crosstalk between the TGF-β, Notch, and Wnt signaling pathways . Additionally, other in vitro and in vivo experiments have confirmed that KLF4 can revert the EMT by suppressing slug expression and that overexpression of KLF4 can reduce HCC cell migration and invasion .
Although some studies have indicated that TNF-α participates in the ontogeny and development of liver injury , TNF-α can also repair liver injury by suppressing cell death, activating stem cells, and promoting epithelial proliferation in the pathological process of liver injury [43–45]. The results of this study also suggest that TNF-α might play a dual role in CCl4-induced liver injury . Previous studies have shown that apelin is overexpressed in HSCs from cirrhotic rats, and that the serum level of apelin is higher in patients or rats with cirrhosis than that in normal individuals [17, 20, 47]. It has been shown that apelin not only powerfully induces proliferation in LX-2 cells but also promotes the synthesis of angiotension-1 (Ang-1), which is a potent proangiogenic factor and contributes to the development of liver injury and fibrosis . The same study showed that the expression of apelin is downregulated in LX-2 cells upon stimulation by TNF-α, although the mechanism underlying this effect still remains unknown. Our in vitro experimental results show that TNF-α not only downregulates apelin expression but also upregulates KLF4 expression at both the mRNA and protein levels in LX-2 cells (Figures 4(a)–4(f)). To further verify the importance of KLF4 in regulating apelin expression, LX-2 cells were either infected with pAd-KLF4 or transfected with si-KLF4 to overexpress or knock down endogenous KLF4, respectively. RT-PCR and Western blotting showed that the overexpression of KLF4 markedly decreased basal apelin expression, while knockdown of KLF4 reversed the decrease in apelin expression induced by TNF-α. These results suggest that KLF4 can negatively regulate apelin expression induced by TNF-α in LX-2 cells. A recent study showed that the silencing of KLF4 in LX-2 cells significantly decreases the expression levels of TNF-α, while significantly upregulating MMP-2 expression . Furthermore, the expression of KLF4 increases substantially upon TNF-α-induced LX-2 cells apoptosis .
In conclusion, we speculate that hepatic apelin acts as a proinflammatory and neoangiogenic factor and so plays an important role in the initiation and maintenance of the inflammatory and hyperplastic processes that occur in acute liver injury. KLF4 exerts a protective effect against injury liver by inhibiting apelin signaling. This study therefore identifies a possible new target pathway for the prevention and therapy of acute liver injury.
The raw data used to support the findings of this study are available from the corresponding author upon request.
Hongyun Shi is the co-first author.
Conflicts of Interest
The authors declare that they have no conflict of interest.
We thank Dr. Wen Jin-Kun (The Key Laboratory of Neural and Vascular Biology, China Administration of Education, Hebei Medical University) for providing pAd-KLF4. This study was supported by the National Natural Science Foundation of China (Grant No. U1404310) and by the Foundation of Science & Technology Department of Henan Province, China (Nos. 192102310107, 182102310371, and 172102310284).
- I. S. Oh and S. H. Park, “Immune-mediated liver injury in hepatitis B virus infection,” Immune Network, vol. 15, pp. 191–198, 2015.
- Y. D. Wang, W. D. Chen, M. Wang, D. Yu, B. M. Forman, and W. Huang, “Farnesoid X receptor antagonizes nuclear factor κB in hepatic inflammatory response,” Hepatology, vol. 48, pp. 1632–1643, 2008.
- O. Park, W. I. Jeong, L. Wang et al., “Diverse roles of invariant natural killer T cells in liver injury and fibrosis induced by carbon tetrachloride,” Hepatology, vol. 49, pp. 1683–1694, 2009.
- T. Khoury, A. A. Rmeileh, L. Yosha, A. A. Benson, S. Daher, and M. Mizrahi, “Drug induced liver injury: review with a focus on genetic factors, tissue diagnosis, and treatment options,” Journal of Clinical and Translational Hepatology, vol. 3, pp. 99–108, 2015.
- C. C. Lin, L. Z. Liu, J. B. Addison, W. F. Wonderlin, A. V. Ivanov, and J. M. Ruppert, “A KLF4-miRNA-206 autoregulatory feedback loop can promote or inhibit protein translation depending upon cell context,” Molecular and Cellular Biology, vol. 31, pp. 2513–2527, 2011.
- C. Bureau, N. Hanoun, J. Torrisani, J. P. Vinel, L. Buscail, and P. Cordelier, “Expression and function of Kruppel like-factors (KLF) in carcinogenesis,” Current Genomics, vol. 10, pp. 353–360, 2009.
- P. Du, Q. Ma, Z. D. Zhu et al., “Mechanism of Corilagin interference with IL-13/STAT6 signaling pathways in hepatic alternative activation macrophages in schistosomiasis-induced liver fibrosis in mouse model,” European Journal of Pharmacology, vol. 793, pp. 119–126, 2016.
- J. K. Lai, H. C. Wu, Y. C. Shen, H. Y. Hsieh, S. Y. Yang, and C. C. Chang, “Kruppel-like factor 4 is involved in cell scattering induced by hepatocyte growth factor,” Journal of Cell Science, vol. 125, pp. 4853–4864, 2012.
- Q. Zhao, W. Cai, X. Zhang et al., “RYBP expression is regulated by KLF4 and Sp1 and is related to hepatocellular carcinoma prognosis,” The Journal of Biological Chemistry, vol. 292, pp. 2143–2158, 2017.
- Q. Li, Y. Gao, Z. Jia et al., “Dysregulated Kruppel-like factor 4 and vitamin D receptor signaling contribute to progression of hepatocellular carcinoma,” Gastroenterology, vol. 143, pp. 799–810 e2, 2012.
- M. T. Sung, H. T. Hsu, C. C. Lee et al., “Krüppel-like factor 4 modulates the migration and invasion of hepatoma cells by suppressing TIMP-1 and TIMP-2,” Oncology Reports, vol. 34, pp. 439–446, 2015.
- P. Yang, C. Read, R. E. Kuc et al., “Elabela/toddler is an endogenous agonist of the apelin APJ receptor in the adult cardiovascular system, and exogenous administration of the peptide compensates for the downregulation of its expression in pulmonary arterial hypertension,” Circulation, vol. 135, pp. 1160–1173, 2017.
- R. Gerbier, R. Alvear-Perez, J. F. Margathe et al., “Development of original metabolically stable apelin-17 analogs with diuretic and cardiovascular effects,” The FASEB Journal, vol. 31, pp. 687–700, 2017.
- J. C. Zhong, Z. Z. Zhang, W. Wang, S. M. McKinnie, J. C. Vederas, and G. Y. Oudit, “Targeting the apelin pathway as a novel therapeutic approach for cardiovascular diseases,” Biochimica et biophysica acta, vol. 1863, pp. 1942–1950, 2016.
- Y. Yang, X. J. Zhang, L. T. Li et al., “Apelin-13 protects against apoptosis by activating AMP-activated protein kinase pathway in ischemia stroke,” Peptides, vol. 75, pp. 96–100, 2016.
- X. Lv, J. Kong, W. D. Chen, and Y. D. Wang, “The role of the apelin/APJ system in the regulation of liver disease,” Frontiers in Pharmacology, vol. 8, p. 221, 2017.
- A. Principe, P. Melgar-Lesmes, G. Fernandez-Varo et al., “The hepatic apelin system: a new therapeutic target for liver disease,” Hepatology, vol. 48, pp. 1193–1201, 2008.
- Y. L. Lim, E. Choi, Y. O. Jang et al., “Clinical implications of the serum apelin level on portal hypertension and prognosis of liver cirrhosis,” Gut and liver, vol. 10, pp. 109–116, 2016.
- H. Yokomori, M. Oda, K. Yoshimura, S. Machida, F. Kaneko, and T. Hibi, “Overexpression of apelin receptor (APJ/AGTRL1) on hepatic stellate cells and sinusoidal angiogenesis in human cirrhotic liver,” Journal of Gastroenterology, vol. 46, pp. 222–231, 2011.
- P. Melgar-Lesmes, G. Casals, M. Pauta et al., “Apelin mediates the induction of profibrogenic genes in human hepatic stellate cells,” Endocrinology, vol. 151, pp. 5306–5314, 2010.
- J. Muto, K. Shirabe, T. Yoshizumi et al., “The apelin-APJ system induces tumor arteriogenesis in hepatocellular carcinoma,” Anticancer Research, vol. 34, pp. 5313–5320, 2014.
- Q. Liu, T. Hu, L. He et al., “Genetic targeting of sprouting angiogenesis using Apln-CreER,” Nature Communications, vol. 6, article 6020, 2015.
- X. R. Lv, B. Zheng, S. Y. Li et al., “Synthetic retinoid Am80 up-regulates apelin expression by promoting interaction of RARα with KLF5 and Sp1 in vascular smooth muscle cells,” Biochemical Journal, vol. 456, pp. 35–46, 2013.
- B. L. Woolbright and H. Jaeschke, “Role of the inflammasome in acetaminophen-induced liver injury and acute liver failure,” Journal of Hepatology, vol. 66, pp. 836–848, 2016.
- R. T. Chung, R. T. Stravitz, R. J. Fontana et al., “Pathogenesis of liver injury in acute liver failure,” Gastroenterology, vol. 143, pp. e1–e7, 2012.
- S. K. Ramaiah and H. Jaeschke, “Role of neutrophils in the pathogenesis of acute inflammatory liver injury,” Toxicologic Pathology, vol. 35, pp. 757–766, 2007.
- Y. D. Wang, W. D. Chen, D. Yu, B. M. Forman, and W. Huang, “The G-protein-coupled bile acid receptor, Gpbar1 (TGR5), negatively regulates hepatic inflammatory response through antagonizing nuclear factor kappa light-chain enhancer of activated B cells (NF-κB) in mice,” Hepatology, vol. 54, pp. 1421–1432, 2011.
- M. Hosoya, Y. Kawamata, S. Fukusumi et al., “Molecular and functional characteristics of APJ. Tissue distribution of mRNA and interaction with the endogenous ligand apelin,” The Journal of Biological Chemistry, vol. 275, pp. 21061–21067, 2000.
- Y. Kawamata, Y. Habata, S. Fukusumi et al., “Molecular properties of apelin: tissue distribution and receptor binding,” Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, vol. 1538, pp. 162–171, 2001.
- J. Chu, H. Zhang, X. Huang et al., “Apelin ameliorates TNF-α-induced reduction of glycogen synthesis in the hepatocytes through G protein-coupled receptor APJ,” PloS one, vol. 8, article e57231, 2013.
- H. Yasuzaki, S. Yoshida, T. Hashimoto et al., “Involvement of the apelin receptor APJ in Fas-induced liver injury,” Liver International, vol. 33, pp. 118–126, 2013.
- A. Drougard, T. Duparc, X. Brenachot et al., “Hypothalamic apelin/reactive oxygen species signaling controls hepatic glucose metabolism in the onset of diabetes,” Antioxidants & Redox Signaling, vol. 20, pp. 557–573, 2014.
- C. N. Ercin, T. Dogru, S. Tapan et al., “Plasma apelin levels in subjects with nonalcoholic fatty liver disease,” Metabolism, vol. 59, pp. 977–981, 2010.
- R. Men, M. Wen, M. Zhao et al., “MircoRNA-145 promotes activation of hepatic stellate cells via targeting Kruppel-like factor 4,” Scientific Reports, vol. 7, article 40468, 2017.
- X. Tian, S. Dai, J. Sun et al., “F-box protein FBXO22 mediates polyubiquitination and degradation of KLF4 to promote hepatocellular carcinoma progression,” Oncotarget, vol. 6, pp. 22767–22775, 2015.
- J. Zhou, P. B. Lai, and S. K. Tsui, “Identification of a non-coding KLF4 transcript generated from intron retention and downregulated in human hepatocellular carcinoma,” International Journal of Oncology, vol. 47, pp. 1554–1562, 2015.
- C. Tian, S. Yao, L. Liu et al., “Klf4 inhibits tumor growth and metastasis by targeting microRNA-31 in human hepatocellular carcinoma,” International Journal of Molecular Medicine, vol. 39, pp. 47–56, 2017.
- Q. Chen, L. Li, Y. Tu et al., “MiR-34a regulates apoptosis in liver cells by targeting the KLF4 gene,” Cellular & Molecular Biology letters, vol. 19, pp. 52–64, 2014.
- S. Yao, C. Tian, Y. Ding et al., “Down-regulation of Krüppel-like factor-4 by microRNA-135a-5p promotes proliferation and metastasis in hepatocellular carcinoma by transforming growth factor-β1,” Oncotarget, vol. 7, pp. 42566–42578, 2016.
- J. Cui, M. Shi, M. Quan, and K. Xie, “Regulation of EMT by KLF4 in gastrointestinal cancer,” Current Cancer Drug Targets, vol. 13, pp. 986–995, 2013.
- Z. S. Lin, H. C. Chu, Y. C. Yen, B. C. Lewis, and Y. W. Chen, “Krüppel-like factor 4, a tumor suppressor in hepatocellular carcinoma cells reverts epithelial mesenchymal transition by suppressing slug expression,” PloS One, vol. 7, article e43593, 2012.
- M. Yin, M. D. Wheeler, H. Kono et al., “Essential role of tumor necrosis factor α in alcohol-induced liver injury in mice,” Gastroenterology, vol. 117, pp. 942–952, 1999.
- A. Kuraishy, M. Karin, and S. I. Grivennikov, “Tumor promotion via injury- and death-induced inflammation,” Immunity, vol. 35, pp. 467–477, 2011.
- C. A. Bradham, J. Plumpe, M. P. Manns, D. A. Brenner, and C. Trautwein, “Mechanisms of hepatic toxicity. I. TNF-induced liver injury,” American Journal of physiology, vol. 275, pp. G387–G392, 1998.
- M. J. Czaja, J. Xu, and E. Alt, “Prevention of carbon tetrachloride-induced rat liver injury by soluble tumor necrosis factor receptor,” Gastroenterology, vol. 108, pp. 1849–1854, 1995.
- Y. Dong, Y. Liu, X. Kou et al., “The protective or damaging effect of tumor necrosis factor-α in acute liver injury is concentration-dependent,” Cell & Bioscience, vol. 6, p. 8, 2016.
- P. Melgar-Lesmes, M. Pauta, V. Reichenbach et al., “Hypoxia and proinflammatory factors upregulate apelin receptor expression in human stellate cells and hepatocytes,” Gut, vol. 60, pp. 1404–1411, 2011.
- T. Li, L. Niu, M. Li et al., “Effects of small interfering RNA-mediated downregulation of the Krüppel-like factor 4 gene on collagen metabolism in human hepatic stellate cells,” Molecular Medicine Reports, vol. 12, pp. 3972–3978, 2015.
- B. Wang, M. Z. Zhao, N. P. Cui et al., “Krüppel-like factor 4 induces apoptosis and inhibits tumorigenic progression in SK-BR-3 breast cancer cells,” FEBS Open Bio, vol. 5, pp. 147–154, 2015.
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