Expression of microRNA-454 in TGF-β1-stimulated hepatic stellate cells and in mouse livers infected with Schistosoma japonicum

• Published in: Parasites & vectors Vol. 7; no. 1; p. 148
• Main Authors: Zhu, Dandan, He, Xue, Duan, Yinong, Chen, Jinling, Wang, Jianxin, Sun, Xiaolei, Qian, Hongyan, Feng, Jinrong, Sun, Wei, Xu, Feifan, Zhang, Lingbo
• Format: Journal Article
• Language: English
• Published: England Springer-Verlag 31.03.2014; BioMed Central Ltd; BioMed Central; BMC
• Subjects: Animals; cell cycle; Cell Line; Cell Proliferation; cytokines; fibrosis; flow cytometry; Gene Expression Regulation; Hepatic fibrosis; Hepatic stellate cell; Hepatic Stellate Cells - drug effects; Hepatic Stellate Cells - metabolism; Humans; lipid metabolism; Liver - metabolism; liver cirrhosis; luciferase; Male; Mice; Mice, Inbred ICR; microRNA; MicroRNAs - genetics; MicroRNAs - metabolism; miR-454; reverse transcriptase polymerase chain reaction; Schistosoma japonicum; Schistosoma japonicum - physiology; Schistosomiasis japonica - metabolism; Schistosomiasis japonica - parasitology; TGF-β1; transforming growth factor beta 1; Transforming Growth Factor beta1 - pharmacology; Western blotting
• ISSN: 1756-3305; 1756-3305
• DOI: 10.1186/1756-3305-7-148

BACKGROUND: In the process of hepatic fibrosis, hepatic stellate cells (HSCs) can be activated by many inflammatory cytokines. The transforming growth factor-β1 (TGF-β1) is one of the main profibrogenic mediators. Recently, some studies have also shown that microRNAs (miRNAs) play essential roles in the progress of liver fibrosis by being involved in the differentiation, fat metabolism and ECM production of HSCs. METHODS: The expression of miR-454 in LX-2 cells treated with TGF-β1 and in the fibrotic livers with Schistosoma japonicum infection was detected by qRT-PCR. The role of miR-454 on LX-2 cells was then analyzed by Western blot, flow cytometry and luciferase assay. RESULTS: The results showed that the expression of miR-454 was down-regulated in the TGF-β1-treated LX-2 cells and miR-454 could inhibit the activation of HSCs by directly targeting Smad4. However, we found that miR-454 had no effect on cell cycle and cell proliferation in TGF-β1-treated LX-2. Besides these, miR-454 was found to be regulated in the process of Schistosoma japonicum infection. CONCLUSIONS: All the results suggested that miR-454 could provide a novel therapeutic approach for treating liver fibrosis, especially the liver fibrosis induced by Schistosoma japonicum.