KMID : 0578320170400030202
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Molecules and Cells 2017 Volume.40 No. 3 p.202 ~ p.210
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Hepatitis C Virus Nonstructural 5A Protein (HCV-NS5A) Inhibits Hepatocyte Apoptosis through the NF-¥êb/miR-503/bcl-2 Pathway
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Xie Zheng Yuan
Xiao Zhi Hua Wang Fen Fen
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Abstract
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The nonstructural protein 5A (NS5A) encoded by the human hepatitis C virus (HCV) RNA genome is a multifunctional phosphoprotein. To analyse the influence of NS5A on apoptosis, we established an Hep-NS5A cell line (HepG2 cells that stably express NS5A) and induced apoptosis using tumour necrosis factor (TNF)-¥á. We utilised the MTT assay to detect cell viability, real-time quantitative polymerase chain reaction and Western blot to analyse gene and protein expression, and a luciferase reporter gene experiment to investigate the targeted regulatory relationship. Chromatin immunoprecipitation was used to identify the combination of NF-¥êB and miR-503. We found that overexpression of NS5A inhibited TNF-¥áinduced hepatocellular apoptosis via regulating miR-503 expression. The cell viability of the TNF-¥á induced Hep-mock cells was significantly less than the viability of the TNF-¥á induced Hep-NS5A cells, which demonstrates that NS5A inhibited TNF-¥á-induced HepG2 cell apoptosis. Under TNF-¥á treatment, miR-503 expression was decreased and cell viability and B-cell lymphoma 2 (bcl-2) expression were increased in the Hep-NS5A cells. Moreover, the luciferase reporter gene experiment verified that bcl-2 was a direct target of miR-503, NS5A inhibited TNF-¥á-induced NF-¥êB activation and NF-¥êB regulated miR-503 transcription by combining with the miR-503 promoter. After the Hep-NS5A cells were transfected with miR-503 mimics, the data indicated that the mimics could reverse TNF-¥á-induced cell apoptosis and blc-2 expression. Collectively, our findings suggest a possible molecular mechanism that may contribute to HCV treatment in which NS5A inhibits NF-¥êB activation to decrease miR-503 expression and increase bcl-2 expression, which leads to a decrease in hepatocellular apoptosis.
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KEYWORD
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bcl-2, HCV-NS5A, hepatocyte apoptosis, miR-503, NF-¥êB
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