病毒学
病毒进入
病毒
乙型肝炎病毒
丁型肝炎
乙型肝炎
癌症研究
丙型肝炎病毒
免疫学
核糖核酸
医学
生物
RNA干扰
病毒复制
遗传学
基因
肝细胞癌
乙型肝炎表面抗原
作者
Éloi R. Verrier,Che C. Colpitts,C Bach,Laura Heydmann,Amélie Weiss,Mickaël Renaud,Sarah Durand,François Habersetzer,David Durantel,Georges Abou-Jaoudé,Maria M. López Ledesma,Daniel J. Felmlee,Magali Soumillon,Tom Croonenborghs,Nathalie Pochet,Michael Nassal,Catherine Schuster,Laurent Brino,Camille Sureau,Mirjam B. Zeisel,Thomas F. Baumert
出处
期刊:Hepatology
[Wiley]
日期:2015-07-30
卷期号:63 (1): 35-48
被引量:148
摘要
Chronic hepatitis B and D infections are major causes of liver disease and hepatocellular carcinoma worldwide. Efficient therapeutic approaches for cure are absent. Sharing the same envelope proteins, hepatitis B virus and hepatitis delta virus use the sodium/taurocholate cotransporting polypeptide (a bile acid transporter) as a receptor to enter hepatocytes. However, the detailed mechanisms of the viral entry process are still poorly understood. Here, we established a high‐throughput infectious cell culture model enabling functional genomics of hepatitis delta virus entry and infection. Using a targeted RNA interference entry screen, we identified glypican 5 as a common host cell entry factor for hepatitis B and delta viruses. Conclusion : These findings advance our understanding of virus cell entry and open new avenues for curative therapies. As glypicans have been shown to play a role in the control of cell division and growth regulation, virus–glypican 5 interactions may also play a role in the pathogenesis of virus‐induced liver disease and cancer. (H epatology 2016;63:35–48)
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