The functional role of sodium taurocholate cotransporting polypeptide NTCP in the life cycle of hepatitis B, C and D viruses

被引:15
作者
Eller, Carla [1 ,2 ]
Heydmann, Laura [1 ,2 ]
Colpitts, Che C. [3 ]
Verrier, Eloi R. [1 ,2 ]
Schuster, Catherine [1 ,2 ]
Baumert, Thomas F. [1 ,2 ,4 ]
机构
[1] INSERM, U1110, Inst Rech Malad Virales & Hepat, 3 Rue Koeberle, F-67000 Strasbourg, France
[2] Univ Strasbourg, F-67000 Strasbourg, France
[3] UCL, Div Infect & Immun, London, England
[4] Nouvel Hop Civil, Pole Hepatodigestif, Inst Hospitalouniv, F-67000 Strasbourg, France
基金
加拿大健康研究院; 美国国家卫生研究院; 欧盟地平线“2020”;
关键词
Liver cell biology; Bile acid transport; Host factor; Anti-viral therapy; Hepatocytes; LARGE SURFACE PROTEIN; SALT EXPORT PUMP; HEPATOBILIARY TRANSPORTER EXPRESSION; BILE-ACID TRANSPORTERS; HEPARAN-SULFATE; CYCLOSPORINE-A; HEPATOCELLULAR-CARCINOMA; NUCLEAR RECEPTORS; ENTRY INHIBITORS; ENVELOPE PROTEIN;
D O I
10.1007/s00018-018-2892-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chronic hepatitis B, C and D virus (HBV, HCV and HDV) infections are a major cause of liver disease and cancer worldwide. Despite employing distinct replication strategies, the three viruses are exclusively hepatotropic, and therefore depend on hepatocyte-specific host factors. The sodium taurocholate co-transporting polypeptide (NTCP), a transmembrane protein highly expressed in human hepatocytes that mediates the transport of bile acids, plays a key role in HBV and HDV entry into hepatocytes. Recently, NTCP has been shown to modulate HCV infection of hepatocytes by regulating innate antiviral immune responses in the liver. Here, we review the current knowledge of the functional role and the molecular and cellular biology of NTCP in the life cycle of the three major hepatotropic viruses, highlight the impact of NTCP as an antiviral target and discuss future avenues of research.
引用
收藏
页码:3895 / 3905
页数:11
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