Stem cell-derived hepatocytes: A novel model for hepatitis E virus replication

JOURNAL OF HEPATOLOGY

卷:64

Article

Helsen, Nicky¹  Debing, Yannick²  Paeshuyse, Jan²  Dallmeier, Kai²  Boon, Ruben¹  Coll, Mar³  Sancho-Bru, Pau³  Claes, Christel¹  Neyts, Johan²  Verfaillie, Catherine M.¹ 

[1] Univ Leuven KU Leuven, Stem Cell Inst, Leuven, Belgium

[2] Univ Leuven KU Leuven, Rega Inst Med Res, Lab Virol & Expt Chemotherapy, Louvain, Belgium

[3] Hosp Clin Barcelona, Inst Invest Biomed August Pi & Sunyer IDIBAPS, Liver Unit, Barcelona, Spain

关键词: Pluripotent stem cells;    Hepatitis E virus;    Cell culture model;    Hepatocytes;   

DOI  :  10.1016/j.jhep.2015.11.013

来源: Elsevier

【 摘 要 】

Background & Aims: Yearly, approximately 20 million people become infected with the hepatitis E virus (HEV) resulting in over 3 million cases of acute hepatitis. Although HEV-mediated hepatitis is usually self-limiting, severe cases of fulminant hepatitis as well as chronic infections have been reported, resulting annually in an estimated 60,000 deaths. We studied whether pluripotent stem cell (PSC)-derived hepatocytes, mesodermal and/or neuroprogenitor cells support HEV replication. Methods: Human PSC were differentiated towards hepatocyte-like cells, mesodermal cells and neuroprogenitors and subsequently infected with HEV. Infection and replication of HEV was analyzed by qRT-PCR, RNA in situ hybridization, negative strand RT-PCR, production of infectious virions and transfection with a transient HEV reporter replicon. Results: PSC-derived hepatocytes supported the complete replication cycle of HEV, as demonstrated by the intracellular presence of positive and negative strand HEV RNA and the production of infectious virions. The replication of the virus in these cells was inhibited by the antiviral drugs ribavirin and interferon-alpha 2b. In contrast to PSC-derived hepatocytes, PSC-derived mesodermal cells and neuroprogenitors only supported HEV replication upon transfection with a HEV subgenomic replicon. Conclusion: We demonstrate that PSC can be used to study the hepatotropism of HEV infection. The complete replication cycle of HEV can be recapitulated in infected PSC-derived hepatocytes. By contrast other germ layer cells support intracellular replication but are not infectable with HEV. Thus the early steps in the viral cycle are the main determinant governing HEV tissue tropism. PSC-hepatocytes offer a physiological relevant tool to study the biology of HEV infection and replication and may aid in the design of therapeutic strategies. (C) 2015 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

【 授权许可】

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