Transgenic expression of hepatitis C virus structural proteins in the mouse

Takao Kawamura, Akihiro Furusaka, Margaret J. Koziel, Raymond T. Chung, Tim C. Wang, Emmett V. Schmidt, T. Jake Liang

Research output: Contribution to journalArticlepeer-review

118 Scopus citations


Although hepatitis C virus (HCV) is a leading cause of morbidity and mortality worldwide, the role of viral cytopathic effects remains unclear. To study the biosynthesis of HCV structural proteins and their pathogenic role, we constructed transgenic mice, expressing type 1b HCV structural proteins (core, E1, and E2) in liver tissues. Two liver-specific promoters were used. The mouse major urinary protein (MUP) promoter has been shown to be developmentally regulated with little or no expression in utero but high- level expression after birth. The albumin (Alb) promoter provides constitutive, high levels of transgenes in liver. Expression of both HCV transgenes was detected in several lines by Northern blots, HCV-specific reverse transcriptase-polymerase chain reactions (RT-PCR), and Western immunoblotting. Alb HCV lines showed higher levels of HCV expression than the MUP HCV lines. Immunohistochemical analysis revealed a predominantly cytoplasmic presence of core protein with occasional nuclear staining, and both cytoplasmic and membrane expression of the E2 protein in the transgenic livers. In both transgenes, the highest levels of both antigens were seen in perivenular hepatocytes, suggesting potential processing specificity in those cells. At six months of age, the livers of all transgenic lineages remained histologically normal. We concluded that HCV structural proteins are not directly cytopathic in this animal model.

Original languageEnglish (US)
Pages (from-to)1014-1021
Number of pages8
Issue number4
StatePublished - 1997
Externally publishedYes

ASJC Scopus subject areas

  • Hepatology


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