Transgenic mice in which the urokinase VX-809 order gene is driven by the human albumin promoter/enhancer were developed and shown to have accelerated hepatocyte death and consequent chronic stimulation of hepatocyte

growth.11 Transplanted rat hepatocytes proliferated and repopulated injured livers in immunodeficient uPA mice, which were produced by mating uPA transgenic mice with scid mice.12 Human hepatocytes were then transplanted into uPA/scid mice; these cells proliferated and replaced the apoptotic mice liver cells (Fig. 1). Such human hepatocyte chimeric mice have been shown to be susceptible to both HBV16 and HCV17 infections. Repopulation levels by human hepatocytes have been estimated by measuring human albumin levels in mouse serum. Replication levels of both HBV13 and HCV17 were higher in mice in which the repopulation index was higher. A unique attempt to remove mouse residual liver cells with the herpes simplex virus type-1 thymidine kinase (HSVtk)/ganciclovir selleck compound (GCV) system failed to result in a higher repopulation rate as a result of damage to the transplanted human hepatocyte caused by bystander effects.18 Despite this, mice with livers that have been highly repopulated with human hepatocytes are susceptible to infection with both HBV and HCV, and as

such comprised the most effective small animal model for chronic hepatitis so far developed.19,20 An example of a highly repopulated mouse liver that we are using in experiments is shown in Figure 2. Highly repopulated mice have been shown to be a valuable model for the study of drug metabolism.21–29 Advances in technology for human hepatocyte transplantation have enabled serial passage of human hepatocytes in uPA/scid selleck kinase inhibitor mice and have been shown to retain infectivity for HBV.30 This mouse model

and other animal models for the study of hepatitis viruses have been summarized in reviews by Meuleman and Leroux-Roels,31 Dandri et al.,32,33 Barth et al.,34 and Kneteman and Toso.35 The present review will focus on key issues and updated information. Since the initial reports of successful transmission of HBV to human hepatocyte chimeric mice in 2001 and 2004,16,27 several researchers have reported transmission of HBV into similar mice.13,36,37 In these studies, passage experiments studies show that HBV replicating in mice retain infectivity.13,36 Further, the presence of viral proteins has been shown immunohistochemically in human hepatocytes transplanted into mouse livers, but these are not present in mouse hepatocytes.13,36,37 Formation of viral particles in infected mouse livers can be shown by electron microscopy.36,37 Genetically engineered viruses lacking HBe-antigen have also been shown to infect chimeric mice, proving that e antigen is dispensable for viral infection and replication.