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Expression of the alternative reading frame protein of Hepatitis C virus induces cytokines involved in hepatic injuries

Marc Fiorucci^1,

Anne Fournillier^1,

Geneviève Inchauspé^1,

Christine Bain^1,

¹ FRE 2736 CNRS-bioMérieux, IFR 128 Biosciences Lyon-Gerland, Lyon, France
² Laboratoire Bioinformatique et RMN Structurales, Institut de Biologie et Chimie des Protéines, UMR 5086 CNRS-UCBL Lyon-I, IFR 128 Biosciences Lyon-Gerland, Lyon, France
³ MRC Virology Unit, Glasgow G11 5JR, UK
⁴ CNRS-Inserm U544, Institut de Virologie, Strasbourg, France
⁵ UMR 2714 CNRS-bioMérieux, IFR 128 Biosciences Lyon-Gerland, Lyon, France

Correspondence
Christine Bain
bain{at}transgene.fr

Hepatitis C virus (HCV) Core has been implicated in immune-mediated mechanisms associated with the development of chronic hepatic diseases. Discovery of different alternative reading frame proteins (ARFPs) expressed from the HCV Core coding sequence challenges properties assigned to Core. This study was designed to evaluate the immunomodulatory functions of Core and ARFPs in monocytes, dendritic cells (DCs), macrophages (M) and hepatocytes, cells that are all capable of supporting HCV replication. THP-1 cells, monocyte-derived M and DCs, and Huh7 cells were infected by using adenoviruses (Ad) encoding Core, CE1E2 and a Core sequence modified so that the Core protein is wild type, but no ARFPs are expressed (CARFP). THP-1 cells and DCs infected with Ad encoding Core or CE1E2 produced significant levels of interleukin-6 (IL-6), IL-8, MCP-1 and MIP-1, whereas production of these chemokines with AdCARFP was reduced or abolished. Similar effects on IL-8 production were observed in Huh7 cells and on IL-6 and MIP-1 in M. Wild-type Core sequence, but not CARFP, could trans-activate the IL-8 promoter and this activation was not associated with activation of p38/p42–44MAPK. This study illustrates, for the first time, the critical importance of ARFP expression in immunomodulatory functions attributed to Core expression and suggests a potential involvement of ARFP in mechanisms associated with HCV pathogenesis.

Present address: Transgene, AFSSA Lyon, 31 avenue Tony Garnier, 69364 Lyon Cedex 07, France.

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