Type I and type II interferon responses in two human liver cell lines (Huh-7 and HuH6)

Most studies investigating the biology of Hepatitis C virus (HCV) have used the human hepatoma cell line Huh-7 or subclones thereof, as these are the most permissive cell lines for HCV infection and replication. Other cell lines also support replication of HCV, most notably the human hepatoblastoma...

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Main Authors: Oliver Grünvogel, Katharina Esser-Nobis, Marc P. Windisch, Michael Frese, Martin Trippler, Ralf Bartenschlager, Volker Lohmann, Marco Binder
Format: Article
Language:English
Published: Elsevier 2016-03-01
Series:Genomics Data
Online Access:http://www.sciencedirect.com/science/article/pii/S2213596015301185
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spelling doaj-c09b8c73cbea4c2788f92047667582e42020-11-25T03:00:02ZengElsevierGenomics Data2213-59602016-03-017166170Type I and type II interferon responses in two human liver cell lines (Huh-7 and HuH6)Oliver Grünvogel0Katharina Esser-Nobis1Marc P. Windisch2Michael Frese3Martin Trippler4Ralf Bartenschlager5Volker Lohmann6Marco Binder7Department of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, GermanyDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, GermanyDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, GermanyDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, GermanyMedical Research Centre, Department of Gastroenterology and Hepatology, University Duisburg-Essen, Essen, GermanyDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany; Division Virus-associated carcinogenesis (F170), German Cancer Research Center (DKFZ), Heidelberg, GermanyDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, GermanyResearch Group “Dynamics of early viral infection and the innate antiviral response”, Division Virus-associated carcinogenesis (F170), German Cancer Research Center (DKFZ), Heidelberg, Germany; Corresponding author.Most studies investigating the biology of Hepatitis C virus (HCV) have used the human hepatoma cell line Huh-7 or subclones thereof, as these are the most permissive cell lines for HCV infection and replication. Other cell lines also support replication of HCV, most notably the human hepatoblastoma cell line HuH6. HCV replication in cell culture is generally highly sensitive to interferons (IFNs) and differences in the IFN-mediated inhibition of virus replication may reflect alterations in the IFN-induced antiviral response inherent to different host cells. For example, HCV replication is highly sensitive to IFN-γ treatment in Huh-7, but not in HuH6 cells. In this study, we used microarray-based gene expression profiling to compare the response of Huh-7 and HuH6 cells to stimulation with IFN-α and IFN-γ. Furthermore, we determined whether the resistance of HCV replication in HuH6 cells can be linked to differences in the expression profile of IFN-regulated genes. Although both cells lines responded to IFNs with rapid changes in gene expression, thereby demonstrating functional type I and type II signaling pathways, differences were observed for a number of genes. Raw and normalized expression data have been deposited in GEO under accession number GSE68927. Keywords: Interferon, IFN-α, IFN-γ, Huh-7, HuH6, Gene expression profilehttp://www.sciencedirect.com/science/article/pii/S2213596015301185
collection DOAJ
language English
format Article
sources DOAJ
author Oliver Grünvogel
Katharina Esser-Nobis
Marc P. Windisch
Michael Frese
Martin Trippler
Ralf Bartenschlager
Volker Lohmann
Marco Binder
spellingShingle Oliver Grünvogel
Katharina Esser-Nobis
Marc P. Windisch
Michael Frese
Martin Trippler
Ralf Bartenschlager
Volker Lohmann
Marco Binder
Type I and type II interferon responses in two human liver cell lines (Huh-7 and HuH6)
Genomics Data
author_facet Oliver Grünvogel
Katharina Esser-Nobis
Marc P. Windisch
Michael Frese
Martin Trippler
Ralf Bartenschlager
Volker Lohmann
Marco Binder
author_sort Oliver Grünvogel
title Type I and type II interferon responses in two human liver cell lines (Huh-7 and HuH6)
title_short Type I and type II interferon responses in two human liver cell lines (Huh-7 and HuH6)
title_full Type I and type II interferon responses in two human liver cell lines (Huh-7 and HuH6)
title_fullStr Type I and type II interferon responses in two human liver cell lines (Huh-7 and HuH6)
title_full_unstemmed Type I and type II interferon responses in two human liver cell lines (Huh-7 and HuH6)
title_sort type i and type ii interferon responses in two human liver cell lines (huh-7 and huh6)
publisher Elsevier
series Genomics Data
issn 2213-5960
publishDate 2016-03-01
description Most studies investigating the biology of Hepatitis C virus (HCV) have used the human hepatoma cell line Huh-7 or subclones thereof, as these are the most permissive cell lines for HCV infection and replication. Other cell lines also support replication of HCV, most notably the human hepatoblastoma cell line HuH6. HCV replication in cell culture is generally highly sensitive to interferons (IFNs) and differences in the IFN-mediated inhibition of virus replication may reflect alterations in the IFN-induced antiviral response inherent to different host cells. For example, HCV replication is highly sensitive to IFN-γ treatment in Huh-7, but not in HuH6 cells. In this study, we used microarray-based gene expression profiling to compare the response of Huh-7 and HuH6 cells to stimulation with IFN-α and IFN-γ. Furthermore, we determined whether the resistance of HCV replication in HuH6 cells can be linked to differences in the expression profile of IFN-regulated genes. Although both cells lines responded to IFNs with rapid changes in gene expression, thereby demonstrating functional type I and type II signaling pathways, differences were observed for a number of genes. Raw and normalized expression data have been deposited in GEO under accession number GSE68927. Keywords: Interferon, IFN-α, IFN-γ, Huh-7, HuH6, Gene expression profile
url http://www.sciencedirect.com/science/article/pii/S2213596015301185
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