Related Experiment Video
Updated: Jul 19, 2026

Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells
Published on: June 5, 2020
High expression of APOBEC3G in patients infected with hepatitis C virus
Yoshihiro Komohara1, Hirohisa Yano, Shigeki Shichijo
1Department of Immunology, Kurume University School of Medicine, Asahi-machi 67, Kurume, Fukuoka 839-0011, Japan.
Insights
Apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3G (APOBEC3G) expression increases in chronic hepatitis C virus (HCV) patients. HCV NS5A gene and interferon also enhance APOBEC3G expression, offering new insights into HCV pathogenesis.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- APOBEC3G (apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3G) is a host-defense protein with cytidine deaminase activity.
- APOBEC3G induces C/G to T/A mutations in viral genomes, including HIV-1 and HBV.
- The role of APOBEC3G in chronic hepatitis C virus (HCV) infection, affecting over 170 million people globally, is not well understood.
Purpose of the Study:
- To investigate APOBEC3G expression levels in patients with chronic HCV infection.
- To explore the impact of HCV components and interferon on APOBEC3G expression.
Main Methods:
- Analysis of APOBEC3G expression in hepatocytes and lymphocytes of chronic HCV patients.
- Transfection of HCV non-structural protein genes (including NS5A) into a hepatocellular carcinoma cell line.
- Incubation of cells with interferon.
Main Results:
- APOBEC3G expression was significantly increased in both hepatocytes and lymphocytes of chronic HCV patients.
- Transfection with the HCV NS5A gene, but not other tested non-structural genes, enhanced APOBEC3G expression in a hepatocellular carcinoma cell line.
- Interferon treatment also led to increased APOBEC3G expression.
Conclusions:
- APOBEC3G expression is upregulated in chronic HCV infection.
- HCV NS5A and interferon may play roles in modulating APOBEC3G expression.
- These findings may offer new perspectives on the pathogenesis of chronic HCV infection.
Abstract:
APOBEC3G (an apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3G; also known as CEM15), a member of the APOBEC family, which possesses cytidine deaminase activity that causes C/G to T/A transition mutations in virus genomes such as human immunodeficiency virus 1 and hepatitis B virus, is reported to play an important role in host-defense mechanisms. However, APOBEC3G expression in patients infected with chronic hepatitis C virus (HCV), of which there are currently more than 170 million worldwide, has not yet been well studied. We investigated this issue herein, and demonstrated an increased expression of APOBEC3G in both hepatocytes and lymphocytes of chronic hepatitis patients infected with HCV. Transfection of the NS5A gene, but not any other non-structural protein genes of HCV tested, to the hepatocellular carcinoma cell line enhanced APOBEC3G expression. Incubation of the cells with interferon also resulted in the augmentation. These results may provide new insight into the pathogenesis of chronic HCV infection.
More Related Videos
10:25"Liver-on-a-Chip" Cultures of Primary Hepatocytes and Kupffer Cells for Hepatitis B Virus Infection
Published on: February 19, 2019
11:34A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
Published on: May 10, 2022
Related Concept Videos
Hepatitis
Viral Hepatitis I: Introduction