Multiple Functions of Cellular FLIP Are Essential for Replication of Hepatitis B Virus

Author:

Lee Ah Ram1,Lim Keo-Heun1,Park Eun-Sook1,Kim Doo Hyun1,Park Yong Kwang1,Park Soree1,Kim Dong-Sik2,Shin Gu-Choul1,Kang Hong Seok1,Won Juhee1,Sim Heewoo1,Ha Yea Na1,Jae Byeongjune1,Choi Seong Il3,Kim Kyun-Hwan145

Affiliation:

1. Department of Pharmacology, Center for Cancer Research and Diagnostic Medicine, IBST, School of Medicine, Konkuk University, Seoul, Republic of Korea

2. Division of HBP Surgery and Liver Transplantation, Department of Surgery, Korea University College of Medicine, Seoul, Republic of Korea

3. Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea

4. KU Open Innovation Center, Konkuk University, Seoul, Republic of Korea

5. Research Institute of Medical Sciences, Konkuk University, Seoul, Republic of Korea

Abstract

Although the chronic hepatitis B virus (HBV) infection still poses a major health concern, the host factors which are required for the replication of HBV are largely uncharacterized. Our studies identify cellular FLICE inhibitory protein (c-FLIP) as an essential factor in HBV replication. We found the dual roles of c-FLIP in regulation of HBV replication: c-FLIP interacts with HBx and enhances its stability and regulates the expression or stability of hepatocyte nuclear factors which are essential for transcription of HBV genome. Our findings may provide a new target for intervention in persistent HBV infection.

Funder

Konkuk University

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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