Functional involvement of endothelial lipase in hepatitis B virus infection.


Journal

Hepatology communications
ISSN: 2471-254X
Titre abrégé: Hepatol Commun
Pays: United States
ID NLM: 101695860

Informations de publication

Date de publication:
01 09 2023
Historique:
received: 25 06 2022
accepted: 05 04 2023
medline: 4 9 2023
pubmed: 1 9 2023
entrez: 1 9 2023
Statut: epublish

Résumé

HBV infection causes chronic liver disease and leads to the development of HCC. To identify host factors that support the HBV life cycle, we previously established the HC1 cell line that maintains HBV infection and identified host genes required for HBV persistence. The present study focused on endothelial lipase (LIPG), which binds to heparan sulfate proteoglycans (HSPGs) in the cell membrane. We found HBV infection was impaired in humanized liver chimeric mouse-derived hepatocytes that were transduced with lentivirus expressing short hairpin RNA against LIPG. Long-term suppression of LIPG combined with entecavir further suppressed HBV replication. LIPG was shown to be involved in HBV attachment to the cell surface by using 2 sodium taurocholate cotransporting peptide (NTCP)-expressing cell lines, and the direct interaction of LIPG and HBV large surface protein was revealed. Heparin and heparinase almost completely suppressed the LIPG-induced increase of HBV attachment, indicating that LIPG accelerated HBV attachment to HSPGs followed by HBV entry through NTCP. Surprisingly, the attachment of a fluorescently labeled NTCP-binding preS1 probe to NTCP-expressing cells was not impaired by heparin, suggesting the HSPG-independent attachment of the preS1 probe to NTCP. Interestingly, attachment of the preS1 probe was severely impaired in LIPG knockdown or knockout cells. Inhibitors of the lipase activity of LIPG similarly impaired the attachment of the preS1 probe to NTCP-expressing cells. LIPG participates in HBV infection by upregulating HBV attachment to the cell membrane by means of 2 possible mechanisms: increasing HBV attachment to HSPGs or facilitating HSPG-dependent or HSPG-independent HBV attachment to NTCP by its lipase activity.

Sections du résumé

BACKGROUND
HBV infection causes chronic liver disease and leads to the development of HCC. To identify host factors that support the HBV life cycle, we previously established the HC1 cell line that maintains HBV infection and identified host genes required for HBV persistence.
METHODS
The present study focused on endothelial lipase (LIPG), which binds to heparan sulfate proteoglycans (HSPGs) in the cell membrane.
RESULTS
We found HBV infection was impaired in humanized liver chimeric mouse-derived hepatocytes that were transduced with lentivirus expressing short hairpin RNA against LIPG. Long-term suppression of LIPG combined with entecavir further suppressed HBV replication. LIPG was shown to be involved in HBV attachment to the cell surface by using 2 sodium taurocholate cotransporting peptide (NTCP)-expressing cell lines, and the direct interaction of LIPG and HBV large surface protein was revealed. Heparin and heparinase almost completely suppressed the LIPG-induced increase of HBV attachment, indicating that LIPG accelerated HBV attachment to HSPGs followed by HBV entry through NTCP. Surprisingly, the attachment of a fluorescently labeled NTCP-binding preS1 probe to NTCP-expressing cells was not impaired by heparin, suggesting the HSPG-independent attachment of the preS1 probe to NTCP. Interestingly, attachment of the preS1 probe was severely impaired in LIPG knockdown or knockout cells. Inhibitors of the lipase activity of LIPG similarly impaired the attachment of the preS1 probe to NTCP-expressing cells.
CONCLUSIONS
LIPG participates in HBV infection by upregulating HBV attachment to the cell membrane by means of 2 possible mechanisms: increasing HBV attachment to HSPGs or facilitating HSPG-dependent or HSPG-independent HBV attachment to NTCP by its lipase activity.

Identifiants

pubmed: 37655967
doi: 10.1097/HC9.0000000000000206
pii: 02009842-202309010-00011
pmc: PMC10476801
pii:
doi:

Substances chimiques

Heparan Sulfate Proteoglycans 0
Heparin 9005-49-6
Lipase EC 3.1.1.3
Lipg protein, mouse EC 3.1.1.3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases.

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Auteurs

Takayoshi Shirasaki (T)

Department of Clinical Laboratory Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

Kazuhisa Murai (K)

Department of Clinical Laboratory Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

Atsuya Ishida (A)

Department of Clinical Laboratory Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

Kazuyuki Kuroki (K)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Kazunori Kawaguchi (K)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Ying Wang (Y)

Department of Clinical Laboratory Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

Souma Yamanaka (S)

Department of Clinical Laboratory Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

Rio Yasukawa (R)

Department of Clinical Laboratory Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

Narumi Kawasaki (N)

Department of Clinical Laboratory Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

Ying-Yi Li (YY)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Tetsuro Shimakami (T)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Ariunaa Sumiyadorj (A)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Kouki Nio (K)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Saiho Sugimoto (S)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Noriaki Orita (N)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Hideo Takayama (H)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Hikari Okada (H)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Phuong Doan Thi Bich (PD)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Sadahiro Iwabuchi (S)

Department of Molecular Pathophysiology, Institute of Advanced Medicine, Wakayama Medical University, Wakayama, Japan.

Shinichi Hashimoto (S)

Department of Molecular Pathophysiology, Institute of Advanced Medicine, Wakayama Medical University, Wakayama, Japan.

Mayuko Ide (M)

Purotech Bio Inc., Kanagawa, Japan.

Noriko Tabata (N)

Purotech Bio Inc., Kanagawa, Japan.

Satoru Ito (S)

Purotech Bio Inc., Kanagawa, Japan.

Kouji Matsushima (K)

Division of Molecular Regulation of Inflammatory and Immune Diseases, Research Institute for Biomedical Sciences, Tokyo University of Science, Chiba, Japan.

Hiroshi Yanagawa (H)

Purotech Bio Inc., Kanagawa, Japan.

Taro Yamashita (T)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Shuichi Kaneko (S)

Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Masao Honda (M)

Department of Clinical Laboratory Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
Department of Gastroenterology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

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