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Establishment of a novel hepatitis B virus culture system using immortalized human hepatocytes
Recent development of hepatitis B virus (HBV) culture systems has made it possible to analyze the almost all steps of the viral life cycle. However, the reproducibility of interaction between HBV and host cells seemed inaccurate in those systems because of utilization of cancer cell lines with a dif...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729873/ https://www.ncbi.nlm.nih.gov/pubmed/33303813 http://dx.doi.org/10.1038/s41598-020-78655-x |
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author | Akahori, Yuichi Kato, Hiroki Fujita, Takashi Moriishi, Kohji Tanaka, Yasuhito Watashi, Koichi Imamura, Michio Chayama, Kazuaki Wakita, Takaji Hijikata, Makoto |
author_facet | Akahori, Yuichi Kato, Hiroki Fujita, Takashi Moriishi, Kohji Tanaka, Yasuhito Watashi, Koichi Imamura, Michio Chayama, Kazuaki Wakita, Takaji Hijikata, Makoto |
author_sort | Akahori, Yuichi |
collection | PubMed |
description | Recent development of hepatitis B virus (HBV) culture systems has made it possible to analyze the almost all steps of the viral life cycle. However, the reproducibility of interaction between HBV and host cells seemed inaccurate in those systems because of utilization of cancer cell lines with a difference from hepatocytes in the majority of cases. In this study, in order to resolve this point, a novel HBV culture system using non-cancer-derived immortalized human hepatocytes derived cell lines, producing exogenous human sodium taurocholate cotransporting polypeptide, was developed. One of the cell clones, E/NtG8 cells, was permissive to both blood-borne HBV (HBVbb) and culture-derived recombinant HBV when cultured in the three-dimensional condition. Furthermore, the production of infectious HBV particles, which showed the similar physicochemical properties to HBVbb, was observed for about a month after HBVbb infection in this system, suggesting that it may reproduce whole steps of the HBV lifecycle under the condition analogous to human liver cells infected with HBV. This system seemed to contribute not only to find novel interactions between HBV and host cells but also to understand mechanism of HBV pathogenesis. |
format | Online Article Text |
id | pubmed-7729873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77298732020-12-14 Establishment of a novel hepatitis B virus culture system using immortalized human hepatocytes Akahori, Yuichi Kato, Hiroki Fujita, Takashi Moriishi, Kohji Tanaka, Yasuhito Watashi, Koichi Imamura, Michio Chayama, Kazuaki Wakita, Takaji Hijikata, Makoto Sci Rep Article Recent development of hepatitis B virus (HBV) culture systems has made it possible to analyze the almost all steps of the viral life cycle. However, the reproducibility of interaction between HBV and host cells seemed inaccurate in those systems because of utilization of cancer cell lines with a difference from hepatocytes in the majority of cases. In this study, in order to resolve this point, a novel HBV culture system using non-cancer-derived immortalized human hepatocytes derived cell lines, producing exogenous human sodium taurocholate cotransporting polypeptide, was developed. One of the cell clones, E/NtG8 cells, was permissive to both blood-borne HBV (HBVbb) and culture-derived recombinant HBV when cultured in the three-dimensional condition. Furthermore, the production of infectious HBV particles, which showed the similar physicochemical properties to HBVbb, was observed for about a month after HBVbb infection in this system, suggesting that it may reproduce whole steps of the HBV lifecycle under the condition analogous to human liver cells infected with HBV. This system seemed to contribute not only to find novel interactions between HBV and host cells but also to understand mechanism of HBV pathogenesis. Nature Publishing Group UK 2020-12-10 /pmc/articles/PMC7729873/ /pubmed/33303813 http://dx.doi.org/10.1038/s41598-020-78655-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Akahori, Yuichi Kato, Hiroki Fujita, Takashi Moriishi, Kohji Tanaka, Yasuhito Watashi, Koichi Imamura, Michio Chayama, Kazuaki Wakita, Takaji Hijikata, Makoto Establishment of a novel hepatitis B virus culture system using immortalized human hepatocytes |
title | Establishment of a novel hepatitis B virus culture system using immortalized human hepatocytes |
title_full | Establishment of a novel hepatitis B virus culture system using immortalized human hepatocytes |
title_fullStr | Establishment of a novel hepatitis B virus culture system using immortalized human hepatocytes |
title_full_unstemmed | Establishment of a novel hepatitis B virus culture system using immortalized human hepatocytes |
title_short | Establishment of a novel hepatitis B virus culture system using immortalized human hepatocytes |
title_sort | establishment of a novel hepatitis b virus culture system using immortalized human hepatocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729873/ https://www.ncbi.nlm.nih.gov/pubmed/33303813 http://dx.doi.org/10.1038/s41598-020-78655-x |
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