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Dynamics of HBV cccDNA expression and transcription in different cell growth phase

BACKGROUND: The covalently closed-circular DNA (cccDNA) of hepatitis B virus (HBV) is associated with viral persistence in HBV-infected hepatocytes. However, the regulation of cccDNA and its transcription in the host cells at different growth stages is not well understood. METHODS: We took advantage...

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Autores principales: Chong, Chin-Liew, Chen, Mong-Liang, Wu, Yi-Chieh, Tsai, Kuen-Nan, Huang, Chien-Chiao, Hu, Cheng-po, Jeng, King-Song, Chou, Yu-Chi, Chang, Chungming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262020/
https://www.ncbi.nlm.nih.gov/pubmed/22208719
http://dx.doi.org/10.1186/1423-0127-18-96
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author Chong, Chin-Liew
Chen, Mong-Liang
Wu, Yi-Chieh
Tsai, Kuen-Nan
Huang, Chien-Chiao
Hu, Cheng-po
Jeng, King-Song
Chou, Yu-Chi
Chang, Chungming
author_facet Chong, Chin-Liew
Chen, Mong-Liang
Wu, Yi-Chieh
Tsai, Kuen-Nan
Huang, Chien-Chiao
Hu, Cheng-po
Jeng, King-Song
Chou, Yu-Chi
Chang, Chungming
author_sort Chong, Chin-Liew
collection PubMed
description BACKGROUND: The covalently closed-circular DNA (cccDNA) of hepatitis B virus (HBV) is associated with viral persistence in HBV-infected hepatocytes. However, the regulation of cccDNA and its transcription in the host cells at different growth stages is not well understood. METHODS: We took advantages of a stably HBV-producing cell line, 1.3ES2, and examine the dynamic changes of HBV cccDNA, viral transcripts, and viral replication intermediates in different cellular growth stages. RESULTS: In this study, we showed that cccDNA increased suddenly in the initial proliferation phase of cell growth, probably attributable to its nuclear replenishment by intracellular nucleocapsids. The amount of cccDNA then decreased dramatically in the cells during their exponential proliferation similar to the loss of extrachromosomal plasmid DNA during cell division, after which it accumulated gradually while the host cells grew to confluency. We found that cccDNA was reduced in dividing cells and could be removed when proliferating cells were subjected to long term of lamivudine (3TC) treatment. The amounts of viral replicative intermediates were rapidly reduced in these proliferating cells and were significantly increased after cells reaching confluency. The expression levels of viral transcripts were increased in parallel with the elevated expression of hepatic transcription factors (HNF4α, CEBPα, PPARα, etc.) during cell growth confluency. The HBV transcripts were transcribed from both integrated viral genome and cccDNA, however the transcriptional abilities of cccDNA was less efficient then that from integrated viral genome in all cell growth stages. We also noted increases in the accumulation of intracellular viral particles and the secretion of mature virions as the cells reached confluency and ceased to grow. CONCLUSIONS: Based on the dynamics of HBV replication, we propose that HBV replication is modulated differently in the different stages of cell growth, and can be divided into three phases (initial proliferation phase, exponential proliferation phase and growth confluency phase) according to the cell growth curve. The regulation of cccDNA in different cell growth phase and its importance regarding HBV replication are discussed.
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spelling pubmed-32620202012-01-20 Dynamics of HBV cccDNA expression and transcription in different cell growth phase Chong, Chin-Liew Chen, Mong-Liang Wu, Yi-Chieh Tsai, Kuen-Nan Huang, Chien-Chiao Hu, Cheng-po Jeng, King-Song Chou, Yu-Chi Chang, Chungming J Biomed Sci Research BACKGROUND: The covalently closed-circular DNA (cccDNA) of hepatitis B virus (HBV) is associated with viral persistence in HBV-infected hepatocytes. However, the regulation of cccDNA and its transcription in the host cells at different growth stages is not well understood. METHODS: We took advantages of a stably HBV-producing cell line, 1.3ES2, and examine the dynamic changes of HBV cccDNA, viral transcripts, and viral replication intermediates in different cellular growth stages. RESULTS: In this study, we showed that cccDNA increased suddenly in the initial proliferation phase of cell growth, probably attributable to its nuclear replenishment by intracellular nucleocapsids. The amount of cccDNA then decreased dramatically in the cells during their exponential proliferation similar to the loss of extrachromosomal plasmid DNA during cell division, after which it accumulated gradually while the host cells grew to confluency. We found that cccDNA was reduced in dividing cells and could be removed when proliferating cells were subjected to long term of lamivudine (3TC) treatment. The amounts of viral replicative intermediates were rapidly reduced in these proliferating cells and were significantly increased after cells reaching confluency. The expression levels of viral transcripts were increased in parallel with the elevated expression of hepatic transcription factors (HNF4α, CEBPα, PPARα, etc.) during cell growth confluency. The HBV transcripts were transcribed from both integrated viral genome and cccDNA, however the transcriptional abilities of cccDNA was less efficient then that from integrated viral genome in all cell growth stages. We also noted increases in the accumulation of intracellular viral particles and the secretion of mature virions as the cells reached confluency and ceased to grow. CONCLUSIONS: Based on the dynamics of HBV replication, we propose that HBV replication is modulated differently in the different stages of cell growth, and can be divided into three phases (initial proliferation phase, exponential proliferation phase and growth confluency phase) according to the cell growth curve. The regulation of cccDNA in different cell growth phase and its importance regarding HBV replication are discussed. BioMed Central 2011-12-30 /pmc/articles/PMC3262020/ /pubmed/22208719 http://dx.doi.org/10.1186/1423-0127-18-96 Text en Copyright © 2011 Chong et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chong, Chin-Liew
Chen, Mong-Liang
Wu, Yi-Chieh
Tsai, Kuen-Nan
Huang, Chien-Chiao
Hu, Cheng-po
Jeng, King-Song
Chou, Yu-Chi
Chang, Chungming
Dynamics of HBV cccDNA expression and transcription in different cell growth phase
title Dynamics of HBV cccDNA expression and transcription in different cell growth phase
title_full Dynamics of HBV cccDNA expression and transcription in different cell growth phase
title_fullStr Dynamics of HBV cccDNA expression and transcription in different cell growth phase
title_full_unstemmed Dynamics of HBV cccDNA expression and transcription in different cell growth phase
title_short Dynamics of HBV cccDNA expression and transcription in different cell growth phase
title_sort dynamics of hbv cccdna expression and transcription in different cell growth phase
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262020/
https://www.ncbi.nlm.nih.gov/pubmed/22208719
http://dx.doi.org/10.1186/1423-0127-18-96
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