Evidence map›Paper›PMID 30232184›Full record

ArticleJournal of virology2018

Robust Human and Murine Hepatocyte Culture Models of Hepatitis B Virus Infection and Replication.

Luhua Qiao, Jianhua Sui, Guangxiang Luo

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Hepatitis B virus covalently closed circular DNA formation in murine hepatic cells uncovers a late entry block.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Hepatitis B virus entry, assembly, and egress.Microbiology and molecular biology reviews : MMBR · 2024
    Review
  5. Progress of Infection and Replication Systems of Hepatitis B Virus.ACS pharmacology & translational science · 2024
    Review
  6. Apolipoprotein E and viral infection: Risks and Mechanisms.Molecular therapy. Nucleic acids · 2023
    Review
  7. Article
  8. All-Viruses · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Luhua QiaoDepartment of Microbiology, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, USA.
Jianhua SuiNational Institute of Biological Sciences, Beijing, China.
Guangxiang LuoDepartment of Microbiology, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, USA gluo@uab.edu.ORCID 0000-0002-0354-6020
University of Alabama at Birmingham · USNational Institute of Biological Sciences, Beijing · CN

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OLAF KUTSCH · 1988 to 2026
$84.1M
NCI NIH HHS P30 CA013148NIAID NIH HHS P30 AI027767
6 · The paper itself

Abstract

Hepatitis B virus (HBV) is a major cause of chronic liver diseases, including hepatitis, cirrhosis, and hepatocellular carcinoma. HBV research has been hampered by the lack of robust cell culture and small animal models of HBV infection. The discovery of sodium taurocholate cotransporting polypeptide (NTCP) as an HBV receptor has been a landmark advance in HBV research in recent years. Ectopic expression of NTCP in nonpermissive HepG2, Huh7, and AML12 cell lines confers HBV susceptibility. However, HBV replication in these human and murine hepatocyte cell lines appeared suboptimal. In the present study, we constructed stable NTCP-expressing HepG2 and AML12 cell lines and found that HBV permissiveness is correlated with NTCP expression. More significantly, we developed robust HBV cell culture models by treating the HBV-infected cells with dimethyl sulfoxide (DMSO) and hydrocortisone, which significantly promoted HBV replication and production. Mechanistic studies suggested that hydrocortisone significantly enhanced the transcription and expression of PGC1α and HNF4α, which are known to promote HBV transcription and replication. These new human and murine hepatocyte culture systems of HBV infection and replication will accelerate the determination of molecular aspects underlying HBV infection, replication, and morphogenesis in human and murine hepatocytes. We anticipate that our HBV cell culture models will also facilitate the discovery and development of antiviral drugs towards the ultimate eradication of chronic hepatitis B virus infection.

Indexed as

AnimalsAnti-Inflammatory AgentsCell Culture TechniquesCryoprotective AgentsDimethyl SulfoxideGene Expression Regulation, ViralHepatitis BHepatitis B virusHepatocytesHep G2 CellsHumansHydrocortisoneMiceOrganic Anion Transporters, Sodium-DependentSymportersVirus InternalizationAnti-Inflammatory AgentsCryoprotective AgentsDimethyl SulfoxideHydrocortisoneOrganic Anion Transporters, Sodium-Dependentsodium-bile acid cotransporterSymportersAML12DMSOHBVhepatitis B virusHepG2hydrocortisoneinfectionmorphogenesisNTCPPHHreplication

Identifiers

PMID30232184
PMCPMC6232483
OpenAlexW2891445108

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.