Evidence map›Paper›PMID 22087337›Full record

ArticlePloS one2011

Innate host response in primary human hepatocytes with hepatitis C virus infection.

Darong Yang, Nianli Liu, Chaohui Zuo, Shoahua Lei, Xinjiao Wu, Fei Zhou, Chen Liu, Haizhen Zhu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. The Journal of biological chemistry · 2020
    Article
  4. Effect of P-body component Mov10 on HCV virus production and infectivity.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Complete replication of hepatitis B virus and hepatitis C virus in a newly developed hepatoma cell line.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. 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

8 authors at 3 institutions in 2 countries.

Darong YangDepartment of Molecular Medicine, College of Biology of Hunan University, Changsha, China.
Nianli Liu
Chaohui Zuo
Shoahua Lei
Xinjiao Wu
Fei Zhou
Chen Liu
Haizhen Zhu
Hunan University · CNHunan Cancer Hospital · CNFlorida College · US

Funding

Role of liver cytokines in hepatitis C viral infectionK08DK002958 · NIDDK · UNIVERSITY OF FLORIDA · PI LIU, CHEN · 2002 to 2006
$584k
NIDDK NIH HHS DK002958NIDDK NIH HHS K08 DK002958
6 · The paper itself

Abstract

BACKGROUND AND

aimThe interaction between hepatitis C virus (HCV) and innate antiviral defense systems in primary human hepatocytes is not well understood. The objective of this study is to examine how primary human hepatocytes response to HCV infection.

methodsAn infectious HCV isolate JFH1 was used to infect isolated primary human hepatocytes. HCV RNA or NS5A protein in the cells was detected by real-time PCR or immunofluorescence staining respectively. Apoptosis was examined with flow cytometry. Mechanisms of HCV-induced IFN-β expression and apoptosis were determined.

resultsPrimary human hepatocytes were susceptible to JFH1 virus and released infectious virus. IFN-α inhibited viral RNA replication in the cells. IFN-β and interferon-stimulated genes were induced in the cells during acute infection. HCV infection induced apoptosis of primary human hepatocytes through the TRAIL-mediated pathway. Silencing RIG-I expression in primary human hepatocytes inhibited IFN-β and TRAIL expression and blocked apoptosis of the cells, which facilitated viral RNA replication in the cells. Moreover, HCV NS34A protein inhibited viral induced IFN-β expression in primary human hepatocytes.

conclusionInnate host response is intact in HCV-infected primary human hepatocytes. RIG-I plays a key role in the induction of IFN and TRAIL by viruses and apoptosis of primary human hepatocytes via activation of the TRAIL-mediated pathway. HCV NS34A protein appears to be capable of disrupting the innate antiviral host responses in primary human hepatocytes. Our study provides a novel mechanism by which primary human hepatocytes respond to natural HCV infection.

Indexed as

Immunity, InnateApoptosisCells, CulturedDEAD Box Protein 58DEAD-box RNA HelicasesHepacivirusHepatitis CHepatocytesHumansInterferon-betaReceptors, ImmunologicRNA, ViralTNF-Related Apoptosis-Inducing LigandTranscriptional ActivationViral ProteinsDEAD Box Protein 58DEAD-box RNA HelicasesInterferon-betaReceptors, ImmunologicRIGI protein, humanRNA, ViralTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanViral Proteins

Identifiers

PMID22087337
PMCPMC3210809
OpenAlexW1968205712

What OpenQuestion holds

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LicenceCC BY
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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.