Evidence map›Paper›PMID 20538002›Full record

ArticleGastroenterology2010

Hepatitis C virus infection of neuroepithelioma cell lines.

Nicola F Fletcher, Jian Ping Yang, Michelle J Farquhar, Ke Hu, Christopher Davis, Qiuchen He, Kimberly Dowd, Stuart C Ray, Sophie E Krieger, Johan Neyts and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Gastroenterology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 67 citations in OpenAlex.

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  10. Brain magnetic resonance spectroscopy and cognitive impairment in chronic hepatitis C patients.The Egyptian journal of neurology, psychiatry and neurosurgery · 2018
    Article
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  17. Hepatitis C virus and neurological damage.World journal of hepatology · 2016
    Review
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  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 4 countries.

Nicola F FletcherHepatitis C Research Group, Institute for Biomedical Research, University of Birmingham, Birmingham, United Kingdom.
Jian Ping Yang
Michelle J Farquhar
Ke Hu
Christopher Davis
Qiuchen He
Kimberly Dowd
Stuart C Ray
Sophie E Krieger
Johan Neyts
Thomas F Baumert
Peter Balfe
Jane A McKeating
Flossie Wong-Staal
University of Birmingham · GBiTherX (United States) · USJohns Hopkins Medicine · USInserm · FRRega Institute for Medical Research · BEUniversité de Strasbourg · FR

Funding

Mechanisms of Hepatitis C Virus EvolutionR01DA024565 · NIDA · JOHNS HOPKINS UNIVERSITY · PI RAY, STUART C · 2007 to 2011
$2.6M
Functional analysis of hepatitis C virus glycoproteinsR01AI050798 · NIAID · UNIVERSITY OF BIRMINGHAM · PI MCKEATING, JANE A. · 2004 to 2008
$1.3M
Medical Research Council G0400802Medical Research Council G0801976NIAID NIH HHS R01 AI050798NIDA NIH HHS R01 DA024565PHS HHS U19 A140034Wellcome Trust
6 · The paper itself

Abstract

BACKGROUND &

aimsHepatitis C virus (HCV) establishes chronic infections in 3% of the world's population. Infection leads to progressive liver disease; hepatocytes are the major site of viral replication in vivo. However, chronic infection is associated with a variety of extrahepatic syndromes, including central nervous system (CNS) abnormalities. We therefore screened a series of neural and brain-derived cell lines for their ability to support HCV entry and replication.

methodsWe used a panel of neural-derived cell lines, HCV pseudoparticles (HCVpp), and an infectious, HCV JFH-1 cell-culture system (HCVcc) to assess viral tropism.

resultsTwo independently derived neuroepithelioma cell lines (SK-N-MC and SK-PN-DW) permitted HCVpp entry. In contrast, several neuroblastoma, glioma, and astrocytoma cell lines were refractory to HCVpp infection. HCVcc infected the neuroepithelioma cell lines and established a productive infection. Permissive neuroepithelioma cells expressed CD81, scavenger receptor BI (SR-BI), and the tight junction proteins Claudin-1 (CLDN1) and occludin, whereas nonpermissive neural cell lines lacked CLDN1 and, in some cases, SR-BI. HCVpp infection of the neuroepithelioma cells was neutralized by antibodies to CD81, SR-BI, CLDN1, and HCV E2. Furthermore, anti-CD81, interferon, and the anti-NS3 protease inhibitor VX-950 significantly reduced HCVcc infection of neuroepithelioma and hepatoma cells.

conclusionsNeuroepithelioma-derived cell lines express functional receptors that support HCV entry at levels comparable to those of hepatoma cells. HCV infection in vitro is not restricted to hepatic-derived cells, so HCV might infect cells of the CNS in vivo.

Indexed as

Antigens, CDCell Line, TumorClaudin-1HepacivirusHumansMembrane ProteinsNeuroectodermal Tumors, Primitive, PeripheralOccludinRNA, ViralScavenger Receptors, Class BTetraspanin 28Viral TropismVirus InternalizationAntigens, CDCD81 protein, humanClaudin-1CLDN1 protein, humanMembrane ProteinsOccludinOCLN protein, humanRNA, ViralSCARB1 protein, humanScavenger Receptors, Class BTetraspanin 28

Identifiers

PMID20538002
PMCPMC3298458
OpenAlexW2093741435

What OpenQuestion holds

Textmetadata
LicenceTDM
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.