Evidence map›Paper›PMID 29544098›Full record

ArticleCell host & microbe2018

Single Particle Imaging of Polarized Hepatoma Organoids upon Hepatitis C Virus Infection Reveals an Ordered and Sequential Entry Process.

Yasmine Baktash, Anisha Madhav, Kelly E Coller, Glenn Randall

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 2 pooled it
7.4field-weighted citation impact, top 2% 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

69 citing papers in PubMed, 2 syntheses or guidelines pooled it, 106 citations in OpenAlex.

  1. Pooled it
  2. Organoids of liver diseases: From bench to bedside.World journal of gastroenterology · 2019
    Pooled it
  3. [Advances in the construction and application of a novel liver organoid model for hepatitis B virus infection].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
    Review
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  7. Organoids: physiologically relevantJournal of virology · 2025
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9 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Yasmine BaktashDepartment of Microbiology, The University of Chicago, Chicago, IL 60637, USA.
Anisha MadhavDepartment of Microbiology, The University of Chicago, Chicago, IL 60637, USA.
Kelly E CollerDepartment of Microbiology, The University of Chicago, Chicago, IL 60637, USA.
Glenn RandallDepartment of Microbiology, The University of Chicago, Chicago, IL 60637, USA. Electronic address: grandall@bsd.uchicago.edu.
University of Chicago · US

Funding

Molecular And Cellular Biology Training ProgramT32GM007183 · NIGMS · UNIVERSITY OF CHICAGO · PI GLICK, BENJAMIN S, RICE, PHOEBE A · 1985 to 2021
$23.9M
Hepatitis C Virus Trafficking in HepatocytesR01AI137514 · NIAID · UNIVERSITY OF CHICAGO · PI Glenn C Randall · 2019 to 2026
$2.7M
Hepatitis C Virus Trafficking in Infected HepatocytesR01AI080703 · NIAID · UNIVERSITY OF CHICAGO · PI RANDALL, GLENN C · 2010 to 2014
$1.7M
Hepatitits C Virus Trafficking in Infected HepatocytesR56AI080703 · NIAID · UNIVERSITY OF CHICAGO · PI RANDALL, GLENN C · 2009 to 2017
$777k
NIAID NIH HHS R01 AI080703NIAID NIH HHS R56 AI080703NIGMS NIH HHS T32 GM007183
6 · The paper itself

Abstract

Hepatitis C virus (HCV) enters hepatocytes via various entry factors, including scavenger receptor BI (SR-B1), cluster of differentiation 81 (CD81), epidermal growth factor receptor (EGFR), claudin-1 (CLDN1), and occludin (OCLN). As CLDN1 and OCLN are not readily accessible due to their tight junctional localization, HCV likely accesses them by either disrupting cellular polarity or migrating to the tight junction. In this study, we image HCV entry into a three-dimensional polarized hepatoma system and reveal that the virus sequentially engages these entry factors through actin-dependent mechanisms. HCV initially localizes with the early entry factors SR-B1, CD81, and EGFR at the basolateral membrane and then accumulates at the tight junction in an actin-dependent manner. HCV associates with CLDN1 and then OCLN at the tight junction and is internalized via clathrin-mediated endocytosis by an active process requiring EGFR. Thus, HCV uses a dynamic and multi-step process to engage and enter host cells.

Indexed as

Virus InternalizationActinsCarcinoma, HepatocellularCell Culture TechniquesCell LineCell MembraneCell SurvivalClaudin-1EndocytosisErbB ReceptorsHepacivirusHepatitis CHost-Pathogen InteractionsHumansImaging, Three-DimensionalOccludinActinsCD81 protein, humanClaudin-1CLDN1 protein, humanErbB ReceptorsNS-5 protein, hepatitis C virusOccludinOCLN protein, humanRNA-Dependent RNA PolymeraseSCARB1 protein, humanScavenger Receptors, Class BTetraspanin 28Viral Nonstructural Proteinsactinclathrin endocytosisEGFR signalingHCV entryorganoidstight junctions

Identifiers

PMID29544098
PMCPMC7169308
OpenAlexW2790122594

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.