Evidence map›Paper›PMID 31132962›Full record

ArticleEmerging microbes & infections2019

Endophilin-A2-mediated endocytic pathway is critical for enterovirus 71 entry into caco-2 cells.

Sheng-Lin Chen, Yan-Gang Liu, Yong-Tao Zhou, Ping Zhao, Hao Ren, Man Xiao, Yong-Zhe Zhu, Zhong-Tian Qi

Open access · goldAbstract read
In one paragraph

Article in Emerging microbes & infections, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

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  12. Application of Fucoidan in Caco-2 Model Establishment.Pharmaceuticals (Basel, Switzerland) · 2022
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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.

Sheng-Lin Chena Department of Microbiology, Shanghai Key Laboratory of Medical Biodefense , Second Military Medical University Shanghai , People's Republic of China.
Yan-Gang Liua Department of Microbiology, Shanghai Key Laboratory of Medical Biodefense , Second Military Medical University Shanghai , People's Republic of China.
Yong-Tao Zhoua Department of Microbiology, Shanghai Key Laboratory of Medical Biodefense , Second Military Medical University Shanghai , People's Republic of China.
Ping Zhaoa Department of Microbiology, Shanghai Key Laboratory of Medical Biodefense , Second Military Medical University Shanghai , People's Republic of China.
Hao Rena Department of Microbiology, Shanghai Key Laboratory of Medical Biodefense , Second Military Medical University Shanghai , People's Republic of China.
Man Xiaob General Hospital of the Tibet Military Area Command , Tibet , People's Republic of China.
Yong-Zhe Zhua Department of Microbiology, Shanghai Key Laboratory of Medical Biodefense , Second Military Medical University Shanghai , People's Republic of China.
Zhong-Tian Qia Department of Microbiology, Shanghai Key Laboratory of Medical Biodefense , Second Military Medical University Shanghai , People's Republic of China.
Second Military Medical University · CNGeneral Hospital of Jinan Military Command · CNMilitary Hospital · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enterovirus 71 (EV71) is typically transmitted by the oral-faecal route and initiates infection upon crossing the intestinal mucosa. Our limited understanding of the mechanisms by which it crosses the intestinal mucosa has hampered the development of effective therapeutic options. Here, using an RNA interference screen combined with chemical inhibitors or the overexpression of dominant negative proteins, we found that EV71 entry into Caco-2 cells, a polarized human intestinal epithelial cell line, does not involve clathrin- and caveolae-dependent endocytic pathways or macropinocytosis but requires GTP-binding protein dynamin 2 and cytoskeleton remodelling. The use of siRNAs targeting endophilin family members revealed that endophlin-A2 is essential for the uptake of EV71 particles by Caco-2 cells. Subcellular analysis revealed that internalized EV71 virions largely colocalized with endophilin-A2 at cytomembrane ruffles and in the perinuclear area. Combined with viral entry kinetics, these data suggest that EV71 enters Caco-2 cells mainly via an endophilin-A2-mediated endocytic (EME) pathway. Finally, we showed that internalized EV71 virions were transported to endosomal sorting complex required for transport (ESCRT)-related multivesicular bodies (MVBs). These data provide attractive therapeutic targets to block EV71 infection.

Indexed as

EndocytosisVirus InternalizationCaco-2 CellsEnterovirus A, HumanEnterovirus InfectionsEpithelial CellsHumansIntestinal MucosaIntracellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsSH3GL1 protein, humanendocytosisendophilinEnterovirus 71intestinal epithelial cellsviral entry

Identifiers

PMID31132962
PMCPMC6542187
OpenAlexW2947175610

What OpenQuestion holds

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LicenceCC BY
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.