Evidence map›Paper›PMID 29100522›Full record

ArticleVirology journal2017

Investigation of antiviral state mediated by interferon-inducible transmembrane protein 1 induced by H9N2 virus and inactivated viral particle in human endothelial cells.

Bo Feng, Lihong Zhao, Wei Wang, Jianfang Wang, Hongyan Wang, Huiqin Duan, Jianjun Zhang, Jian Qiao

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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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 1 country.

Bo FengDepartment of Pathophysiology, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, People's Republic of China.
Lihong ZhaoDepartment of Pathophysiology, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, People's Republic of China.
Wei WangDepartment of Microbiology and Immunology, Shanxi Medical University, Taiyuan, 030001, Shanxi, People's Republic of China.
Jianfang WangBeijing Key Laboratory of Traditional Chinese Veterinary Medicine, Beijing University of Agriculture, Beijing, 102206, People's Republic of China.
Hongyan WangDepartment of Pathophysiology, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, People's Republic of China.
Huiqin DuanBeijing Key Laboratory of Traditional Chinese Veterinary Medicine, Beijing University of Agriculture, Beijing, 102206, People's Republic of China.
Jianjun ZhangBeijing Key Laboratory of Traditional Chinese Veterinary Medicine, Beijing University of Agriculture, Beijing, 102206, People's Republic of China.
Jian QiaoDepartment of Pathophysiology, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, People's Republic of China. qiaojian@cau.edu.cn.
China Agricultural University · CNBeijing University of Agriculture · CNShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndothelial cells are believed to play an important role in response to virus infection. Our previous microarray analysis showed that H9N2 virus infection and inactivated viral particle inoculation increased the expression of interferon-inducible transmembrane protein 1 (IFITM1) in human umbilical vein endothelial cells (HUVECs). In present study, we deeply investigated the expression patterns of IFITM1 and IFITM1-mediated antiviral response induced by H9N2 virus infection and inactivated viral particle inoculation in HUVECs. Epithelial cells that are considered target cells of the influenza virus were selected as a reference control.

methodsFirst, we quantified the expression levels of IFITM1 in HUVECs induced by H9N2 virus infection or viral particle inoculation using quantitative real-time PCR and western blot. Second, we observed whether hemagglutinin or neuraminidase affected IFITM1 expression in HUVECs. Finally, we investigated the effect of induced-IFITM1 on the antiviral state in HUVECs by siRNA and activation plasmid transfection.

resultsBoth H9N2 virus infection and viral particle inoculation increased the expression of IFITM1 without elevating the levels of interferon-ɑ/β in HUVECs. HA or NA protein binding alone is not sufficient to increase the levels of IFITM1 and interferon-ɑ/β in HUVECs. IFITM1 induced by viral particle inoculation significantly decreased the virus titers in culture supernatants of HUVECs.

conclusionsOur results showed that inactivated viral particle inoculation increased the expression of IFITM1 at mRNA and protein levels. Moreover, the induction of IFITM1 expression mediated the antiviral state in HUVECs.

Indexed as

Antigens, DifferentiationAntiviral AgentsCell LineHost-Pathogen InteractionsHumansHuman Umbilical Vein Endothelial CellsImmunity, InnateInfluenza A Virus, H9N2 SubtypeInterferon-alphaInterferon-betaRNA, Small InterferingVirionVirus InactivationAntigens, DifferentiationAntiviral AgentsInterferon-alphaInterferon-betaleu-13 antigenRNA, Small InterferingAntiviral stateH9N2 influenza virusHuman endothelial cellsHuman epithelial cellsIFITM1Inactivated viral particle

Identifiers

PMID29100522
PMCPMC5670731
OpenAlexW2765531046

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.