Evidence map›Paper›PMID 32308197›Full record

ArticleVirology2020

Increased expression of microRNA-155-5p by alveolar type II cells contributes to development of lethal ARDS in H1N1 influenza A virus-infected mice.

Parker S Woods, Lauren M Doolittle, Lucia E Rosas, S Patrick Nana-Sinkam, Esmerina Tili, Ian C Davis

Open access · greenAbstract read
In one paragraph

Article in Virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Parker S WoodsDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
Lauren M DoolittleDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
Lucia E RosasDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA.
S Patrick Nana-SinkamDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine, Wexner Medical Center, Columbus, OH, USA.
Esmerina TiliDepartment of Cancer Biology and Genetics, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Ian C DavisDepartment of Veterinary Biosciences, College of Veterinary Medicine, Columbus, OH, USA. Electronic address: davis.2448@osu.edu.
The Ohio State University Wexner Medical Center · USThe Ohio State University · US

Funding

Role of alterations in the ATII cell lipidome in influenza pathogenesisR01HL137090 · NHLBI · OHIO STATE UNIVERSITY · PI DAVIS, IAN CHRISTOPHER · 2017 to 2020
$2.5M
The role of adenosine in the pathogenesis of influenzaR01HL102469 · NHLBI · OHIO STATE UNIVERSITY · PI DAVIS, IAN CHRISTOPHER · 2010 to 2014
$1.9M
Elucidating the role of miR-155 in the development of paralysis consecutive to spinal cord damage caused by thoracic-abdominal aortic aneurysm repair surgeryR03NS102861 · NINDS · OHIO STATE UNIVERSITY · PI TILI, ESMERINA · 2017 to 2018
$156k
NHLBI NIH HHS R01 HL102469NHLBI NIH HHS R01 HL137090NINDS NIH HHS R03 NS102861
6 · The paper itself

Abstract

Alveolar type II (ATII) cells are essential to lung function and a primary site of influenza A virus (IAV) replication. Effects of IAV infection on ATII cell microRNA (miR) expression have not been comprehensively investigated. Infection of C57BL/6 mice with 10,000 or 100 pfu/mouse of IAV A/WSN/33 (H1N1) significantly altered expression of 73 out of 1908 mature murine miRs in ATII cells at 2 days post-infection (d.p.i.) and 253 miRs at 6 d.p.i. miR-155-5p (miR-155) showed the greatest increase in expression within ATII cells at both timepoints and the magnitude of this increase correlated with inoculum size and pulmonary edema severity. Influenza-induced lung injury was attenuated in C57BL/6-congenic miR-155-knockout mice without affecting viral replication. Attenuation of lung injury was dependent on deletion of miR-155 from stromal cells and was recapitulated in ATII cell-specific miR-155-knockout mice. These data suggest that ATII cell miR-155 is a potential therapeutic target for IAV-induced ARDS.

Indexed as

Alveolar Epithelial CellsAnimalsFemaleHumansInfluenza A Virus, H1N1 SubtypeInfluenza, HumanMiceMice, Inbred C57BLMice, KnockoutMicroRNAsRespiratory Distress SyndromeMicroRNAsMirn155 microRNA, mouseAcute respiratory distress syndromeAlveolar type II cellInfluenza A virusmicroRNAMouse

Identifiers

PMID32308197
PMCPMC7199462
OpenAlexW3012909412

What OpenQuestion holds

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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.