Evidence map›Paper›PMID 22879901›Full record

ArticlePloS one2012

Scavenger receptors in human airway epithelial cells: role in response to double-stranded RNA.

Audrey Dieudonné, David Torres, Simon Blanchard, Solenne Taront, Pascale Jeannin, Yves Delneste, Muriel Pichavant, François Trottein, Philippe Gosset

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
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  8. Experimental challenges regarding the in vitro investigation of the nanoparticle-biocorona in disease states.Toxicology in vitro : an international journal published in association with BIBRA · 2018
    Article
  9. Smoking-Dependent Distal-to-Proximal Repatterning of the Adult Human Small Airway Epithelium.American journal of respiratory and critical care medicine · 2017
    Article
  10. Article
  11. Article
  12. Formation of a protein corona on silver nanoparticles mediates cellular toxicity via scavenger receptors.Toxicological sciences : an official journal of the Society of Toxicology · 2015
    Article
  13. Innate receptors and cellular defense against pulmonary infections.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Review
  14. 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

9 authors at 4 institutions in 1 country.

Audrey DieudonnéInstitut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
David Torres
Simon Blanchard
Solenne Taront
Pascale Jeannin
Yves Delneste
Muriel Pichavant
François Trottein
Philippe Gosset
Inserm · FRCenter for Infection and Immunity of Lille · FRUniversité Nantes Angers Le Mans · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scavenger receptors and Toll-like receptors (TLRs) cooperate in response to danger signals to adjust the host immune response. The TLR3 agonist double stranded (ds)RNA is an efficient activator of innate signalling in bronchial epithelial cells. In this study, we aimed at defining the role played by scavenger receptors expressed by bronchial epithelial cells in the control of the innate response to dsRNA both in vitro and in vivo. Expression of several scavenger receptor involved in pathogen recognition was first evaluated in human bronchial epithelial cells in steady-state and inflammatory conditions. Their implication in the uptake of dsRNA and the subsequent cell activation was evaluated in vitro by competition with ligand of scavenger receptors including maleylated ovalbumin and by RNA silencing. The capacity of maleylated ovalbumin to modulate lung inflammation induced by dsRNA was also investigated in mice. Exposure to tumor necrosis factor-α increased expression of the scavenger receptors LOX-1 and CXCL16 and the capacity to internalize maleylated ovalbumin, whereas activation by TLR ligands did not. In contrast, the expression of SR-B1 was not modulated in these conditions. Interestingly, supplementation with maleylated ovalbumin limited dsRNA uptake and inhibited subsequent activation of bronchial epithelial cells. RNA silencing of LOX-1 and SR-B1 strongly blocked the dsRNA-induced cytokine production. Finally, administration of maleylated ovalbumin in mice inhibited the dsRNA-induced infiltration and activation of inflammatory cells in bronchoalveolar spaces and lung draining lymph nodes. Together, our data characterize the function of SR-B1 and LOX-1 in bronchial epithelial cells and their implication in dsRNA-induced responses, a finding that might be relevant during respiratory viral infections.

Indexed as

Administration, IntranasalAnimalsBronchiBronchoalveolar Lavage FluidCell MembraneCytokinesEndocytosisEpithelial CellsGene SilencingHumansLigandsMiceMice, Inbred C57BLOvalbuminPoly I-CReceptors, ScavengerCytokinesLigandsOvalbuminPoly I-CReceptors, ScavengerRNA, Double-StrandedRNA, Messenger

Identifiers

PMID22879901
PMCPMC3413698
OpenAlexW2024994521

What OpenQuestion holds

Textmetadata
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.