Evidence map›Paper›PMID 28542361›Full record

ArticlePloS one2017

Granulocyte colony-stimulating factor blockade enables dexamethasone to inhibit lipopolysaccharide-induced murine lung neutrophils.

Jesus Banuelos, Yun Cao, Soon Cheon Shin, Bruce S Bochner, Pedro Avila, Shihong Li, Xin Jiang, Mark W Lingen, Robert P Schleimer, Nick Z Lu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Circadian variation in pulmonary inflammatory responses is independent of rhythmic glucocorticoid signaling in airway epithelial cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
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

10 authors at 2 institutions in 1 country.

Jesus BanuelosDivision of Allergy-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Yun CaoDivision of Allergy-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Soon Cheon ShinDivision of Allergy-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Bruce S BochnerDivision of Allergy-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Pedro AvilaDivision of Allergy-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Shihong LiDepartment of Pharmacology and Human Tissue Resource Center, The University of Chicago, Chicago, Illinois, United States of America.
Xin JiangDepartment of Pharmacology and Human Tissue Resource Center, The University of Chicago, Chicago, Illinois, United States of America.
Mark W LingenDepartment of Pharmacology and Human Tissue Resource Center, The University of Chicago, Chicago, Illinois, United States of America.
Robert P SchleimerDivision of Allergy-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Nick Z LuDivision of Allergy-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.ORCID http://orcid.org/0000-0003-0679-3999
Northwestern University · USUniversity of Chicago · US

Funding

Glucocorticosteroid Action In Inflammatory DiseaseR37HL068546 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHLEIMER, ROBERT P · 2009 to 2018
$3.5M
Glucocorticoid induced G-CSF in lung inflammationR56HL133058 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LU, NICK · 2016 to 2016
$391k
NHLBI NIH HHS R37 HL068546NHLBI NIH HHS R56 HL133058
6 · The paper itself

Abstract

Glucocorticoids promote neutrophilic inflammation, the mechanisms of which are poorly characterized. Using a lipopolysaccharide (LPS)-induced acute murine lung injury model, we determined the role of granulocyte colony-stimulating factor (G-CSF) in mouse lung neutrophil numbers in the absence and presence of dexamethasone, a potent glucocorticoid. G-CSF was blocked using a neutralizing antibody. Airway neutrophil numbers, cytokine levels, and lung injury parameters were measured. Glucocorticoid treatment maintained LPS-induced airway G-CSF while suppressing TNF and IL-6. The addition of anti-G-CSF antibodies enabled dexamethasone to decrease airway G-CSF, neutrophils, and lung injury scores. In LPS-challenged murine lungs, structural cells and infiltrating leukocytes produced G-CSF. In vitro using BEAS 2B bronchial epithelial cells, A549 lung epithelial cells, human monocyte-derived macrophages, and human neutrophils, we found that dexamethasone and proinflammatory cytokines synergistically induced G-CSF. Blocking G-CSF production in BEAS 2B cells using shRNAs diminished the ability of BEAS 2B cells to protect neutrophils from undergoing spontaneous apoptosis. These data support that G-CSF plays a role in upregulation of airway neutrophil numbers by dexamethasone in the LPS-induced acute lung injury model.

Indexed as

AnimalsCells, CulturedCytokinesDexamethasoneGlucocorticoidsGranulocyte Colony-Stimulating FactorHumansLipopolysaccharidesLungLung InjuryMacrophagesMiceMice, Inbred BALB CNeutrophilsCytokinesDexamethasoneGlucocorticoidsGranulocyte Colony-Stimulating FactorLipopolysaccharides

Identifiers

PMID28542361
PMCPMC5438114
OpenAlexW2614724526

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.