Evidence map›Paper›PMID 30361541›Full record

ArticleScientific reports2018

Fibroblast gene expression following asthmatic bronchial epithelial cell conditioning correlates with epithelial donor lung function and exacerbation history.

Stephen R Reeves, Kaitlyn A Barrow, Tessa K Kolstad, Maria P White, Lucille M Rich, Thomas N Wight, Jason S Debley

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Circadian disruption in lung fibroblasts enhances NF-κB activity to exacerbate neutrophil recruitment.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
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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

7 authors at 3 institutions in 1 country.

Stephen R ReevesDivision of Pulmonary and Sleep Medicine, Seattle Children's Hospital, Seattle, WA, USA.
Kaitlyn A BarrowCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, USA.
Tessa K KolstadCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, USA.
Maria P WhiteCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, USA.
Lucille M RichCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, USA.
Thomas N WightMatrix Biology Program, Benaroya Research Institute, Seattle, WA, USA.
Jason S DebleyDivision of Pulmonary and Sleep Medicine, Seattle Children's Hospital, Seattle, WA, USA. jason.debley@seattlechildrens.org.ORCID http://orcid.org/0000-0001-6438-9535
Matrix Research (United States) · USSeattle Children's Hospital · USUniversity of Washington · US

Funding

Regulation of the Innate Immune Response by the Epithelium in AsthmaU19AI125378 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J · 2016 to 2020
$9.2M
Dysregulated Airway Epithelial Signaling as a Driver of Airway Remodeling in Asthmatic ChildrenR01HL128361 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI DEBLEY, JASON S · 2016 to 2018
$1.4M
Airway epithelial regulation of fibroblast hyaluronan and versican production in asthmatic airway inflammationK08HL135266 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI REEVES, STEPHEN R · 2017 to 2021
$812k
NHLBI NIH HHS K08 HL135266NHLBI NIH HHS R01 HL128361NIAID NIH HHS U19 AI125378U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) K08HL135266U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL128361U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) U19AI125378
6 · The paper itself

Abstract

Airway remodeling may contribute to decreased lung function in asthmatic children. Bronchial epithelial cells (BECs) may regulate fibroblast expression of extracellular matrix (ECM) constituents and fibroblast-to-myofibroblast transition (FMT). Our objective was to determine if human lung fibroblast (HLF) expression of collagen I (COL1A1), hyaluronan synthase 2 (HAS2), and the FMT marker alpha-smooth muscle actin (α-SMA) by HLFs conditioned by BECs from asthmatic and healthy children correlate with lung function measures and exacerbation history among BEC donors. BECs from asthmatic (n = 23) and healthy children (n = 15) were differentiated at an air-liquid interface (ALI) and then co-cultured with HLFs for 96 hours. Expression of COL1A1, HAS2, and α-SMA by HLFs was determined by quantitative polymerase chain reaction (qPCR). FMT was quantified by measuring HLF cytoskeletal α-SMA by flow cytometry. Pro-collagen Iα1, hyaluronan (HA), and PGE

Indexed as

Gene Expression RegulationTissue DonorsActinsAdolescentAsthmaBronchiChildCollagen Type ICytoskeletonDinoprostoneEpithelial CellsFemaleFibroblastsHumansHyaluronan SynthasesHyaluronic AcidACTA2 protein, humanActinsCollagen Type IDinoprostoneHyaluronan SynthasesHyaluronic Acid

Identifiers

PMID30361541
PMCPMC6202408
OpenAlexW2896089169

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.