Evidence map›Paper›PMID 28912382›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2017

Versican is produced by Trif- and type I interferon-dependent signaling in macrophages and contributes to fine control of innate immunity in lungs.

Mary Y Chang, Inkyung Kang, Michael Gale, Anne M Manicone, Michael G Kinsella, Kathleen R Braun, Tara Wigmosta, William C Parks, William A Altemeier, Thomas N Wight and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

44 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The mouse pubic symphysis: a narrative review.Frontiers in physiology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Defining the versican interactome in lung health and disease.American journal of physiology. Cell physiology · 2022
    Review
  14. Proteoglycans in Toll-like receptor responses and innate immunity.American journal of physiology. Cell physiology · 2022
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review
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

11 authors at 3 institutions in 1 country.

Mary Y ChangComparative Pathology Program, Department of Comparative Medicine, University of Washington School of Medicine, Seattle, Washington.
Inkyung KangMatrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington.
Michael GaleDepartment of Immunology, University of Washington School of Medicine, Seattle, Washington.
Anne M ManiconeDivision of Pulmonary and Critical Care Medicine, Department of Medicine, University of Washington School of Medicine, Seattle, Washington; and.
Michael G KinsellaMatrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington.
Kathleen R BraunMatrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington.
Tara WigmostaComparative Pathology Program, Department of Comparative Medicine, University of Washington School of Medicine, Seattle, Washington.
William C ParksDivision of Pulmonary and Critical Care Medicine, Department of Medicine, University of Washington School of Medicine, Seattle, Washington; and.
William A AltemeierDivision of Pulmonary and Critical Care Medicine, Department of Medicine, University of Washington School of Medicine, Seattle, Washington; and.
Thomas N WightMatrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington.
Charles W FrevertComparative Pathology Program, Department of Comparative Medicine, University of Washington School of Medicine, Seattle, Washington; cfrevert@uw.edu.ORCID http://orcid.org/0000-0002-1037-3244
University of Washington · USVirginia Mason Medical Center · USCedars-Sinai Medical Center · US

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Karin E Bornfeldt · 1986 to 2026
$41.4M
West Nile Virus and host control of innate defensesU19AI083019 · NIAID · UNIVERSITY OF WASHINGTON · PI DIAMOND, MICHAEL S · 2009 to 2018
$22.5M
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
Impact of versican deficiency on the innate immune response to influenza virusR01AI136468 · NIAID · UNIVERSITY OF WASHINGTON · PI ALTEMEIER, WILLIAM A, FREVERT, CHARLES WAYNE · 2018 to 2022
$3.1M
MMP28 Regulation Of Macrophage Recruitment and PolarizationR01HL116514 · NHLBI · UNIVERSITY OF WASHINGTON · PI MANICONE, ANNE M. · 2014 to 2018
$2.2M
PDGFR-beta+ stromal cells as critical regulators of immune response to tissue injuryR01HL122895 · NHLBI · UNIVERSITY OF WASHINGTON · PI ALTEMEIER, WILLIAM A · 2015 to 2018
$1.7M
Gene-targeted mouse models to study the function of versicanR21RR030249 · NCRR · UNIVERSITY OF WASHINGTON · PI FREVERT, CHARLES WAYNE · 2010 to 2011
$388k
NCRR NIH HHS R21 RR030249NHLBI NIH HHS R01 HL116514NHLBI NIH HHS R01 HL122895NIAID NIH HHS R01 AI136468NIAID NIH HHS U19 AI083019NIAID NIH HHS U19 AI125378NIDDK NIH HHS P30 DK017047
6 · The paper itself

Abstract

Growing evidence suggests that versican is important in the innate immune response to lung infection. Our goal was to understand the regulation of macrophage-derived versican and the role it plays in innate immunity. We first defined the signaling events that regulate versican expression, using bone marrow-derived macrophages (BMDMs) from mice lacking specific Toll-like receptors (TLRs), TLR adaptor molecules, or the type I interferon receptor (IFNAR1). We show that LPS and polyinosinic-polycytidylic acid [poly(I:C)] trigger a signaling cascade involving TLR3 or TLR4, the Trif adaptor, type I interferons, and IFNAR1, leading to increased expression of versican by macrophages and implicating versican as an interferon-stimulated gene. The signaling events regulating versican are distinct from those for hyaluronan synthase 1 (HAS1) and syndecan-4 in macrophages. HAS1 expression requires TLR2 and MyD88. Syndecan-4 requires TLR2, TLR3, or TLR4 and both MyD88 and Trif. Neither HAS1 nor syndecan-4 is dependent on type I interferons. The importance of macrophage-derived versican in lungs was determined with LysM/

Indexed as

Immunity, InnateAdaptor Proteins, Vesicular TransportAnimalsHyaluronan SynthasesInterferon-betaInterleukin-10LipopolysaccharidesLungMacrophages, AlveolarMiceMice, KnockoutReceptor, Interferon alpha-betaSyndecan-4Toll-Like ReceptorsVersicansAdaptor Proteins, Vesicular TransportHyaluronan SynthasesIfnar1 protein, mouseIL10 protein, mouseInterferon-betaInterleukin-10lipopolysaccharide, Escherichia coli O111 B4LipopolysaccharidesReceptor, Interferon alpha-betaSdc4 protein, mouseSyndecan-4Ticam1 protein, mouseToll-Like ReceptorsVcan protein, mouseVersicanshyaluronan synthase 1inflammationtype I interferonsversican, syndecan-4

Identifiers

PMID28912382
PMCPMC5814701
OpenAlexW2755496644

What OpenQuestion holds

Textmetadata
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.