Evidence map›Paper›PMID 25291985›Full record

ArticleMucosal immunology2015

Maturation of mast cell progenitors to mucosal mast cells during allergic pulmonary inflammation in mice.

L G Bankova, D F Dwyer, A Y Liu, K F Austen, M F Gurish

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

45 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Observational
  20. 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

5 authors at 2 institutions in 1 country.

L G BankovaDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
D F DwyerDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
A Y LiuDivision of Immunology and Allergy, Department of Pediatrics, Stanford University School of Medicine, Palo Alto, California, USA.
K F AustenDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
M F GurishDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Brigham and Women's Hospital · USStanford University · US

Funding

THE ROLE OF NATURAL ANTIBODY IN REPERFUSION INJURYP50GM052585 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI MOORE, FRANCIS D · 1995 to 2011
$17.1M
IMMUNOLOGIC BASIS OF RESISTANCE AND HYPERSENSITIVITYT32AI007306 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Nora Amanda Barrett, Joshua A Boyce · 1985 to 2026
$12.2M
Mechanisms of Pulmonary Mast Cell Recruitment and MaturationR01AI083516 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI GURISH, MICHAEL FAGERSTEN · 2009 to 2012
$1.6M
NIAID NIH HHS R01 AI083516NIAID NIH HHS R01-AI083516NIAID NIH HHS T32 AI007306NIAID NIH HHS T32-AI007306NIGMS NIH HHS P50 GM052585NIGMS NIH HHS P50-GM52585
6 · The paper itself

Abstract

In contrast to resident constitutive mast cells (CMCs), mucosal MCs (MMCs) appear in the lung and trachea of sensitized mice only following inhalation challenge. We monitored the influx and maturation of MCs by their expression of Kit, FcɛRI, β7-integrin and side scatter (SSC) by flow cytometry. Influx of MC progenitors (MCps) (FcɛRI(lo), Kit(int), β7(hi), and SSC(lo)) peaks 1 day after challenges and subsides to baseline by day 7 after challenge. The mature MMCs appear as a distinct population on day 7 and peak at day 14 with higher SSC and FcɛRI expression, but lower β7 and Kit expression. A distinct transitional population is present between 1 and 7 days after challenge. Maturation occurs more rapidly in the trachea. The resident tracheal CMCs had higher SSC, FcɛRI, and Kit and lower β7-integrin expression than the MMCs. By histology, the MMCs follow similar kinetics to the flow cytometry-identified mature MMCs and are notably persistent for >42 days. Steroid treatment reduced inflammation and MCp influx but had no effect on established MMCs. Thus, changes in SSC, FcɛRI, and Kit together with the expression of αE/α4:β7-integrins characterizes the development of induced MMCs from MCps and distinguishes them from resident CMCs in the trachea and large airways.

Indexed as

AnimalsAnti-Inflammatory AgentsCell DifferentiationGene Expression ProfilingGene Expression RegulationIntegrin beta ChainsMast CellsMiceMice, Inbred BALB COvalbuminPneumoniaPrednisoneProto-Oncogene Proteins c-kitReceptors, IgERespiratory HypersensitivitySignal TransductionAnti-Inflammatory Agentsintegrin beta7Integrin beta ChainsOvalbuminPrednisoneProto-Oncogene Proteins c-kitReceptors, IgE

Identifiers

PMID25291985
PMCPMC4390399
OpenAlexW2090205957

What OpenQuestion holds

Textmetadata
LicenceTDM
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.