Evidence map›Paper›PMID 26192732›Full record

ArticleAmerican journal of respiratory cell and molecular biology2016

CD11b(+) Mononuclear Cells Mitigate Hyperoxia-Induced Lung Injury in Neonatal Mice.

Laurie C Eldredge, Piper M Treuting, Anne M Manicone, Steven F Ziegler, William C Parks, John K McGuire

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Single-Cell Profiling of Premature Neonate Airways Reveals a Continuum of Myeloid Differentiation.American journal of respiratory cell and molecular biology · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Lung CD103American journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  11. Early origins of lung disease: towards an interdisciplinary approach.European respiratory review : an official journal of the European Respiratory Society · 2020
    Review
  12. Phenotypes of Bronchopulmonary Dysplasia.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. CD11bPhysiological reports · 2018
    Article
  17. Article
  18. Review
  19. Oxygen-dependent changes in lung development do not affect epithelial infection with influenza A virus.American journal of physiology. Lung cellular and molecular physiology · 2017
    Article
  20. Stat5 Is Required for CD103Journal of immunology (Baltimore, Md. : 1950) · 2017
    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

6 authors at 3 institutions in 5 countries.

Laurie C Eldredge1 Center for Lung Biology, and Department of Pediatrics, Divisions of.
Piper M Treuting3 Department of Comparative Medicine.
Anne M Manicone1 Center for Lung Biology, and Department of Pediatrics, Divisions of.
Steven F Ziegler6 Department of Immunology, University of Washington, Seattle, Washington; and.
William C Parks1 Center for Lung Biology, and Department of Pediatrics, Divisions of.
John K McGuire1 Center for Lung Biology, and Department of Pediatrics, Divisions of.
German Center for Lung Research · DEBritish Institute of International and Comparative Law · GBUniversity of Washington · US

Funding

E-cadherin shedding in chronic lung injuryR01HL093022 · NHLBI · UNIVERSITY OF WASHINGTON · PI MCGUIRE, JOHN K · 2010 to 2014
$2.0M
NHLBI NIH HHS R01 HL093022
6 · The paper itself

Abstract

Bronchopulmonary dysplasia (BPD) is a common consequence of life-saving interventions for infants born with immature lungs. Resident tissue myeloid cells regulate lung pathology, but their role in BPD is poorly understood. To determine the role of lung interstitial myeloid cells in neonatal responses to lung injury, we exposed newborn mice to hyperoxia, a neonatal mouse lung injury model with features of human BPD. In newborn mice raised in normoxia, we identified a CD45(+) F4/80(+) CD11b(+), Ly6G(lo-int) CD71(+) population of cells in lungs of neonatal mice present in significantly greater percentages than in adult mice. In response to hyperoxia, surface marker and gene expression in whole lung macrophages/monocytes was biased to an alternatively activated phenotype. Partial depletion of these CD11b(+) mononuclear cells using CD11b-diphtheria toxin (DT) receptor transgenic mice resulted in 60% mortality by 40 hours of hyperoxia exposure with more severe lung injury, perivascular edema, and alveolar hemorrhage compared with DT-treated CD11b-DT receptor-negative controls, which displayed no mortality. These results identify an antiinflammatory population of CD11b(+) mononuclear cells that are protective in hyperoxia-induced neonatal lung injury in mice, and suggest that enhancing their beneficial functions may be a treatment strategy in infants at risk for BPD.

Indexed as

AnimalsAnimals, NewbornBronchopulmonary DysplasiaCD11b AntigenDisease Models, AnimalHeparin-binding EGF-like Growth FactorHyperoxiaInflammation MediatorsLungLung InjuryMacrophage ActivationMacrophagesMice, Inbred C57BLMice, TransgenicPhenotypePulmonary EdemaCD11b AntigenHeparin-binding EGF-like Growth FactorInflammation Mediatorshyperoxiainterstitial macrophagelung developmentlung injurymacrophage polarization

Identifiers

PMID26192732
PMCPMC4821040
OpenAlexW1944756777

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.