Evidence map›Paper›PMID 17641296›Full record

ArticleAmerican journal of respiratory cell and molecular biology2007

Antigen-presenting cell population dynamics during murine silicosis.

Celine A Beamer, Andrij Holian

Abstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.6field-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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. The role of inflammation in silicosis.Frontiers in pharmacology · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Chronic endotoxin exposure produces airflow obstruction and lung dendritic cell expansion.American journal of respiratory cell and molecular biology · 2012
    Article
  16. Aryl hydrocarbon receptor (AhR) regulates silica-induced inflammation but not fibrosis.Toxicological sciences : an official journal of the Society of Toxicology · 2012
    Article
  17. Review
  18. Critical role of MARCO in crystalline silica-induced pulmonary inflammation.Toxicological sciences : an official journal of the Society of Toxicology · 2009
    Article
  19. Differential binding of inorganic particles to MARCO.Toxicological sciences : an official journal of the Society of Toxicology · 2009
    Article
  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

2 authors at 1 institution in 1 country.

Celine A BeamerCenter for Environmental Health Sciences, Department of Biomedical and Pharmaceutical Sciences, School of Pharmacy and Allied Health Sciences, University of Montana, Missoula, Montana 59812, USA. celine.beamer@umontana.edu
Andrij Holian
Center for Environmental Health · US

Funding

THE ROLE OF PULMONARY SUBPOPULATIONS AND TH2 IMMUNITY IN BALB/C SILICOSIS MODELP20RR017670 · NCRR · UNIVERSITY OF MONTANA · PI ROBERTS, KEVAN · 2002 to 2011
$22.0M
Molecular Histology and Fluorescent ImagingP30GM103338 · NIGMS · UNIVERSITY OF MONTANA · PI HOLIAN, ANDRIJ · 2013 to 2017
$5.6M
Defining the roles of macrophages subsets and NK lymphocytes in silicosisR01ES015294 · NIEHS · UNIVERSITY OF MONTANA · PI HOLIAN, ANDRIJ · 2007 to 2011
$1.6M
Akt activation sustains silica induced inflammationF32ES013044 · NIEHS · UNIVERSITY OF MONTANA · PI BEAMER, CELINE A · 2004 to 2006
$149k
NCRR NIH HHS P20 RR017670NCRR NIH HHS P20 RR17670NIEHS NIH HHS ES-013044NIEHS NIH HHS ES-015294NIEHS NIH HHS F32 ES013044NIEHS NIH HHS R01 ES015294NIGMS NIH HHS P30 GM103338
6 · The paper itself

Abstract

Silicosis is an occupational lung disease resulting from the inhalation of silica particles over prolonged periods of time, which causes chronic inflammation and progressive pulmonary fibrosis. Alveolar macrophages (AM) are critical effector cells, while less is known about the role and function of pulmonary dendritic cells (DC) in silicosis. We hypothesize that a balance exists between the suppressive nature of AM and the stimulatory capacity of DC to regulate lung immunity, and that this equilibrium may be overcome by silica exposure in vivo. Our results demonstrate that in response to silica exposure, both the percent and absolute number of AM significantly decreased over time, with a concomitant significant increase in DC. Both AM and DC exhibited cellular activation in response to silica, indicated by increased expression of cell surface markers. In the absence of silica-induced AM apoptosis (TNFR 1/2-null and Gld mice), no change was observed in the percent or absolute number of either cell type. Furthermore, bone marrow-derived DC, but not bone marrow-derived macrophages, migrated from the alveoli into the lung parenchyma in response to silica, resulting in significantly increased numbers of activated T lymphocytes. Collectively, the results demonstrate that AM and DC are distinct antigen-presenting cells within the respiratory tract that respond to silica exposure in vivo in unique ways, with significant implications for immune reactivity of the lung in response to environmental pathogens.

Indexed as

Administration, IntranasalAnimalsAntigen-Presenting CellsBone Marrow CellsBronchoalveolar Lavage FluidCD11c AntigenCell CountCell MovementCytokinesDendritic CellsFas Ligand ProteinKineticsLungMacrophages, AlveolarMiceMice, Inbred C57BLCD11c AntigenCytokinesFas Ligand ProteinReceptors, Tumor Necrosis Factor, Type IReceptors, Tumor Necrosis Factor, Type IISilicon DioxideTnfrsf1a protein, mouse

Identifiers

PMID17641296
PMCPMC2219550
OpenAlexW1988689331

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.