Evidence map›Paper›PMID 27784615›Full record

ArticleBiochimica et biophysica acta. General subjects2017

Quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by alveolar macrophages.

Trudy Padmore, Carahline Stark, Leonid A Turkevich, Julie A Champion

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta. General subjects, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Review
  6. Article
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  15. Environmental science. Nano · 2024
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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

4 authors at 2 institutions in 1 country.

Trudy PadmoreChemical & Biomolecular Engineering, Georgia Institute of Technology, United States.
Carahline StarkChemical & Biomolecular Engineering, Georgia Institute of Technology, United States.
Leonid A TurkevichCEMB/DART/NIOSH/CDC, United States.
Julie A ChampionChemical & Biomolecular Engineering, Georgia Institute of Technology, United States. Electronic address: julie.champion@chbe.gatech.edu.
Georgia Institute of Technology · USNational Institute for Occupational Safety and Health · US

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

backgroundIn the lung, macrophages attempt to engulf inhaled high aspect ratio pathogenic materials, secreting inflammatory molecules in the process. The inability of macrophages to remove these materials leads to chronic inflammation and disease. How the biophysical and biochemical mechanisms of these effects are influenced by fiber length remains undetermined. This study evaluates the role of fiber length on phagocytosis and molecular inflammatory responses to non-cytotoxic fibers, enabling development of quantitative length-based models.

methodsMurine alveolar macrophages were exposed to short and long populations of JM-100 glass fibers, produced by successive sedimentation and repeated crushing, respectively. Interactions between fibers and macrophages were observed using time-lapse video microscopy, and quantified by flow cytometry. Inflammatory biomolecules (TNF-α, IL-1α, COX-2, PGE

resultsUptake of short fibers occurred more readily than for long, but long fibers were more potent stimulators of inflammatory molecules. Stimulation resulted in dose-dependent secretion of inflammatory biomolecules but no cytotoxicity or strong ROS production. Linear cytokine dose-response curves evaluated with length-dependent potency models, using measured fiber length distributions, resulted in identification of critical fiber lengths that cause frustrated phagocytosis and increased inflammatory biomolecule production.

conclusionShort fibers played a minor role in the inflammatory response compared to long fibers. The critical lengths at which frustrated phagocytosis occurs can be quantified by fitting dose-response curves to fiber distribution data. GENERAL SIGNIFICANCE: The single physical parameter of length can be used to directly assess the contributions of length against other physicochemical fiber properties to disease endpoints.

Indexed as

AnimalsCells, CulturedCyclooxygenase 2DinoprostoneEvaluation Studies as TopicGlassInflammationInterleukin-1alphaMacrophagesMacrophages, AlveolarMicePhagocytosisReactive Oxygen SpeciesTumor Necrosis Factor-alphaCyclooxygenase 2DinoprostonefiberglassInterleukin-1alphaReactive Oxygen SpeciesTumor Necrosis Factor-alphaFrustrated phagocytosisGlass fibersLengthMacrophageTNF-α: Tumor necrosis factor-α

Identifiers

PMID27784615
PMCPMC5228597
OpenAlexW2535627036

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.