Evidence map›Paper›PMID 28385809›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2017

Free actin impairs macrophage bacterial defenses via scavenger receptor MARCO interaction with reversal by plasma gelsolin.

Christine M Ordija, Terry Ting-Yu Chiou, Zhiping Yang, Glen M Deloid, Melina de Oliveira Valdo, Zhi Wang, Alice Bedugnis, Terry L Noah, Samuel Jones, Henry Koziel and 1 more

Open access · bronzeAbstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

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  13. Low Admission Plasma Gelsolin Concentrations Identify Community-acquired Pneumonia Patients at High Risk for Severe Outcomes.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
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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

11 authors at 4 institutions in 2 countries.

Christine M OrdijaDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Terry Ting-Yu ChiouDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Zhiping YangDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Glen M DeloidDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Melina de Oliveira ValdoDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Zhi WangDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Alice BedugnisDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Terry L NoahDepartment of Pediatrics, Pulmonology Division, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Samuel JonesDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and.
Henry KozielDivision of Pulmonary, Critical Care, and Sleep Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Lester KobzikDepartment of Environmental Health, Harvard T. H. Chan School of Public Health, Boston, Massachusetts; lkobzik@hsph.harvard.edu.
Harvard University · USUniversity of North Carolina at Chapel Hill · USBeth Israel Deaconess Medical Center · USChang Gung University · TW

Funding

Translational Research Support CoreP30ES000002 · NIEHS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI SUSAN A KORRICK · 1985 to 2026
$44.6M
Training Program in Molecular and Integrative Physiological SciencesT32HL007118 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI LU, QUAN · 1985 to 2025
$14.3M
Plasma Gelsolin and Host Defense After Lung InjuryR01HL115778 · NHLBI · HARVARD SCHOOL OF PUBLIC HEALTH · PI KOBZIK, LESTER · 2013 to 2016
$1.6M
NHLBI NIH HHS R01 HL115778NHLBI NIH HHS T32 HL007118NIEHS NIH HHS P30 ES000002
6 · The paper itself

Abstract

Lung injury can release intracellular actin into the alveolar milieu and is also associated with increased susceptibility to secondary infections. We investigated the effect of free (extracellular) actin on lung macrophage host defense functions. Western blot analysis demonstrated free actin release into the lung lavage fluids of mouse models of ozone injury, influenza infection, and secondary pneumococcal pneumonia and in samples from patients following burn and inhalation injury. Using levels comparable with those observed in lung injury, we found that free actin markedly inhibited murine lung macrophage binding and uptake in vitro of

Indexed as

ActinsAnimalsBacteriaFemaleGelsolinHumansLung InjuryMacrophages, AlveolarMaleMice, Inbred C57BLProtein BindingReceptors, ImmunologicReceptors, ScavengerActinsGelsolinMarco protein, mouseReceptors, ImmunologicReceptors, Scavengeractinalveolar macrophagesplasma gelsolinscavenger receptors

Identifiers

PMID28385809
PMCPMC5495953
OpenAlexW2604164147

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.