Evidence map›Paper›PMID 32376590›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2020

[Phagocytosis of alveolar macrophages is suppressed in a mouse model of lipopolysaccharide-induced acute lung injury].

Qian Yang, Peiyu Gao, Mimi Mu, Xiangnan Tao, Jing He, Fengjiao Wu, Shujun Guo, Zhongqing Qian, Chuanwang Song

Open access · greenAbstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 59% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Emerging Effects of IL-33 on COVID-19.International journal of molecular sciences · 2022
    Review
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

9 authors at 2 institutions in 1 country.

Qian YangDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical College; Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu 233030, China.
Peiyu GaoDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical College; Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu 233030, China.
Mimi MuDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical College; Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu 233030, China.
Xiangnan TaoDepartment of Clinical Laboratory, Second Affiliated Hospital of Bengbu Medical College, Bengbu 233040, China.
Jing HeDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical College; Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu 233030, China.
Fengjiao WuDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical College; Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu 233030, China.
Shujun GuoDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical College; Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu 233030, China.
Zhongqing QianDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical College; Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu 233030, China.
Chuanwang SongDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical College; Anhui Provincial Key Laboratory of Infection and Immunity, Bengbu 233030, China.
Bengbu Medical College · CNThe Second Affiliated Hospital of Bengbu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the changes in phagocytic function of alveolar macrophages (AMs) in mice with lipopolysaccharide (LPS)-induced acute lung injury (ALI) and explore the possible mechanism.

methodsKunming mice were randomly divided into normal control group and ALI (induced by LPS instillation in the airway) model group. AMs were obtained from bronchoalveolar lavage fluid in both groups, and phagocytosis of the AMs was observed using flow cytometry and fluorescence microscopy. Western blotting and ELISA were used to detect the expression and secretion of IL-33 in the lung tissue of the mice. We also detected the secretion of IL-33 by an alveolar epithelial cell line MLE-12 in response to stimulation with different concentrations of LPS. The AMs from the normal control mice were treated with different concentrations of LPS and IL-33, and the changes in the phagocytic activity of the cells were observed.

resultsCompared with those in normal control group, the percentage of AMs phagocytosing fluorescent microspheres was significantly decreased, and the expression of IL-33 in lung tissue and IL-33 level in the bronchoalveolar lavage fluid were significantly increased in ALI mice (

conclusionsThe phagocytic activity of AMs is weakened in ALI mice possibly due to direct LPS stimulation and the inhibitory effect of the alarmin IL-33 produced by LPS-stimulated alveolar epithelial cells.

Indexed as

Acute Lung InjuryMacrophages, AlveolarAnimalsLipopolysaccharidesLungMicePhagocytosisLipopolysaccharidesacute lung injuryalveolar macrophageinterleukin-33lipopolysaccharidephagocytosis

Identifiers

PMID32376590
PMCPMC7167316
OpenAlexW3026804745

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.