Evidence map›Paper›PMID 25105760›Full record

ArticlePloS one2014

PI3K/Akt signaling pathway modulates influenza virus induced mouse alveolar macrophage polarization to M1/M2b.

Xiangfeng Zhao, Jianping Dai, Xuejun Xiao, Liqi Wu, Jun Zeng, Jiangtao Sheng, Jinghua Su, Xiaoxuan Chen, Gefei Wang, Kangsheng Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed, 60 citations in OpenAlex.

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  15. Extracellular vesicles ofFrontiers in immunology · 2023
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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

10 authors at 3 institutions in 1 country.

Xiangfeng ZhaoDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Jianping DaiDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Xuejun XiaoDepartment of Nursing, Guilin Medical University, Guilin, Guangxi, China.
Liqi WuDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Jun ZengDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Jiangtao ShengDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Jinghua SuDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Xiaoxuan ChenDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Gefei WangDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Kangsheng LiDepartment of Microbiology and Immunology, Shantou University Medical College, College, Shantou, Guangdong, China.
Shantou University Medical College · CNShantou University · CNGuilin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages polarized to M1 (pro-inflammation) or M2 (anti-inflammation) phenotypes in response to environmental signals. In this study, we examined the polarization of alveolar macrophage (AM), following induction by different influenza virus strains (ST169 (H1N1), ST602 (H3N2) and HKG9 (H9N2)). Macrophages from other tissues or cell line exert alternative responding pattern, and AM is necessary for investigating the respiratory system. AM polarized toward the M1 phenotype after 4 hours of infection by all three virus strains, and AM to presented M2b phenotype after 8 hours induction, and immunosuppressive phenotype after 24 hours of induction. Protein expression assay showed similar results as the gene expression analysis for phenotype verification. The ELISA assay showed that TNF-α secretion was up-regulated after 4 and 8 hours of infection by influenza viruses, and it returned to basal levels after 24 hours of infection. IL-10 expression was elevated after 8 and 24 hours of infection. Immunofluorescence showed that iNOS expression was up-regulated but not Arg1 expression. Influenza virus notably increased phospho-Akt but not phospho-Erk1/2 or phospho-p38, and the AM polarization pattern have been changed by LY294002 (PI3K inhibitor). In conclusion, our results demonstrate the dynamic polarization of AM induced by influenza viruses, and suggested that PI3K/Akt signaling pathway modulates AM polarization to M1/M2b.

Indexed as

AnimalsFemaleHumansInfluenza A virusInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInfluenza A Virus, H9N2 SubtypeInfluenza, HumanInterleukin-10Macrophages, AlveolarMiceMice, Inbred C57BLNitric Oxide Synthase Type IIOrthomyxoviridae InfectionsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktInterleukin-10Nitric Oxide Synthase Type IIPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTumor Necrosis Factor-alpha

Identifiers

PMID25105760
PMCPMC4126709
OpenAlexW2043216363

What OpenQuestion holds

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Registered trials

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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.