Evidence map›Paper›PMID 25953901›Full record

ArticleThe Journal of biological chemistry2015

Nuclear Receptor Nr4a2 Promotes Alternative Polarization of Macrophages and Confers Protection in Sepsis.

Sahil Mahajan, Ankita Saini, Vemika Chandra, Ravikanth Nanduri, Rashi Kalra, Ella Bhagyaraj, Neeraj Khatri, Pawan Gupta

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

58 citing papers in PubMed, 88 citations in OpenAlex.

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  13. Profiling Genome-Wide Methylation Patterns in Cattle Infected withInternational journal of molecular sciences · 2024
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  19. IGF2-NR4A2 Signaling Regulates Macrophage Subtypes to Attenuate Liver Cirrhosis.Journal of clinical and translational hepatology · 2023
    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

8 authors at 1 institution in 1 country.

Sahil MahajanFrom the Institute of Microbial Technology, Council of Scientific and Industrial Research, Chandigarh 160036, India.
Ankita SainiFrom the Institute of Microbial Technology, Council of Scientific and Industrial Research, Chandigarh 160036, India.
Vemika ChandraFrom the Institute of Microbial Technology, Council of Scientific and Industrial Research, Chandigarh 160036, India.
Ravikanth NanduriFrom the Institute of Microbial Technology, Council of Scientific and Industrial Research, Chandigarh 160036, India.
Rashi KalraFrom the Institute of Microbial Technology, Council of Scientific and Industrial Research, Chandigarh 160036, India.
Ella BhagyarajFrom the Institute of Microbial Technology, Council of Scientific and Industrial Research, Chandigarh 160036, India.
Neeraj KhatriFrom the Institute of Microbial Technology, Council of Scientific and Industrial Research, Chandigarh 160036, India.
Pawan GuptaFrom the Institute of Microbial Technology, Council of Scientific and Industrial Research, Chandigarh 160036, India pawan@imtech.res.in.
Council of Scientific and Industrial Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The orphan nuclear receptor Nr4a2 is known to modulate both inflammatory and metabolic processes, but the mechanism by which it regulates innate inflammatory homeostasis has not been adequately addressed. This study shows that exposure to ligands for Toll-like receptors (TLRs) robustly induces Nr4a2 and that this induction is tightly regulated by the PI3K-Akt signaling axis. Interestingly, exogenous expression of Nr4a2 in macrophages leads to their alternative phenotype with induction of genes that are prototypical M2 markers. Moreover, Nr4a2 transcriptionally activates arginase 1 expression by directly binding to its promoter. Adoptive transfer experiments revealed that increased survival of animals in endotoxin-induced sepsis is Nr4a2-dependent. Thus our data identify a previously unknown role for Nr4a2 in the regulation of macrophage polarization.

Indexed as

AnimalsCell PolarityGene Expression RegulationHumansInflammationLigandsLipopolysaccharidesMacrophagesMiceNuclear Receptor Subfamily 4, Group A, Member 2Phosphatidylinositol 3-KinasesPromoter Regions, GeneticProtein BindingProto-Oncogene Proteins c-aktSepsisSignal TransductionLigandsLipopolysaccharidesNr4a2 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 2Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktToll-Like ReceptorsArginase 1gene transcriptioninflammationM2 macrophagesmacrophageNr4a2nuclear receptorsepsis

Identifiers

PMID25953901
PMCPMC4513091
OpenAlexW1603125704

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.