Evidence map›Paper›PMID 30072431›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Nur77 serves as a molecular brake of the metabolic switch during T cell activation to restrict autoimmunity.

Marie Liebmann, Stephanie Hucke, Kathrin Koch, Melanie Eschborn, Julia Ghelman, Achmet I Chasan, Shirin Glander, Martin Schädlich, Meike Kuhlencord, Niklas M Daber and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 122 citations in OpenAlex.

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  5. Coincident epithelial signals restrain commensal-specific CD8αβbioRxiv : the preprint server for biology · 2026
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  12. Controversy and multiple roles of the solitary nucleus receptor Nur77 in disease and physiology.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
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12 more citing papers are in PubMed but not listed here.

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

20 authors at 4 institutions in 1 country.

Marie LiebmannDepartment of Neurology with Institute of Translational Neurology, University Hospital Muenster, 48149 Muenster, Germany.
Stephanie HuckeDepartment of Neurology with Institute of Translational Neurology, University Hospital Muenster, 48149 Muenster, Germany.
Kathrin KochDepartment of Neurology with Institute of Translational Neurology, University Hospital Muenster, 48149 Muenster, Germany.
Melanie EschbornDepartment of Neurology with Institute of Translational Neurology, University Hospital Muenster, 48149 Muenster, Germany.
Julia GhelmanInstitute of Neuropathology, University Hospital Muenster, 48149 Muenster, Germany.
Achmet I ChasanInstitute of Immunology, University of Muenster, 48149 Muenster, Germany.
Shirin GlanderDepartment of Genetic Epidemiology, Institute of Human Genetics, University of Muenster, 48149 Muenster, Germany.
Martin SchädlichDepartment of Genetic Epidemiology, Institute of Human Genetics, University of Muenster, 48149 Muenster, Germany.
Meike KuhlencordInstitute of Immunology, University of Muenster, 48149 Muenster, Germany.
Niklas M DaberInstitute of Immunology, University of Muenster, 48149 Muenster, Germany.
Maria EveslageInstitute of Biostatistics and Clinical Research, University of Muenster, 48149 Muenster, Germany.
Marc BeyerDepartment of Genomics and Immunoregulation, Life and Medical Sciences Institute, University of Bonn, 53115 Bonn, Germany.
Michael DietrichDepartment of Neurology, University of Düsseldorf, 40225 Düsseldorf, Germany.
Philipp AlbrechtDepartment of Neurology, University of Düsseldorf, 40225 Düsseldorf, Germany.
Monika StollDepartment of Genetic Epidemiology, Institute of Human Genetics, University of Muenster, 48149 Muenster, Germany.
Karin B BuschInstitute for Molecular Cell Biology, University of Muenster, 48149 Muenster, Germany.
Heinz WiendlDepartment of Neurology with Institute of Translational Neurology, University Hospital Muenster, 48149 Muenster, Germany.
Johannes RothInstitute of Immunology, University of Muenster, 48149 Muenster, Germany.
Tanja KuhlmannInstitute of Neuropathology, University Hospital Muenster, 48149 Muenster, Germany.
Luisa KlotzDepartment of Neurology with Institute of Translational Neurology, University Hospital Muenster, 48149 Muenster, Germany; luisa.klotz@ukmuenster.de.
University Hospital Münster · DEHeinrich Heine University Düsseldorf · DEGerman Center for Neurodegenerative Diseases · DEInstitute of Molecular Biology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cells critically depend on reprogramming of metabolic signatures to meet the bioenergetic demands during activation and clonal expansion. Here we identify the transcription factor Nur77 as a cell-intrinsic modulator of T cell activation. Nur77-deficient T cells are highly proliferative, and lack of Nur77 is associated with enhanced T cell activation and increased susceptibility for T cell-mediated inflammatory diseases, such as CNS autoimmunity, allergic contact dermatitis and collagen-induced arthritis. Importantly, Nur77 serves as key regulator of energy metabolism in T cells, restricting mitochondrial respiration and glycolysis and controlling switching between different energy pathways. Transcriptional network analysis revealed that Nur77 modulates the expression of metabolic genes, most likely in close interaction with other transcription factors, especially estrogen-related receptor α. In summary, we identify Nur77 as a transcriptional regulator of T cell metabolism, which elevates the threshold for T cell activation and confers protection in different T cell-mediated inflammatory diseases.

Indexed as

AutoimmunityLymphocyte ActivationMitochondriaNuclear Receptor Subfamily 4, Group A, Member 1T-LymphocytesAnimalsCentral Nervous SystemERRalpha Estrogen-Related ReceptorGene Expression ProfilingInflammationMiceMice, KnockoutOxygen ConsumptionReceptors, EstrogenERRalpha Estrogen-Related ReceptorNr4a1 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 1Receptors, EstrogenautoimmunityimmunometabolismNur77T cells

Identifiers

PMID30072431
PMCPMC6112725
OpenAlexW2885687576

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.