Evidence map›Paper›PMID 34954109›Full record

ArticleMolecular metabolism2022

Glucocorticoids coordinate macrophage metabolism through the regulation of the tricarboxylic acid cycle.

Ulrich Stifel, Eva-Maria Wolfschmitt, Josef Vogt, Ulrich Wachter, Sabine Vettorazzi, Daniel Tews, Melanie Hogg, Fabian Zink, Nora Maria Koll, Sandra Winning and 6 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

47 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
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  3. Immunometabolic Remodeling in Ischemic and Non-Ischemic Heart Failure.Journal of cardiovascular translational research · 2026
    Review
  4. Article
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  7. Timing of Glucocorticoid Treatment Dictates Glucocorticoid Receptor Actions Modulating the NLRP3-Inflammasome Activation in Macrophages.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  8. Article
  9. Review
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  13. Review
  14. Glucocorticoids regulate the human non-coding genome.bioRxiv : the preprint server for biology · 2025
    Article
  15. Weight Loss-Associated Remodeling of Adipose Tissue Immunometabolism.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Review
  16. Article
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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

16 authors at 6 institutions in 2 countries.

Ulrich StifelInstitute of Comparative Molecular Endocrinology (CME), Ulm University, Ulm, Germany.
Eva-Maria WolfschmittInstitute for Anesthesiological Pathophysiology and Process Engineering, and Department of Anesthesiology, University Hospital, Ulm, Germany.
Josef VogtInstitute for Anesthesiological Pathophysiology and Process Engineering, and Department of Anesthesiology, University Hospital, Ulm, Germany.
Ulrich WachterInstitute for Anesthesiological Pathophysiology and Process Engineering, and Department of Anesthesiology, University Hospital, Ulm, Germany.
Sabine VettorazziInstitute of Comparative Molecular Endocrinology (CME), Ulm University, Ulm, Germany.
Daniel TewsDivision of Pediatric Endocrinology and Diabetes, Department of Pediatric and Adolescent Medicine, Ulm University Medical Center, Ulm, Germany.
Melanie HoggInstitute for Anesthesiological Pathophysiology and Process Engineering, and Department of Anesthesiology, University Hospital, Ulm, Germany.
Fabian ZinkInstitute for Anesthesiological Pathophysiology and Process Engineering, and Department of Anesthesiology, University Hospital, Ulm, Germany.
Nora Maria KollInstitut fürPhysiologie, Universitätsklinikum Essen, Universität Duisburg-Essen, 45122, Essen, Germany.
Sandra WinningInstitut fürPhysiologie, Universitätsklinikum Essen, Universität Duisburg-Essen, 45122, Essen, Germany.
Rémi MounierInstitut NeuroMyoGène, Université Claude Bernard Lyon 1, CNRS UMR 5310, INSERM U1217, Université Lyon, Lyon, France.
Bénédicte ChazaudInstitut NeuroMyoGène, Université Claude Bernard Lyon 1, CNRS UMR 5310, INSERM U1217, Université Lyon, Lyon, France.
Peter RadermacherInstitute for Anesthesiological Pathophysiology and Process Engineering, and Department of Anesthesiology, University Hospital, Ulm, Germany.
Pamela Fischer-PosovszkyDepartment of Pediatric and Adolescent Medicine, Ulm University Medical Center, Ulm, Germany.
Giorgio CarattiInstitute of Comparative Molecular Endocrinology (CME), Ulm University, Ulm, Germany. Electronic address: giorgio.caratti@uni-ulm.de.
Jan TuckermannInstitute of Comparative Molecular Endocrinology (CME), Ulm University, Ulm, Germany. Electronic address: jan.tuckermann@uni-ulm.de.
Universität Ulm · DEUniversity Hospital Ulm · DECentre National de la Recherche Scientifique · FREssen University Hospital · DEInstitut NeuroMyoGène · FRUniversity of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesGlucocorticoids (GCs) are one of the most widely prescribed anti-inflammatory drugs. By acting through their cognate receptor, the glucocorticoid receptor (GR), GCs downregulate the expression of pro-inflammatory genes and upregulate the expression of anti-inflammatory genes. Metabolic pathways have recently been identified as key parts of both the inflammatory activation and anti-inflammatory polarization of macrophages, immune cells responsible for acute inflammation and tissue repair. It is currently unknown whether GCs control macrophage metabolism, and if so, to what extent metabolic regulation by GCs confers anti-inflammatory activity.

methodsUsing transcriptomic and metabolomic profiling of macrophages, we identified GC-controlled pathways involved in metabolism, especially in mitochondrial function.

resultsMetabolic analyses revealed that GCs repress glycolysis in inflammatory myeloid cells and promote tricarboxylic acid (TCA) cycle flux, promoting succinate metabolism and preventing intracellular accumulation of succinate. Inhibition of ATP synthase attenuated GC-induced transcriptional changes, likely through stalling of TCA cycle anaplerosis. We further identified a glycolytic regulatory transcription factor, HIF1α, as regulated by GCs, and as a key regulator of GC responsiveness during inflammatory challenge.

conclusionsOur findings link metabolism to gene regulation by GCs in macrophages.

Indexed as

Citric Acid CycleGlucocorticoidsHumansInflammationMacrophagesReceptors, GlucocorticoidGlucocorticoidsReceptors, GlucocorticoidGlucocorticoidsImmunometabolismMacrophageSuccinateTCA Cycle

Identifiers

PMID34954109
PMCPMC8783148
OpenAlexW4200196970

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.