Evidence map›Paper›PMID 41099430›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2025

Preadipocyte Uncoupling Protein 1 Expression Invoked by Fibroblast Growth Factors Imprints on Post-Differentiation White and Brown Adipocyte Phenotype.

Katharina Kuellmer, Carolin Mönch, Wilma Roch, Christine Wurmser, Patricia S S Petersen, Hildigunnur Hermannsdóttir, Mersiha Hasic, Brice Emanuelli, Tobias Fromme

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Katharina KuellmerChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
Carolin MönchChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
Wilma RochChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
Christine WurmserChair of Animal Physiology and Immunology, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
Patricia S S PetersenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Hildigunnur HermannsdóttirChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
Mersiha HasicChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
Brice EmanuelliNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Tobias FrommeChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.ORCID https://orcid.org/0000-0001-9150-2513

Funding

Deutsche Forschungsgemeinschaft (DFG) 450149205Deutsche Forschungsgemeinschaft (DFG) TRR333/1Novo Nordisk Foundation Center for Basic Metabolic Research (NovoNordisk Foundation Center for Basic Metabolic Research) NNF18CC0034900Novo Nordisk Foundation Center for Basic Metabolic Research (NovoNordisk Foundation Center for Basic Metabolic Research) NNF23SA0084103
6 · The paper itself

Abstract

Uncoupling protein 1 (UCP1) is a hallmark of thermogenic adipocytes and enables heat production by dissipating energy from mitochondrial proton motive force as heat. The purpose of its recently discovered presence in preadipocytes in response to certain fibroblast growth factors (FGFs) remains elusive. In this study, we systematically investigated the potential of all paracrine FGFs to invoke UCP1 expression in murine preadipocytes derived from interscapular brown and inguinal white adipose tissue. FGF2, FGF4, FGF8, and FGF9 induced UCP1 expression in undifferentiated preadipocytes, with FGF2 acting most potently and rapidly. This premature UCP1 induction did not translate into increased UCP1 thermogenic activity after complete adipogenic differentiation. Notably, preadipocyte treatment with FGFs and parallel UCP1 expression led to a sustained suppression of interferon-stimulated genes after differentiation. Preadipocyte UCP1 was required and sufficient for this lasting imprint. Thus, FGF-induced UCP1 expression in preadipocytes programs a lasting post-differentiation anti-inflammatory status.

Indexed as

Adipocytes, BrownAdipocytes, WhiteCell DifferentiationFibroblast Growth FactorsUncoupling Protein 1AdipogenesisAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsCells, CulturedMiceMice, Inbred C57BLPhenotypeThermogenesisFibroblast Growth FactorsUcp1 protein, mouseUncoupling Protein 1adipocyte differentiationfibroblast growth factor signalinginflammatory signalingnon‐thermogenic UCP1preadipocyte programmingsingle‐cell RNA‐sequencinguncoupling protein 1

Identifiers

PMID41099430
PMCPMC12529888

What Socratic 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 Socratic graph.