Evidence map›Paper›PMID 35920128›Full record

ArticleCell proliferation2022

GDF11 inhibits adipogenesis and improves mature adipocytes metabolic function via WNT/β-catenin and ALK5/SMAD2/3 pathways.

Jan Frohlich, Kristina Kovacovicova, Marco Raffaele, Tereza Virglova, Eliska Cizkova, Jan Kucera, Julie Bienertova-Vasku, Martin Wabitsch, Marion Peyrou, Francesca Bonomini and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Activin Actions in Adipocytes.The Journal of clinical endocrinology and metabolism · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. GDF11: An emerging therapeutic target for liver diseases and fibrosis.Journal of cellular and molecular medicine · 2024
    Review
  13. Article
  14. Article
  15. 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

17 authors at 8 institutions in 6 countries.

Jan FrohlichInternational Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
Kristina KovacovicovaInternational Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
Marco RaffaeleInternational Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
Tereza VirglovaInternational Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
Eliska CizkovaInternational Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
Jan KuceraResearch Center for Toxic Compounds in the Environment (RECETOX), Masaryk University, Brno, Czech Republic.
Julie Bienertova-VaskuResearch Center for Toxic Compounds in the Environment (RECETOX), Masaryk University, Brno, Czech Republic.
Martin WabitschDivision of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University of Ulm, Ulm, Germany.
Marion PeyrouDepartament de Bioquímica i Biomedicina Molecular and Institut de Biomedicina, Universitat de Barcelona, Barcelona, Spain.
Francesca BonominiAnatomy and Physiopathology Division, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
Rita RezzaniAnatomy and Physiopathology Division, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
George N ChaldakovDepartment of Translational Stem Cell Biology, Research Institute of the Medical University, Varna, Bulgaria.
Anton B TonchevDepartment of Translational Stem Cell Biology, Research Institute of the Medical University, Varna, Bulgaria.
Michelino Di RosaDepartment of Biomedical and Biotechnological Sciences, Human Anatomy and Histology Section, School of Medicine, University of Catania, Catania, Italy.
Nicolas BlavetCEITEC-Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
Vaclav HejretCEITEC-Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
Manlio VinciguerraInternational Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.ORCID https://orcid.org/0000-0002-1768-3894
University Hospital Brno · CZMedical University of Varna · BGCentral European Institute of Technology · CZMasaryk University · CZUniversity of Brescia · ITHospital Sant Joan de Déu Barcelona · ESUniversität Ulm · DEUniversity of Catania · IT

Funding

European Regional Development Fund CZ.02.1.01/0.0/0.0/15_003/0000492Horizon 2020 Framework Programme Project 856871-TRANSTEM
6 · The paper itself

Abstract

objectiveGDF11 is a member of the TGF-β superfamily that was recently implicated as potential "rejuvenating" factor, which can ameliorate metabolic disorders. The main objective of the presented study was to closely characterize the role of GDF11 signaling in the glucose homeostasis and in the differentiation of white adipose tissue.

methodsWe performed microscopy imaging, biochemical and transcriptomic analyses of adipose tissues of 9 weeks old ob/ob mice and murine and human pre-adipocyte cell lines.

resultsOur in vivo experiments employing GDF11 treatment in ob/ob mice showed improved glucose/insulin homeostasis, decreased weight gain and white adipocyte size. Furthermore, GDF11 treatment inhibited adipogenesis in pre-adipocytes by ALK5-SMAD2/3 activation in cooperation with the WNT/β-catenin pathway, whose inhibition resulted in adipogenic differentiation. Lastly, we observed significantly elevated levels of the adipokine hormone adiponectin and increased glucose uptake by mature adipocytes upon GDF11 exposure.

conclusionWe show evidence that link GDF11 to adipogenic differentiation, glucose, and insulin homeostasis, which are pointing towards potential beneficial effects of GDF11-based "anti-obesity" therapy.

Indexed as

Adipogenesisbeta CateninAdipocytesAdiponectinAnimalsBone Morphogenetic ProteinsCell DifferentiationGlucoseGrowth Differentiation FactorsHumansInsulinMiceReceptor, Transforming Growth Factor-beta Type ISmad2 ProteinSmad3 ProteinSmad Proteins, Receptor-RegulatedAdiponectinbeta CateninBone Morphogenetic ProteinsGDF11 protein, humanGdf11 protein, mouseGlucoseGrowth Differentiation FactorsInsulinReceptor, Transforming Growth Factor-beta Type ISmad2 ProteinSMAD2 protein, humanSmad2 protein, mouseSmad3 ProteinSMAD3 protein, humanSmad3 protein, mouseSmad Proteins, Receptor-RegulatedTGFBR1 protein, humanTgfbr1 protein, mouseTransforming Growth Factor beta

Identifiers

PMID35920128
PMCPMC9528760
OpenAlexW4289711902

What OpenQuestion holds

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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.