Evidence map›Paper›PMID 32473405›Full record

ArticleMolecular metabolism2020

STAT5 is required for lipid breakdown and beta-adrenergic responsiveness of brown adipose tissue.

Doris Kaltenecker, Katrin Spirk, Frank Ruge, Florian Grebien, Marco Herling, Anne Rupprecht, Lukas Kenner, Elena E Pohl, Kristina M Mueller, Richard Moriggl

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2020. 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
1.9field-weighted citation impact, top 14% 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, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Adipose tissue lipid metabolism: lipolysis.Current opinion in genetics & development · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. STAT5 as a Key Protein of Erythropoietin Signalization.International journal of molecular sciences · 2021
    Review
  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

10 authors at 5 institutions in 2 countries.

Doris KalteneckerInstitute of Animal Breeding and Genetics, University of Veterinary Medicine, 1210, Vienna, Austria; Ludwig Boltzmann Institute for Cancer Research, 1090, Vienna, Austria; Institute for Diabetes and Cancer (IDC), Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Katrin SpirkInstitute of Animal Breeding and Genetics, University of Veterinary Medicine, 1210, Vienna, Austria; Ludwig Boltzmann Institute for Cancer Research, 1090, Vienna, Austria.
Frank RugeInstitute of Animal Breeding and Genetics, University of Veterinary Medicine, 1210, Vienna, Austria; Ludwig Boltzmann Institute for Cancer Research, 1090, Vienna, Austria.
Florian GrebienLudwig Boltzmann Institute for Cancer Research, 1090, Vienna, Austria; Institute for Medical Biochemistry, University of Veterinary Medicine, 1210, Vienna, Austria.
Marco HerlingLaboratory of Lymphocyte Signaling and Oncoproteome, Department I of Internal Medicine, CIO Aachen-Bonn-Cologne-Duesseldorf, Excellence Cluster for Cellular Stress Response and Aging-Associated Diseases (CECAD), Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
Anne RupprechtUnit of Physiology and Biophysics, University of Veterinary Medicine, 1210, Vienna, Austria.
Lukas KennerUnit of Pathology of Laboratory Animals, University of Veterinary Medicine, Vienna, 1210, Vienna, Austria; Department of Pathology, Medical University Vienna, 1090, Vienna, Austria; Christian Doppler Laboratory for Applied Metabolomics, Medical University Vienna, 1090, Vienna, Austria.
Elena E PohlUnit of Physiology and Biophysics, University of Veterinary Medicine, 1210, Vienna, Austria.
Kristina M MuellerInstitute of Animal Breeding and Genetics, University of Veterinary Medicine, 1210, Vienna, Austria; Ludwig Boltzmann Institute for Cancer Research, 1090, Vienna, Austria.
Richard MorigglInstitute of Animal Breeding and Genetics, University of Veterinary Medicine, 1210, Vienna, Austria; Ludwig Boltzmann Institute for Cancer Research, 1090, Vienna, Austria. Electronic address: richard.moriggl@vetmeduni.ac.at.
University of Veterinary Medicine Vienna · ATLudwig Boltzmann Institute for Cancer Research · ATCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEHelmholtz Zentrum München · DEMedical University of Vienna · AT

Funding

Austrian Science Fund FWF I 4157European Research Council 636855
6 · The paper itself

Abstract

objectiveIncreasing energy expenditure through activation of brown adipose tissue (BAT) thermogenesis is an attractive approach to counteract obesity. It is therefore essential to understand the molecular mechanisms that control BAT functions. Until now several members of the Janus kinase (JAK) - signal transducer and activator of transcription (STAT) pathway have been implicated as being relevant for BAT physiology. However, whether the STAT family member STAT5 is important for the thermogenic property of adipose tissues is unknown. Therefore, we have investigated the role of STAT5 in thermogenic fat in this paper.

methodsWe performed metabolic and molecular analyses using mice that harbor an adipocyte-specific deletion of Stat5a/b alleles.

resultsWe found that STAT5 is necessary for acute cold-induced temperature maintenance and the induction of lipid mobilization in BAT following β

conclusionWe conclude that STAT5 is essential for the functionality and the β-adrenergic responsiveness of thermogenic adipose tissue.

Indexed as

AdipocytesAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsCold-Shock ResponseEnergy MetabolismFemaleLipid MetabolismLipidsLipolysisMaleMiceMice, Inbred C57BLMice, KnockoutMitochondriaObesityLipidsReceptors, Adrenergic, betaStat5a protein, mouseSTAT5 Transcription FactorJAK-STATTemperature maintenanceThermogenesisβ-adrenergic signalling

Identifiers

PMID32473405
PMCPMC7322099
OpenAlexW3028969822

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.