Evidence map›Paper›PMID 32203115›Full record

ArticleInternational journal of obesity (2005)2020

The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance.

Tomáš Suchý, Christian Zieschang, Yulia Popkova, Isabell Kaczmarek, Juliane Weiner, Aenne-Dorothea Liebing, Mehmet Volkan Çakir, Kathrin Landgraf, Martin Gericke, John Andrew Pospisilik and 7 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of obesity (2005), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Glucose sensing and homeostasis by adipocyte GPCR.Frontiers in endocrinology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Methylation profiles at birth linked to early childhood obesity.Journal of developmental origins of health and disease · 2024
    Article
  15. Methylation profiles at birth linked to early childhood obesity.medRxiv : the preprint server for health sciences · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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 5 institutions in 2 countries.

Tomáš Suchý *Rudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany.
Christian Zieschang *Rudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany.
Yulia PopkovaInstitute for Medical Physics and Biophysics, Medical Faculty, Leipzig University, Leipzig, Germany.
Isabell KaczmarekRudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany.
Juliane WeinerDepartment of Endocrinology, Medical Faculty, Leipzig University, Leipzig, Germany.
Aenne-Dorothea LiebingRudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany.
Mehmet Volkan ÇakirRudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany.
Kathrin LandgrafCenter for Pediatric Research Leipzig, Hospital for Children & Adolescents, Medical Faculty, Leipzig University, Leipzig, Germany.ORCID http://orcid.org/0000-0002-6878-6033
Martin GerickeInstitute for Anatomy and Cell biology, Medical Faculty, Halle University, Halle (Saale), Germany.
John Andrew PospisilikVan Andel Research Institute, Grand Rapids, MI, 49503, USA.
Antje KörnerCenter for Pediatric Research Leipzig, Hospital for Children & Adolescents, Medical Faculty, Leipzig University, Leipzig, Germany.ORCID http://orcid.org/0000-0001-6001-0356
John T HeikerIFB Adiposity Diseases, Leipzig University, Leipzig, Germany.
Dirk DannenbergerLeibniz Institute for Farm Animal Biology, Institute of Muscle Biology and Growth, Dummerstorf, Germany.
Jürgen SchillerInstitute for Medical Physics and Biophysics, Medical Faculty, Leipzig University, Leipzig, Germany.
Torsten SchönebergRudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany.
Ines Liebscher *Rudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany. ines.liebscher@medizin.uni-leipzig.de.
Doreen Thor *Rudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany. doreen.thor@medizin.uni-leipzig.de.ORCID http://orcid.org/0000-0002-9522-5098
Leipzig University · DEHelmholtz Zentrum München · DEResearch Institute for Farm Animal Biology (FBN) · DEUniversity Hospital Leipzig · DEVan Andel Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundG protein-coupled receptors (GPCR) are well-characterized regulators of a plethora of physiological functions among them the modulation of adipogenesis and adipocyte function. The class of Adhesion GPCR (aGPCR) and their role in adipose tissue, however, is poorly studied. With respect to the demand for novel targets in obesity treatment, we present a comprehensive study on the expression and function of this enigmatic GPCR class during adipogenesis and in mature adipocytes.

methodsThe expression of all aGPCR representatives was determined by reanalyzing RNA-Seq data and by performing qPCR in different mouse and human adipose tissues under low- and high-fat conditions. The impact of aGPCR expression on adipocyte differentiation and lipid accumulation was studied by siRNA-mediated knockdown of all expressed members of this receptor class. The biological characteristics and function of mature adipocytes lacking selected aGPCR were analyzed by mass spectrometry and biochemical methods (lipolysis, glucose uptake, adiponectin secretion).

resultsMore than ten aGPCR are significantly expressed in visceral and subcutaneous adipose tissues and several aGPCR are differentially regulated under high-caloric conditions in human and mouse. Receptor knockdown of six receptors resulted in an impaired adipogenesis indicating their expression is essential for proper adipogenesis. The altered lipid composition was studied in more detail for two representatives, ADGRG2/GPR64 and ADGRG6/GPR126. While GPR126 is mainly involved in adipocyte differentiation, GPR64 has an additional role in mature adipocytes by regulating metabolic processes.

conclusionsAdhesion GPCR are significantly involved in qualitative and quantitative adipocyte lipid accumulation and can control lipolysis. Factors driving adipocyte formation and function are governed by signaling pathways induced by aGPCR yielding these receptors potential targets for treating obesity.

Indexed as

Adipogenesis3T3-L1 CellsAdipocytesAnimalsHumansLipid MetabolismLipolysisMaleMiceMice, Inbred C57BLReceptors, G-Protein-CoupledRNA-SeqReceptors, G-Protein-Coupled

Identifiers

PMID32203115
PMCPMC7508673
OpenAlexW3010698941

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.