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

BACKGROUND: G 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...

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Autores principales: Suchý, Tomáš, Zieschang, Christian, Popkova, Yulia, Kaczmarek, Isabell, Weiner, Juliane, Liebing, Aenne-Dorothea, Çakir, Mehmet Volkan, Landgraf, Kathrin, Gericke, Martin, Pospisilik, John Andrew, Körner, Antje, Heiker, John T., Dannenberger, Dirk, Schiller, Jürgen, Schöneberg, Torsten, Liebscher, Ines, Thor, Doreen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508673/
https://www.ncbi.nlm.nih.gov/pubmed/32203115
http://dx.doi.org/10.1038/s41366-020-0570-2
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author Suchý, Tomáš
Zieschang, Christian
Popkova, Yulia
Kaczmarek, Isabell
Weiner, Juliane
Liebing, Aenne-Dorothea
Çakir, Mehmet Volkan
Landgraf, Kathrin
Gericke, Martin
Pospisilik, John Andrew
Körner, Antje
Heiker, John T.
Dannenberger, Dirk
Schiller, Jürgen
Schöneberg, Torsten
Liebscher, Ines
Thor, Doreen
author_facet Suchý, Tomáš
Zieschang, Christian
Popkova, Yulia
Kaczmarek, Isabell
Weiner, Juliane
Liebing, Aenne-Dorothea
Çakir, Mehmet Volkan
Landgraf, Kathrin
Gericke, Martin
Pospisilik, John Andrew
Körner, Antje
Heiker, John T.
Dannenberger, Dirk
Schiller, Jürgen
Schöneberg, Torsten
Liebscher, Ines
Thor, Doreen
author_sort Suchý, Tomáš
collection PubMed
description BACKGROUND: G 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. METHODS: The 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). RESULTS: More 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. CONCLUSIONS: Adhesion 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.
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spelling pubmed-75086732020-10-05 The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance Suchý, Tomáš Zieschang, Christian Popkova, Yulia Kaczmarek, Isabell Weiner, Juliane Liebing, Aenne-Dorothea Çakir, Mehmet Volkan Landgraf, Kathrin Gericke, Martin Pospisilik, John Andrew Körner, Antje Heiker, John T. Dannenberger, Dirk Schiller, Jürgen Schöneberg, Torsten Liebscher, Ines Thor, Doreen Int J Obes (Lond) Article BACKGROUND: G 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. METHODS: The 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). RESULTS: More 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. CONCLUSIONS: Adhesion 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. Nature Publishing Group UK 2020-03-19 2020 /pmc/articles/PMC7508673/ /pubmed/32203115 http://dx.doi.org/10.1038/s41366-020-0570-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Suchý, Tomáš
Zieschang, Christian
Popkova, Yulia
Kaczmarek, Isabell
Weiner, Juliane
Liebing, Aenne-Dorothea
Çakir, Mehmet Volkan
Landgraf, Kathrin
Gericke, Martin
Pospisilik, John Andrew
Körner, Antje
Heiker, John T.
Dannenberger, Dirk
Schiller, Jürgen
Schöneberg, Torsten
Liebscher, Ines
Thor, Doreen
The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance
title The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance
title_full The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance
title_fullStr The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance
title_full_unstemmed The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance
title_short The repertoire of Adhesion G protein-coupled receptors in adipocytes and their functional relevance
title_sort repertoire of adhesion g protein-coupled receptors in adipocytes and their functional relevance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508673/
https://www.ncbi.nlm.nih.gov/pubmed/32203115
http://dx.doi.org/10.1038/s41366-020-0570-2
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