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Protein kinase D1 deletion in adipocytes enhances energy dissipation and protects against adiposity

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-176093
  • Nutrient overload in combination with decreased energy dissipation promotes obesity and diabetes. Obesity results in a hormonal imbalance, which among others, activates G-protein coupled receptors utilizing diacylglycerol (DAG) as secondary messenger. Protein kinase D1 (PKD1) is a DAG effector which integrates multiple nutritional and hormonal inputs, but its physiological role in adipocytes is unknown. Here, we show that PKD1 promotes lipogenesis and suppresses mitochondrial fragmentation, biogenesis, respiration, and energy dissipation in anNutrient overload in combination with decreased energy dissipation promotes obesity and diabetes. Obesity results in a hormonal imbalance, which among others, activates G-protein coupled receptors utilizing diacylglycerol (DAG) as secondary messenger. Protein kinase D1 (PKD1) is a DAG effector which integrates multiple nutritional and hormonal inputs, but its physiological role in adipocytes is unknown. Here, we show that PKD1 promotes lipogenesis and suppresses mitochondrial fragmentation, biogenesis, respiration, and energy dissipation in an AMP-activated protein kinase (AMPK)-dependent manner. Moreover, mice lacking PKD1 in adipocytes are resistant to diet-induced obesity due to elevated energy expenditure. Beiging of adipocytes promotes energy expenditure and counteracts obesity. Consistently, deletion of PKD1 promotes expression of the β3-adrenergic receptor (ADRB3) in a CCAAT/enhancerbinding protein (C/EBP)-α and δ-dependent manner, which leads to the elevated expression of beige markers in adipocytes and subcutaneous adipose tissue. Finally, deletion of PKD1 in adipocytes improves insulin sensitivity and ameliorates liver steatosis. Thus, loss of PKD1 in adipocytes increases energy dissipation by several complementary mechanisms and might represent an attractive strategy to treat obesity and its related complications.zeige mehrzeige weniger

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Autor(en): Mona C. LöfflerORCiD, Alexander E. Mayer, Jonathan Trujillo Viera, Angel Loza Valdes, Rabih El-Merahib, Carsten P. Ade, Till Karwen, Werner Schmitz, Anja Slotta, Manuela Erk, Sudha Janaki-Raman, Nuria Matesanz, Jorge L. Torres, Miguel Marcos, Guadalupe Sabio, Martin EilersORCiD, Almut Schulze, Grzegorz SumaraORCiD
URN:urn:nbn:de:bvb:20-opus-176093
Dokumentart:Preprint (Vorabdruck)
Institute der Universität:Medizinische Fakultät / Theodor-Boveri-Institut für Biowissenschaften
Fakultät für Biologie / Rudolf-Virchow-Zentrum
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):The EMBO Journal
Erscheinungsjahr:2018
Originalveröffentlichung / Quelle:The EMBO Journal (2018) 37, e99182. DOI 10.15252/embj.201899182
Allgemeine fachliche Zuordnung (DDC-Klassifikation):5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 572 Biochemie
6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):AMP-activated protein kinase (AMPK); Beige adipocytes; C/EBP; Protein kinase D1 (PKD1); β3 adrenergic receptor (ADRB3)
Datum der Freischaltung:21.02.2019
Embargo-Datum:15.05.2019
EU-Projektnummer / Contract (GA) number:260464
EU-Projektnummer / Contract (GA) number:678119
OpenAIRE:OpenAIRE
Lizenz (Deutsch):License LogoDeutsches Urheberrecht