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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Institute for Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands
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for 24 h. Cells were harvested in Tripure for further RT-PCR analysis of GR-responsive transcripts. Murine-immortalized brown adipocytes were generated and cultured as previously published ( Kroon et al . 2018 ) and exposure with DHT and
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mM glucose, 100 mM HEPES, 4% BSA, 1.5 mg/mL collagenase A (Sigma), 100 U/mL penicillin and 100 µg/mL streptomycin. Cells were expanded in DMEM supplemented with 15% FBS and were used within two passages. For SVF differentiation into brown adipocytes
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Park-Klinik Weissensee, Internal Medicine – Gastroenterology, Berlin, Germany
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processes are conferred via UCP1 protein ( Nicholls et al . 1978 ). The capacity of brown adipocytes to generate heat is precisely controlled by orchestration of environmental and hormonal factors as well as the sympathetic nervous system ( Richard et al
Department of Physiology, Naval Medical University, Shanghai, China
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NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Tianjin Medical University Chu Hsien-I Memorial Hospital and Tianjin Institute of Endocrinology, Tianjin, China
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, Rowland et al . 2015 , Bal et al . 2017 ). Mitochondrial function is the basis for NST of brown adipocytes. Mature mitochondria are highly dynamic with fission and fusion processes, which are essential for mitochondrion renewal and activity. There are
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-1 is induced in brown adipocytes by isoproterenol We tested whether isoproterenol’s effect on TIMP-1 mRNA is specific for 3T3-L1 adipocytes. For this purpose, differentiated immortalized brown adipocytes were treated with 10 μM
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β-adrenergic agonists or thiazolidinediones ( Ohno et al . 2012 , Wu et al . 2012 , Schulz & Tseng 2013 ). Brite adipocytes not only present gene expression signatures similar to those of canonical brown adipocytes (i.e. uncoupling protein 1
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gene profiling approaches have indicated that interscapular brown fat from human infants and neck brown fat from human adults shares features with classical murine brown adipocytes, while supraclavicular fat of adult humans mainly consists of beige
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or ARC increases food intake and RQ ( Currie et al . 2005 ). Therefore, the central effect of ghrelin on energy homeostasis may be mediated through the activation of GHS-R1a in the PVN and ARC. Brown adipocytes are important in the regulation of
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. 2009 , Zingaretti et al . 2009 ) and confirmed the existence of an inverse correlation between BMI and BAT activity. These observations have aroused considerable interest in the therapeutic potential of brown adipocytes for inducing weight loss, and
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adipogenic media, suggesting that this concentration (10 −5 M) may have a different effect to the other concentrations, possibly involving anti-differentiation, pro-apoptotic and/or toxic effects. Expression of gene markers of brown adipocytes As 1,25(OH) 2