Nature Communications · 2016 · 117 citations · 27 references
Life SciencesMolecular BiologyPhysiologyCell SignalingMolecular PhysiologySignal TransductionAdipocyte DifferentiationAdipose TissueCell Signaling NetworksG Protein-coupled Receptor SignalingMetabolic EndocrinologyMetabolic SignalingAdipocyte BiologyBrown Adipose Tissue BioenergeticsDifferentiationEndothelin Receptor SignalingG-protein-coupled ReceptorsUncoupling ProteinsWhite Adipose Tissue BiologyWhole-body Energy Expenditure
Brown adipose tissue (BAT) dissipates nutritional energy as heat via the uncoupling protein-1 (UCP1) and BAT activity correlates with leanness in human adults. Here we profile G protein-coupled receptors (GPCRs) in brown adipocytes to identify druggable regulators of BAT. Twenty-one per cent of the GPCRs link to the Gq family, and inhibition of Gq signalling enhances differentiation of human and murine brown adipocytes. In contrast, activation of Gq signalling abrogates brown adipogenesis. We further identify the endothelin/Ednra pathway as an autocrine activator of Gq signalling in brown adipocytes. Expression of a constitutively active Gq protein in mice reduces UCP1 expression in BAT, whole-body energy expenditure and the number of brown-like/beige cells in white adipose tissue (WAT). Furthermore, expression of Gq in human WAT inversely correlates with UCP1 expression. Thus, our data indicate that Gq signalling regulates brown/beige adipocytes and inhibition of Gq signalling may be a novel therapeutic approach to combat obesity.
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