BMP8B Increases Brown Adipose Tissue Thermogenesis through Both Central and Peripheral Actions

Andrew J. Whittle(University of Cambridge), Stefania Carobbio(University of Cambridge), Luís Martins(Universidade de Santiago de Compostela), Marc Slawik(University of Cambridge), Elayne Hondares(Centro de Investigación Biomédica en Red), María J. Vázquez(Universidade de Santiago de Compostela), Donald A. Morgan(University of Iowa), Robert I. Csikasz(Stockholm University), Rosalı́a Gallego(Universidade de Santiago de Compostela), Sergio Rodríguez‐Cuenca(University of Cambridge), Martin Dale(University of Cambridge), Sam Virtue(University of Cambridge), Francesc Villarroya(Centro de Investigación Biomédica en Red), Barbara Cannon(Royal Veterinary College), Kamal Rahmouni(University of Iowa), Miguel López(Universidade de Santiago de Compostela), Antonio Vidal‐Puig(University of Cambridge)
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Abstract

Thermogenesis in brown adipose tissue (BAT) is fundamental to energy balance and is also relevant for humans. Bone morphogenetic proteins (BMPs) regulate adipogenesis, and, here, we describe a role for BMP8B in the direct regulation of thermogenesis. BMP8B is induced by nutritional and thermogenic factors in mature BAT, increasing the response to noradrenaline through enhanced p38MAPK/CREB signaling and increased lipase activity. Bmp8b(-/-) mice exhibit impaired thermogenesis and reduced metabolic rate, causing weight gain despite hypophagia. BMP8B is also expressed in the hypothalamus, and Bmp8b(-/-) mice display altered neuropeptide levels and reduced phosphorylation of AMP-activated protein kinase (AMPK), indicating an anorexigenic state. Central BMP8B treatment increased sympathetic activation of BAT, dependent on the status of AMPK in key hypothalamic nuclei. Our results indicate that BMP8B is a thermogenic protein that regulates energy balance in partnership with hypothalamic AMPK. BMP8B may offer a mechanism to specifically increase energy dissipation by BAT.


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