BMP8B Increases Brown Adipose Tissue Thermogenesis through Both Central and Peripheral Actions
Author(s) -
Andrew J. Whittle,
Stefania Carobbio,
Luís Martins,
Marc Slawik,
Elayne Hondares,
María J. Vázquez,
Donald A. Morgan,
Robert I. Csikasz,
Rosalı́a Gallego,
Sergio Rodrı́guez-Cuenca,
Martin Dale,
Sam Virtue,
Francesc Villarroya,
Barbara Can,
Kamal Rahmouni,
Miguel López,
António Vidal-Puig
Publication year - 2012
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2012.02.066
Subject(s) - thermogenesis , biology , ampk , endocrinology , medicine , brown adipose tissue , protein kinase a , amp activated protein kinase , adipose tissue , phosphorylation , microbiology and biotechnology
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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