Adipocyte-secreted BMP8b mediates adrenergic-induced remodeling of the neuro-vascular network in adipose tissue

Vanessa Pellegrinelli(University of Cambridge), Vivian Peirce(University of Cambridge), Laura Howard(Cardiff University), Sam Virtue(University of Cambridge), Dénes Türei(European Bioinformatics Institute), Martina Senzacqua(Marche Polytechnic University), Andrea Frontini(University of Pavia), Jeffrey W. Dalley(University of Cambridge), Antony Horton(Cardiff University), Guillaume Bidault(University of Cambridge), Ilenia Severi(Marche Polytechnic University), Andrew J. Whittle(University of Cambridge), Kamal Rahmouni(University of Iowa), Julio Sáez-Rodríguez(European Bioinformatics Institute), Saverio Cinti(Marche Polytechnic University), Alun M. Davies(Cardiff University), Antonio Vidal‐Puig(Wellcome Sanger Institute)
Nature Communications
November 20, 2018
Cited by 129Open Access
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Abstract

Activation of brown adipose tissue-mediated thermogenesis is a strategy for tackling obesity and promoting metabolic health. BMP8b is secreted by brown/beige adipocytes and enhances energy dissipation. Here we show that adipocyte-secreted BMP8b contributes to adrenergic-induced remodeling of the neuro-vascular network in adipose tissue (AT). Overexpression of bmp8b in AT enhances browning of the subcutaneous depot and maximal thermogenic capacity. Moreover, BMP8b-induced browning, increased sympathetic innervation and vascularization of AT were maintained at 28 °C, a condition of low adrenergic output. This reinforces the local trophic effect of BMP8b. Innervation and vascular remodeling effects required BMP8b signaling through the adipocytes to 1) secrete neuregulin-4 (NRG4), which promotes sympathetic axon growth and branching in vitro, and 2) induce a pro-angiogenic transcriptional and secretory profile that promotes vascular sprouting. Thus, BMP8b and NRG4 can be considered as interconnected regulators of neuro-vascular remodeling in AT and are potential therapeutic targets in obesity.


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