dissipating capacity but how BAT modulates vascular function and atherosclerosis through
endocrine mechanisms remains poorly understood. Here we show that BAT-derived
neuregulin-4 (Nrg4) ameliorates atherosclerosis in mice. BAT-specific Nrg4 deficiency
accelerates vascular inflammation and adhesion responses, endothelial dysfunction and
apoptosis and atherosclerosis in male mice. BAT-specific Nrg4 restoration alleviates …