摘要：SummaryBrown adipose tissue (BAT) has a role in maintaining systemic metabolic health in rodents and humans. Here, we show that metabolic stress induces BAT to produce coagulation factors, which then—together with molecules derived from the circulation—promote BAT dysfunction and systemic glucose intolerance. When mice were fed a high-fat diet (HFD), the levels of tissue factor, coagulation Factor VII (FVII), activated coagulation Factor X (FXa), and protease-activated receptor 1 (PAR1) expression increased significantly in BAT. Genetic or pharmacological suppression of coagulation factor-PAR1 signaling in BAT ameliorated its whitening and improved thermogenic response and systemic glucose intolerance in mice with dietary obesity. Conversely, the activation of coagulation factor-PAR1 signaling in BAT caused mitochondrial dysfunction in brown adipocytes and systemic glucose intolerance in mice fed normal chow. These results indicate that BAT produces endogenous coagulation factors that mediate pleiotropic effects via PAR1 signaling under metabolic stress.Graphical abstractDisplay OmittedHighlights•Coagulation factors and protease-activated receptor 1 (PAR1) are upregulated in brown adipose tissue (BAT) under metabolic stress•Inhibition of coagulation factor-PAR1 signaling in BAT improves metabolic dysfunction•Activation of coagulation factor-PAR1 signaling in BAT causes metabolic dysfunctionBiological sciences; Human Physiology; Human metabolism; Cell biology
