Increased Reliance on Muscle-based Thermogenesis upon Acute Minimization of Brown Adipose Tissue Function

• Published in: The Journal of biological chemistry 2016-08, Vol.291 (33), p.17247-17257
• Main Authors: Bal, Naresh C., Maurya, Santosh K., Singh, Sushant, Wehrens, Xander H.T., Periasamy, Muthu
• Format: Article
• Language: English
• Subjects: Adipose Tissue, Brown - metabolism; Animals; brown adipose tissue; Calcium Signaling - physiology; calcium transport; cold adaptation; Cold Temperature; core body temperature; Male; Metabolism; Mice; mitochondria; mitochondrial dynamics; mitochondrial metabolism; Muscle, Skeletal - metabolism; Oxygen Consumption - physiology; sarcoplasmic reticulum (SR); skeletal muscle; Thermogenesis - physiology
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M116.728188

Skeletal muscle has been suggested as a site of nonshivering thermogenesis (NST) besides brown adipose tissue (BAT). Studies in birds, which do not contain BAT, have demonstrated the importance of skeletal muscle-based NST. However, muscle-based NST in mammals remains poorly characterized. We recently reported that sarco/endoplasmic reticulum Ca2+ cycling and that its regulation by SLN can be the basis for muscle NST. Because of the dominant role of BAT-mediated thermogenesis in rodents, the role of muscle-based NST is less obvious. In this study, we investigated whether muscle will become an important site of NST when BAT function is conditionally minimized in mice. We surgically removed interscapular BAT (iBAT, which constitutes ∼70% of total BAT) and exposed the mice to prolonged cold (4 °C) for 9 days. The iBAT-ablated mice were able to maintain optimal body temperature (∼35–37 °C) during the entire period of cold exposure. After 4 days in the cold, both sham controls and iBAT-ablated mice stopped shivering and resumed routine physical activity, indicating that they are cold-adapted. The iBAT-ablated mice showed higher oxygen consumption and decreased body weight and fat mass, suggesting an increased energy cost of cold adaptation. The skeletal muscles in these mice underwent extensive remodeling of both the sarcoplasmic reticulum and mitochondria, including alteration in the expression of key components of Ca2+ handling and mitochondrial metabolism. These changes, along with increased sarcolipin expression, provide evidence for the recruitment of NST in skeletal muscle. These studies collectively suggest that skeletal muscle becomes the major site of NST when BAT activity is minimized.