Transcriptome profiling of brown adipose tissue during cold exposure reveals extensive regulation of glucose metabolism

• Published in: American journal of physiology: endocrinology and metabolism Vol. 308; no. 5; pp. E380 - E392
• Main Authors: Hao, Qin, Yadav, Rachita, Basse, Astrid L, Petersen, Sidsel, Sonne, Si B, Rasmussen, Simon, Zhu, Qianhua, Lu, Zhike, Wang, Jun, Audouze, Karine, Gupta, Ramneek, Madsen, Lise, Kristiansen, Karsten, Hansen, Jacob B
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.03.2015
• Subjects: Acclimatization - genetics; Adipose Tissue, Brown - metabolism; Adipose Tissue, White - metabolism; Animals; Body fat; Body Temperature Regulation - genetics; Carbohydrate Metabolism - genetics; Cells, Cultured; Cold Temperature; Gene expression; Gene Expression Profiling; Glucose; Glucose - metabolism; Glycolysis - genetics; Male; Metabolism; Mice; Mice, Inbred C57BL; Ribonucleic acid; RNA; Rodents; Stress, Physiological - genetics; Transcriptome; pyruvate dehydrogenase; thermogenesis; glycolysis
• ISSN: 0193-1849; 1522-1555
• DOI: 10.1152/ajpendo.00277.2014

We applied digital gene expression profiling to determine the transcriptome of brown and white adipose tissues (BAT and WAT, respectively) during cold exposure. Male C57BL/6J mice were exposed to cold for 2 or 4 days. A notable induction of genes related to glucose uptake, glycolysis, glycogen metabolism, and the pentose phosphate pathway was observed in BAT from cold-exposed animals. In addition, glycerol-3-phosphate dehydrogenase 1 expression was induced in BAT from cold-challenged mice, suggesting increased synthesis of glycerol from glucose. Similarly, expression of lactate dehydrogenases was induced by cold in BAT. Pyruvate dehydrogenase kinase 2 (Pdk2) and Pdk4 were expressed at significantly higher levels in BAT than in WAT, and Pdk2 was induced in BAT by cold. Of notice, only a subset of the changes detected in BAT was observed in WAT. Based on changes in gene expression during cold exposure, we propose a model for the intermediary glucose metabolism in activated BAT: 1) fluxes through glycolysis and the pentose phosphate pathway are induced, the latter providing reducing equivalents for de novo fatty acid synthesis; 2) glycerol synthesis from glucose is increased, facilitating triacylglycerol synthesis/fatty acid re-esterification; 3) glycogen turnover and lactate production are increased; and 4) entry of glucose carbon into the tricarboxylic acid cycle is restricted by PDK2 and PDK4. In summary, our results demonstrate extensive and diverse gene expression changes related to glucose handling in activated BAT.