|Title||ANGPTL4 mediates shuttling of lipid fuel to brown adipose tissue during sustained cold exposure|
|Author(s)||Dijk, Wieneke; Heine, Markus; Vergnes, Laurent; Boon, Mariëtte R.; Schaart, Gert; Hesselink, Matthijs K.C.; Reue, Karen; Marken Lichtenbelt, Wouter D. van; Olivecrona, Gunilla; Rensen, Patrick C.N.; Heeren, Joerg; Kersten, Sander|
|Source||eLife 4 (2015). - ISSN 2050-084X - 23 p.|
Chair Nutrition Metabolism and Genomics
|Publication type||Refereed Article in a scientific journal|
Brown adipose tissue (BAT) activation via cold exposure is increasingly scrutinized as a potential approach to ameliorate cardio-metabolic risk. Transition to cold temperatures requires changes in the partitioning of energy substrates, re-routing fatty acids to BAT to fuel non-shivering thermogenesis. However, the mechanisms behind the redistribution of energy substrates to BAT remain largely unknown. Angiopoietin-like 4 (ANGPTL4), a protein that inhibits lipoprotein lipase (LPL) activity, is highly expressed in BAT. Here, we demonstrate that ANGPTL4 is part of a shuttling mechanism that directs fatty acids derived from circulating triglyceride-rich lipoproteins to BAT during cold. Specifically, we show that cold markedly down-regulates ANGPTL4 in BAT, likely via activation of AMPK, enhancing LPL activity and uptake of plasma triglyceride-derived fatty acids. In contrast, cold up-regulates ANGPTL4 in WAT, abolishing a cold-induced increase in LPL activity. Together, our data indicate that ANGPTL4 is an important regulator of plasma lipid partitioning during sustained cold.