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Loss of UCP1 function augments recruitment of futile lipid cycling for thermogenesis in murine brown fat

产热 产热素 褐色脂肪组织 脂滴 脂肪酸 生物 脂肪甘油三酯脂肪酶 脂肪酸合成 甘油三酯 白色脂肪组织 生物化学 内分泌学 化学 内科学
作者
Josef Oeckl,Petra Janovska,Katerina Adamcova,Kristina Bardova,Sarah Brunner,Sebastian Dieckmann,Josef Ecker,Tobias Fromme,Jiri Funda,Thomas Gantert,Piero Giansanti,Maria Soledad Hidrobo,Ondrej Kuda,Bernhard Kuster,Yongguo Li,Radek Pohl,Sabine Schmitt,Sabine Schweizer,Hans Zischka,Petr Zouhar,Jan Kopecky,Martin Klingenspor
出处
期刊:Molecular metabolism [Elsevier]
卷期号:: 101499-101499
标识
DOI:10.1016/j.molmet.2022.101499
摘要

Classical ATP-independent non-shivering thermogenesis enabled by uncoupling protein 1 (UCP1) in brown adipose tissue (BAT) is activated, but not essential for survival, in the cold. It has long been suspected that futile ATP-consuming substrate cycles also contribute to thermogenesis and can partially compensate for the genetic ablation of UCP1 in mouse models. Futile ATP-dependent thermogenesis could thereby enable survival in the cold even when brown fat is less abundant or missing. In this study, we explore different potential sources of UCP1-independent thermogenesis and identify a futile ATP-consuming triglyceride/fatty acid cycle as the main contributor to cellular heat production in brown adipocytes lacking UCP1. We uncover the mechanism on a molecular level and pinpoint the key enzymes involved using pharmacological and genetic interference. ATGL is the most important lipase in terms of releasing fatty acids from lipid droplets, while DGAT1 accounts for the majority of fatty acid re-esterification in UCP1-ablated brown adipocytes. Furthermore, we demonstrate that chronic cold exposure causes a pronounced remodeling of adipose tissues and leads to the recruitment of lipid cycling capacity specifically in BAT of UCP1-knockout mice, possibly fueled by fatty acids from white fat. Quantification of triglyceride/fatty acid cycling clearly shows that UCP1-ablated animals significantly increase turnover rates at room temperature and below. Our results suggest an important role for futile lipid cycling in adaptive thermogenesis and total energy expenditure. • A futile ATP-consuming triglyceride/fatty acid cycle is the main contributor to cellular heat production in brown adipocytes lacking UCP1. • ATGL is the most important lipase in terms of releasing fatty acids from lipid droplets, while DGAT1 accounts for the majority of fatty acid re-esterification. • UCP1-ablated animals significantly increase triglyceride/fatty acid cycling crates at room temperature and below.
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