A-FABP mediates adaptive thermogenesis by promoting intracellular activation of thyroid hormones in brown adipocytes

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作者
Lingling Shu
Ruby L. C. Hoo
Xiaoping Wu
Yong Pan
Ida P. C. Lee
Lai Yee Cheong
Stefan R Bornstein
Xianglu Rong
Jiao Guo
Aimin Xu
机构
[1] State Key Laboratory of Pharmaceutical Biotechnology,Department of Medicine
[2] LKS Faculty of Medicine,Department of Pharmacology and Pharmacy
[3] The University of Hong Kong,Department of Medicine
[4] LKS Faculty of Medicine,undefined
[5] The University of Hong Kong,undefined
[6] LKS Faculty of Medicine,undefined
[7] The University of Hong Kong,undefined
[8] University of Dresden,undefined
[9] Joint Laboratory of Guangdong and Hong Kong on Metabolic Diseases,undefined
[10] Guangdong Pharmaceutical University,undefined
来源
Nature Communications | / 8卷
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摘要
The adipokine adipocyte fatty acid-binding protein (A-FABP) has been implicated in obesity-related cardio-metabolic complications. Here we show that A-FABP increases thermogenesis by promoting the conversion of T4 to T3 in brown adipocytes. We find that A-FABP levels are increased in both white (WAT) and brown (BAT) adipose tissues and the bloodstream in response to thermogenic stimuli. A-FABP knockout mice have reduced thermogenesis and whole-body energy expenditure after cold stress or after feeding a high-fat diet, which can be reversed by infusion of recombinant A-FABP. Mechanistically, A-FABP induces the expression of type-II iodothyronine deiodinase in BAT via inhibition of the nuclear receptor liver X receptor α, thereby leading to the conversion of thyroid hormone from its inactive form T4 to active T3. The thermogenic responses to T4 are abrogated in A-FABP KO mice, but enhanced by A-FABP. Thus, A-FABP acts as a physiological stimulator of BAT-mediated adaptive thermogenesis.
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