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A-FABP mediates adaptive thermogenesis by promoting intracellular activation of thyroid hormones in brown adipocytes.
- Source :
-
Nature communications [Nat Commun] 2017 Jan 27; Vol. 8, pp. 14147. Date of Electronic Publication: 2017 Jan 27. - Publication Year :
- 2017
-
Abstract
- 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.<br />Competing Interests: The authors declare no competing financial interests.
- Subjects :
- Adipose Tissue, Brown cytology
Adipose Tissue, Brown metabolism
Adipose Tissue, White metabolism
Animals
Cells, Cultured
Cytoplasm metabolism
Diet, High-Fat adverse effects
Disease Models, Animal
Energy Metabolism physiology
Fatty Acid-Binding Proteins genetics
Humans
Iodide Peroxidase metabolism
Liver X Receptors metabolism
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Obesity etiology
Obesity metabolism
Primary Cell Culture
Signal Transduction physiology
Iodothyronine Deiodinase Type II
Adipocytes, Brown metabolism
Fatty Acid-Binding Proteins physiology
Thermogenesis physiology
Thyroxine metabolism
Triiodothyronine metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 8
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 28128199
- Full Text :
- https://doi.org/10.1038/ncomms14147