301. Adipose Tissue CLK2 Promotes Energy Expenditure during High-Fat Diet Intermittent Fasting.
- Author
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Hatting M, Rines AK, Luo C, Tabata M, Sharabi K, Hall JA, Verdeguer F, Trautwein C, and Puigserver P
- Subjects
- Adipocytes, Brown metabolism, Adipose Tissue metabolism, Adipose Tissue, Brown metabolism, Animals, Cyclic AMP Response Element-Binding Protein metabolism, Disease Progression, Feeding Behavior, Mice, Knockout, Obesity enzymology, Obesity pathology, Organ Specificity, Oxygen Consumption, Phosphorylation, Protein Phosphatase 2 metabolism, Protein Serine-Threonine Kinases deficiency, Protein-Tyrosine Kinases deficiency, Uncoupling Protein 1 metabolism, Up-Regulation, Adipose Tissue enzymology, Diet, High-Fat, Energy Metabolism, Fasting metabolism, Protein Serine-Threonine Kinases metabolism, Protein-Tyrosine Kinases metabolism
- Abstract
A promising approach to treating obesity is to increase diet-induced thermogenesis in brown adipose tissue (BAT), but the regulation of this process remains unclear. Here we find that CDC-like kinase 2 (CLK2) is expressed in BAT and upregulated upon refeeding. Mice lacking CLK2 in adipose tissue exhibit exacerbated obesity and decreased energy expenditure during high-fat diet intermittent fasting. Additionally, tissue oxygen consumption and protein levels of UCP1 are reduced in CLK2-deficient BAT. Phosphorylation of CREB, a transcriptional activator of UCP1, is markedly decreased in BAT cells lacking CLK2 due to enhanced CREB dephosphorylation. Mechanistically, CREB dephosphorylation is rescued by the inhibition of PP2A, a phosphatase that targets CREB. Our results suggest that CLK2 is a regulatory component of diet-induced thermogenesis in BAT through increased CREB-dependent expression of UCP1., (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Published
- 2017
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