The FASEB Journal · 2018 · 13 citations · 50 references
Life SciencesEndocrinologyPhysiologyMetabolic PhysiologyMetabolic RegulationMetabolismAdipose TissueFatty Acid MetabolismHormonal Control Of MetabolismInsulin ResistanceLipid MetabolismMetabolic SignalingAdipocyte Lipid MetabolismAdipocyte MetabolismAdipose Tissue Gene Expression ResponsesAdipose Tissue Lipid MetabolismBrown Adipose Tissue MetabolismLipid Metabolism RegulationMetabolic Rate RegulationThyroid Hormone Effects On Metabolic Rate
ABSTRACT Secretory phospholipase A 2 group IIA (PLA2G2A) is a phospholipase which has a role in inflammation, atherogenesis, and host defense. Previously, we found that PLA2G2A protects mice on high‐fat diets from weight gain and insulin resistance. Here, we examined the regulation of PLA2G2A and the metabolic changes that occur in response to variations in thyroid status. In particular, the impact of PLA2G2A on the brown adipose tissue (BAT) thermogenic gene expression was explored. We induced hypothyroidism in C57BL/6 and PLA2G2A‐overexpressing (IIA+) mice over a 10 wk period or treated them with thyroid hormone (T 3 ) for 5 wk. There were no significant changes in PLA2G2A abundance in response to thyroid status. The energy expenditure of hypothyroid IIA+ mice did not increase; however, the energy expenditure, substrate utilization, insulin sensitivity, and glucose tolerance were all elevated in the IIA+ mice given T 3 . Moreover, white adipocytes from IIA+ mice were much more prone to “beiging,” including increased expression of brown adipose thermogenic markers such as uncoupling protein 1 (UCP1), PR domain containing 16, and early B cell factor 2. Finally, the BAT of IIA+ mice had increased UCP1 and other proteins indicative of mitochondrial uncoupling and nonshivering adaptive thermogenesis. These data reveal a novel role for PLA2G2A on adipose tissue thermogenesis depending on thyroid status.—Kuefner, M. S., Deng, X., Stephenson, E. J., Pham, K., Park, E. A. Secretory phospholipase A2 group IIA enhances the metabolic rate and increases glucose utilization in response to thyroid hormone. FASEB J. 33, 738–749 (2019). www.fasebj.org
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