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Publication : Deletion of fatty acid transport protein 2 (FATP2) in the mouse liver changes the metabolic landscape by increasing the expression of PPARα-regulated genes.

First Author  Perez VM Year  2020
Journal  J Biol Chem Volume  295
Issue  17 Pages  5737-5750
PubMed ID  32188695 Mgi Jnum  J:289840
Mgi Id  MGI:6436444 Doi  10.1074/jbc.RA120.012730
Citation  Perez VM, et al. (2020) Deletion of fatty acid transport protein 2 (FATP2) in the mouse liver changes the metabolic landscape by increasing the expression of PPARalpha-regulated genes. J Biol Chem 295(17):5737-5750
abstractText  Fatty acid transport protein 2 (FATP2) is highly expressed in the liver, small intestine, and kidney, where it functions in both the transport of exogenous long-chain fatty acids and the activation of very-long-chain fatty acids. Here, using a murine model, we investigated the phenotypic impacts of deleting FATP2, followed by a transcriptomic analysis using unbiased RNA-Seq to identify concomitant changes in the liver transcriptome. WT and FATP2-null (Fatp2 (-/-)) mice (5 weeks) were maintained on a standard chow diet for 6 weeks. The Fatp2 (-/-) mice had reduced weight gain, lowered serum triglyceride, and increased serum cholesterol levels and attenuated dietary fatty acid absorption. Transcriptomic analysis of the liver revealed 258 differentially expressed genes in male Fatp2 (-/-) mice and a total of 91 in female Fatp2 (-/-) mice. These genes mapped to the following gene ontology categories: fatty acid degradation, peroxisome biogenesis, fatty acid synthesis, and retinol and arachidonic acid metabolism. Targeted RT-quantitative PCR verified the altered expression of selected genes. Of note, most of the genes with increased expression were known to be regulated by peroxisome proliferator-activated receptor alpha (PPARalpha), suggesting that FATP2 activity is linked to a PPARalpha-specific proximal ligand. Targeted metabolomic experiments in the Fatp2 (-/-) liver revealed increases of total C16:0, C16:1, and C18:1 fatty acids; increases in lipoxin A4 and prostaglandin J2; and a decrease in 20-hydroxyeicosatetraenoic acid. We conclude that the expression of FATP2 in the liver broadly affects the metabolic landscape through PPARalpha, indicating that FATP2 provides an important role in liver lipid metabolism through its transport or activation activities.
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