4.6 Article

Regulation of fatty acid trafficking in liver by thioesterase superfamily member 1

Journal

JOURNAL OF LIPID RESEARCH
Volume 59, Issue 2, Pages 368-379

Publisher

ELSEVIER
DOI: 10.1194/jlr.M081455

Keywords

lipids; nonalcoholic fatty liver disease; obesity; triglycerides; fatty acid/metabolism; fatty acid/oxidation; very low density lipoprotein; fatty acyl-CoA

Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases [R01 DK103046]
  2. Harvard Digestive Diseases Center [P30 DK034854]
  3. American Liver Foundation

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Thioesterase superfamily member 1 (Them1) is an acyl-CoA thioesterase that is highly expressed in brown adipose tissue, where it functions to suppress energy expenditure. Lower Them1 expression levels in the liver are upregulated in response to high-fat feeding. Them1(-/-) mice are resistant to diet-induced obesity, hepatic steatosis, and glucose intolerance, but the contribution of Them1 in liver is unclear. To examine its liver-specific functions, we created conditional transgenic mice, which, when bred to Them1(-/-) mice and activated, expressed Them1 exclusively in the liver. Mice with liver-specific Them1 expression exhibited no changes in energy expenditure. Rates of fatty acid oxidation were increased, whereas hepatic VLDL triglyceride secretion rates were decreased by hepatic Them1 expression. When fed a high-fat diet, Them1 expression in liver promoted excess steatosis in the setting of reduced rates of fatty acid oxidation and preserved glycerolipid synthesis. Liver-specific Them1 expression did not influence glucose tolerance or insulin sensitivity, but did promote hepatic gluconeogenesis in high-fat-fed animals. This was attributable to the generation of excess fatty acids, which activated PPAR. and promoted expression of gluconeogenic genes. These findings reveal a regulatory role for Them1 in hepatocellular fatty acid trafficking.

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