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硫酯酶超家族成员 1 对肝脏脂肪酸转运的调节作用。

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

机构信息

Joan & Sanford I. Weill Department of Medicine, Weill Cornell Medical College, New York, NY 10021.

Department of Biochemistry, Boston University School of Medicine, Boston, MA 02118.

出版信息

J Lipid Res. 2018 Feb;59(2):368-379. doi: 10.1194/jlr.M081455. Epub 2017 Dec 5.

Abstract

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. 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 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 PPARα and promoted expression of gluconeogenic genes. These findings reveal a regulatory role for Them1 in hepatocellular fatty acid trafficking.

摘要

硫酯酶超家族成员 1(Them1)是一种酰基辅酶 A 硫酯酶,在棕色脂肪组织中高度表达,其功能是抑制能量消耗。高脂喂养时肝脏中 Them1 的表达水平降低。在肝脏中,高脂肪喂养会引起 Them1 表达水平升高。 Them1 敲除小鼠对饮食诱导的肥胖、肝脂肪变性和葡萄糖不耐受具有抗性,但 Them1 在肝脏中的作用尚不清楚。为了研究其肝脏特异性功能,我们构建了条件性转基因小鼠,当与 Them1 敲除小鼠杂交并激活时,它们在肝脏中特异性表达 Them1。具有肝脏特异性 Them1 表达的小鼠能量消耗没有变化。脂肪酸氧化率增加,而肝脏 VLDL 甘油三酯分泌率降低。当给予高脂肪饮食时,肝脏中 Them1 的表达促进了脂肪过量堆积,同时降低了脂肪酸氧化率并维持了甘油脂质的合成。肝脏特异性 Them1 表达不影响葡萄糖耐量或胰岛素敏感性,但在高脂肪喂养的动物中促进了肝糖异生。这归因于过量脂肪酸的产生,其激活了 PPARα 并促进了糖异生基因的表达。这些发现揭示了 Them1 在肝细胞脂肪酸转运中的调节作用。

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