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Analysis of vanin-1 upregulation and lipid accumulation in hepatocytes in response to a high-fat diet and free fatty acids

机译:高脂饮食和游离脂肪酸对Vanin-1上调和肝细胞脂质积累的分析

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摘要

High-fat diet is one of the causes of nonalcoholic fatty liver disease. We have previously demonstrated that high-fat diet induces upregulation of adipose differentiation-related protein mRNA expression accompanied by lipid droplet formation in mouse liver. Vanin-1 is a ubiquitous epithelial ectoenzyme that has pantetheinase activity and produces cysteamine, a potent endogenous antioxidant. In the present study, we analyzed the expression of hepatic vanin-1 mRNA following the administration of a high-fat diet in mice as well as free fatty acids in hepatocyte cultures and speculated its possible mechanism. Vanin-1 mRNA levels in the livers of mice were upregulated within a day of the high-fat diet, even before the expression of adipose differentiation-related protein mRNA and lipid accumulation. An in vitro analysis using HuH-7 cells revealed a significant upregulation of vanin-1 mRNA by as low as 0.01 mM oleic acid; however, lipid accumulation in hepatocytes was not affected at this concentration. Furthermore, vanin-1 mRNA was differentially upregulated by various free fatty acids irrespective of the grade of lipid accumulation. These findings indicate that the upregulation of vanin-1 precedes lipid accumulation and is differentially mediated by various types of free fatty acids in the model, presenting vanin-1 as a novel player in the pathogenesis of nonalcoholic fatty liver disease.
机译:高脂饮食是非酒精性脂肪肝的原因之一。我们以前已经证明,高脂饮食会诱导脂肪分化相关蛋白mRNA表达的上调,并伴随小鼠肝脏中脂质滴的形成。 Vanin-1是一种普遍存在的上皮外切酶,具有泛酶活性并产生半胱胺(一种有效的内源性抗氧化剂)。在本研究中,我们分析了高脂饮食对小鼠以及肝细胞培养物中游离脂肪酸给药后肝Vanin-1 mRNA表达的影响,并推测了其可能的机制。在高脂饮食的一天之内,甚至在脂肪分化相关蛋白的mRNA表达和脂质蓄积之前,小鼠肝脏中Vanin-1 mRNA的水平就会上调。使用HuH-7细胞进行的体外分析显示,低至0.01 mM的油酸可显着上调Vanin-1 mRNA;但是,在此浓度下,肝细胞中的脂质蓄积不受影响。此外,vanin-1 mRNA被各种游离脂肪酸差异上调,而与脂质积累的等级无关。这些发现表明,vanin-1的上调先于脂质蓄积,并由模型中的各种类型的游离脂肪酸差异介导,从而将vanin-1视为非酒精性脂肪肝疾病发病机理中的新型角色。

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