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Induction of Lipin1 by ROS-Dependent SREBP-2 Activation

机译:ROS依赖性SREBP-2激活诱导Lipin1

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摘要

Lipin1 was identified as a phosphatidate phosphatase enzyme, and it plays a key role in lipid metabolism. Since free radicals contribute to metabolic diseases in the liver, this study investigated the effects of free radicals on the regulation of Lipin1 expression in Huh7 and AML12 cells. Hydrogen peroxide induced mRNA and protein expression of Lipin1 in Huh7 cells, which was assayed by quantitative RT-PCR and immunoblotting, respectively. Induction of Lipin1 by hydrogen peroxide was confirmed in AML12 cells. Hydrogen peroxide treatment significantly increased expression of sterol regulatory element-binding protein (SREBP)-2, but not SREBP-1. Moreover, nuclear translocation of SREBP-2 was detected after hydrogen peroxide treatment. Hydrogen peroxide-induced Lipin1 or SREBP-2 expression was significantly reduced by N-acetyl-l-cysteine treatment, indicating that reactive oxygen species (ROS) were implicated in Lipin1 expression. Next, we investigated whether the hypoxic environments that cause endogenous ROS production in mitochondria in metabolic diseases affect the expression of Lipin1. Exposure to hypoxia also increased Lipin1 expression. In contrast, pretreatment with antioxidants attenuated hypoxia-induced Lipin1 expression. Collectively, our results show that ROS activate SREBP-2, which induces Lipin1 expression.
机译:Lipin1被鉴定为磷脂酰磷酸酶,在脂质代谢中起关键作用。由于自由基促成肝脏的代谢性疾病,因此本研究调查了自由基对Huh7和AML12细胞中Lipin1表达调控的影响。过氧化氢诱导Huh7细胞中Lipin1的mRNA和蛋白表达,分别通过定量RT-PCR和免疫印迹法进行检测。在AML12细胞中证实过氧化氢诱导Lipin1。过氧化氢处理显着增加了固醇调节元件结合蛋白(SREBP)-2的表达,但不增加SREBP-1的表达。此外,在过氧化氢处理后检测到SREBP-2的核易位。 N-乙酰基-1-半胱氨酸处理显着降低了过氧化氢诱导的Lipin1或SREBP-2的表达,表明活性氧(ROS)与Lipin1的表达有关。接下来,我们研究了在代谢性疾病的线粒体中引起内源性ROS产生的低氧环境是否会影响Lipin1的表达。暴露于缺氧也会增加Lipin1表达。相反,用抗氧化剂进行的预处理减弱了缺氧诱导的Lipin1表达。总体而言,我们的结果表明ROS激活SREBP-2,从而诱导Lipin1表达。

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