Bahitham Wesam, Watts Russell, Nelson Randal, Lian Jihong, Lehner Richard
Group on Molecular and Cell Biology of Lipids, University of Alberta, Edmonton, Alberta T6G 2S2, Canada; Department of Pediatrics, University of Alberta, Edmonton, Alberta T6G 2S2, Canada; King Abdullah International Medical Research Center (KAIMRC), Jeddah, Saudi Arabia.
Group on Molecular and Cell Biology of Lipids, University of Alberta, Edmonton, Alberta T6G 2S2, Canada; Department of Pediatrics, University of Alberta, Edmonton, Alberta T6G 2S2, Canada.
Biochim Biophys Acta. 2016 May;1861(5):482-90. doi: 10.1016/j.bbalip.2016.03.009. Epub 2016 Mar 11.
Ces1g/Es-x deficiency in mice results in weight gain, insulin resistance, fatty liver and hyperlipidemia through upregulation of de novo lipogenesis and oversecretion of triacylglycerol (TG)-rich lipoproteins. Here, we show that restoration of Ces1g/Es-x expression only in the liver significantly reduced hepatic TG concentration accompanied by decreased size of lipid droplets, reduced secretion of very low-density lipoproteins and improved insulin-mediated signal transduction in the liver. Collectively, these results demonstrate that hepatic Ces1g/Es-x plays a critical role in limiting hepatic steatosis, very low-density lipoprotein assembly and in augmenting insulin sensitivity.
小鼠体内Ces1g/Es-x缺乏会通过上调从头脂肪生成和富含三酰甘油(TG)的脂蛋白过度分泌,导致体重增加、胰岛素抵抗、脂肪肝和高脂血症。在此,我们表明仅在肝脏中恢复Ces1g/Es-x表达可显著降低肝脏TG浓度,同时伴随着脂滴大小减小、极低密度脂蛋白分泌减少以及肝脏中胰岛素介导的信号转导改善。总体而言,这些结果表明肝脏中的Ces1g/Es-x在限制肝脏脂肪变性、极低密度脂蛋白组装以及增强胰岛素敏感性方面发挥着关键作用。