Tiwari Samata, Siddiqi Shaila, Zhelyabovska Olga, Siddiqi Shadab A
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida 32827.
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida 32827.
J Biol Chem. 2016 Jun 10;291(24):12514-12526. doi: 10.1074/jbc.M115.705269. Epub 2016 Apr 15.
The transport of nascent very low density lipoprotein (VLDL) particles from the endoplasmic reticulum (ER) to the Golgi determines their secretion by the liver and is mediated by a specialized ER-derived vesicle, the VLDL transport vesicle (VTV). Our previous studies have shown that the formation of ER-derived VTV requires proteins in addition to coat complex II proteins. The VTV proteome revealed that a 9-kDa protein, small valosin-containing protein-interacting protein (SVIP), is uniquely present in these specialized vesicles. Our biochemical and morphological data indicate that the VTV contains SVIP. Using confocal microscopy and co-immunoprecipitation assays, we show that SVIP co-localizes with apolipoprotein B-100 (apoB100) and specifically interacts with VLDL apoB100 and coat complex II proteins. Treatment of ER membranes with myristic acid in the presence of cytosol increases SVIP recruitment to the ER in a concentration-dependent manner. Furthermore, we show that myristic acid treatment of hepatocytes increases both VTV budding and VLDL secretion. To determine the role of SVIP in VTV formation, we either blocked the SVIP protein using specific antibodies or silenced SVIP by siRNA in hepatocytes. Our results show that both blocking and silencing of SVIP lead to significant reduction in VTV formation. Additionally, we show that silencing of SVIP reduces VLDL secretion, suggesting a physiological role of SVIP in intracellular VLDL trafficking and secretion. We conclude that SVIP acts as a novel regulator of VTV formation by interacting with its cargo and coat proteins and has significant implications in VLDL secretion by hepatocytes.
新生极低密度脂蛋白(VLDL)颗粒从内质网(ER)向高尔基体的转运决定了它们由肝脏分泌,并且由一种特殊的源自内质网的囊泡——VLDL转运囊泡(VTV)介导。我们之前的研究表明,源自内质网的VTV的形成除了需要II型被膜小泡蛋白外还需要其他蛋白质。VTV蛋白质组显示,一种9 kDa的蛋白质,即小含缬酪肽蛋白相互作用蛋白(SVIP),独特地存在于这些特殊的囊泡中。我们的生化和形态学数据表明,VTV含有SVIP。利用共聚焦显微镜和免疫共沉淀分析,我们发现SVIP与载脂蛋白B-100(apoB100)共定位,并特异性地与VLDL apoB100和II型被膜小泡蛋白相互作用。在胞质溶胶存在的情况下用肉豆蔻酸处理内质网膜,会以浓度依赖的方式增加SVIP向内质网的募集。此外,我们发现用肉豆蔻酸处理肝细胞会增加VTV出芽和VLDL分泌。为了确定SVIP在VTV形成中的作用我们要么使用特异性抗体阻断SVIP蛋白,要么在肝细胞中通过小干扰RNA(siRNA)使SVIP沉默。我们的结果表明,阻断和沉默SVIP都会导致VTV形成显著减少。此外,我们发现沉默SVIP会减少VLDL分泌,这表明SVIP在细胞内VLDL运输和分泌中具有生理作用。我们得出结论,SVIP通过与其货物蛋白和被膜蛋白相互作用,作为VTV形成的一种新型调节因子,并且对肝细胞分泌VLDL具有重要意义。