Krijnse-Locker J, Ericsson M, Rottier P J, Griffiths G
Institute of Virology, Faculty of Veterinary Medicine, University of Utrecht, The Netherlands.
J Cell Biol. 1994 Jan;124(1-2):55-70. doi: 10.1083/jcb.124.1.55.
Mouse hepatitis coronavirus (MHV) buds into pleomorphic membrane structures with features expected of the intermediate compartment between the ER and the Golgi complex. Here, we characterize the MHV budding compartment in more detail in mouse L cells using streptolysin O (SLO) permeabilization which allowed us to better visualize the membrane structures at the ER-Golgi boundary. The MHV budding compartment shares membrane continuities with the rough ER as well as with cisternal elements on one side of the Golgi stack. It also labeled with p58 and rab2, two markers of the intermediate compartment, and with PDI, usually considered to be a marker of the rough ER. The membranes of the budding compartment, as well as the budding virions themselves, but not the rough ER, labeled with the N-acetyl-galactosamine (GalNAc)-specific lectin Helix pomatia. When the SLO-permeabilized cells were treated with guanosine 5'-(3-O-thio)triphosphate (GTP gamma S), the budding compartment accumulated a large number of beta-cop-containing buds and vesicular profiles. Complementary biochemical experiments were carried out to determine whether vesicular transport was required for the newly synthesized M protein, that contains only O-linked oligosaccharides, to acquire first, GalNAc and second, the Golgi modifications galactose and sialic acid. The results from both in vivo studies and from the use of SLO-permeabilized cells showed that, while GalNAc addition occurred under conditions which block vesicular transport, both cytosol and ATP were prerequisites for the M protein oligosaccharides to acquire Golgi modifications. Collectively, our data argue that transport from the rough ER to the Golgi complex requires only one vesicular transport step and that the intermediate compartment is a specialized domain of the endoplasmatic reticulum that extends to the first cisterna on the cis side of the Golgi stack.
小鼠肝炎冠状病毒(MHV)出芽进入多形性膜结构,这些结构具有内质网(ER)和高尔基体复合体之间中间区室的预期特征。在此,我们利用链球菌溶血素O(SLO)通透化技术,更详细地对小鼠L细胞中的MHV出芽区室进行了表征,这使我们能够更好地观察内质网 - 高尔基体边界处的膜结构。MHV出芽区室与糙面内质网以及高尔基体堆叠一侧的扁平囊泡元件共享膜连续性。它还标记有中间区室的两个标志物p58和rab2,以及通常被认为是糙面内质网标志物的蛋白二硫键异构酶(PDI)。出芽区室的膜以及出芽的病毒粒子本身,而非糙面内质网,标记有N - 乙酰半乳糖胺(GalNAc)特异性凝集素苹果蜗牛凝集素。当用鸟苷5'-(3 - O - 硫代)三磷酸(GTPγS)处理经SLO通透化的细胞时,出芽区室积累了大量含β - 衔接蛋白的芽和囊泡样结构。我们进行了补充性生化实验,以确定仅含有O - 连接寡糖的新合成M蛋白首先获得GalNAc,其次获得高尔基体修饰半乳糖和唾液酸是否需要囊泡运输。体内研究和使用经SLO通透化细胞的研究结果均表明,虽然在阻断囊泡运输的条件下会发生GalNAc添加,但胞质溶胶和ATP都是M蛋白寡糖获得高尔基体修饰的先决条件。总体而言,我们的数据表明从糙面内质网到高尔基体复合体的运输仅需要一个囊泡运输步骤,并且中间区室是内质网的一个特化区域,延伸至高尔基体堆叠顺面的第一个扁平囊泡。