Griffiths G, Pepperkok R, Locker J K, Kreis T E
European Molecular Biology Laboratory, Heidelberg, Germany.
J Cell Sci. 1995 Aug;108 ( Pt 8):2839-56. doi: 10.1242/jcs.108.8.2839.
Recent data strongly suggest that the coatomer (COP) complex is involved in membrane transport between the ER and Golgi complex. This vesicular coat has been implicated in ER to Golgi, in intra Golgi as well as in Golgi to ER traffic. In this study we present a detailed immunocytochemical analysis of the distribution of beta-COP in different tissue culture cells. Our results extend previous studies by showing, using electron microscopy, that beta-COP accumulates on vesicular profiles and buds in the intermediate compartment (IC) under conditions that block ER to Golgi transport (15 degrees C). Importantly, under these conditions beta-COP co-localizes on these structures with a passenger protein, the membrane glycoprotein of vesicular stomatis virus (ts-O45-G). Furthermore, quantitative immunofluorescence microscopy of cells with ts-045-G accumulated in the ER, IC and trans-Golgi network, shifted briefly to the permissive temperature, showed that beta-COP was associated with many of the putative transport intermediates containing the viral glycoprotein which is in transit between the ER/IC and the cis-Golgi. The simplest interpretation of these data is that COP-coated vesicles are involved in anterograde transport of ts-045-G from the IC to the Golgi complex. Since many putative COP vesicle lacked the G protein following release of the 15 degrees C block this pool could be involved in retrograde transport. We also show that beta-COP is present on the membranes of the trans-Golgi network. However, in contrast to the ER-Golgi boundary, we could find no convincing evidence that this pool of beta-COP is associated with buds or trans-Golgi network-derived transport vesicles.
最近的数据有力地表明,外被体(COP)复合体参与内质网和高尔基体复合体之间的膜运输。这种囊泡外被与从内质网到高尔基体、高尔基体内部以及从高尔基体到内质网的运输都有关联。在本研究中,我们对不同组织培养细胞中β-COP的分布进行了详细的免疫细胞化学分析。我们的结果扩展了先前的研究,通过电子显微镜显示,在阻断内质网到高尔基体运输的条件下(15摄氏度),β-COP在内质网中间腔(IC)的囊泡轮廓和芽上积累。重要的是,在这些条件下,β-COP与一种搭载蛋白——水泡性口炎病毒的膜糖蛋白(ts-O45-G)在这些结构上共定位。此外,对ts-045-G在内质网、IC和反式高尔基体网络中积累的细胞进行定量免疫荧光显微镜观察,短暂转移到允许温度后发现,β-COP与许多含有病毒糖蛋白的假定运输中间体相关联,这些中间体正在内质网/IC和顺式高尔基体之间转运。对这些数据最简单的解释是,COP包被的囊泡参与了ts-045-G从IC到高尔基体复合体的顺向运输。由于在解除15摄氏度阻断后,许多假定的COP囊泡缺乏G蛋白,这个池可能参与逆行运输。我们还表明,β-COP存在于反式高尔基体网络的膜上。然而,与内质网-高尔基体边界不同,我们没有找到令人信服的证据表明这个β-COP池与芽或反式高尔基体网络衍生的运输囊泡有关联。