Martinez-Menárguez J A, Prekeris R, Oorschot V M, Scheller R, Slot J W, Geuze H J, Klumperman J
Department of Cell Biology, School of Medicine, University of Murcia, 30071 Murcia, Spain.
J Cell Biol. 2001 Dec 24;155(7):1213-24. doi: 10.1083/jcb.200108029. Epub 2001 Dec 17.
A cisternal progression mode of intra-Golgi transport requires that Golgi resident proteins recycle by peri-Golgi vesicles, whereas the alternative model of vesicular transport predicts anterograde cargo proteins to be present in such vesicles. We have used quantitative immuno-EM on NRK cells to distinguish peri-Golgi vesicles from other vesicles in the Golgi region. We found significant levels of the Golgi resident enzyme mannosidase II and the transport machinery proteins giantin, KDEL-receptor, and rBet1 in coatomer protein I-coated cisternal rims and peri-Golgi vesicles. By contrast, when cells expressed vesicular stomatitis virus protein G this anterograde marker was largely absent from the peri-Golgi vesicles. These data suggest a role of peri-Golgi vesicles in recycling of Golgi residents, rather than an important role in anterograde transport.
高尔基体内运输的池状进展模式要求高尔基驻留蛋白通过高尔基周围小泡进行循环,而囊泡运输的另一种模型则预测顺行货物蛋白会存在于此类小泡中。我们利用对NRK细胞进行的定量免疫电镜技术,将高尔基周围小泡与高尔基区域的其他小泡区分开来。我们发现,在包被蛋白I包被的池状边缘和高尔基周围小泡中,高尔基驻留酶甘露糖苷酶II以及运输机制蛋白巨蛋白、KDEL受体和rBet1的水平显著。相比之下,当细胞表达水泡性口炎病毒蛋白G时,这种顺行标记物在高尔基周围小泡中基本不存在。这些数据表明高尔基周围小泡在高尔基驻留蛋白的循环中发挥作用,而非在顺行运输中起重要作用。