Iversen T G, Skretting G, Llorente A, Nicoziani P, van Deurs B, Sandvig K
Institute for Cancer Research, The Norwegian Radium Hospital, Montebello 0310 Oslo, Norway.
Mol Biol Cell. 2001 Jul;12(7):2099-107. doi: 10.1091/mbc.12.7.2099.
The plant toxin ricin is transported to the Golgi and the endoplasmic reticulum before translocation to the cytosol where it inhibits protein synthesis. The toxin can therefore be used to investigate pathways leading to the Golgi apparatus. Except for the Rab9-mediated transport of mannose 6-phosphate receptors from endosomes to the trans-Golgi network (TGN), transport routes between endosomes and the Golgi apparatus are still poorly characterized. To investigate endosome to Golgi transport, we have used here a modified ricin molecule containing a tyrosine sulfation site and quantified incorporation of radioactive sulfate, a TGN modification. A tetracycline-inducible mutant Rab9S21N HeLa cell line was constructed and characterized to study whether Rab9 was involved in transport of ricin to the TGN and, if not, to further investigate the route used by ricin. Induced expression of Rab9S21N inhibited Golgi transport of mannose 6-phosphate receptors but did not affect the sulfation of ricin, suggesting that ricin is transported to the TGN via a Rab9-independent pathway. Moreover, because Rab11 is present in the endosomal recycling compartment and the TGN, studies of transient transfections with mutant Rab11 were performed. The results indicated that routing of ricin from endosomes to the TGN occurs by a Rab11-independent pathway. Finally, because clathrin has been implicated in early endosome to TGN transport, ricin transport was investigated in cells with inducible expression of antisense to clathrin heavy chain. Importantly, endosome to TGN transport (sulfation of endocytosed ricin) was unchanged when clathrin function was abolished. In conclusion, ricin is transported from endosomes to the Golgi apparatus by a Rab9-, Rab11-, and clathrin-independent pathway.
植物毒素蓖麻毒素在转运至胞质溶胶抑制蛋白质合成之前,会先被转运至高尔基体和内质网。因此,该毒素可用于研究通向高尔基体的途径。除了Rab9介导的甘露糖6-磷酸受体从内体到反式高尔基体网络(TGN)的转运外,内体与高尔基体之间的运输途径仍不太清楚。为了研究内体到高尔基体的运输,我们在此使用了一种含有酪氨酸硫酸化位点的修饰蓖麻毒素分子,并对放射性硫酸盐(一种TGN修饰)的掺入进行了定量。构建并鉴定了四环素诱导型突变体Rab9S21N HeLa细胞系,以研究Rab9是否参与蓖麻毒素向TGN的运输,如果不参与,则进一步研究蓖麻毒素所使用的途径。Rab9S21N的诱导表达抑制了甘露糖6-磷酸受体的高尔基体运输,但不影响蓖麻毒素的硫酸化,这表明蓖麻毒素是通过一条不依赖Rab9的途径转运至TGN的。此外,由于Rab11存在于内体循环区室和TGN中,因此进行了突变体Rab11瞬时转染的研究。结果表明,蓖麻毒素从内体到TGN的转运是通过一条不依赖Rab11的途径进行的。最后,由于网格蛋白与早期内体到TGN的运输有关,因此在可诱导表达网格蛋白重链反义RNA的细胞中研究了蓖麻毒素的运输。重要的是,当网格蛋白功能被消除时,内体到TGN的运输(内吞蓖麻毒素的硫酸化)没有改变。总之,蓖麻毒素通过一条不依赖Rab9、Rab11和网格蛋白的途径从内体转运至高尔基体。