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Nocodazole-dependent transport and brefeldin A--sensitive processing and sorting of newly synthesized membrane proteins in cultured neurons

机译:在培养的神经元中新合成膜蛋白的诺考达唑依赖性转运和布雷菲德菌素A敏感的加工和分类

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摘要

The envelope glycoproteins of Semliki Forest virus (SFV), Vesicular Stomatitis virus (VSV), and Influenza Fowl Plague virus (FPV) are vectorially targeted in neurons to the plasma membrane of dendrites (SFV and VSV) and axons (FPV). To gain insight into the mechanisms responsible for such polarized delivery we have examined the effects on neurons of nocodazole and brefeldin A (BFA), which are known to cause microtubule depolymerization and disassembly of the Golgi apparatus, respectively. Nocodazole treatment blocked transport of all viral glycoproteins to both axons and dendrites. BFA treatment induced disruption of the Golgi complex, including the trans-Golgi network (TGN), and tubulation of endosomes. However, the delivery of the SFV and FPV glycoproteins to the cell surface was not affected significantly by BFA, although processing and sorting were altered, as revealed by surface biotinylation and immunofluorescence microscopy of fixed nonpermeabilized cells. These results demonstrate the involvement of microtubules in axonal and dendritic transport of integral membrane glycoproteins, and the existence of a BFA-sensitive component in the sorting but not in the transport machinery.
机译:Semliki森林病毒(SFV),水泡性口腔炎病毒(VSV)和禽流感病毒(FPV)的包膜糖蛋白在神经元中被矢量靶向树突(SFV和VSV)和轴突(FPV)的质膜。为了深入了解造成这种极化传递的机制,我们检查了诺考达唑和布雷菲德菌素A(BFA)对神经元的作用,已知它们分别引起微管解聚和高尔基体分解。诺考达唑处理可阻断所有病毒糖蛋白向轴突和树突的转运。 BFA处理可导致高尔基复合体(包括反式高尔基体网络(TGN))的破坏和内体小管的形成。但是,SFF和FPV糖蛋白向细胞表面的递送不受BFA的显着影响,尽管加工和分选发生了变化,如固定的非透化细胞的表面生物素化和免疫荧光显微镜检查所揭示。这些结果表明微管参与完整的膜糖蛋白的轴突和树突状运输,以及在分选中但在运输机械中不存在BFA敏感成分。

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