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A resident Golgi protein is excluded from peri-Golgi vesicles in NRK cells

机译:NRK细胞中高尔基体周围囊泡中不存在高尔基体蛋白

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To understand the structure and the function of the Golgi apparatus, it is essential to establish how resident Golgi enzymes are localized in only a few Golgi cisternae. In particular it is crucial to establish whether Golgi enzymes are retained specifically in cisternae, or if they are continuously transported from cisterna to cisterna. Here we report that a resident Golgi enzyme is largely excluded from peri-Golgi transport vesicles in normal rat kidney cells, a cell type in which conflicting results have been reported. Analysis of the lateral distribution of two markers within Golgi cisternae led to the same conclusion: a protein incorporated in vesicles (KDEL receptor) is concentrated at the rims of cisternae where vesicles form, while mannosidase II is not. These results suggest that localization of resident Golgi enzymes is achieved primarily by selective retention within cisternae and exclusion from transport vesicles. These observations cannot easily be reconciled with the vision of rapidly maturing Golgi cisternae as the principal means of intra-Golgi transport.
机译:要了解高尔基体的结构和功能,必须确定驻留的高尔基体酶是如何仅在少数高尔基池中定位的。特别重要的是确定高尔基酶是否特异性地保留在池中,或者是否从池中连续转移到池中。在这里我们报道,在正常大鼠肾脏细胞中,常高尔基转运小泡中基本上排除了常驻高尔基体酶,这种细胞类型已报道了相互矛盾的结果。对高尔基池中两个标记的横向分布的分析得出了相同的结论:囊泡中掺入的蛋白质(KDEL受体)集中在形成囊泡的池突边缘,而甘露糖苷酶II则不存在。这些结果表明,驻留高尔基体酶的定位主要是通过在池中选择性保留和从运输囊泡中排除而实现的。这些观察结果不容易与迅速成熟的高尔基蓄水池作为高尔基体内运输的主要手段的愿景相吻合。

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