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Associations of elements of the Golgi apparatus with microtubules

机译:高尔基体的元素与微管的关联

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摘要

The intracellular spatial relationships between elements of the Golgi apparatus (GA) and microtubules in interphase cells have been explored by double immunofluorescence microscopy. By using cultured cells infected with the temperature-sensitive Orsay-45 mutant of vesicular stomatitis virus and a temperature shift-down protocol, we visualized functional elements of the GA by immunolabeling of the G protein of the virus that was arrested in the GA during its intracellular passage to the plasma membrane 13 min after the temperature shift-down. Complete disassembly of the cytoplasmic microtubules by nocodazole at the nonpermissive temperature before the temperature shift led to the dispersal of the GA elements, from their normal compact perinuclear configuration close to the microtubule-organizing center (MTOC) into the cell periphery. Washout of the nocodazole that led to the reassembly of the microtubules from the MTOC also led to the recompaction of the GA elements to their normal configuration. During this recompaction process, GA elements were seen in close lateral apposition to microtubules. In cells treated with nocodazole followed by taxol, an MTOC developed, but most of the microtubules were free of the MTOC and were assembled into bundles in the cell periphery. Under these circumstances, the GA elements that had been dispersed into the cell periphery by the nocodazole treatment remained dispersed despite the presence of an MTOC. In cells treated directly with taxol, free microtubules were seen in the cytoplasm in widely different, bundled configurations from one cell to another, but, in each case, elements of the GA appeared to be associated with one of the two end regions of the microtubule bundles, and to be uncorrelated with the locations of the vimentin intermediate filaments in these cells. These results are interpreted to suggest two types of associations of elements of the GA with microtubules: one lateral, and the other (more stable) end-on. The end-on association is suggested to involve the minus-end regions of microtubules, and it is proposed that this accounts for the GA-MTOC association in normal cells.
机译:通过双重免疫荧光显微镜研究了高尔基体(GA)的元素和相间细胞中的微管之间的细胞内空间关系。通过使用感染了水疱性口炎病毒的温敏性Orsay-45突变体和温度下移方案的培养细胞,我们通过免疫标记被捕集在GA中的病毒G蛋白来可视化GA的功能元件温度下降后13分钟,细胞内进入质膜。在温度转变之前,诺考达唑在非许可温度下完全分解了细胞质微管,导致GA元素从其正常的紧密核周构型靠近微管组织中心(MTOC)扩散到细胞周围。诺考达唑的冲洗导致MTOC中的微管重新组装,还导致GA元素重新组合成其正常构型。在重新压实过程中,发现GA元素与微管的侧向并列紧密。在用诺考达唑和紫杉醇处理的细胞中,出现了MTOC,但大多数微管中没有MTOC,并在细胞外围组装成束。在这种情况下,尽管存在MTOC,但通过Nocodazole处理分散到细胞周围的GA元素仍然保持分散状态。在直接用紫杉醇处理的细胞中,在细胞质中看到游离的微管,其形态从一个细胞到另一个细胞都大不相同,成束排列,但是在每种情况下,GA的成分似乎都与微管的两个末端区域之一相关。束,并与波形蛋白中间丝在这些细胞中的位置无关。这些结果被解释为暗示了GA元素与微管的两种关联:一种是侧向的,另一种是(更稳定的)末端连接。建议该末端连接涉及微管的负末端区域,并且提出这解释了正常细胞中GA-MTOC的连接。

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