腮腺腺泡细胞中的高尔基体芽。

Hideaki Tamaki, Akihisa Segawa, Shohei Yamashina
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引用次数: 1

摘要

高尔基体(GA)是一种膜质细胞器,由堆叠的贮池和相关的囊泡组成。本研究旨在确定其在大鼠腮腺腺泡细胞中的来源。GA的形态发生可以在发育过程和细胞有丝分裂过程中被识别。EM研究描述了在出生后发育或有丝分裂的早期阶段小泡的聚集,这似乎是GA的基本要素。Brefeldin A诱导池结构迅速降解为泡状聚集体。在去除药物后,观察到基于这些残余囊泡的GA结构重建。微管破坏后,可以观察到类似的膜组装。这些膜状聚集体可能相当于腮腺腺泡细胞中的“腺芽”。然而,在这种未成熟的赤霉病细胞中没有检测到常规的赤霉病细胞化学标记。我们发现GA基质蛋白GM130和锇还原性(一个经典的顺式高尔基元件标记)一致定位于GA元件中。因此,我们在各种动态条件下研究了GM130的免疫组织化学分布和锇浸渍腮腺腺泡细胞,这些动态条件产生了GA的结构修饰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Buds of the Golgi apparatus in parotid acinar cells.

The Golgi apparatus (GA) is a membranous organelle composed of stacked cisterns with associated vesicles. This study was undertaken to determine its origin in rat parotid acinar cells. The morphogenesis of the GA could be recognized in the developmental process as well as in mitotic division of cells. EM studies depicted an aggregation of small vesicles in the early stage of postnatal development or mitosis, that appeared to be the rudimental element of GA. Brefeldin A induced rapid degradation of the cisternal structure to vesicular aggregates. Reconstruction of the GA structure based on these remnant vesicles was observed upon removal of the drug. Similar membranous assembly could be observed after destruction of microtubules. These membranous aggregates presumably corresponded to 'buds of the GA' in parotid acinar cells. However, conventional cytochemical markers for GA were not detected on such immature form of GA. We found that the GA matrix protein GM130 and osmium reductivity (a classical marker for cis-Golgi elements) were consistently localized in the GA elements. Therefore, immunohistochemical distribution of GM130 and osmium impregnation of parotid acinar cells were studied under various dynamic conditions that produced structural modification of the GA.

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