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体外培养的星形胶质细胞中乙酰化微管、胶质纤维和线粒体的共定位。

Colocalisation of acetylated microtubules, glial filaments, and mitochondria in astrocytes in vitro.

作者信息

Cambray-Deakin M A, Robson S J, Burgoyne R D

机构信息

Physiological Laboratory, University of Liverpool, England.

出版信息

Cell Motil Cytoskeleton. 1988;10(3):438-49. doi: 10.1002/cm.970100311.

DOI:10.1002/cm.970100311
PMID:3052874
Abstract

We have recently shown that acetylated alpha-tubulin containing microtubules (acetyl-MTs; labeled by antibody 6-11B-1) constitute a cold-stable subset of the microtubule network of nonneuronal cells in rat primary forebrain cultures [Cambray-Deakin and Burgoyne: Cell Motil. 8(3):284-291, 1987b]. In contrast, tyrosinated alpha-tubulin containing MTs (tyr-MTs; labeled by antibody YL1/2) are cold-labile. Here we have examined the distribution of acetyl-MTs and tyr-MTs in cultures of newborn rat forebrain astrocytes and simultaneously investigated the distribution of mitochondria and glial filaments. In double-label immunofluorescence experiments a marked colocalisation of acetyl-MTs and glial filament bundles was observed. Tyr-MTs did not show a similar colocalisation with glial filament bundles. Furthermore, the distribution of mitochondria closely followed that of the acetyl-MT and glial filament bundles. When cells were exposed to short-term (30-min) treatments with MT-disrupting agents such as colchicine and nocodazole, the tyr-MT network was removed but the distributions of acetyl-MTs, glial filaments, and mitochondria were unchanged. Increased exposure to colchicine (9-16 hr) caused a progressive disruption of the acetyl-MTs and the collapse of glial filaments and mitochondria to the perinuclear region. These results suggest that acetyl-MTs and glial filaments but not tyr-MTs may be involved in the intracellular transport of organelles and/or in the control of their cytoplasmic distribution.

摘要

我们最近发现,含有乙酰化α-微管蛋白的微管(乙酰化微管;用抗体6-11B-1标记)构成大鼠原代前脑培养物中非神经元细胞微管网络的一个冷稳定亚群[坎布雷-迪金和伯戈因:《细胞运动》。8(3):284 - 291, 1987b]。相比之下,含有酪氨酸化α-微管蛋白的微管(酪氨酸化微管;用抗体YL1/2标记)对冷不稳定。在此,我们研究了新生大鼠前脑星形胶质细胞培养物中乙酰化微管和酪氨酸化微管的分布,同时研究了线粒体和胶质丝的分布。在双标记免疫荧光实验中,观察到乙酰化微管与胶质丝束有明显的共定位。酪氨酸化微管与胶质丝束未显示出类似的共定位。此外,线粒体的分布与乙酰化微管和胶质丝束的分布密切相关。当细胞用秋水仙碱和诺考达唑等微管破坏剂进行短期(30分钟)处理时,酪氨酸化微管网络被去除,但乙酰化微管、胶质丝和线粒体的分布未改变。增加秋水仙碱处理时间(9 - 16小时)会导致乙酰化微管逐渐破坏,胶质丝和线粒体向核周区域塌陷。这些结果表明,乙酰化微管和胶质丝而非酪氨酸化微管可能参与细胞器的细胞内运输和/或其细胞质分布的控制。

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