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注入少突胶质细胞的外源性髓鞘碱性蛋白信使核糖核酸的转运与定位

Transport and localization of exogenous myelin basic protein mRNA microinjected into oligodendrocytes.

作者信息

Ainger K, Avossa D, Morgan F, Hill S J, Barry C, Barbarese E, Carson J H

机构信息

Department of Biochemistry, University of Connecticut Health Center, Farmington 06030.

出版信息

J Cell Biol. 1993 Oct;123(2):431-41. doi: 10.1083/jcb.123.2.431.

Abstract

We have studied transport and localization of MBP mRNA in oligodendrocytes in culture by microinjecting labeled mRNA into living cells and analyzing the intracellular distribution of the injected RNA by confocal microscopy. Injected mRNA initially appears dispersed in the perikaryon. Within minutes, the RNA forms granules which, in the case of MBP mRNA, are transported down the processes to the periphery of the cell where the distribution again becomes dispersed. In situ hybridization shows that endogenous MBP mRNA in oligodendrocytes also appears as granules in the perikaryon and processes and dispersed in the peripheral membranes. The granules are not released by extraction with non-ionic detergent, indicating that they are associated with the cytoskeletal matrix. Three dimensional visualization indicates that MBP mRNA granules are often aligned in tracks along microtubules traversing the cytoplasm and processes. Several distinct patterns of granule movement are observed. Granules in the processes undergo sustained directional movement with a velocity of approximately 0.2 micron/s. Granules at branch points undergo oscillatory motion with a mean displacement of 0.1 micron/s. Granules in the periphery of the cell circulate randomly with a mean displacement of approximately 1 micron/s. The results are discussed in terms of a multi-step pathway for transport and localization of MBP mRNA in oligodendrocytes. This work represents the first characterization of intracellular movement of mRNA in living cells, and the first description of the role of RNA granules in transport and localization of mRNA in cells.

摘要

我们通过将标记的mRNA显微注射到培养的少突胶质细胞中,并利用共聚焦显微镜分析注射RNA的细胞内分布,研究了髓鞘碱性蛋白(MBP)mRNA在少突胶质细胞中的运输和定位。注射的mRNA最初在核周呈分散状态。几分钟内,RNA形成颗粒,对于MBP mRNA而言,这些颗粒沿突起向下运输至细胞周边,在那里分布再次变得分散。原位杂交显示,少突胶质细胞内源性MBP mRNA在核周和突起中也呈颗粒状,并分散于周边膜中。这些颗粒不会因用非离子去污剂提取而释放,表明它们与细胞骨架基质相关。三维可视化显示,MBP mRNA颗粒常沿穿过细胞质和突起的微管排列成轨迹。观察到几种不同的颗粒运动模式。突起中的颗粒以约0.2微米/秒的速度进行持续的定向运动。分支点处的颗粒进行振荡运动,平均位移为0.1微米/秒。细胞周边的颗粒以约1微米/秒的平均位移随机循环。本文根据MBP mRNA在少突胶质细胞中运输和定位的多步骤途径对结果进行了讨论。这项工作首次描述了活细胞中mRNA的细胞内运动,以及RNA颗粒在细胞中mRNA运输和定位中的作用。

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