Okabe S, Hirokawa N
Department of Anatomy and Cell Biology, School of Medicine, University of Tokyo, Japan.
Nature. 1990 Feb 1;343(6257):479-82. doi: 10.1038/343479a0.
The cytoskeleton has an important role in the generation and maintenance of the structure of the axon. Microtubules, neurofilaments and actin, together with various kinds of associated proteins, form highly organized dynamic cytoskeletal structures. Because tubulin and actin molecules are essential cytoskeletal components and are transported down the axon, it is important to understand their dynamic behaviour within the axon. Although previous pulse-labelling studies have indicated that the axonal cytoskeleton is a static complex travelling down the axon, this view has been challenged by the results of several recent experiments. We have now addressed this question by analysing the recovery of fluorescence after photobleaching fluorescent analogues of tubulin and actin in the axons of cultured neurons. We did not observe movement or spreading of bleached zones along the axon, both in neurons injected with fluorescein-labelled tubulin and actin. All bleached zones recovered their fluorescence gradually, however, indicating that microtubules and actin filaments are not static polymers moving forward within the axon, but are dynamic structures that continue to assemble along the length of the axon.
细胞骨架在轴突结构的形成和维持中起着重要作用。微管、神经丝和肌动蛋白,连同各种相关蛋白,形成高度有组织的动态细胞骨架结构。由于微管蛋白和肌动蛋白分子是重要的细胞骨架成分,并沿着轴突运输,因此了解它们在轴突内的动态行为很重要。尽管先前的脉冲标记研究表明轴突细胞骨架是一个沿轴突下行的静态复合体,但这一观点已受到最近几项实验结果的挑战。我们现在通过分析培养神经元轴突中微管蛋白和肌动蛋白荧光类似物光漂白后荧光的恢复情况来解决这个问题。在注射了荧光素标记的微管蛋白和肌动蛋白的神经元中,我们均未观察到漂白区域沿轴突移动或扩散。然而,所有漂白区域的荧光都逐渐恢复,这表明微管和肌动蛋白丝不是在轴突内向前移动的静态聚合物,而是沿着轴突长度持续组装的动态结构。