Baas Peter W, Vidya Nadar C, Myers Kenneth A
Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 W. Queen Lane, Philadelphia, PA 19129, USA.
Traffic. 2006 May;7(5):490-8. doi: 10.1111/j.1600-0854.2006.00392.x.
Recent studies on cultured neurons have demonstrated that microtubules are transported down the axon in the form of short polymers. The transport of these microtubules is bidirectional, intermittent, asynchronous, and occurs at the fast rate of known motors. The majority of the microtubule mass in the axon exists in the form of longer immobile microtubules. We have proposed a model called 'cut and run', in which the longer microtubules are mobilized by enzymes that sever them into shorter mobile polymers. In this view, the molecular motors that transport microtubules are not selective for short microtubules but rather impinge upon microtubules irrespective of their length. In the case of the longer microtubules, these motor-driven forces do not transport the microtubules in a rapid and concerted fashion but presumably affect them nonetheless. Here, we discuss the mechanisms by which the short microtubules are transported and suggest possibilities for how analogous mechanisms may align and organize the longer microtubules and functionally integrate them with each other and with the actin cytoskeleton.
最近对培养神经元的研究表明,微管以短聚合物的形式沿轴突运输。这些微管的运输是双向的、间歇性的、异步的,并且以已知马达的快速速率发生。轴突中大部分微管物质以较长的固定微管形式存在。我们提出了一个名为“切断并运行”的模型,其中较长的微管被酶动员,这些酶将它们切割成较短的可移动聚合物。按照这种观点,运输微管的分子马达对短微管没有选择性,而是不论微管长度都作用于它们。对于较长的微管,这些马达驱动力不会以快速和协同的方式运输微管,但可能仍然会对它们产生影响。在这里,我们讨论短微管运输的机制,并提出类似机制如何排列和组织较长微管以及如何使它们彼此之间以及与肌动蛋白细胞骨架在功能上整合的可能性。