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运动蛋白在建立轴突和树突的微管阵列中的作用。

The role of motor proteins in establishing the microtubule arrays of axons and dendrites.

作者信息

Baas P W

机构信息

Department of Anatomy, The University of Wisconsin Medical School, Madison 53706, USA.

出版信息

J Chem Neuroanat. 1998 Jun;14(3-4):175-80. doi: 10.1016/s0891-0618(98)00012-x.

Abstract

Neurons generate two distinct types of processes called axons and dendrites, both of which rely on highly organized arrays of microtubules for their growth and maintenance. Axonal microtubules are uniformly oriented with their plus-ends distal to the cell body, while dendritic microtubules are nonuniformly oriented. In neither case are the microtubules attached to the centrosome or any detectable structure that could establish their distinct patterns of polarity orientation. Here I describe several lines of evidence from my laboratory that support a model for the establishment of these microtubule arrays based on microtubule transport by motor proteins. Microtubules destined for axons and dendrites are nucleated at the centrosome within the cell body of the neuron, and rapidly released. The released microtubules are then transported into the developing processes. Early in neuronal development, the microtubules are transported with their plus-ends-leading into the developing axon and into the immature processes that will develop into dendrites. In the case of the developing dendrites, the plus-end-distal microtubules are later joined by a population of microtubules that are transported into these processes with their minus-ends-leading. Implicit in this model is that there are molecular motor proteins that transport microtubules with the appropriate orientation into each type of process. There is precedent for molecular motor proteins transporting microtubules during mitosis, and our results suggest that the same or similar motors are utilized during the development of axons and dendrites after a neuroblast becomes terminally postmitotic.

摘要

神经元产生两种不同类型的突起,即轴突和树突,二者的生长和维持都依赖于高度有序排列的微管。轴突微管的正端远离细胞体,呈均匀排列,而树突微管的排列则不均匀。在这两种情况下,微管都不附着于中心体或任何可检测到的能确立其独特极性排列模式的结构。在此,我将描述来自我实验室的几条证据,这些证据支持一个基于驱动蛋白介导的微管运输来建立这些微管阵列的模型。发往轴突和树突的微管在神经元细胞体的中心体处成核,然后迅速释放。释放后的微管随后被运输到正在发育的突起中。在神经元发育早期,微管以其正端在前的方式被运输到正在发育的轴突以及将发育为树突的未成熟突起中。就正在发育的树突而言,正端远离的微管后来会与另一群微管会合,这群微管是以负端在前的方式被运输到这些突起中的。该模型隐含的意思是,存在分子驱动蛋白,它们以适当的方向将微管运输到每种类型的突起中。在有丝分裂期间有分子驱动蛋白运输微管的先例,我们的结果表明,在神经母细胞进入终末有丝分裂后期后,轴突和树突发育过程中利用的是相同或相似的驱动蛋白。

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