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间期小鼠成纤维细胞外周的微管正端构象与动力学

Microtubule plus-end conformations and dynamics in the periphery of interphase mouse fibroblasts.

作者信息

Zovko Sandra, Abrahams Jan Pieter, Koster Abraham J, Galjart Niels, Mommaas A Mieke

机构信息

Section Electron Microscopy, Department of Molecular Cell Biology, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands.

出版信息

Mol Biol Cell. 2008 Jul;19(7):3138-46. doi: 10.1091/mbc.e07-07-0681. Epub 2008 May 14.

Abstract

The plus ends of microtubules (MTs) alternate between phases of growth, pause, and shrinkage, a process called "dynamic instability." Cryo-EM of in vitro-assembled MTs indicates that the dynamic state of the plus end corresponds with a particular MT plus-end conformation. Frayed ("ram's horn like"), blunt, and sheet conformations are associated with shrinking, pausing, and elongating plus ends, respectively. A number of new conformations have recently been found in situ but their dynamic states remained to be confirmed. Here, we investigated the dynamics of MT plus ends in the peripheral area of interphase mouse fibroblasts (3T3s) using electron microscopical and tomographical analysis of cryo-fixed, freeze-substituted, and flat-embedded sections. We identified nine morphologically distinct plus-end conformations. The frequency of these conformations correlates with their proximity to the cell border, indicating that the dynamic status of a plus end is influenced by features present in the periphery. Shifting dynamic instability toward depolymerization with nocodazole enabled us to address the dynamic status of these conformations. We suggest a new transition path from growth to shrinkage via the so-called sheet-frayed and flared ends, and we present a kinetic model that describes the chronology of events taking place in nocodazole-induced MT depolymerization.

摘要

微管(MTs)的正端在生长、暂停和收缩阶段之间交替变化,这一过程称为“动态不稳定性”。体外组装微管的冷冻电镜显示,正端的动态状态与特定的微管正端构象相对应。磨损状(“羊角状”)、钝端和片状构象分别与收缩、暂停和伸长的正端相关。最近在原位发现了一些新的构象,但其动态状态仍有待证实。在这里,我们使用冷冻固定、冷冻替代和平板包埋切片的电子显微镜和断层扫描分析,研究了间期小鼠成纤维细胞(3T3s)周边区域微管正端的动态变化。我们识别出了九种形态上不同的正端构象。这些构象的频率与其与细胞边界的接近程度相关,表明正端的动态状态受周边区域特征的影响。用诺考达唑使动态不稳定性向解聚转变,使我们能够确定这些构象的动态状态。我们提出了一条从生长到收缩的新转变途径,即通过所谓的片状-磨损状和喇叭状末端,并提出了一个动力学模型,描述了诺考达唑诱导的微管解聚过程中发生的事件顺序。

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