EB1 identifies sites of microtubule polymerisation during neurite development

被引:59
作者
Morrison, EE [1 ]
Moncur, PM [1 ]
Askham, JM [1 ]
机构
[1] St James Univ Hosp, Mol Med Unit, Leeds LS9 7TF, W Yorkshire, England
来源
MOLECULAR BRAIN RESEARCH | 2002年 / 98卷 / 1-2期
基金
英国医学研究理事会;
关键词
microtubules; axon elongation; optical imaging;
D O I
10.1016/S0169-328X(01)00290-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
EB1 is a microtubule associated protein which interacts with the APC tumour suppressor protein and components of the cytoplasmic dynein/dynactin complex. EB1 is also a specific marker of growing microtubule tips. Here we demonstrate that EB1 protein levels are increased during axon but not dendrite formation in differentiated N2A neuroblastoma cells, and that EB1 localises to microtubule tips throughout extending neurites in these cells. In N2A axons, analysis of the ratio of EB1/beta-tubulin fluorescence demonstrated that the distal tip region contained the highest proportion of polymerising microtubules. Time-lapse confocal imaging of an EB1-GFP fusion protein in transfected N2A cells directly revealed the dynamics of microtubule extension in neurites, and demonstrated the existence of unusual, discrete knots of microtubule polymerisation at the periphery of non-process bearing cells which may represent an early event in neurite outgrowth. We conclude that EB1 localisation can be used to identify and analyse sites of microtubule polymerisation at a high resolution during neurite development, a process to which it may contribute. (C) 2002 Elsevier Science B.V.. All rights reserved.
引用
收藏
页码:145 / 152
页数:8
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