Suppr超能文献

塌陷反应介导蛋白-2参与微管动力学的证据。

Evidence that collapsin response mediator protein-2 is involved in the dynamics of microtubules.

作者信息

Gu Y, Ihara Y

机构信息

Department of Neuropathology, Faculty of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

J Biol Chem. 2000 Jun 16;275(24):17917-20. doi: 10.1074/jbc.C000179200.

Abstract

Collapsin response mediator protein-2 (CRMP-2) is a member of the CRMP/TOAD/Ulip/DRP family of cytosolic phosphoproteins involved in neuronal differentiation and axonal guidance. CRMP-2 mediates the intracellular response to collapsin 1/semaphorin 3A, a repulsive extracellular guidance cue for axonal outgrowth. The mutation of UNC-33, a Caenorhabditis elegans homolog of CRMP-2, results in abnormality of microtubules in neurites, but the mechanism of CRMP-2 action remains to be clarified. Here, we report that overexpression of human CRMP-2 in Neuro2a cells, a mouse neuroblastoma cell line, results in blebbing of the cytoplasm. Furthermore, some cells exhibited intranuclear inclusions, which were labeled with antibodies to CRMP-2 and tubulin. CRMP-2 was found to be associated with microtubule bundles in the spindles at the metaphase and in the midbodies at the late telophase in mitotic cells. Thus, it is most likely that failure of complete disassembly of the spindle microtubules during mitosis is responsible for the formation of these intranuclear inclusions. We suggest that CRMP-2 functions by regulating the dynamics of microtubules.

摘要

塌陷反应介导蛋白2(CRMP-2)是CRMP/TOAD/Ulip/DRP家族的胞质磷蛋白成员,参与神经元分化和轴突导向。CRMP-2介导细胞内对塌陷蛋白1/信号素3A的反应,塌陷蛋白1/信号素3A是一种对轴突生长具有排斥作用的细胞外导向因子。CRMP-2在秀丽隐杆线虫中的同源物UNC-33发生突变会导致神经突中微管异常,但CRMP-2的作用机制仍有待阐明。在此,我们报告在小鼠神经母细胞瘤细胞系Neuro2a细胞中过表达人CRMP-2会导致细胞质起泡。此外,一些细胞表现出核内包涵体,这些包涵体用抗CRMP-2和微管蛋白的抗体标记。我们发现CRMP-2在有丝分裂细胞的中期纺锤体微管束和末期后期中间体中与微管束相关。因此,很可能是有丝分裂期间纺锤体微管未能完全拆卸导致了这些核内包涵体的形成。我们认为CRMP-2通过调节微管的动力学发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验