Suppr超能文献

僵硬的微管与神经元形态

Stiff microtubules and neuronal morphology.

作者信息

Matus A

机构信息

Friedrich Miescher Institute, Basel, Switzerland.

出版信息

Trends Neurosci. 1994 Jan;17(1):19-22. doi: 10.1016/0166-2236(94)90030-2.

Abstract

Neuronal processes contain high concentrations of two related microtubule-associated proteins, MAP2 and tau. When MAP2 is expressed in non-neuronal cells the microtubules appear to be stiffer than those in control cells that do not express MAP2. A stiffening effect of MAP2 is further suggested by recent experiments with microtubules reassembled in vitro and by the fact that, under appropriate circumstances, MAP2-expressing cells can be induced to form processes that are long and cylindrical. Both MAP2 and tau contain homologous microtubule-binding domains, consisting of three or four repeats of an 18 amino acid sequence, which we believe are responsible for the stiffening effect. Our hypothesis is that each repeat binds to a neighbouring tubulin subunit in the wall of the microtubule, tethering them together and reducing their freedom of movement relative to one another. Based on these considerations, we suggest that MAP2 and tau may contribute to the support of neuronal processes by making the microtubules they contain longer, more stable and stiffer than those in non-neuronal cells.

摘要

神经元突起中含有高浓度的两种相关的微管相关蛋白,即微管相关蛋白2(MAP2)和tau蛋白。当MAP2在非神经元细胞中表达时,微管似乎比未表达MAP2的对照细胞中的微管更硬。体外重新组装微管的最新实验以及在适当情况下可诱导表达MAP2的细胞形成长而圆柱形的突起这一事实,进一步表明了MAP2的硬化作用。MAP2和tau蛋白都含有同源的微管结合结构域,由18个氨基酸序列的三个或四个重复序列组成,我们认为这些重复序列负责这种硬化作用。我们的假设是,每个重复序列与微管壁中的相邻微管蛋白亚基结合,将它们拴在一起,并减少它们相对于彼此的移动自由度。基于这些考虑,我们认为MAP2和tau蛋白可能通过使它们所含的微管比非神经元细胞中的微管更长、更稳定和更硬,从而有助于支持神经元突起。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验