Kosik K S, McConlogue L
Harvard Medical School, Department of Medicine, Brigham and Women's Hospital, Boston.
Cell Motil Cytoskeleton. 1994;28(3):195-8. doi: 10.1002/cm.970280302.
The phenotypes induced by the expression of neuronal microtubule-associated proteins (MAPs) in Sf9 cells have provided data on the in situ function of these proteins. Both MAP2 and tau can induce long processes in Sf9 cells, and the processes contain bundles of microtubules. In both cases the microtubules are aligned with their plus ends distal. Tau expression usually induces a single process that is unbranched and of uniform caliber. Processes can form even when the cells are grown in suspension. Microtubules do not extend all the way to the tip; instead the terminal region contains an actin-rich meshwork. Taxol treatment of Sf9 cells also induces the assembly of microtubules into bundles but does not induce process formation in Sf9 cells. Therefore the in vitro properties of tau as a molecule capable of assembling, stabilizing, and bundling microtubules do not fully account for the in vivo ability of tau alone to transduce microtubule assembly into a change in cell shape. The morphological features of the processes induced by MAP2 differ in highly informative ways.
神经元微管相关蛋白(MAPs)在Sf9细胞中表达所诱导的表型,为这些蛋白的原位功能提供了数据。MAP2和tau都能在Sf9细胞中诱导长出长突起,且这些突起含有微管束。在这两种情况下,微管的正端都朝向远端排列。tau的表达通常诱导出一个单一的、无分支且管径均匀的突起。即使细胞在悬浮状态下生长,也能形成突起。微管并非一直延伸到突起顶端;相反,末端区域含有富含肌动蛋白的网络。用紫杉醇处理Sf9细胞也能诱导微管组装成束,但不会在Sf9细胞中诱导突起形成。因此,tau作为一种能够组装、稳定和捆绑微管的分子,其体外特性并不能完全解释tau单独在体内将微管组装转化为细胞形状变化的能力。由MAP2诱导的突起的形态特征在很多方面具有高度信息性。