Division of Biological Science, Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan.
J Cell Biol. 2013 Jul 8;202(1):25-33. doi: 10.1083/jcb.201304031. Epub 2013 Jul 1.
The formation of a functional spindle requires microtubule (MT) nucleation from within the spindle, which depends on augmin. How augmin contributes to MT formation and organization is not known because augmin-dependent MTs have never been specifically visualized. In this paper, we identify augmin-dependent MTs and their connections to other MTs by electron tomography and 3D modeling. In metaphase spindles of human cells, the minus ends of MTs were located both around the centriole and in the body of the spindle. When augmin was knocked down, the latter population of MTs was significantly reduced. In control cells, we identified connections between the wall of one MT and the minus end of a neighboring MT. Interestingly, the connected MTs were nearly parallel, unlike other examples of end-wall connections between cytoskeletal polymers. Our observations support the concept of augmin-dependent MT nucleation at the walls of existing spindle MTs. Furthermore, they suggest a mechanism for maintaining polarized MT organization, even when noncentrosomal MT initiation is widespread.
功能性纺锤体的形成需要纺锤体内微管(MT)的核形成,这取决于微管相关蛋白复合物。然而,微管相关蛋白复合物如何促进 MT 的形成和组织尚不清楚,因为从未专门观察到微管相关蛋白复合物依赖性 MT。在本文中,我们通过电子断层扫描和 3D 建模来鉴定微管相关蛋白复合物依赖性 MT 及其与其他 MT 的连接。在人类细胞的中期纺锤体中,MT 的负端既位于中心粒周围,也位于纺锤体的主体中。当微管相关蛋白复合物被敲低时,后者的 MT 群体明显减少。在对照细胞中,我们鉴定了一个 MT 的壁与相邻 MT 的负端之间的连接。有趣的是,连接的 MT 几乎是平行的,与细胞骨架聚合物之间其他末端壁连接的例子不同。我们的观察结果支持在现有纺锤体 MT 的壁上进行微管相关蛋白复合物依赖性 MT 核形成的概念。此外,它们还提出了一种即使非中心体 MT 起始广泛存在也能维持极化 MT 组织的机制。