Sluder G, Rieder C L
J Cell Biol. 1985 Mar;100(3):887-96. doi: 10.1083/jcb.100.3.887.
The reproduction of spindle poles is a key event in the cell's preparation for mitosis. To gain further insight into how this process is controlled, we systematically characterized the ultrastructure of spindle poles whose reproductive capacity had been experimentally altered. In particular, we wanted to determine if the ability of a pole to reproduce before the next division is related to the number of centrioles it contains. We used mercaptoethanol to indirectly induce the formation of monopolar spindles in sea urchin eggs. We followed individually treated eggs in vivo with a polarizing microscope during the induction and development of monopolar spindles. We then fixed each egg at one of three predetermined key stages and serially semithick sectioned it for observation in a high-voltage electron microscope. We thus know the history of each egg before fixation and, from earlier studies, what that cell would have done had it not been fixed. We found that spindle poles that would have given rise to monopolar spindles at the next mitosis have only one centriole whereas spindle poles that would have formed bipolar spindles at the next division have two centrioles. By serially sectioning each egg, we were able to count all centrioles present. In the twelve cells examined, we found no cases of acentriolar spindle poles or centriole reduplication. Thus, the reproductive capacity of a spindle pole is linked to the number of centrioles it contains. Our experimental results also show, contrary to existing reports, that the daughter centriole of a centrosome can acquire pericentriolar material without first becoming a parent. Furthermore, our results demonstrate that the splitting apart of mother and daughter centrioles is an event that is distinct from, and not dependent on, centriole duplication.
纺锤极的复制是细胞为有丝分裂做准备的关键事件。为了更深入了解这一过程是如何被控制的,我们系统地描述了其复制能力经实验改变的纺锤极的超微结构。具体而言,我们想确定一个纺锤极在下一次分裂前进行复制的能力是否与其所含中心粒的数量有关。我们使用巯基乙醇间接诱导海胆卵中形成单极纺锤体。在单极纺锤体的诱导和发育过程中,我们用偏光显微镜在体内跟踪各个处理过的卵。然后,我们在三个预先确定的关键阶段之一固定每个卵,并对其进行连续半薄切片,以便在高压电子显微镜下观察。因此,我们知道每个卵在固定前的情况,并且根据早期研究,我们知道如果该细胞没有被固定会发生什么。我们发现,在下一次有丝分裂时会产生单极纺锤体的纺锤极只有一个中心粒,而在下一次分裂时会形成双极纺锤体的纺锤极有两个中心粒。通过对每个卵进行连续切片,我们能够数出所有存在的中心粒。在检查的12个细胞中,我们没有发现无中心粒纺锤极或中心粒复制的情况。因此,纺锤极的复制能力与其所含中心粒的数量有关。我们的实验结果还表明,与现有报道相反,中心体的子中心粒可以在不先成为母中心粒的情况下获得中心粒周围物质。此外,我们的结果表明,母中心粒和子中心粒的分离是一个与中心粒复制不同且不依赖于中心粒复制的事件。