Kuriyama R, Borisy G G
J Cell Biol. 1981 Dec;91(3 Pt 1):814-21. doi: 10.1083/jcb.91.3.814.
In interphase Chinese hamster ovary (CHO) cells, the centrosome is attached to the nucleus very firmly. This nuclear-centrosome complex is isolated as a coherent structure by lysis and extraction of cells with Triton X-100 in a low ionic strength medium. Under these conditions, the ultrastructure of the centrioles attached to the nucleus can be discerned by electron microscopy of whole-mount preparations. The structural changes of the centrioles as a function of the cell cycle were monitored by this technique. Specifically, centriolar profiles were placed into six categories according to their orientation and the length ratio of daughter and parent centrioles. The proportion of centrioles in each category was plotted as a frequency histogram. The morphological changes in the centriole cycle were characterized by three distinguishable events: nucleation, elongation, and disorientation. The progress of centrioles through these stages was determined in synchronous populations of cells starting from S or M phase, in cells inhibited in DNA synthesis by addition of thymidine, and in cytoplasts. The results provide a quantitative description of the events of the centriole cycle. They also show that, in complete cells, nucleation, elongation, and disorientation are not dependent upon DNA synthesis. However, in cytoplasts, although elongation and disorientation occur as in normal cells, nucleation is blocked. Procentriole formation appeared to be inhibited by the removal of the nucleus. We suggest that coordination of centriole replication and nuclear replication may depend upon a signal arising from the nucleus.
在间期的中国仓鼠卵巢(CHO)细胞中,中心体与细胞核紧密相连。通过在低离子强度介质中用Triton X-100裂解和提取细胞,可将这种核-中心体复合体作为一个连贯结构分离出来。在这些条件下,通过整装标本的电子显微镜观察,可以辨别附着在细胞核上的中心粒的超微结构。利用该技术监测了中心粒作为细胞周期函数的结构变化。具体而言,根据中心粒的方向以及子代和亲代中心粒的长度比,将中心粒轮廓分为六类。将每类中心粒的比例绘制成频率直方图。中心粒周期中的形态变化以三个可区分的事件为特征:成核、伸长和取向紊乱。从S期或M期开始,在同步细胞群体中,在通过添加胸苷抑制DNA合成的细胞中,以及在细胞质体中,确定了中心粒在这些阶段的进展。结果提供了中心粒周期事件的定量描述。它们还表明,在完整细胞中,成核、伸长和取向紊乱不依赖于DNA合成。然而,在细胞质体中,虽然伸长和取向紊乱与正常细胞中一样发生,但成核受到阻断。原中心粒的形成似乎因细胞核的去除而受到抑制。我们认为中心粒复制和细胞核复制的协调可能取决于来自细胞核的信号。