Witt P L, Ris H, Borisy G G
Chromosoma. 1981;83(4):523-40. doi: 10.1007/BF00328277.
To understand how microtubules interact in forming the mitotic apparatus and orienting and moving chromosomes, the precise arrangement of microtubules in kinetochore fibers in Chinese hamster ovary cells was examined. Individual microtubules were traced, using high voltage electron microscopy of serial 0.25 micron sections, from the kinetochore toward the pole. Microtubule arrangement in kinetochore fibers in untreated mitotic cells and in cells recovering from Colcemid arrest were similar in two respects: the number of microtubules per kinetochore (mean 14 and 12, respectively) and the nearest neighbor intermicrotubule distance (mean approximately 90 nm). In Colcemid recovered cells, over 90% of the microtubules in kinetochore fibers were attached to the kinetochore (i.e. kinetochore microtubules) are extended most or all of the distance to the pole. Few free microtubules were present in the kinetochore fibers; most non-kinetochore microtubules terminated in the pole. Since kinetochores in this Colcemid-recovered system have been demonstrated to nucleate microtubules (Witt et al., 1980), it seems likely that most if not all of these kinetochore microtubules originated at the kinetochore. Some of the reconstructed kinetochore fibers were attached to chromosomes with bipolar orientation, suggesting that kinetochore microtubules need not interact with many polar microtubules for orientation to occur. In Colcemid recovered cells lysed to reduce cytoplasmic background, microtubules in kinetochore fibers were preferentially preserved. The parallel and near-hexagonal order typical of microtubules in kinetochore fibers was maintained, as was the number of kinetochore microtubules (mean, 13). The intermicrotubule distance was slightly reduced in lysed cells (mean, 60 nm). Crossbridges about 5 nm wide and 30-40 nm long were visible in kinetochore fibers of lysed cells. Such crossbridges probably contribute to the stabilization and parallel order of microtubules in kinetochore fibers, any may have a functional role as well.
为了解微管如何相互作用以形成有丝分裂器并使染色体定向和移动,我们检测了中国仓鼠卵巢细胞中动粒纤维微管的精确排列。使用连续0.25微米切片的高压电子显微镜,从动粒向极追踪单个微管。未处理的有丝分裂细胞和从秋水仙酰胺阻滞中恢复的细胞中的动粒纤维微管排列在两个方面相似:每个动粒的微管数量(分别平均为14和12)以及最近邻微管间距离(平均约90纳米)。在从秋水仙酰胺中恢复的细胞中,动粒纤维中超过90%的微管附着于动粒(即动粒微管),并延伸至极的大部分或全部距离。动粒纤维中几乎没有游离微管;大多数非动粒微管在极处终止。由于在这个从秋水仙酰胺中恢复的系统中,动粒已被证明能使微管成核(维特等人,1980年),所以似乎这些动粒微管中的大多数(如果不是全部的话)起源于动粒。一些重建的动粒纤维以双极方向附着于染色体,这表明动粒微管在发生定向时无需与许多极微管相互作用。在为减少细胞质背景而裂解的从秋水仙酰胺中恢复的细胞中,动粒纤维中的微管被优先保留。动粒纤维中微管典型的平行和近六边形排列得以维持,动粒微管数量(平均为13)也保持不变。裂解细胞中的微管间距离略有减小(平均为60纳米)。在裂解细胞的动粒纤维中可见宽约5纳米、长30 - 40纳米的交叉桥。这种交叉桥可能有助于动粒纤维中微管的稳定和平行排列,也可能具有功能作用。