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中心体在组织间期微管阵列中的作用:含有或缺乏中心体的细胞质体的特性

Role of the centrosome in organizing the interphase microtubule array: properties of cytoplasts containing or lacking centrosomes.

作者信息

Karsenti E, Kobayashi S, Mitchison T, Kirschner M

出版信息

J Cell Biol. 1984 May;98(5):1763-76. doi: 10.1083/jcb.98.5.1763.

Abstract

To study the role of the centrosome in microtubule organization in interphase cells, we developed a method for obtaining cytoplasts (cells lacking a nucleus) that did or did not contain centrosomes. After drug-induced microtubule depolymerization, cytoplasts with centrosomes made from sparsely plated cells reconstituted a microtubule array typical of normal cells. Under these conditions cytoplasts without centrosomes formed only a few scattered microtubules. This difference in degree of polymerization suggests that centrosomes affect not only the distribution but the amount of microtubules in cells. To our surprise, the extent of microtubules assembled increased with the cell density of the original culture. At confluent density, cytoplasts without centrosomes had many microtubules, equivalent to cytoplasts with centrosomes. The additional microtubules were arranged peripherally and differed from the centrosomal microtubules in their sensitivity to nocodazole. These and other results suggest that the centrosome stabilizes microtubules in the cell, perhaps by capping one end. Microtubules with greater sensitivity to nocodazole arise by virtue of change in the growth state of the cell and may represent free or uncapped polymers. These experiments suggest that the spatial arrangement of microtubules may change by shifting the total tubulin concentration or the critical concentration for assembly.

摘要

为了研究中心体在间期细胞微管组织中的作用,我们开发了一种获取含有或不含有中心体的胞质体(无细胞核的细胞)的方法。在药物诱导微管解聚后,由稀疏接种的细胞制成的含有中心体的胞质体重构了典型的正常细胞微管阵列。在这些条件下,不含中心体的胞质体仅形成少数分散的微管。这种聚合程度的差异表明,中心体不仅影响微管在细胞内的分布,还影响其数量。令我们惊讶的是,组装的微管数量随着原始培养物的细胞密度增加而增加。在汇合密度下,不含中心体的胞质体有许多微管,与含有中心体的胞质体相当。额外的微管排列在周边,并且在对诺考达唑的敏感性方面与中心体微管不同。这些以及其他结果表明,中心体可能通过封闭一端来稳定细胞内的微管。对诺考达唑更敏感的微管是由于细胞生长状态的改变而产生的,可能代表游离的或未封闭的聚合物。这些实验表明,微管的空间排列可能通过改变总微管蛋白浓度或组装的临界浓度而发生变化。

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