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从诺考达唑阻滞中释放后,PtK细胞有丝分裂和胞质分裂的快速完成。

Rapid completion of mitosis and cytokinesis in PtK cells following release from nocodazole arrest.

作者信息

Hamilton B T, Snyder J A

出版信息

Eur J Cell Biol. 1982 Oct;28(2):190-4.

PMID:7173218
Abstract

Mitotic PtK1 cells were arrested at nuclear envelope breakdown with the rapidly reversible microtubule inhibitor nocodazole. Addition of 1 microgram/ml nocodazole for 20 min resulted in complete blockage of spindle microtubule assembly but permitted other mitotic events to proceed such as chromosome condensation and cell rounding, typical of a c-mitosis. Upon release from nocodazole, mitosis and cytokinesis were completed approximately 35% faster than in a normal mitosis. The duration of each mitotic stage was compared in untreated and treated and released cells. Metaphase and cytokinesis were dramatically shortened while anaphase was unaffected. Cells treated for shorter periods of time with nocodazole and then released also reduced the length of time to complete mitosis and cytokinesis. The reduction in duration of these events was equivalent to the period of interruption of the mitotic cycle by nocodazole. With respect to the cell division cycle, PtK1 cells display a timing mechanism which is independent of the presence of microtubules.

摘要

有丝分裂的PtK1细胞用快速可逆的微管抑制剂诺考达唑阻滞在核膜破裂阶段。添加1微克/毫升诺考达唑20分钟导致纺锤体微管组装完全受阻,但允许其他有丝分裂事件继续进行,如染色体凝聚和细胞变圆,这是c-有丝分裂的典型特征。从诺考达唑中释放后,有丝分裂和胞质分裂的完成速度比正常有丝分裂快约35%。比较了未处理、处理并释放的细胞中每个有丝分裂阶段的持续时间。中期和胞质分裂显著缩短,而后期不受影响。用诺考达唑处理较短时间然后释放的细胞也减少了完成有丝分裂和胞质分裂的时间。这些事件持续时间的减少相当于诺考达唑对有丝分裂周期的中断时间。就细胞分裂周期而言,PtK1细胞显示出一种与微管存在无关的定时机制。

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