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Roles for microtubule and microfilament cytoskeletons in animal cell cytokinesis

机译:微管和微丝细胞骨架在动物细胞胞质分裂中的作用

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Microtubule and microfilament cytoskeletons play key roles in the whole process of cytokinesis. Although a number of hypotheses have been proposed to elucidate the mechanism of cytokinesis by microtubule and actin filament cytoskeletons, many reports are conflicting. In our study, combining the cytoskeletons drug treatments with the time-lapse video technology, we retested the key roles of microtubule and actin filament in cytokinesis. The results showed that depolymerization of microtubules by Nocodazole after the initiation of furrowing would not inhibit the furrow ingression, but obviously decrease the stiffness of daughter cells. Depolymerizing actin filaments by Cytochalasin B before metaphase would inhibit the initiation of furrowing but not chromosome segregation, resulting in the formation of binucleate cells; however, depolymerize actin filaments during anaphase would prevent furrowing and lead to the regress of established furrow, also resulting in the formation of binucleate cells. Further, depolymerizing microtubules and actin filaments simultaneously after metaphase would cause the quick regress of the furrow and the formation of binucleate cells. From these results we propose a successful cytokinesis requires functions and coordination of both the microtubule and actin filament cytoskeletons. Microtubule cytoskeleton may function in the positioning and initiation of cleavage furrow, and the actin filament cytoskeleton may play key roles in the initiation and ingression of the furrow.
机译:微管和微丝细胞骨架在胞质分裂的整个过程中起关键作用。尽管已经提出了许多假说来阐明微管和肌动蛋白丝细胞骨架的胞质分裂机制,但许多报道相互矛盾。在我们的研究中,将细胞骨架药物治疗与延时视频技术相结合,我们重新测试了微管和肌动蛋白丝在胞质分裂中的关键作用。结果表明,犁沟开始后诺考达唑对微管的解聚不会抑制犁沟的进入,但明显降低了子代细胞的刚度。在中期之前,通过细胞松弛素B使肌动蛋白丝解聚将抑制犁沟的开始,但不能抑制染色体分离,从而导致双核细胞的形成。然而,在后期使肌动蛋白丝解聚将防止犁沟并导致犁沟的退缩,也导致双核细胞的形成。此外,在中期后同时使微管和肌动蛋白丝解聚将引起沟的快速消退和双核细胞的形成。根据这些结果,我们提出成功的胞质分裂需要微管和肌动蛋白丝细胞骨架的功能和协调。微管细胞骨架可能在切割沟的定位和起始中起作用,而肌动蛋白丝细胞骨架可能在沟的起始和进入中起关键作用。

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