1,2-二辛烷甘油酯随其添加时间的增加而加速或延缓花蕊毛细胞的有丝分裂进程。

P M Larsen, S M Wolniak
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引用次数: 15

摘要

我们用0.5微克/毫升或60微克/毫升的1,2-二辛烷甘油(一种有效的蛋白激酶C的渗透激活剂)处理了来自蜘蛛草植物Tradescantia virginia的活的、完整的雄蕊毛细胞,并观察了有丝分裂从前期到后期的进展速度。我们发现,除了使用的浓度外,1,2-二辛烷酰甘油初始处理的时间决定了细胞的反应。当这种双甘油酯在正常核膜破裂时间前0 ~约8分钟加入细胞时,细胞迅速发生核膜破裂。后期发生在核膜破裂后28分钟,而不是在未处理的细胞中观察到的33分钟间隔。如果细胞在中期前期用0.5微克/毫升1,2-二辛烷酰甘油处理,直至核膜破裂后15分钟,也可观察到细胞快速进展到中期。在核膜破裂后约26分钟加入0.5微克/毫升的1,2-二辛烷甘油,导致姐妹染色单体的分离时间略早于正常时间,在核膜破裂后33分钟,在早熟细胞板泡聚集中,比未处理的细胞早3-5分钟。在核膜破裂前0至约5分钟的时间内,用60微克/毫升的1,2-二辛烷甘油处理细胞,可导致早熟进入后期。如果细胞在核膜破裂前20分钟用0.5微克/毫升或60微克/毫升1,2-二辛烷甘油处理,细胞不会进入有丝分裂,而是恢复到间期而不分裂。当1,2-二辛烷甘油在有丝分裂期间的其他时间添加时,随后的有丝分裂进程的速度显着减慢;细胞从核膜破裂到后期开始需要超过55分钟的时间,尽管一旦进入后期,细胞以正常速率继续进行细胞质分裂。在前期、中期或中期的任何时候用1,3-二辛烷甘油处理细胞对随后的有丝分裂进展速率没有影响。细胞在特定时间用1,2-二辛烷酰甘油在中期和中期处理后的反应变化可能表明在后期开始之前存在一个或多个调节开关点(即检查点)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
1,2-Dioctanoylglycerol accelerates or retards mitotic progression in Tradescantia stamen hair cells as a function of the time of its addition.

We have treated living, intact stamen hair cells from the spiderwort plant, Tradescantia virginiana, with 0.5 microgram/ml or 60 micrograms/ml 1,2-dioctanoylglycerol, a potent and permeant activator of protein kinase C, and have observed the rates of progression of mitosis from prophase through anaphase. We have found that in addition to the concentration used, the time of initial treatment with 1,2-dioctanoylglycerol defines the response by the cells. The cells rapidly undergo nuclear envelope breakdown when this diglyceride is added in very late prophase, 0 to approximately 8 min prior to the time of normal nuclear envelope breakdown. Anaphase onset occurs 28 min after nuclear envelope breakdown, rather than after the 33 min interval observed in untreated cells. Rapid progression through metaphase is also observed if cells are treated with 0.5 microgram/ml 1,2-dioctanoylglycerol during prometaphase, up to 15 min after nuclear envelope breakdown. The addition of 0.5 microgram/ml 1,2-dioctanoylglycerol in late metaphase, approximately 26 min after nuclear envelope breakdown, results in sister chromatid separation slightly ahead of its normal time, 33 min after nuclear envelope breakdown, and in precocious cell plate vesicle aggregation, 3-5 min earlier than that observed in untreated cells. Treatment of cells with 60 micrograms/ml of 1,2-dioctanoylglycerol at any point during the interval from 0 to approximately 5 min prior to nuclear envelope breakdown results in precocious entry into anaphase. If cells are treated with either 0.5 microgram/ml or 60 micrograms/ml 1,2-dioctanoylglycerol earlier than 20 min before nuclear envelope breakdown, they do not enter mitosis, but instead revert to interphase without dividing. When 1,2-dioctanoylglycerol is added at other times during mitosis, the rate of subsequent mitotic progression is dramatically slowed; the cells require greater than 55 min to progress from nuclear envelope breakdown to anaphase onset, though once in anaphase, the cells progress onward to cytokinesis at normal rates. Treatments o of cells with 1,3-dioctanoylglycerol at any point during prophase, prometaphase, or metaphase are without effect on the rate of subsequent mitotic progression. The shifts in response by cells treated at specific times with 1,2-dioctanoylglycerol during mid- and late metaphase may be indicative of the existence of one or more regulatory switch points (i.e., checkpoints) just prior to anaphase onset.

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