Larsen P M, Wolniak S M
Department of Botany, University of Maryland, College Park 20742.
Cell Motil Cytoskeleton. 1990;16(3):190-203. doi: 10.1002/cm.970160306.
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.
我们用0.5微克/毫升或60微克/毫升的1,2 - 二辛酰甘油(一种强效且可渗透的蛋白激酶C激活剂)处理了紫露草(Tradescantia virginiana)植株中活的、完整的雄蕊毛细胞,并观察了从前期到后期的有丝分裂进程速率。我们发现,除了所使用的浓度外,用1,2 - 二辛酰甘油进行初始处理的时间也决定了细胞的反应。当在非常晚的前期(即正常核膜破裂前0至约8分钟)添加这种二酰甘油时,细胞会迅速经历核膜破裂。核膜破裂后28分钟发生后期起始,而不是像未处理细胞那样在33分钟的间隔后发生。如果在前期向后期过渡阶段(核膜破裂后长达15分钟)用0.5微克/毫升的1,2 - 二辛酰甘油处理细胞,也会观察到中期的快速进程。在中期后期(核膜破裂后约26分钟)添加0.5微克/毫升的1,2 - 二辛酰甘油,会导致姐妹染色单体分离比正常时间(核膜破裂后33分钟)略早,并且细胞板小泡聚集提前,比未处理细胞提前3 - 5分钟。在核膜破裂前0至约5分钟的任何时间用60微克/毫升的1,2 - 二辛酰甘油处理细胞,会导致提前进入后期。如果在核膜破裂前20分钟之前用0.5微克/毫升或60微克/毫升的1,2 - 二辛酰甘油处理细胞,它们不会进入有丝分裂,而是恢复到间期不分裂。当在有丝分裂的其他时间添加1,2 - 二辛酰甘油时,随后的有丝分裂进程速率会显著减慢;细胞从核膜破裂到后期起始需要超过55分钟,不过一旦进入后期,细胞会以正常速率继续进行到胞质分裂。在前期、前期向后期过渡阶段或中期的任何时间用1,3 - 二辛酰甘油处理细胞,对随后的有丝分裂进程速率没有影响。在中期后期特定时间用1,2 - 二辛酰甘油处理的细胞反应变化,可能表明在后期起始前存在一个或多个调节转换点(即检查点)。