Sluder G
J Cell Biol. 1976 Jul;70(1):75-85. doi: 10.1083/jcb.70.1.75.
Spindle assembly is studied in the eggs of the sea urchin Lytechinus variegatus by experimentally varying the amount of polymerizable tubulin within the egg. Aliquots of fertilized eggs from the same female are individually pulsed for 1-6 min with 1 X 10(-6) M Colcemid at least 20 min before first nuclear envelope breakdown. This treatment inactivates a portion of the cellular tubulin before the spindle is formed. Upon entering mitosis, treated eggs form functional spindles that are reduced in length and birefringent retardation but not width. With increased exposure to Colcemid, the length and retardation of the metaphase spindles are progressively reduced. Similar results are obtained by pulsing the eggs with Colcemid before fertilization, which demonstrates that the tubulin found in unfertilized sea urchin eggs is later used in spindle formation. Spindles, once assembled, are responsive to increases in the amount of polymerizable tubulin within the cell. Rapid increases in the amount of polymerizable tubulin within a Colcemid-treated cell can be experimentally effected by irradiating the cells with 366-nm light. This treatment photochemically inactivates the Colcemid, thereby freeing the tubulin to polymerize. Upon irradiation, the small prometaphase spindles of Colcemid-treated cells immediately increase in length and retardation. In these irradiated cells, spindle length and retardation increase as much as four times faster than they do during prometaphase for normal spindles. This suggests that the rate of the normal prometaphase increase in retardation and spindle size may be determined by factors other than the maximum rate of tubulin polymerization in the cell.
通过实验改变海胆(Lytechinus variegatus)卵内可聚合微管蛋白的量,对纺锤体组装进行了研究。在第一次核膜破裂前至少20分钟,用1×10⁻⁶ M秋水仙酰胺对来自同一雌性的受精鸡蛋等分试样分别脉冲处理1 - 6分钟。这种处理在纺锤体形成之前使一部分细胞微管蛋白失活。进入有丝分裂后,经处理的卵形成功能性纺锤体,其长度和双折射延迟减小,但宽度不变。随着秋水仙酰胺暴露时间增加,中期纺锤体的长度和延迟逐渐减小。在受精前用秋水仙酰胺对卵进行脉冲处理也得到了类似结果,这表明未受精海胆卵中的微管蛋白后来用于纺锤体形成。纺锤体一旦组装完成,就会对细胞内可聚合微管蛋白量的增加做出反应。通过用366纳米光照射细胞,可以在实验中使秋水仙酰胺处理的细胞内可聚合微管蛋白量快速增加。这种处理通过光化学作用使秋水仙酰胺失活,从而使微管蛋白能够聚合。照射后,秋水仙酰胺处理细胞的小前中期纺锤体的长度和延迟立即增加。在这些照射的细胞中,纺锤体长度和延迟的增加速度比正常纺锤体在前中期增加速度快四倍之多。这表明正常前中期延迟增加和纺锤体大小增加的速率可能由细胞内微管蛋白聚合的最大速率以外的因素决定。