Brown D L, Bouck G B
J Cell Biol. 1973 Feb;56(2):360-78. doi: 10.1083/jcb.56.2.360.
The proposal made in the preceding paper that the species-specific shape of Ochromonas is mediated by cytoplasmic microtubules which are related to two nucleating sites has been experimentally verified. Exposure of cells to colchicine or hydrostatic pressure causes microtubule disassembly and a correlative loss of cell shape in a posterior to anterior direction. Upon removal of colchicine or release of pressure, cell shape regenerates and microtubules reappear, first in association with the kineto-beak site concomitant with regeneration of the anterior asymmetry, and later at the rhizoplast site concomitant with formation of the posterior tail. It is concluded that two separate sets of cytoplasmic tubules function in formation and maintenance of specific portions of the total cell shape. On the basis of the following observations, we further suggest that the beak and rhizoplast sites could exert control over the position and timing of the appearance, the orientation, and the pattern of microtubule distribution in Ochromonas. (a) the two sites are accurately positioned in the cell relative to other cell organelles; (b) in regenerating cells microtubules reform first at these sites and appear to elongate to the cell posterior; (c) microtubules initially reappear in the orientation characteristic of the fully differentiated cell; (d) the two sets of tubules are polymerized at different times, in the same sequence, during reassembly or resynthesis of the microtubular system. Experiments using cycloheximide, after a treatment with colchicine, have demonstrated that Ochromonas cannot reassume its normal shape without new protein synthesis. This suggests that microtubule protein once exposed to colchicine cannot be reassembled into microtubules. Pressure-treated cells, on the other hand, reassemble tubules and regenerate the normal shape in the presence or absence of cycloheximide. The use of these two agents in analyzing nucleating site function and the independent processes of synthesis and assembly of microtubules is discussed.
在前一篇论文中提出的关于赭纤虫物种特异性形状由与两个成核位点相关的细胞质微管介导的提议已得到实验验证。将细胞暴露于秋水仙碱或静水压力下会导致微管解体,并沿前后方向相应地失去细胞形状。去除秋水仙碱或解除压力后,细胞形状会再生,微管重新出现,首先与动喙位点相关,伴随着前部不对称性的再生,随后在根丝体位点出现,伴随着后部尾巴的形成。可以得出结论,两组独立的细胞质微管在整个细胞形状特定部分的形成和维持中发挥作用。基于以下观察结果,我们进一步认为喙和根丝体位点可以控制赭纤虫中微管出现的位置和时间、方向以及微管分布模式。(a) 这两个位点相对于其他细胞器在细胞中定位准确;(b) 在再生细胞中,微管首先在这些位点重新形成,并似乎向细胞后部延伸;(c) 微管最初以完全分化细胞的特征方向重新出现;(d) 在微管系统的重新组装或再合成过程中,两组微管以相同顺序在不同时间聚合。在用秋水仙碱处理后使用放线菌酮的实验表明,没有新的蛋白质合成,赭纤虫就无法恢复其正常形状。这表明一旦暴露于秋水仙碱,微管蛋白就不能重新组装成微管。另一方面,经压力处理的细胞在有或没有放线菌酮的情况下都会重新组装微管并恢复正常形状。讨论了使用这两种试剂分析成核位点功能以及微管合成和组装的独立过程。