Gunning B E, Wick S M
J Cell Sci Suppl. 1985;2:157-79. doi: 10.1242/jcs.1985.supplement_2.9.
Features of preprophase bands (PPBs) of microtubules (MTs), and the spatial relationship between phragmosomes, PPB sites, and developing phragmoplasts during cytokinesis, are reviewed, setting new observations in the context of current knowledge. PPBs in onion root tip cells are present by the beginning of the G2 period of the cell cycle. They are at first wide, but later become more compact, narrower bands. MTs traverse the cytoplasm between the band at the cell cortex and the nuclear envelope. This whole assemblage of nucleus, PPB and intervening MTs remains together when the cell is ruptured during preparation for examination by immunofluorescence microscopy. Double bands are occasionally seen in early stages of PPB development, perhaps as a consequence of double induction from neighbouring cells. Calmodulin is not present in PPBs at a higher concentration than in the general cytoplasm, but it is more abundant in parts of the spindle and in the phragmoplast. The PPB MTs disappear at prophase, but nevertheless the new cell plate fuses with the parental cell walls at the PPB site. This spatial relationship can be disrupted by treatment with CIPC. Another experimental disruption of the relationship, accomplished by making minute wounds in the PPB site of mitotic cells in Tradescantia stamen hairs, is described. In other experiments on these cells the phragmoplast is shown to become tethered to the PPB site when the cell plate is half to three-quarters developed, although the telophase nuclei are free to move. Rhodamine-labelled phalloidin reveals putative F-actin in the phragmoplast of Tradescantia, but not in the gap between the extending phragmoplast and the PPB site. Rhodamine-labelled phalloidin also stains cytoplasmic strands that exist when cytoplasmic streaming occurs before and after (but not during) mitosis. Cytochalasin B treatment blocks incorporation of actin into the phragmoplast, which, however, can still develop, though usually abnormally. The F-actin of the phragmoplast may function in consolidation of the cell plate, rather than in spatial guidance of its growth toward the PPB site at the cell surface.
本文综述了微管(MTs)的前有丝分裂带(PPBs)的特征,以及胞质分裂过程中膜体、PPB位点和正在发育的成膜体之间的空间关系,并将新的观察结果置于当前知识背景下进行探讨。洋葱根尖细胞中的PPBs在细胞周期的G2期开始时出现。它们起初较宽,但后来变得更加紧密、更窄。微管横穿细胞皮层的带与核膜之间的细胞质。当细胞在免疫荧光显微镜检查的制备过程中破裂时,细胞核、PPB和中间的微管的整个组合会保持在一起。在PPB发育的早期阶段偶尔会看到双带,这可能是相邻细胞双重诱导的结果。钙调蛋白在PPBs中的浓度并不比在一般细胞质中更高,但在纺锤体的部分区域和成膜体中含量更丰富。PPB微管在前期消失,但新的细胞板仍在PPB位点与亲代细胞壁融合。这种空间关系可以通过用氯苯胺灵(CIPC)处理而被破坏。本文还描述了另一种对这种关系的实验性破坏,即通过在紫露草雄蕊毛的有丝分裂细胞的PPB位点制造微小伤口来实现。在对这些细胞的其他实验中,当细胞板发育到一半至四分之三时,成膜体被显示为与PPB位点相连,尽管末期细胞核可以自由移动。罗丹明标记的鬼笔环肽揭示了紫露草成膜体中存在假定的F-肌动蛋白,但在延伸的成膜体与PPB位点之间的间隙中不存在。罗丹明标记的鬼笔环肽还会对有丝分裂之前和之后(但不是在有丝分裂期间)发生细胞质流动时存在的细胞质丝进行染色。细胞松弛素B处理会阻止肌动蛋白掺入成膜体,然而,成膜体仍然可以发育,尽管通常发育异常。成膜体的F-肌动蛋白可能在巩固细胞板方面发挥作用,而不是在其向细胞表面的PPB位点生长的空间引导方面发挥作用。