Osumi M, Sato M, Ishijima S A, Konomi M, Takagi T, Yaguchi H
Faculty of Science, Graduate School of Science, Institute of Electron Microscopy, Japan Women's University, 2-8-1, Mejirodai Bunkyo-ku, Tokyo, 112-8681, Japan.
Fungal Genet Biol. 1998 Jun-Jul;24(1-2):178-206. doi: 10.1006/fgbi.1998.1067.
Studies on the dynamics of surface and intracellular structures during cell wall formation from the reverting protoplast of Schizosaccharomyces pombe were reviewed, and the correlation between cell wall formation and actin cytoskeleton, which is the most important conductor of the mechanism, is described in this paper. A close spatial and temporal relationship between actin cytoskeleton and cell wall formation was found by using wild type and actin point-mutant cps8 of S. pombe. Concomitant with the cell wall formation, dynamic behavior of the intracellular secretion machinery, especially the Golgi apparatus and secretory vesicles, was analyzed by three-dimensional reconstruction of 40 to 80 serial sections at five reverting stages. Total reverting protoplast volume increased by 3.8 and 4.3 times at 3 and 5 h, respectively, and the volume of the Golgi apparatus in the corresponding stages increased 2.3- and 2. 5-fold over the same periods. The number of secretory vesicles also markedly increased by 3.4 and 5.8 times over that of the corresponding reverting protoplasts. Actin point-mutant cps8 cells have abnormal structure in the cell wall and septum, and the distribution pattern of the actin cytoskeleton during the reversion process was different from wild-type protoplasts. The profiles of actin showed one or two thick cables and patches in the cytoplasm which remained throughout reversion. The development of crosslinkage of the glucan fibrils which are beta-1,3-glucan in nature on the reverting protoplast surface was defective; the glucan networks consisted of thin, rope-shaped fibrils up to 30 nm in width which formed a ribbon-shape 200 nm wide in wild-type reverting protoplasts. The intrafibrillar space is not filled with amorphous particles of alpha-galactomannan in nature. The secretion machinery was seen to have a similar profile as the wild type. The above results suggest that actin cytoskeleton may control secretion of beta-1,6-glucan and other cell wall substances such as alpha-glucan and alpha-galactomannan rather than beta-1,3-glucan. Study of the role of actin cytoskeleton in the cell wall formation is contributing to the development of antifungal agents together with basic cell biology.
综述了粟酒裂殖酵母原生质体回复过程中细胞壁形成期间表面和细胞内结构的动力学研究,本文描述了细胞壁形成与肌动蛋白细胞骨架之间的相关性,肌动蛋白细胞骨架是该机制最重要的传导者。通过使用粟酒裂殖酵母的野生型和肌动蛋白点突变体cps8,发现肌动蛋白细胞骨架与细胞壁形成之间存在密切的空间和时间关系。伴随着细胞壁的形成,通过对五个回复阶段的40至80个连续切片进行三维重建,分析了细胞内分泌机制,特别是高尔基体和分泌囊泡的动态行为。回复原生质体的总体积在3小时和5小时时分别增加了3.8倍和4.3倍,相应阶段高尔基体的体积在同一时期增加了2.3倍和2.5倍。分泌囊泡的数量也比相应的回复原生质体显著增加了3.4倍和5.8倍。肌动蛋白点突变体cps8细胞的细胞壁和隔膜结构异常,回复过程中肌动蛋白细胞骨架的分布模式与野生型原生质体不同。肌动蛋白的轮廓在整个回复过程中在细胞质中显示出一条或两条粗索和斑块。回复原生质体表面上本质上是β-1,3-葡聚糖的葡聚糖原纤维的交联发育存在缺陷;葡聚糖网络由宽度达30nm的细的、绳状原纤维组成,在野生型回复原生质体中形成200nm宽的带状。原纤维内空间没有填充本质上是α-半乳甘露聚糖的无定形颗粒。分泌机制的情况与野生型相似。上述结果表明,肌动蛋白细胞骨架可能控制β-1,6-葡聚糖和其他细胞壁物质如α-葡聚糖和α-半乳甘露聚糖的分泌,而不是β-1,3-葡聚糖。研究肌动蛋白细胞骨架在细胞壁形成中的作用,与基础细胞生物学一起,有助于抗真菌剂的开发。