Sibley J T, Paul M D, Hanson E D
J Protozool. 1977 Nov;24(4):595-604. doi: 10.1111/j.1550-7408.1977.tb01022.x.
Paramecium aurelia syngen 4, stock 57 (sensitve) cultivated in Cerophyl infusion were exposed to cytochalasin B (CB) and dimethylsulfoxide (DMSO), the solvent for CB, to distinquish between the effects of these agents on a cellular system. DMSO significantly inhibited survival, fission rate,, [3H]leucine incorporation, and cell size. CB-treated cells generally and slower division and poorer survival rates than cells exposed to the equivalent DMSO concentration, although the [3H]leucine incorporation was generally greater at the lower CB concentrations than for DMSO alone. As seen by electron microscopy and a new glycerination technic for observing polysomes, DMSO caused nuclear (nucleolar, chromatin) abnormalities as well as membrane degradation and polysomal breakdown: CB caused the formation of aberrant membrane structures and ribosomal tetramers, crystals, and tubes.
在瑟洛菲尔浸出液中培养的尾草履虫同宗配合4型,品系57(敏感型)被暴露于细胞松弛素B(CB)和CB的溶剂二甲基亚砜(DMSO)中,以区分这些试剂对细胞系统的影响。DMSO显著抑制了存活率、分裂率、[3H]亮氨酸掺入以及细胞大小。与暴露于同等DMSO浓度的细胞相比,CB处理的细胞通常分裂较慢且存活率较低,尽管在较低CB浓度下[3H]亮氨酸掺入通常比单独使用DMSO时更高。通过电子显微镜和一种用于观察多核糖体的新甘油化技术可以看出,DMSO导致细胞核(核仁、染色质)异常以及膜降解和多核糖体解体:CB导致异常膜结构以及核糖体四聚体、晶体和管状物的形成。