Pollera M, Malvaldi G
Tumori. 1980 Oct 31;66(5):529-48. doi: 10.1177/030089168006600502.
The results of an electron microscopic study of the changes in hepatocytes induced by chronic intoxication with thioacetamide are reported. During the poisoning aspecific toxic changes are intermingled with progressive, preneoplastic ones. The main cell subpopulations identified are: 1) large hepatocytes with smooth endoplasmic reticulum (SER) hypertrophy, with or without rough endoplasmic reticulum (RER) neoformation and glycogen storage, which is starvation resistant; 2) smaller hepatocytes, where RER hypertrophy and ribosome accumulation are the prominent features. Such a pattern persists for months. After the withdrawal of the drug most of the cell changes disappear. However, during this time a simplification of the liver structure and cell composition takes place, allowing a sequence of cell events which seem relevant for establishment of neoplastic progression. The SER-hypertrophied cell appears first and gives rise, via several intermediate stages, to the RER-hypertrophied one, which is believed to play a key role as the ultimate precursor of cancer cells.
本文报道了硫代乙酰胺慢性中毒诱导肝细胞变化的电子显微镜研究结果。中毒期间,非特异性毒性变化与进行性、肿瘤前变化相互交织。鉴定出的主要细胞亚群有:1)内质网(SER)肥大的大肝细胞,有或无粗面内质网(RER)新生及糖原储存,具有抗饥饿能力;2)较小的肝细胞,其突出特征是RER肥大和核糖体积累。这种模式持续数月。停药后,大多数细胞变化消失。然而,在此期间肝脏结构和细胞组成发生简化,使得一系列细胞事件发生,这些事件似乎与肿瘤进展的建立相关。SER肥大的细胞首先出现,并通过几个中间阶段产生RER肥大的细胞,后者被认为作为癌细胞的最终前体发挥关键作用。