Piersma A H, Roelen B, Roest P, Haakmat-Hoesenie A S, van Achterberg T A, Mummery C L
Unit Teratology, Endocrinology, and Perinatal Screening, National Institute of Public Health and Environmental Protection, The Netherlands.
Teratology. 1993 Oct;48(4):335-41. doi: 10.1002/tera.1420480407.
Murine embryonal carcinoma cells have been used in in vitro models to study the effects of cadmium chloride on proliferation and differentiation of early embryonic cells. This approach allows the various cell types within the early embryo as well as several developmental mechanisms to be dissected and studied in isolation using larger numbers of cells than would be readily available from the embryo itself. The present study shows that both embryonal carcinoma cell proliferation and differentiation into parietal endoderm are inhibited by cadmium chloride. The effects are counteracted by the additional presence of zinc chloride. The uptake of cadmium into the cells is inhibited in the presence of zinc chloride, suggesting that competition between these metals for passage into the cells contributes to the mechanism underlying the protective effect of zinc. In addition, metallothionein gene expression is enhanced more rapidly after simultaneous incubation with zinc chloride, indicating that the attenuating effect of zinc on cadmium toxicity is also partly attributable to detoxification by metallothioneins.
小鼠胚胎癌细胞已被用于体外模型,以研究氯化镉对早期胚胎细胞增殖和分化的影响。这种方法能够剖析并单独研究早期胚胎中的各种细胞类型以及多种发育机制,使用的细胞数量比从胚胎本身获取的要多。本研究表明,氯化镉会抑制胚胎癌细胞的增殖以及向滋养层内胚层的分化。氯化锌的额外存在可抵消这些影响。在氯化锌存在的情况下,细胞对镉的摄取受到抑制,这表明这些金属在进入细胞过程中的竞争作用是锌具有保护作用的潜在机制之一。此外,与氯化锌同时孵育后,金属硫蛋白基因表达更快增强,这表明锌对镉毒性的减弱作用也部分归因于金属硫蛋白的解毒作用。