Greenberg J H
Teratog Carcinog Mutagen. 1982;2(3-4):319-23. doi: 10.1002/1520-6866(1990)2:3/4<319::aid-tcm1770020313>3.0.co;2-3.
We have tested the effects of teratogenic and nonteratogenic compounds on cultures of differentiating embryonic neural crest cells. Compounds were evaluated for their effects on the growth or differentiation of the cells based on morphologic criteria or on quantitative changes in biochemical markers for the differentiated cells. When metabolic activation may be required, compounds were incubated in the cultures in the presence of the postmitochondrial supernatant fraction of rat liver microsomes. Nine of 11 compounds with proven teratogenic effects in vivo induced readily detectable morphologic changes in differentiating cultures. In contrast, none of the nonteratogenic compounds tested had an effect on these cultures. The use of differentiating cell cultures as a screening system for teratogens is discussed.
我们已经测试了致畸和非致畸化合物对分化中的胚胎神经嵴细胞培养物的影响。根据形态学标准或分化细胞生化标志物的定量变化,评估化合物对细胞生长或分化的影响。当可能需要代谢活化时,将化合物与大鼠肝微粒体的线粒体后上清液组分一起在培养物中孵育。11种在体内已证实有致畸作用的化合物中有9种在分化培养物中诱导出易于检测到的形态学变化。相比之下,所测试的非致畸化合物均对这些培养物没有影响。本文讨论了使用分化细胞培养物作为致畸剂筛选系统的情况。