Honegger P, Werffeli P
Institute of Physiology, University of Lausanne, Switzerland.
Experientia. 1988 Oct 15;44(10):817-23. doi: 10.1007/BF01941177.
Relatively simple techniques are now available which allow the preparation of large quantities of highly reproducible aggregate cultures from fetal rat brain or liver cells, and to grow them in a chemically defined medium. Since these cultures exhibit extensive histotypic cellular reorganization and maturation, they offer unique possibilities for developmental studies. Therefore, the purpose of the present study was to investigate the usefulness of these cultures in developmental toxicology. Aggregating brain cell cultures were exposed at different developmental stages to model drugs (i.e., antimitotic, neurotoxic, and teratogenic agents) and assayed for their responsiveness by measuring a set of biochemical parameters (i.e., total protein and DNA content, cell type-specific enzyme activities) which permit a monitoring of cellular growth and maturation. It was found that each test compound elicited a distinct, dose-dependent response pattern, which may ultimately serve to screen and classify toxic drugs by using mechanistic criteria. In addition, it could be shown that aggregating liver cell cultures are capable of toxic drug activation, and that they can be used in co-culture with brain cell aggregates, providing a potential model for complementary toxicological and metabolic studies.
现在已有相对简单的技术,可用于从胎鼠脑细胞或肝细胞制备大量高度可重复的聚集培养物,并在化学成分明确的培养基中培养它们。由于这些培养物表现出广泛的组织型细胞重组和成熟,它们为发育研究提供了独特的可能性。因此,本研究的目的是探讨这些培养物在发育毒理学中的实用性。将聚集的脑细胞培养物在不同发育阶段暴露于模型药物(即抗有丝分裂剂、神经毒性剂和致畸剂),并通过测量一组生化参数(即总蛋白和DNA含量、细胞类型特异性酶活性)来检测它们的反应性,这些参数可用于监测细胞生长和成熟。结果发现,每种测试化合物都引发了独特的、剂量依赖性的反应模式,这最终可能有助于通过使用机制标准对有毒药物进行筛选和分类。此外,还可以证明,聚集的肝细胞培养物能够激活有毒药物,并且它们可以与脑细胞聚集体共同培养,为互补的毒理学和代谢研究提供一个潜在的模型。