Westenend P J, Dahmen R, Charles R, Lamers W H
Department of Anatomy and Embryology, University of Amsterdam, The Netherlands.
Acta Morphol Neerl Scand. 1986;24(3):165-80.
In monolayer cultures, hepatocyte-specific enzymes are inducible by hormones as soon as hepatocytes differentiate from the embryonic foregut (15-somite stage). Though offering an excellent opportunity for quantitative studies, several features of a normal cell environment are lost in such a model system. To determine the inducibility of such tissue-specific enzymes in intact organisms, rat embryos were cultured in vitro for 48 h and exposed to the hormonal factors that had been found effective in monolayer culture, viz. dexamethasone, triiodothyronine and dibutyryl cyclic AMP. Normal development of the embryos during culture in vitro was assessed by general criteria reflecting growth, morphogenesis and cytodifferentiation. Development of external features, organogenesis, the distribution of cell divisions and the appearance of tissue-specific proteins such as alpha-fetoprotein and glutamate dehydrogenase served as parameters. Despite undisturbed development of the embryos as judged by these criteria, irrespective of whether the culture was started at day 10 or at day 11 of gestation (just before, respectively after the appearance of the liver primordium), induction of hepatocyte-specific enzymes like carbamoylphosphate synthetase by hormones could not be demonstrated immunohistochemically. However, induction of this enzyme by hormones could be demonstrated in monolayers of hepatocytes isolated from such embryos after 48 h of culture, providing yet another demonstration of the adequate culture conditions. In addition, an adequate uptake of hormones by the embryo during culture could be shown with radio-actively labeled dexamethasone and triiodothyronine and with a radioreceptor assay for cyclic AMP. Therefore, the presence of factors in young embryos that inhibit tissue-specific enzyme synthesis has to be postulated.
在单层培养中,一旦肝细胞从胚胎前肠(15体节期)分化出来,肝细胞特异性酶就可被激素诱导。尽管这种模型系统为定量研究提供了绝佳机会,但正常细胞环境的几个特征在此模型系统中丧失了。为了确定完整生物体中此类组织特异性酶的可诱导性,将大鼠胚胎体外培养48小时,并暴露于在单层培养中已发现有效的激素因子,即地塞米松、三碘甲状腺原氨酸和二丁酰环磷腺苷。通过反映生长、形态发生和细胞分化的一般标准评估胚胎在体外培养期间的正常发育。外部特征的发育、器官发生、细胞分裂的分布以及组织特异性蛋白质如甲胎蛋白和谷氨酸脱氢酶的出现作为参数。尽管根据这些标准判断胚胎发育未受干扰,无论培养是在妊娠第10天还是第11天开始(分别在肝原基出现之前和之后),但通过免疫组织化学无法证明激素对肝细胞特异性酶如氨甲酰磷酸合成酶的诱导作用。然而,在培养48小时后从此类胚胎分离的肝细胞单层中可证明激素对该酶的诱导作用,这再次证明了培养条件的适宜性。此外,通过放射性标记的地塞米松和三碘甲状腺原氨酸以及环磷腺苷的放射受体测定法可显示胚胎在培养期间对激素的充分摄取。因此,必须假定年轻胚胎中存在抑制组织特异性酶合成的因子。