肝特异性酶在培养大鼠胚胎中的激素诱导作用。

P J Westenend, R Dahmen, R Charles, W H Lamers
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引用次数: 0

摘要

在单层培养中,当肝细胞从胚胎前肠(15体期)分化时,肝细胞特异性酶被激素诱导。虽然为定量研究提供了极好的机会,但在这种模型系统中失去了正常细胞环境的几个特征。为了确定这些组织特异性酶在完整生物体中的诱导性,将大鼠胚胎体外培养48小时,并暴露于单层培养有效的激素因子中,即地塞米松、三碘甲状腺原氨酸和二丁基环AMP。通过反映生长、形态发生和细胞分化的一般标准来评估体外培养期间胚胎的正常发育。外部特征的发展、器官发生、细胞分裂的分布以及组织特异性蛋白(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,但无论在妊娠第10天还是第11天(分别在肝原基出现之前和之后)开始培养,激素对肝细胞特异性酶(如氨甲酰磷酸合成酶)的诱导作用在免疫组织化学上都无法证明。然而,在培养48小时后,从这种胚胎中分离出来的肝细胞单层中可以证明激素对这种酶的诱导作用,这又一次证明了培养条件是适当的。此外,胚胎在培养过程中可以通过放射性标记的地塞米松和三碘甲状腺原氨酸以及环AMP的放射性受体试验来充分摄取激素。因此,必须假设年轻胚胎中存在抑制组织特异性酶合成的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hormonal inducibility of liver-specific enzymes in cultured rat embryos.

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.

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