King W J, Greene G L
Nature. 1984;307(5953):745-7. doi: 10.1038/307745a0.
Although it is widely accepted that specific intracellular receptor proteins are involved in the oestrogenic regulation of gene expression and growth in reproductive tissues, the precise nature of the regulation is poorly understood. Among the unresolved issues are the distribution and dynamics of the oestrogen receptor protein (oestrophilin) in target tissues in the presence and absence of oestrogens and antioestrogens. The use of radiolabelled and unlabelled receptor ligands to detect and measure oestrogen receptors in tissues has been complicated by the presence of other intracellular steroid-binding proteins and by the low concentration of receptors in responsive tissues. We report here the development of an immunocytochemical procedure that is suitable for localizing oestrophilin directly in frozen tissue sections or cells from human and several non-human sources. When monoclonal antibodies to oestrophilin were used to detect receptor in various oestrogen-sensitive tissues, specific staining was confined to the nucleus of all stained cells, suggesting that both cytosol and nuclear forms of the receptor protein may reside in the nuclear compartment.
尽管人们普遍认为特定的细胞内受体蛋白参与生殖组织中基因表达和生长的雌激素调节,但对这种调节的确切性质却知之甚少。尚未解决的问题包括在存在和不存在雌激素及抗雌激素的情况下,雌激素受体蛋白(雌激素亲和蛋白)在靶组织中的分布和动态变化。由于存在其他细胞内类固醇结合蛋白以及反应性组织中受体浓度较低,使用放射性标记和未标记的受体配体来检测和测量组织中的雌激素受体变得复杂。我们在此报告一种免疫细胞化学方法的开发,该方法适用于直接在来自人类和几种非人类来源的冷冻组织切片或细胞中定位雌激素亲和蛋白。当使用针对雌激素亲和蛋白的单克隆抗体来检测各种雌激素敏感组织中的受体时,特异性染色局限于所有染色细胞的细胞核,这表明受体蛋白的胞质溶胶和核形式可能都存在于核区室中。