Ikeda Yayoi, Tanaka Hideo, Esaki Michiyo
Department of Histology and Cell Biology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama 236-0004, Japan.
Endocrinology. 2008 Aug;149(8):3970-9. doi: 10.1210/en.2007-1599. Epub 2008 Apr 24.
To study the effects of gestational exposure to estrogen on early gonadal differentiation, pregnant mice were treated by sc injection of diethylstilbestrol (DES) or vehicle from embryonic day (E) 8.5 to E14.5, and gonads at E11.5, E12.5, and E14.5 were examined. Quantitative real-time RT-PCR and in situ hybridization revealed that mRNA levels of steroidogenic factor 1 (SF-1), a key regulator of gonadal differentiation, and several male gonad-specific genes, including Müllerian-inhibiting substance (MIS), steroidogenic acute regulatory protein, cholesterol side-chain cleavage cytochrome P450, and Cerebellin 1 precursor protein, were significantly decreased in the DES-treated testis, compared with the control testis at E12.5 and/or E14.5. Immunohistochemistry demonstrated that the staining intensities for SF-1 and MIS in Sertoli cells were apparently reduced in the DES-treated testis, compared with those of the controls, at E12.5 and E14.5. Because MIS, steroidogenic acute regulatory protein, cholesterol side-chain cleavage cytochrome P450, and Cerebellin 1 precursor protein are activated under the regulation of SF-1, the down-regulation of these factors may be due to reduced SF-1 expression. Immunohistochemistry for laminin-1 demonstrated that ovigerous cords in the DES-treated ovary were smaller than those in controls at E14.5. Moreover, the number of 5-bromo-2'deoxyuridine-5-monophosphate-labeled cells in the DES-treated testis was significantly reduced at E12.5 and E14.5, compared with controls, and that in the DES-treated ovary remained higher than that in the control ovary at E14.5. The results suggest that exogenous estrogens can alter sex-specific genetic pathways governing early differentiation and cell proliferation of both male and female gonads.
为研究孕期暴露于雌激素对早期性腺分化的影响,在胚胎期第(E)8.5天至E14.5天,通过皮下注射己烯雌酚(DES)或赋形剂处理怀孕小鼠,并检查E11.5、E12.5和E14.5时的性腺。定量实时逆转录聚合酶链反应(RT-PCR)和原位杂交显示,与E12.5和/或E14.5时的对照睾丸相比,DES处理的睾丸中,性腺分化的关键调节因子类固醇生成因子1(SF-1)以及几个雄性性腺特异性基因的mRNA水平显著降低,这些雄性性腺特异性基因包括苗勒管抑制物质(MIS)、类固醇生成急性调节蛋白、胆固醇侧链裂解细胞色素P450和小脑素1前体蛋白。免疫组织化学表明,与对照组相比,在E12.5和E14.5时,DES处理的睾丸中支持细胞中SF-1和MIS的染色强度明显降低。由于MIS、类固醇生成急性调节蛋白、胆固醇侧链裂解细胞色素P450和小脑素1前体蛋白在SF-1的调节下被激活,这些因子的下调可能是由于SF-1表达降低所致。层粘连蛋白-1的免疫组织化学显示,在E14.5时,DES处理的卵巢中的卵泡索比对照组的小。此外,与对照组相比,DES处理的睾丸中5-溴-2'-脱氧尿苷-5-单磷酸标记细胞的数量在E12.5和E14.5时显著减少,而在E14.5时,DES处理的卵巢中该细胞数量仍高于对照卵巢。结果表明,外源性雌激素可改变控制雄性和雌性性腺早期分化和细胞增殖的性别特异性遗传途径。