Martikainen P M, Mäkelä S I, Santti R S, Härkönen P L, Suominen J J
Department of Anatomy, University of Turku, Finland.
Prostate. 1987;11(4):291-303. doi: 10.1002/pros.2990110402.
The organ culture of the rat ventral prostate was chosen as a model to determine whether any of the estrogen effects in vivo on the prostate are direct and expressed at the hormone concentrations normally found in the male. During 2 weeks of culture, estradiol at the high concentration of 10(-5) M blocked the androgenic activation of [3H]thymidine incorporation into DNA. The inhibition was localized in epithelium. Protein content of testosterone-treated explants and the accumulation of prostatein in the medium were considerably decreased, indicating inhibition of secretion. Antiandrogenic effects were not seen in morphology of estrogen-treated explants. The lower concentrations (from 10(-9) M to 10(-6) M) of estradiol increased the volume density of epithelium from day 7 onwards. The height of epithelium was concomitantly increased. The volume density of epithelium as well as the percentage of acini with metaplastic changes were significantly increased. These epithelial changes were less pronounced in the presence of androgen, suggesting that physiological concentrations of androgen prevent the expression of estrogen action in the morphology of the prostate. A change in staining with peanut (PNA)- and wheat germ agglutinin (WGA)-lectins indicated defective secretory capacity in metaplastic epithelium. In spite of the increased protein content in the explants, no constant pattern of the changes in prostatein accumulation could be recorded. Although the concentrations of estrogen required to induce squamous metaplasia were still unphysiological, the occurrence of this abnormal differentiation of the prostatic epithelium suggests that the cooperative action of estrogen is involved in androgen-dependent normal epithelial growth and possibly also in promoting growth of prostatic neoplasia.
选用大鼠腹侧前列腺器官培养作为模型,以确定雌激素在体内对前列腺的任何作用是否直接,并在雄性动物体内正常存在的激素浓度下得以表达。在培养的2周时间里,浓度为10(-5)M的高浓度雌二醇阻断了[3H]胸腺嘧啶核苷掺入DNA的雄激素激活作用。这种抑制作用定位于上皮细胞。经睾酮处理的外植体的蛋白质含量以及培养基中前列腺蛋白的积累量均显著降低,表明分泌受到抑制。在经雌激素处理的外植体形态中未观察到抗雄激素作用。从第7天起,较低浓度(从10(-9)M到10(-6)M)的雌二醇增加了上皮细胞的体积密度。上皮细胞高度随之增加。上皮细胞的体积密度以及发生化生改变的腺泡百分比均显著增加。在雄激素存在的情况下,这些上皮细胞变化不太明显,这表明生理浓度的雄激素可阻止雌激素作用在前列腺形态中的表达。花生凝集素(PNA)和麦胚凝集素(WGA)染色的变化表明化生上皮细胞的分泌能力存在缺陷。尽管外植体中的蛋白质含量有所增加,但前列腺蛋白积累的变化并没有恒定的模式。虽然诱导鳞状化生所需的雌激素浓度仍不符合生理状态,但前列腺上皮这种异常分化的发生表明雌激素的协同作用参与了雄激素依赖性正常上皮生长,也可能参与促进前列腺肿瘤的生长。