Yuasa H, Ono Y, Ohma C, Shimizu N, Yamanaka H, Uchida T, Mizunuma H, Aoki K, Suzuki K
Department of Urology, Gunma University School of Medicine, Japan.
Hinyokika Kiyo. 1996 Jan;42(1):33-7.
We have already reported that estrogen treatment given to immature castrated rats caused proliferative changes in both collagen and smooth muscle in the seminal vesicles of immature rats detected by light microscopy. Herein, we studied the estrogen-induced changes in estrogen receptor (ER) in the seminal vesicles of immature castrated rats by means of enzyme immunoassay, an immunohistochemical method and RT-PCR, to clarify the mechanism of estrogen induced proliferation of collagen and smooth muscle. Immature rats (3 weeks old) were castrated and left untreated for 3 weeks and then injected subcutaneously with estradiol-17 beta (E2-17 beta, 5 micrograms/day) for 7 days before they were killed. The nuclear ER content per gland, mg tissue and mg protein in the seminal vesicles of castrated rats increased markedly compared with those of non-treated rats. Castration also enhanced ERmRNA expression. The immunohistochemical analysis demonstrated the obvious tissue distribution by which the nuclear ER positive cells were densely distributed in the periglandular stroma. The nuclear ER contents per gland, mg tissue and mg protein in the seminal vesicles of estrogen-treated castrated rats were greater than those in castrated rats. Estrogen treatment further enhanced ERmRNA expression in the castrated rats. The immunohistochemical studies demonstrated that the nuclear ER positive cells appeared among the glandular epithelial cells, basal cells and the peripheral stromal cells, in addition to the periglandular stromal cells. These findings suggest that ER is related to the estrogen induced proliferation of collagen and smooth muscle in the seminal vesicles of immature castrated rats.
我们已经报道,对未成熟去势大鼠给予雌激素治疗,通过光学显微镜检测发现,未成熟大鼠精囊中的胶原蛋白和平滑肌均出现增殖性变化。在此,我们通过酶免疫测定、免疫组织化学方法和逆转录聚合酶链反应,研究未成熟去势大鼠精囊中雌激素诱导的雌激素受体(ER)变化,以阐明雌激素诱导胶原蛋白和平滑肌增殖的机制。未成熟大鼠(3周龄)去势后3周不进行处理,然后皮下注射17β-雌二醇(E2-17β,5微克/天),持续7天,之后处死。与未处理大鼠相比,去势大鼠精囊中每个腺体、每毫克组织和每毫克蛋白质的核ER含量显著增加。去势也增强了ERmRNA的表达。免疫组织化学分析显示出明显的组织分布,核ER阳性细胞密集分布在腺体周围的基质中。雌激素处理的去势大鼠精囊中每个腺体、每毫克组织和每毫克蛋白质的核ER含量高于去势大鼠。雌激素处理进一步增强了去势大鼠中ERmRNA的表达。免疫组织化学研究表明,除了腺体周围的基质细胞外,核ER阳性细胞还出现在腺上皮细胞、基底细胞和外周基质细胞中。这些发现表明,ER与未成熟去势大鼠精囊中雌激素诱导的胶原蛋白和平滑肌增殖有关。