Jung-Testas I, Groyer M T, Bruner-Lorand J, Hechter O, Baulieu E E, Robel P
Endocrinology. 1981 Oct;109(4):1287-9. doi: 10.1210/endo-109-4-1287.
Estrogen and androgen receptors have been investigated in rat ventral prostate epithelium and stoma. High speed supernatants were prepared from unfractionated or fractionated prostates. Cytosols from intact rats were incubated with 2 nM 3H-estradiol (E2) in presence of 80 nM dihydrotestosterone (DHT), and cytosols from 1 day castrated rats were incubated with 2 nM 3H-DHT, at 0 C for 4 h. They were submitted to ultracentrifugation on glycerol-Tris gradients. The amounts of hormones bound to the saturable 8S binding components were determined on a comparative basis. The values for E2-receptor in intact rats were 2.3, 15.4 and 5.9 fmol/mg cytosol protein in unfractionated prostate, stroma and epithelium, respectively. The corresponding values for DHT-binding were 31.9, 17.2 and 29.2 fmol/mg protein. In addition, Scatchard analysis of saturable E2 and DHT binding, using the protamine precipitation technique, essentially confirmed the results of glycerol gradients, and led to the conclusion that, contrary to androgen receptor, the major part of estradiol receptor is localized in stroma.
已对大鼠腹侧前列腺上皮和基质中的雌激素和雄激素受体进行了研究。从未分级或分级的前列腺中制备高速上清液。将完整大鼠的胞质溶胶与2 nM 3H-雌二醇(E2)在80 nM二氢睾酮(DHT)存在下于0℃孵育4小时,将去势1天大鼠的胞质溶胶与2 nM 3H-DHT于0℃孵育4小时。将它们在甘油-三羟甲基氨基甲烷梯度上进行超速离心。在比较的基础上测定与可饱和的8S结合成分结合的激素量。完整大鼠中未分级前列腺、基质和上皮中E2受体的值分别为2.3、15.4和5.9 fmol/mg胞质溶胶蛋白。DHT结合的相应值为31.9、17.2和29.2 fmol/mg蛋白。此外,使用鱼精蛋白沉淀技术对可饱和的E2和DHT结合进行Scatchard分析,基本证实了甘油梯度的结果,并得出结论,与雄激素受体相反,雌二醇受体的主要部分位于基质中。