Sutherland R L, Baulieu E E
Eur J Biochem. 1976 Nov 15;70(2):531-41. doi: 10.1111/j.1432-1033.1976.tb11045.x.
(3H)Oestradiol exchange techniques were developed for the determination of specific oestrogen receptor site concentrations in the cytoplasm and nuclei of chick oviduct cells. Non-labelled, receptor-bound oestrogens were exchanged with (3H)oestradiol during a 24-h incubation at 20 degrees C, 2 h at 30 degrees C or 45 min at 3 degrees C. Both "soluble" and "insoluble" nuclear receptors were stable for at least 6 h at 30 degrees C and 3 degrees C but a proportion (approx. 30%) of cytoplasmic sites from withdrawn chickens were inactivated after 2 h at 20 degrees C. The magnum of 4-week-old immature chickens (weight = 15 mg) contained 0.20 pmol of oestrogen receptor which corresponds to 4275 receptor sites/cell, when it is assumed that all magnum cells have equal concentrations of receptor. In primarily stimulated chickens of similar age which had received 10x1 mg of oestradiol benzoate/day, the magnum weighed approximately 800 mg and contained 8.65 pmol of oestrogen receptor (4610 sites/cell). Withdrawal from primary oestrogenic stimulation for 3-6 weeks resulted in a 110 mg magnum which contained 1.20 pmol of receptor (2225 sites/cell). Oviducts from immature and withdrawn chickens had the majority (73-77%) of their oestrogen receptors sites in the receptor sites in the cytoplasmic fraction, while in primary stimulated chicken oviducts the majority (82%) of receptor sites were located in the nucleus. A single secondary injection of oestradiol, to oestrogen-withdrawn chickens, resulted in apparent translocation of cytoplasmic receptors to the nucleus during the first hour after injection. The magnitude of the decline in cytoplasmic receptor, and the concurrent increase in nuclear receptor concentration, was dose-dependent between 2 and 100 mug oestradiol/kg body weight. Larger doses of oestradiol up to 1 mg/kg did not increase the concentration of nuclear receptor above the maximum level seen at 100 mug oestradiol/kg. The initial rapid accumulation of nuclear receptor sites was followed by a period of progressive decline. The initial rapid accumulation of nuclear receptor sites was followed by a period of progressive decline. By 15 h after an injection of 100 mug oestradiol/kg, the concentration of nuclear sites had reached pre-injection levels. During the same time period, the depleted cytoplasmic receptor levels were replenished such that they reached control values by 12 h and were about 150% of the pre-injection level at 24 h.
(3H)雌二醇交换技术被开发用于测定鸡输卵管细胞胞质和细胞核中特异性雌激素受体位点的浓度。在20℃孵育24小时、30℃孵育2小时或3℃孵育45分钟期间,未标记的、与受体结合的雌激素与(3H)雌二醇进行交换。“可溶性”和“不可溶性”核受体在30℃和3℃下至少6小时保持稳定,但来自已撤雌激素的鸡的一部分(约30%)胞质位点在20℃下2小时后失活。假设所有输卵管细胞的受体浓度相等,4周龄未成熟鸡(体重=15毫克)的输卵管含有0.20皮摩尔雌激素受体,相当于每个细胞4275个受体位点。在年龄相似、每天接受10×1毫克苯甲酸雌二醇的初次刺激鸡中,输卵管重约800毫克,含有8.65皮摩尔雌激素受体(每个细胞4610个位点)。从初次雌激素刺激中撤药3至6周后,输卵管重110毫克,含有1.20皮摩尔受体(每个细胞2225个位点)。未成熟和已撤雌激素鸡的输卵管中,其雌激素受体位点的大部分(73 - 77%)位于胞质部分的受体位点,而在初次刺激的鸡输卵管中,大部分(82%)受体位点位于细胞核。对已撤雌激素的鸡单次二次注射雌二醇,导致注射后第一小时内胞质受体明显向细胞核转运。在2至100微克雌二醇/千克体重之间,胞质受体下降的幅度以及核受体浓度的同时增加呈剂量依赖性。高达1毫克/千克的更大剂量雌二醇并未使核受体浓度高于100微克雌二醇/千克时所见的最高水平。核受体位点最初的快速积累之后是一个逐渐下降的时期。在注射100微克雌二醇/千克后15小时,核位点浓度已达到注射前水平。在同一时间段内,耗尽的胞质受体水平得到补充,以至于在12小时时达到对照值,在24小时时约为注射前水平的150%。