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抗雌激素对雌激素受体定位与补充的体内效应

In vivo effect of anti-estrogens on the localisation and replenishment of estrogen receptor.

作者信息

Capony F, Rochefort H

出版信息

Mol Cell Endocrinol. 1975 Sep;3(3):233-51. doi: 10.1016/0303-7207(75)90047-7.

Abstract

Interactions between estrogen recpetors and triaryl ethylene anti-estrogens (U-11100A, MER 25 and CI 628) were tested on immature rat uteri. The accessible and the total (accessible and occupied) estrogen receptor sites were assayed in the cytosol and nuclear extracts using charcoal adsorption. After in vivo administration of anti-estrogens, the estradiol receptor sites were occupied and subsequently transferred to the nuclear compartment. The nuclear localisation of the receptor induced by the antagonist lasted for several days, during which replenishment of the cytosol receptor occurred. The nuclear receptors transferred by anti-estrogens and labelled in vitro with [3H]estradiol, were similar to the nuclear receptor-estradiol complex formed in vivo as far as their sedimentation constants and extractability from nuclei were concerned. Although these anti-estrogens are capable to translocate the estrogen receptor to the nucleus and to induce the replenishment of the cytosol receptor, the mechanism of their antagonism and of their weak estrogenic activity is still not clear.

摘要

在未成熟大鼠子宫上测试了雌激素受体与三芳基乙烯抗雌激素(U-11100A、MER 25和CI 628)之间的相互作用。使用活性炭吸附法测定了胞质溶胶和核提取物中可及的以及总的(可及的和被占据的)雌激素受体位点。在体内给予抗雌激素后,雌二醇受体位点被占据,随后转移至核区室。拮抗剂诱导的受体核定位持续数天,在此期间胞质溶胶受体发生补充。经抗雌激素转移并在体外用[3H]雌二醇标记的核受体,就其沉降常数和从细胞核中的可提取性而言,与体内形成的核受体-雌二醇复合物相似。尽管这些抗雌激素能够将雌激素受体转运至细胞核并诱导胞质溶胶受体的补充,但其拮抗作用机制及其微弱的雌激素活性机制仍不清楚。

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