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糖皮质激素拮抗剂在培养的肝癌细胞中的核定位。

Nuclear localization of a glucocorticoid antagonist in cultured hepatoma cells.

作者信息

Golaz S, Beck G

出版信息

Biochem Biophys Res Commun. 1983 Feb 10;110(3):719-25. doi: 10.1016/0006-291x(83)91020-3.

Abstract

The binding characteristics of promegestone, a typical antagonist of glucocorticoid action, has been investigated. We localized [3H] promegestone in the nuclei purified from steroid-treated HTC cells but the radioactivity specifically bound to the nucleus was much lower for the antagonist than for an inducer steroid, for instance dexamethasone. We attempted to define the nature of the "nuclear" activity and found that promegestone does not bind to the perinuclear membrane but is associated with the chromatin fraction.

摘要

已对典型的糖皮质激素作用拮抗剂普美孕酮的结合特性进行了研究。我们在从用类固醇处理过的HTC细胞中纯化得到的细胞核中定位了[3H]普美孕酮,但该拮抗剂与细胞核特异性结合的放射性远低于诱导性类固醇,例如地塞米松。我们试图确定“核”活性的性质,发现普美孕酮不与核周膜结合,而是与染色质部分相关。

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