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17β-羟基类固醇脱氢酶在外周组织内分泌性甾体激素生成中的作用

Role of 17 beta-hydroxysteroid dehydrogenases in sex steroid formation in peripheral intracrine tissues.

作者信息

Labrie F, Luu-The V, Lin S X, Simard J, Labrie C

机构信息

Oncology and Molecular Endocrinology Research Center, Laval University Hospital (CHUL) and Laval University, 2705, Laurier Boulevard, Québec, Canada G1V 4G2.

出版信息

Trends Endocrinol Metab. 2000 Dec;11(10):421-7. doi: 10.1016/s1043-2760(00)00342-8.

Abstract

In postmenopausal women, almost 100% of active sex steroids are synthesized in peripheral target tissues from inactive steroid precursors and, in adult men, approximately 50% of androgens are made locally in target tissues. This new field of endocrinology has been called intracrinology. The last and key step in the formation of all estrogens and androgens is catalyzed by a series of substrate-specific, cell-specific and unidirectional 17 beta-hydroxysteroid dehydrogenases (17 beta-HSDs). To date, seven human 17 beta-HSDs have been cloned, sequenced and characterized. The 17 beta-HSDs provide each cell with the means of precisely controlling the intracellular concentration of each sex steroid according to local needs.

摘要

在绝经后女性中,几乎100%的活性甾体激素是由无活性的甾体前体在外周靶组织中合成的;而在成年男性中,约50%的雄激素是在靶组织中局部生成的。内分泌学的这一新领域被称为“细胞内内分泌学”。所有雌激素和雄激素形成过程的最后关键步骤由一系列底物特异性、细胞特异性且单向的17β-羟基类固醇脱氢酶(17β-HSDs)催化。迄今为止,已克隆、测序并鉴定出7种人类17β-HSDs。17β-HSDs使每个细胞能够根据局部需求精确控制每种甾体激素的细胞内浓度。

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