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大鼠子宫细胞摄取雌二醇的机制及雌二醇与子宫质膜结合的研究。

Studies on the mechanism of estradiol uptake by rat uterine cells and on estradiol binding to uterine plasma membranes.

作者信息

Muller R E, Johnston T C, Traish A M, Wotiz H H

出版信息

Adv Exp Med Biol. 1979;117:401-21. doi: 10.1007/978-1-4757-6589-2_22.

DOI:10.1007/978-1-4757-6589-2_22
PMID:474287
Abstract

A method for the preparation of viable uterine cell suspensions is described. Using this system the kinetics of estradiol uptake were studied in order to asses whether the steroid enters uterine cells by passive diffusion (1) or protein mediated diffusion (2). The data presented show that a) the rates of estradiol entry are nonsaturable; b) temperature dependence of uptake kinetics gives a linear Arrhenius plot; c) E2-6-CMO-BSA does not inhibit 3H-E2 uptake; d) uterine plasma membranes do not contain specific estrogen binding sites. Thus, estrogen uptake occures by passive diffusion.

摘要

本文描述了一种制备有活力的子宫细胞悬液的方法。利用该系统研究了雌二醇摄取的动力学,以评估该类固醇是通过被动扩散(1)还是蛋白质介导的扩散(2)进入子宫细胞。所呈现的数据表明:a)雌二醇进入的速率是不饱和的;b)摄取动力学的温度依赖性给出线性的阿伦尼乌斯图;c)E2-6-CMO-BSA不抑制3H-E2的摄取;d)子宫质膜不含有特异性雌激素结合位点。因此,雌激素的摄取是通过被动扩散发生的。

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1
Studies on the mechanism of estradiol uptake by rat uterine cells and on estradiol binding to uterine plasma membranes.大鼠子宫细胞摄取雌二醇的机制及雌二醇与子宫质膜结合的研究。
Adv Exp Med Biol. 1979;117:401-21. doi: 10.1007/978-1-4757-6589-2_22.
2
Effects of chlorpromazine on the inhibition and artifactual elevation of [3H]estradiol binding to estrogen receptors in rat uterine cytosol.氯丙嗪对大鼠子宫胞质溶胶中[3H]雌二醇与雌激素受体结合的抑制及人为升高作用。
J Steroid Biochem. 1984 Oct;21(4):475-6. doi: 10.1016/0022-4731(84)90315-7.
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CDRI-85/287: studies on competition to estrogen binding sites in the immature rat uterus.
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Analysis of binding of [3H]Estradiol to the cytosol fraction of rat pancreas: comparison with sites in the cytosol of uterus.[3H]雌二醇与大鼠胰腺胞浆部分结合的分析:与子宫胞浆中位点的比较。
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Interaction of estradiol and estriol with uterine estrogen receptor in vivo and in excised uteri or cell suspensions at 37 C: noncooperative estradiol binding and absence of estriol inhibition of estradiol-induced receptor activation and transformation.雌二醇和雌三醇在体内、37℃下的离体子宫或细胞悬液中与子宫雌激素受体的相互作用:雌二醇结合不具有协同性,且雌三醇不抑制雌二醇诱导的受体激活和转化。
Endocrinology. 1985 Nov;117(5):1839-47. doi: 10.1210/endo-117-5-1839.
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Two binding sites for estradiol in rat uterine nuclei: relationship to uterotropic response.大鼠子宫细胞核中雌二醇的两个结合位点:与子宫生长反应的关系。
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Endocrinology. 1982 Mar;110(3):741-8. doi: 10.1210/endo-110-3-741.
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[Multi-component system of estrogen binding proteins from the liver: characterization of binding properties of high molecular weight protein from rat liver similar to uterine estradiol receptors].[肝脏雌激素结合蛋白的多组分系统:大鼠肝脏中与子宫雌二醇受体相似的高分子量蛋白结合特性的表征]
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Progesterone action in hamster uterus: rapid inhibition of 3H-estradiol retention by the nuclear fraction.孕酮在仓鼠子宫中的作用:核组分对³H-雌二醇保留的快速抑制。
Endocrinology. 1980 Oct;107(4):1261-3. doi: 10.1210/endo-107-4-1261.
10
Differentiation of estradiol receptors in rat uterine cytosol by sensitivity to tamoxifen.
Biochem Biophys Res Commun. 1979 Mar 30;87(2):550-8. doi: 10.1016/0006-291x(79)91830-8.

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