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子宫内膜异位组织和子宫子宫内膜中雌激素和孕激素结合的组织化学证明:一项比较研究。

Histochemical demonstration of estrogen and progesterone binding in endometriotic tissue and in uterine endometrium: A comparative study.

作者信息

Bergqvist A, Jeppsson S, Ljungberg O

出版信息

J Histochem Cytochem. 1985 Feb;33(2):155-61. doi: 10.1177/33.2.3968421.

DOI:10.1177/33.2.3968421
PMID:3968421
Abstract

Estrogen and progesterone binding to endometriotic and endometrial tissue was studied histochemically using estradiol and progesterone fluorochrome derivatives (E2-bovine serum albumin-fluorescein isothiocyanate and progesterone-bovine serum albumin-tetramethylrhodamine isothiocyanate). Thirty endometriotic samples from 21 women were studied, together with endometrial specimens obtained simultaneously from 14 of the women. In 77% of the endometriotic samples binding of the estrogen conjugate was indicated by specific fluorescence in more than half of the epithelial cell population, and in 20% in less than half. The corresponding figures for the progesterone conjugate binding were 75 and 18%, respectively. Blocking studies indicated a reasonable degree of ligand specificity. In endometrial tissue the corresponding figures were 64 and 29%, respectively, for binding of the estrogen conjugate and 54 and 38%, respectively, for binding of the progesterone conjugate. In 7 of 13 cases where evaluable samples of both tissues had been obtained, the relative proportion of fluorescent cells, with either reagent, was similar in the two tissue types. Our results suggest that the cytoplasm of epithelial cells in endometriotic tissue and in uterine endometrium contains specific binding sites for both estrogen and progesterone. The binding pattern of the two conjugates in endometriotic tissue was unrelated to the menstrual phase.

摘要

使用雌二醇和孕酮荧光染料衍生物(雌二醇 - 牛血清白蛋白 - 异硫氰酸荧光素和孕酮 - 牛血清白蛋白 - 异硫氰酸四甲基罗丹明)对子宫内膜异位症组织和子宫内膜组织中的雌激素和孕酮结合进行了组织化学研究。研究了来自21名女性的30个子宫内膜异位症样本,以及同时从其中14名女性获得的子宫内膜标本。在77%的子宫内膜异位症样本中,超过一半的上皮细胞群体出现特异性荧光,表明雌激素结合物与之结合,20%的样本中少于一半的上皮细胞群体出现特异性荧光。孕酮结合物结合的相应数字分别为75%和18%。阻断研究表明配体具有合理程度的特异性。在子宫内膜组织中,雌激素结合物结合的相应数字分别为64%和29%,孕酮结合物结合的相应数字分别为54%和38%。在13例同时获得两种组织可评估样本的病例中,有7例两种组织类型中使用任何一种试剂时荧光细胞的相对比例相似。我们的结果表明,子宫内膜异位症组织和子宫内膜上皮细胞的细胞质中都含有雌激素和孕酮的特异性结合位点。子宫内膜异位症组织中两种结合物的结合模式与月经周期无关。

相似文献

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Histochemical demonstration of estrogen and progesterone binding in endometriotic tissue and in uterine endometrium: A comparative study.子宫内膜异位组织和子宫子宫内膜中雌激素和孕激素结合的组织化学证明:一项比较研究。
J Histochem Cytochem. 1985 Feb;33(2):155-61. doi: 10.1177/33.2.3968421.
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Histochemical localization of specific estrogen and progesterone binding in human endometrium and endometriotic tissue. A preliminary report.人子宫内膜和子宫内膜异位组织中特异性雌激素和孕激素结合的组织化学定位。初步报告。
Acta Obstet Gynecol Scand Suppl. 1984;123:15-6. doi: 10.3109/00016348409156973.
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Deficient 17beta-hydroxysteroid dehydrogenase type 2 expression in endometriosis: failure to metabolize 17beta-estradiol.子宫内膜异位症中2型17β-羟基类固醇脱氢酶表达缺陷:无法代谢17β-雌二醇。
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Binding of estrogen and progesterone to human endometrium in the different phases of the menstrual cycle. A histochemical study.雌激素和孕激素在月经周期不同阶段与人类子宫内膜的结合。一项组织化学研究。
Am J Clin Pathol. 1985 Apr;83(4):444-9. doi: 10.1093/ajcp/83.4.444.
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Estrogen receptor beta and matrix metalloproteinase 1 are coexpressed in uterine endometrium and endometriotic lesions of patients with endometriosis.雌激素受体β和基质金属蛋白酶1在子宫内膜异位症患者的子宫内膜及异位内膜病灶中共同表达。
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Progesterone receptor isoform A but not B is expressed in endometriosis.孕激素受体A亚型而非B亚型在子宫内膜异位症中表达。
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[Fundamental and clinical studies on biochemical properties of endometriosis in comparison with endometrium].[子宫内膜异位症与子宫内膜生化特性的基础及临床研究]
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Oestrogen and progesterone receptors in endometriotic tissue and endometrium: comparison of different cycle phases and ages.子宫内膜异位症组织和子宫内膜中的雌激素和孕激素受体:不同周期阶段和年龄的比较。
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Histochemical localization of estrogen and progesterone receptors: evaluation of a method.雌激素和孕激素受体的组织化学定位:一种方法的评估
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Metabolism of estrone sulfate in endometriotic tissue and in uterine endometrium in proliferative and secretory cycle phase.硫酸雌酮在子宫内膜异位症组织以及增殖期和分泌期子宫子宫内膜中的代谢。
Fertil Steril. 1988 Feb;49(2):229-33. doi: 10.1016/s0015-0282(16)59707-6.

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Cell Tissue Res. 1988 Jun;252(3):625-30. doi: 10.1007/BF00216650.