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正常人子宫内膜细胞中雌激素和孕激素细胞内定位的免疫荧光分析(作者译)

[Immunofluorescent analysis of intracellular localization of estrogen and progesterone in normal human endometrial cells (author's transl)].

作者信息

Kato Y, Kimura J, Harada K, Hirose T, Nawa M, Okada H

出版信息

Acta Obstet Gynaecol Jpn. 1980 Dec;32(12):1999-2006.

PMID:7010879
Abstract

Intracellular localization and the heat-dependent redistribution of estrogen and progesterone in human endometrial cells have been investigated by a fluorescent steroid-antibody technique. The dispersed endometrial cells were incubated with 5 X 10(-8) M estradiol-17 beta and progesterone in TC medium 199 containing 10% calf serum for 1--3 hr at 4 degrees C or 37 degrees C. An indirect immunofluorescent technique using FITC-labeled anti-rabbit IgG and steroid antibodies raised from rabbits immunizing with estradiol-6-oxime-BSA and progesterone-3-oxime-BSA was applied to the smear specimens. In normal endometrial cells in both proliferative and secretory stages, specific fluorescences to estradiol and progesterone were generally observed in the cytoplasm after incubation with the steroids at 4 degrees C for 1 hr. When these cells were incubated with the steroids at 37 degrees C for 1 hr, cytoplasmic and predominant nuclear fluorescences were detected, whereas the 3 hr-incubation at 37 degrees C resulted in disappearance of cytoplasmic fluorescence, remaining nuclear fluorescence alone. These fluorescences were remarkedly eliminated when endometrial cells were incubated with diethylstilbestrol and R-5020 prior to the incubation with estradiol and progesterone, respectively. These results indicate that the fluorescent steroid-antibody technique used in this study enables us to visualize subcellular localization of estradiol and progesterone possibly bound to receptors in each endometrial cell.

摘要

通过荧光甾体抗体技术研究了雌激素和孕激素在人子宫内膜细胞中的细胞内定位以及热依赖性再分布。将分散的子宫内膜细胞在含有10%小牛血清的TC 199培养基中,于4℃或37℃下与5×10⁻⁸M的雌二醇-17β和孕酮孵育1 - 3小时。将使用异硫氰酸荧光素标记的抗兔IgG以及用雌二醇-6-肟-牛血清白蛋白和孕酮-3-肟-牛血清白蛋白免疫兔子产生的甾体抗体的间接免疫荧光技术应用于涂片标本。在增殖期和分泌期的正常子宫内膜细胞中,在4℃下与甾体孵育1小时后,通常在细胞质中观察到对雌二醇和孕酮的特异性荧光。当这些细胞在37℃下与甾体孵育1小时时,检测到细胞质和主要的核荧光,而在37℃下孵育3小时导致细胞质荧光消失,仅留下核荧光。当子宫内膜细胞分别在与雌二醇和孕酮孵育之前,先与己烯雌酚和R-5020孵育时,这些荧光明显消除。这些结果表明,本研究中使用的荧光甾体抗体技术使我们能够观察到可能与每个子宫内膜细胞中的受体结合的雌二醇和孕酮的亚细胞定位。

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