Zaino R J, Clarke C L, Feil P D, Satyaswaroop P G
Department of Pathology, Pennsylvania State University, Hershey 17033.
Endocrinology. 1989 Nov;125(5):2728-34. doi: 10.1210/endo-125-5-2728.
The action of sex steroids on the growth and differentiation of target tissues requires the presence of specific intracellular receptors. We compared the distribution of cells containing estrogen receptor (ER) and/or progesterone receptor (PR) in rabbit uterus by immunohistochemistry using monoclonal antibodies directed against these receptors. Initial experiments using serial cryostat sections surprisingly revealed the intensity of staining for ER to be inversely proportional to that of PR, as follows: ER, luminal and glandular epithelium greater than myometrium greater than stroma; PR, stroma greater than myometrium greater than glands greater than luminal epithelium. Localization was strictly confined to the nuclei of target cells. Single and dual immunofluorescent labeling of ER and PR in cryostat sections was accomplished using fluorochromes with differing emission spectra. Individual fields of dual labeled sections were examined for red [phycoerythrin (ER)] and green [fluorescein (PR)] fluorescence, with the same distribution as noted by single antibody immunohistochemistry. Myometrial nuclei displayed fluorescence of equivalent relative intensity for both antibodies. Further, sequential exposure photomicrography (exposure first in the spectrum of phycoerythrin emission, followed by exposure in the spectrum of fluorescein emission) revealed the presence of occasional stromal cells staining only for PR and some luminal cells staining only for ER. This differential distribution of ER and PR within various cell populations of rabbit is a novel observation and challenges current concepts of receptor regulation. Dual immunofluorescent localization of both ER and PR within individual cells provides a unique perspective from which to investigate the interactive influences of these sex steroid receptors at the cellular level.
性类固醇对靶组织生长和分化的作用需要特定细胞内受体的存在。我们使用针对这些受体的单克隆抗体,通过免疫组织化学方法比较了兔子宫中含雌激素受体(ER)和/或孕激素受体(PR)的细胞分布。最初使用连续冰冻切片的实验令人惊讶地发现,ER染色强度与PR染色强度呈反比,具体如下:ER,腔上皮和腺上皮大于肌层大于基质;PR,基质大于肌层大于腺体大于腔上皮。定位严格局限于靶细胞的细胞核。使用具有不同发射光谱的荧光染料对冰冻切片中的ER和PR进行单重和双重免疫荧光标记。对双重标记切片的各个视野检查红色[藻红蛋白(ER)]和绿色[荧光素(PR)]荧光,其分布与单抗体免疫组织化学所观察到的相同。肌层细胞核对两种抗体均显示出相对强度相当的荧光。此外,顺序曝光显微摄影(先在藻红蛋白发射光谱中曝光,然后在荧光素发射光谱中曝光)显示,偶尔有仅对PR染色的基质细胞和一些仅对ER染色的腔细胞存在。兔不同细胞群体中ER和PR的这种差异分布是一项新的观察结果,对当前的受体调节概念提出了挑战。ER和PR在单个细胞内的双重免疫荧光定位提供了一个独特的视角,可据此在细胞水平研究这些性类固醇受体的相互影响。