Okada A, Ohta Y, Inoue S, Hiroi H, Muramatsu M, Iguchi T
Safety Research Laboratories, Yamanouchi Pharmaceutical Co., Ltd, Itabashi, Tokyo 174-8511, Japan.
J Mol Endocrinol. 2003 Jun;30(3):301-15. doi: 10.1677/jme.0.0300301.
To determine expression and localization of receptors for estrogen (ER), progesterone (PR) and androgen (AR), detailed immunohistochemical evaluations were performed in the Sprague-Dawley rat oviduct during pre- and neonatal development, estrous cycle and pre-implantation period. In addition, real-time RT-PCR studies were conducted to evaluate changes in ERalpha, ERbeta, total PR (PR-A+B), PR-B and AR mRNA expressions. All receptors except for ERbeta were detected in epithelial, and stromal or mesenchymal cells of the fetal and neonatal oviduct, and increased with development. During the estrous cycle and early pregnancy, ERalpha and PR-A+B were expressed in epithelial, stromal and muscle cells throughout the oviduct region, and showed changes in expression predominantly in the isthmus. Only a few epithelial cells in the infundibulum (inf) and ampulla (AMP) showed ERbeta staining. AR was detected in stromal and muscle cells throughout the oviduct region, and in epithelial cells of the inf/AMP. Taken together, ERalpha, PR-A+B and AR were detected in the epithelium of the inf/AMP region, but all of these receptors were expressed in a distinct subset of epithelial cells which were negative for beta-tubulin IV, a ciliated epithelial cell marker. These results contribute to a better understanding of the respective roles of ERs, PRs and AR in the rat oviduct.
为了确定雌激素(ER)、孕激素(PR)和雄激素(AR)受体的表达及定位,我们在Sprague-Dawley大鼠输卵管的产前和新生儿发育、发情周期及着床前期进行了详细的免疫组织化学评估。此外,还进行了实时逆转录聚合酶链反应(RT-PCR)研究,以评估ERα、ERβ、总PR(PR-A+B)、PR-B和AR mRNA表达的变化。除ERβ外,所有受体均在胎儿和新生儿输卵管的上皮细胞、基质细胞或间充质细胞中检测到,并随发育而增加。在发情周期和妊娠早期,ERα和PR-A+B在整个输卵管区域的上皮细胞、基质细胞和肌肉细胞中表达,并主要在峡部显示出表达变化。漏斗部(inf)和壶腹部(AMP)只有少数上皮细胞显示ERβ染色。AR在整个输卵管区域的基质细胞和肌肉细胞以及inf/AMP的上皮细胞中检测到。综上所述,在inf/AMP区域的上皮细胞中检测到ERα、PR-A+B和AR,但所有这些受体均在β-微管蛋白IV(一种纤毛上皮细胞标记物)阴性的上皮细胞亚群中表达。这些结果有助于更好地理解ERs、PRs和AR在大鼠输卵管中的各自作用。