Yamada A T
Department of Anatomy and Cell Biology, Shinshu University School of Medicine, Matsumoto, Japan.
Cell Mol Biol (Noisy-le-grand). 1993 Feb;39(1):1-12.
Many efforts have been made to correlate the morphological and biochemical evidences with changes on physiological state of the uterus during activation of the implantation window. However, the exact mechanism involved in such a phenomenon remains to be determined. The present experiment used the radioautographic approach to determine whether, chronological and/or topological variations of proteins synthesis occur in the peri-implanting endometrium. Pregnant mice submitted to ovariectomy, received exogenous supply of nidatory estradiol. After 0 to 18 hrs. of time-lapsed estradiol effects, each animal received intraperitoneally, 1 hr. pulse 3H-leucine. The uterine fragments embedded in epoxy resin, were processed for light and electron microscope radioautography. The pattern of 3H-leucine incorporation in the luminal epithelium varied according to their relation with the blastocyst present in the uterine lumen. The highest incorporation ratio was seen in the epithelium just around the conceptus 6 hrs. after estradiol treatment, while in the cells localized at interimplantation site no peak of incorporation was seen. At ultrastructural level, cell organelles involved in protein synthesis were found to be labelled. Accumulation of silver grains occurred at apical portion of the epithelial cells showed accumulation of silver grains after 6 hrs. of estradiol treatment, but not on cell surface. The endometrial stromal cells localized around the blastocyst also showed a peak of 3H-leucine incorporation 6 hrs. after estradiol, but not in the cells localized at interimplantation sites. No increased labeling was seen on the components of extra-cellular matrix at ultrastructural level. The present radioautographic experiment showed that epithelial and stromal cells localized in the endometrium of implantation chamber, changed their pattern of protein synthesis under nidatory estradiol effects. This evidence suggests that the phenomenon of implantation window induced by estradiol, is not a systemic response of the whole pregnant endometrium. The activation involves only a specific population of the endometrial cells localized just around the conceptus.
人们已做出许多努力,将形态学和生化证据与着床窗激活期间子宫生理状态的变化联系起来。然而,这种现象所涉及的确切机制仍有待确定。本实验采用放射自显影方法,以确定蛋白质合成的时间和/或拓扑变化是否发生在植入前的子宫内膜中。接受卵巢切除术的怀孕小鼠接受了着床期雌二醇的外源供应。在雌二醇作用0至18小时后,每只动物腹腔注射1小时脉冲的3H-亮氨酸。将子宫片段嵌入环氧树脂中,进行光镜和电镜放射自显影处理。3H-亮氨酸掺入腔上皮的模式根据其与子宫腔内存在的胚泡的关系而有所不同。在雌二醇处理6小时后,在胚泡周围的上皮中观察到最高掺入率,而在着床间位点的细胞中未观察到掺入峰值。在超微结构水平上,发现参与蛋白质合成的细胞器被标记。上皮细胞顶端部分出现银粒积累,雌二醇处理6小时后显示银粒积累,但细胞表面没有。胚泡周围的子宫内膜基质细胞在雌二醇处理6小时后也显示3H-亮氨酸掺入峰值,但着床间位点的细胞中没有。在超微结构水平上,细胞外基质成分未观察到标记增加。本放射自显影实验表明,着床腔子宫内膜中的上皮和基质细胞在着床期雌二醇作用下改变了蛋白质合成模式。这一证据表明,雌二醇诱导的着床窗现象不是整个妊娠子宫内膜的全身性反应。激活仅涉及位于胚泡周围的特定子宫内膜细胞群。