Yamada A T, Nagata T
Department of Anatomy and Cell Biology, Shinshu University, School of Medicine, Matsumoto, Japan.
Cell Mol Biol (Noisy-le-grand). 1992 Nov;38(7):763-74.
Pregnant mice were ovariectomized at pre-implantation stage and exogenous nidatory estradiol was administered to evaluate the DNA synthesis of the endometrial cells during activation of uterine receptivity for blastocyst implantation. After 0, 3, 6, 12 and 18 hrs. of estradiol treatment, the animals received 3H-thymidine injection, sacrificed 1 hr. later, and the uteri were prepared for light and electron microscopic radioautography. At time 0, no labelled stromal or epithelial cells was found in the endometrium. According to the time-lapse after estradiol induction, a gradual increase of labelled stromal and endothelial cells was seen in the endometrium. The highest labeling index was observed at the antimesometrial side of the implantation sites and the lowest value was found at the interimplantation site. The cells found at mesometrial side of the implantation site showed an intermediate labeling index. Eighteen hrs. after estradiol treatment, the labelled stromal cells found near the implantation chamber resembled the morphology of decidual cells while those labelled cells localized at the interimplantation sites were similar to the fibroblast. The uterine luminal epithelial cells showed low DNA synthesis after estradiol treatment resulting in only a few labelled cells at the interimplantation sites and no labelled cells at the implantation sites. A similar labeling pattern was seen in the glandular epithelium. The distribution of labelled cells seen among the regions of pregnant endometrium under estradiol effect suggest that DNA synthesis related to uterine activation for blastocyst implantation is a focal reaction, where the luminal epithelium does nt proliferate while the stromal and endothelial cells around the conceptus increase the DNA synthesis to prepare the endometrial decidualization.
在植入前阶段对怀孕小鼠进行卵巢切除术,并给予外源性着床雌二醇,以评估在子宫对胚泡着床的接受性激活过程中子宫内膜细胞的DNA合成。在雌二醇处理0、3、6、12和18小时后,给动物注射3H-胸腺嘧啶核苷,1小时后处死,然后制备子宫用于光镜和电镜放射自显影。在时间0时,子宫内膜中未发现标记的基质细胞或上皮细胞。根据雌二醇诱导后的时间推移,子宫内膜中标记的基质细胞和内皮细胞逐渐增加。在着床部位的反系膜侧观察到最高的标记指数,在着床间隙部位发现最低值。在着床部位系膜侧发现的细胞显示出中等标记指数。雌二醇处理18小时后,在着床腔附近发现的标记基质细胞类似于蜕膜细胞的形态,而那些位于着床间隙部位的标记细胞类似于成纤维细胞。雌二醇处理后子宫腔上皮细胞显示低DNA合成,导致在着床间隙部位只有少数标记细胞,而在着床部位没有标记细胞。在腺上皮中也观察到类似的标记模式。在雌二醇作用下,怀孕子宫内膜各区域中标记细胞的分布表明,与子宫对胚泡着床的激活相关的DNA合成是一种局灶性反应,其中腔上皮不增殖,而围绕孕体的基质细胞和内皮细胞增加DNA合成以准备子宫内膜蜕膜化。