Yoshida A, Newbold R R, Dixon D
Laboratory of Experimental Pathology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.
Toxicol Pathol. 1999 May-Jun;27(3):325-33. doi: 10.1177/019262339902700308.
The effects of neonatal diethylstilbestrol (DES) exposure on the morphology and proliferating patterns of endometrial epithelial cells were investigated at various stages of development in mice. Female CD-1 mice were given daily subcutaneous injections of 2 micrograms of DES in corn oil or corn oil alone (control) at 1-5 days of age and were killed at 5, 6, 7, 8, 15, and 22 days of age. At 5 days of age, the uteri of DES-treated mice had expanded lumina and undulated luminal surfaces lined by slightly elongated epithelial cells. At 6-8 days of age, marked infolding of clusters of hypertrophic elongated luminal epithelial cells was present; uteri had disorganized endometrial stromal and myometrial layers. At 15 and 22 days of age, the tissues from DES-treated mice had decreased numbers of endometrial glands, minimal stromal fibrosis, and smaller uterine horns than did the controls. Ultrastructurally, the endometrial epithelial cells of DES-treated mice at 5 and 8 days of age had distorted nuclei with condensed matrix and abundant secretory granules associated with rough endoplasmic reticulum and Golgi apparatus. At 8 days of age, an accumulation of fingerlike cytoplasmic processes that extended into the separated intercellular spaces and along the basal aspects of the endometrial epithelial cells were also observed. At 5-8 days of age, the proliferative activity of endometrial epithelial cells in DES-treated mice, identified by bromodeoxyuridine labeling, was significantly lower (10.5-1.7%) than that of the controls (25.5-19.8%). In situ analysis of endometrial luminal epithelial cells for DNA fragmentation representing apoptosis revealed < or = 0.1% and > 10% in the DES-treated and control mice at 5-8 days of age, respectively. The data show that cell cycle kinetics, in addition to changes in morphology, are altered in the developing mouse uterus following neonatal exposure to DES.
研究了新生小鼠暴露于己烯雌酚(DES)对子宫内膜上皮细胞形态和增殖模式在不同发育阶段的影响。雌性CD-1小鼠在1-5日龄时每天皮下注射2微克DES溶于玉米油中或仅注射玉米油(对照),并在5、6、7、8、15和22日龄时处死。5日龄时,DES处理组小鼠的子宫腔扩大,管腔表面呈波浪状,内衬稍拉长的上皮细胞。6-8日龄时,出现肥厚拉长的管腔上皮细胞簇明显内折;子宫的子宫内膜基质层和肌层紊乱。15和22日龄时,DES处理组小鼠的组织中子宫内膜腺体数量减少,基质纤维化轻微,子宫角比对照组小。超微结构上,5和8日龄DES处理组小鼠的子宫内膜上皮细胞核扭曲,基质浓缩,有丰富的分泌颗粒,与粗面内质网和高尔基体相关。8日龄时,还观察到指状细胞质突起积聚,延伸到分离的细胞间隙并沿着子宫内膜上皮细胞的基底部分。5-8日龄时,通过溴脱氧尿苷标记鉴定,DES处理组小鼠子宫内膜上皮细胞的增殖活性显著低于对照组(分别为10.5-1.7%和25.5-19.8%)。对代表凋亡的DNA片段化进行的子宫内膜管腔上皮细胞原位分析显示,5-8日龄时DES处理组和对照组小鼠分别为≤0.1%和>10%。数据表明,新生小鼠暴露于DES后,发育中的小鼠子宫除形态变化外,细胞周期动力学也发生改变。