Bigsby R M, Cunha G R
Endocrinology. 1986 Jul;119(1):390-6. doi: 10.1210/endo-119-1-390.
Autoradiographic studies from this laboratory have previously indicated that the uterine epithelium of the neonatal mouse is devoid of estrogen receptors. The neonatal murine uterus is composed of an undifferentiated mesenchyme and a simple columnar epithelium lining the lumen. In the present study, a method for measuring whole cell uptake of 16 alpha-[125I]iodoestradiol ([125I]iodo-E2) was developed and applied to enzymatically separated, isolated epithelial and mesenchymal cells of neonatal (4-5 days postnatal) uteri. Epithelial cells and fibromuscular cells (stromal and myometrial cells) from uteri of 21-day-old animals were used to validate the assay method. A component of the uptake of [125I]iodo-E2 by cells from 21-day-old uteri was shown to be specific, saturable, and of high affinity. Kd values for specific uptake by uterine mesenchymal and epithelial cells were 1.2-1.3 nM. Maximal specific uptake was 9.3 and 4.2 fmol/micrograms DNA for epithelial and mesenchymal cells, respectively. The uterine epithelial cells of 4- and 5-day-old mice showed no measurable specific uptake of [125I]iodo-E2, while the mesenchymal cells from these animals had a maximal specific uptake of 7.9 fmol/micrograms DNA, with a Kd of 1.3 nM. DNA synthesis increased within the uterine epithelium of neonatal mice after estrogen treatment. The thymidine labeling index was doubled 10 h after a single dose of diethylstilbestrol (DES) and returned to pretreatment values by 18 h. The epithelial mitotic index was also 2-fold higher than control values 16-18 h after DES treatment. The increase in the thymidine labeling index was specific to estrogen treatment. DES did not induce the production of estrogen receptors in neonatal uterine epithelium. Epithelial cells of 5-day-old mice that were treated with DES showed no specific [125I]iodo-E2 uptake, while whole cell uptake by mesenchymal cells from these animals exhibited a specific, high affinity component, with a maximal binding of 8.4 fmol/micrograms DNA. Autoradiographic analysis of [3H]estradiol uptake by uterine tissues from 5-day-old mice 12 h after DES treatment did not show nuclear concentration of the steroid in the epithelial cells. These results indicate that the uterine epithelium of the neonatal mouse is indeed devoid of estrogen receptors, and yet the rate of DNA synthesis within this tissue is responsive to estrogen stimulation. The epithelial cells remain devoid of estrogen receptors after DES stimulation, indicating that intraepithelial estrogen receptors are not required for induction of DNA synthesis in these cells in situ. Possible mechanisms by which this phenomenon may occur are discussed.
该实验室先前的放射自显影研究表明,新生小鼠的子宫上皮细胞缺乏雌激素受体。新生小鼠子宫由未分化的间充质和衬于管腔的单层柱状上皮组成。在本研究中,开发了一种测量全细胞摄取16α-[125I]碘雌二醇([125I]碘-E2)的方法,并将其应用于酶分离的新生(出生后4 - 5天)子宫上皮细胞和间充质细胞。使用21日龄动物子宫的上皮细胞和纤维肌细胞(基质细胞和肌层细胞)来验证该检测方法。结果表明,21日龄子宫细胞对[125I]碘-E2的摄取具有特异性、可饱和性且亲和力高。子宫间充质细胞和上皮细胞特异性摄取的Kd值为1.2 - 1.3 nM。上皮细胞和间充质细胞的最大特异性摄取量分别为9.3和4.2 fmol/μg DNA。4日龄和5日龄小鼠的子宫上皮细胞未检测到[125I]碘-E2的特异性摄取,而这些动物的间充质细胞最大特异性摄取量为7.9 fmol/μg DNA,Kd为1.3 nM。雌激素处理后,新生小鼠子宫上皮细胞内的DNA合成增加。单次给予己烯雌酚(DES)10小时后,胸苷标记指数翻倍,18小时后恢复到预处理值。DES处理后16 - 18小时,上皮有丝分裂指数也比对照值高2倍。胸苷标记指数的增加对雌激素处理具有特异性。DES未诱导新生子宫上皮细胞产生雌激素受体。用DES处理的5日龄小鼠上皮细胞未显示出特异性[125I]碘-E2摄取,而这些动物间充质细胞的全细胞摄取表现出特异性、高亲和力成分,最大结合量为8.4 fmol/μg DNA。DES处理12小时后,对5日龄小鼠子宫组织[3H]雌二醇摄取的放射自显影分析未显示上皮细胞中有类固醇的核浓集。这些结果表明,新生小鼠的子宫上皮细胞确实缺乏雌激素受体,然而该组织内的DNA合成速率对雌激素刺激有反应。DES刺激后上皮细胞仍缺乏雌激素受体,表明原位诱导这些细胞中的DNA合成不需要上皮内雌激素受体。讨论了这种现象可能发生的潜在机制。