Malayer J R, Woods V M
Department of Infectious Disease and Physiology, College of Veterinary Medicine, Oklahoma State University, Stillwater 74078-0350, USA.
J Reprod Fertil. 1998 Mar;112(2):289-300. doi: 10.1530/jrf.0.1120289.
The objective of the present study was to determine the temporal expression of oestrogen receptor alpha in the uterus of the developing bovine fetus. Bovine fetuses were collected and approximate gestational age was determined by crown-rump measurement. Fetal uteri were either snap frozen in dry ice-ethanol, or placed in sterile Dulbecco's modified Eagle's medium. Fetal uteri (n = 20) were homogenized and cytosolic oestrogen receptor measured by [3H]ligand binding assay. Total RNA was extracted from fetal uteri (n = 53) and amplified by reverse transcription-polymerase chain reaction using primers specific for the oestrogen receptor, progesterone receptor, interleukin 1 alpha, interleukin 6, transforming growth factor beta, prolactin receptor, epidermal growth factor receptor, retinoic acid receptor isoforms alpha, beta, and gamma, or glyceraldehyde-3-phosphate dehydrogenase (loading control). Expressed as a ratio with glyceraldehyde-3-phosphate dehydrogenase, mRNA encoding oestrogen receptor was identified in fetal uteri throughout the period from day 65 to day 200, and was increased from day 100 to day 185 (P < 0.003); uterine samples from day 100 to day 200 expressed interleukin 1 alpha, interleukin 6, transforming growth factor beta, prolactin receptor, epidermal growth factor receptor and retinoic acid receptor isoforms alpha, beta, and gamma, but did not express detectable mRNA encoding progesterone receptor. Despite the presence of mRNA encoding oestrogen receptor, [3H]oestradiol binding was not detected until after day 155. Fetal uterine explants collected at days 100-110 (n = 3) or at days 185-200 (n = 3) were cultured in the presence of oestradiol (1.0 nmol l-1, or vehicle); there was a significant effect of oestradiol treatment on specific mRNA expression at days 185-200 (P < 0.014), but not at days 100-110 (P = 0.71). It is concluded that mRNA encoding oestrogen receptor is constitutively expressed at least from day 65 in the uterus of the bovine fetus, but that oestrogen receptor alpha protein and a functional oestrogen response are not present until late in the second third of pregnancy.
本研究的目的是确定雌激素受体α在发育中的牛胎儿子宫内的时序表达。收集牛胎儿并通过顶臀长度测量确定大致的妊娠年龄。将胎儿子宫要么在干冰 - 乙醇中速冻,要么置于无菌的杜氏改良 Eagle 培养基中。将胎儿子宫(n = 20)匀浆,通过[³H]配体结合测定法测量胞质雌激素受体。从胎儿子宫(n = 53)中提取总 RNA,并使用针对雌激素受体、孕激素受体、白细胞介素 1α、白细胞介素 6、转化生长因子β、催乳素受体、表皮生长因子受体、视黄酸受体亚型α、β和γ或甘油醛 - 3 - 磷酸脱氢酶(上样对照)的引物,通过逆转录 - 聚合酶链反应进行扩增。以与甘油醛 - 3 - 磷酸脱氢酶的比值表示,在整个第65天至第200天期间,胎儿子宫中均鉴定出编码雌激素受体的mRNA,并且从第100天至第185天有所增加(P < 0.003);第100天至第200天的子宫样本表达白细胞介素1α、白细胞介素6、转化生长因子β、催乳素受体、表皮生长因子受体和视黄酸受体亚型α、β和γ,但未检测到编码孕激素受体的可检测mRNA。尽管存在编码雌激素受体的mRNA,但直到第155天后才检测到[³H]雌二醇结合。在第100 - 110天(n = 3)或第185 - 200天(n = 3)收集的胎儿子宫外植体在雌二醇(1.0 nmol l⁻¹,或溶剂)存在下培养;雌二醇处理对第185 - 200天的特异性mRNA表达有显著影响(P < 0.014),但对第100 - 110天无显著影响(P = 0.71)。结论是,至少从第65天起,牛胎儿子宫中就组成性表达编码雌激素受体的mRNA,但直到妊娠第二个三分之一后期才出现雌激素受体α蛋白和功能性雌激素反应。