Agras Koray, Willingham Emily, Shiroyanagi Yoshiyuki, Minasi Petros, Baskin Laurence S
Institute for the Study and Treatment of Hypospadias, Department of Urology, UCSF Children's Medical Center, University of California-San Francisco, San Francisco, CA, USA.
J Urol. 2007 Jun;177(6):2386-92. doi: 10.1016/j.juro.2007.01.111.
We examined the ontogenic and sex specific expression of estrogen receptor-alpha and beta in mouse genital tubercles and assessed the effects of in utero estrogen exposure on these parameters.
Expression of the 2 genes was detected in mouse genital tubercles from fetuses collected on gestational days 12, 14, 16 and 18, and from newborns using immunohistochemistry and quantitative polymerase chain reaction. Pregnant dams were exposed to ethinyl estradiol or corn oil as the control.
Estrogen receptor-alpha and beta proteins first appeared on gestational days 12 and 14, respectively. The 2 proteins were expressed in the urethral plate and mesenchyma. Staining intensity was more prominent in the mesenchyma for estrogen receptor-alpha and in the urethral plate for estrogen receptor-beta. Female genital tubercles expressed more estrogen receptor-alpha than male genital tubercles (p <0.01), while estrogen receptor-alpha expression increased gradually in the 2 sexes until birth. Estrogen receptor-beta expression did not differ between males and females, and it showed no notable variation during fetal life. Ethinyl estradiol led to a 2.1 and 3.8-fold increase in estrogen receptor-alpha expression in females and in males with hypospadias (p = 0.002 and 0.04, respectively). Estrogen receptor-beta expression did not change in response to ethinyl estradiol.
This study provides in vivo evidence that estrogen receptor-alpha expression in the genital tubercles of each sex increases until parturition but estrogen receptor-beta expression does not, implying genital tubercle sensitivity to estrogen increases during fetal life. Exogenous administration of estrogens results in a response of increased expression of estrogen receptor-alpha but not of estrogen receptor-beta. These differential findings for estrogen receptor-alpha and beta imply that the 2 receptors may have different roles in normal or anomalous genital tubercle development.
我们研究了雌激素受体α和β在小鼠生殖结节中的个体发生及性别特异性表达,并评估了子宫内雌激素暴露对这些参数的影响。
使用免疫组织化学和定量聚合酶链反应,在妊娠第12、14、16和18天收集的胎儿以及新生儿的小鼠生殖结节中检测这两种基因的表达。将怀孕母鼠暴露于乙炔雌二醇或玉米油作为对照。
雌激素受体α和β蛋白分别在妊娠第12天和14天首次出现。这两种蛋白在尿道板和间充质中表达。雌激素受体α在间充质中的染色强度更明显,而雌激素受体β在尿道板中的染色强度更明显。雌性生殖结节比雄性生殖结节表达更多的雌激素受体α(p<0.01),而雌激素受体α在两性中的表达在出生前逐渐增加。雌激素受体β的表达在雄性和雌性之间没有差异,并且在胎儿期没有明显变化。乙炔雌二醇导致雌性和患有尿道下裂的雄性中雌激素受体α表达分别增加2.1倍和3.8倍(分别为p = 0.002和0.04)。雌激素受体β的表达对乙炔雌二醇没有反应。
本研究提供了体内证据,表明各性别生殖结节中雌激素受体α的表达在分娩前增加,但雌激素受体β的表达没有增加,这意味着胎儿期生殖结节对雌激素的敏感性增加。外源性给予雌激素会导致雌激素受体α表达增加,但不会导致雌激素受体β表达增加。雌激素受体α和β这些不同的发现表明,这两种受体在正常或异常生殖结节发育中可能具有不同的作用。