Stewart M D, Johnson G A, Gray C A, Burghardt R C, Schuler L A, Joyce M M, Bazer F W, Spencer T E
Center for Animal Biotechnology and Genomics, Albert B. Alkek Institute of Biosciences and Technology, Texas A&M University System Health Science Center and Department of Animal Science, Texas A&M University, College Station, Texas 77843-2471, USA.
Biol Reprod. 2000 Jun;62(6):1779-89. doi: 10.1095/biolreprod62.6.1779.
Lactogenic hormones regulate epithelial proliferation, differentiation, and function in a variety of epitheliomesenchymal organs. During pregnancy, the ovine uterus is a potential site for endocrine and paracrine actions of lactogenic hormones in the form of pituitary prolactin (PRL) and placental lactogen (PL). These studies determined temporal and spatial alterations in PRL receptor (PRL-R) and expression of uterine milk proteins (UTMP), a marker of endometrial secretory activity, in the ovine endometrium during the estrous cycle and pregnancy. Slot-blot hybridization analysis indicated that steady-state levels of endometrial PRL-R mRNA increased during pregnancy. In situ hybridization and immunohistochemical analyses indicated that PRL-R mRNA and protein were exclusively expressed in the endometrial glandular epithelium (GE). No PRL-R mRNA expression was detected in luminal epithelium, stroma, myometrium, or conceptus trophectoderm. Reverse transcription-polymerase chain reaction analyses determined that the endometrial GE expressed both long and short alternative splice forms of the ovine PRL-R gene. Slot-blot hybridization analysis indicated that steady-state levels of intercaruncular endometrial UTMP mRNA increased about 3-fold between Days 20 and 60, increased another 3-fold between Days 60 and 80, and then declined slightly to Day 120. In pregnant ewes, UTMP mRNA expression was restricted to the endometrial GE in the stratum spongiosum (sGE), increased substantially between Days 15 and 17, and, between Days 17 to 50 of gestation, was markedly higher in upper than lower sGE. After Day 50, hyperplasia of the sGE was accompanied by increased UTMP mRNA expression by all sGE. Collectively, results indicate that 1) endometrial sGE is a primary target for actions of lactogenic hormones and 2) UTMP mRNA expression is correlated with PL production by the trophectoderm and state of sGE differentiation during pregnancy. It is proposed that activation of PRL-R signal transduction pathways by PRL and PL plays a major role in endometrial GE remodeling and differentiated function during pregnancy in support of conceptus growth and development.
催乳激素在多种上皮间充质器官中调节上皮细胞的增殖、分化及功能。在妊娠期间,绵羊子宫是催乳激素以垂体催乳素(PRL)和胎盘催乳素(PL)形式进行内分泌和旁分泌作用的潜在场所。这些研究确定了发情周期和妊娠期间绵羊子宫内膜中PRL受体(PRL-R)的时空变化以及子宫乳蛋白(UTMP)的表达情况,UTMP是子宫内膜分泌活动的一个标志物。狭缝印迹杂交分析表明,妊娠期间子宫内膜PRL-R mRNA的稳态水平升高。原位杂交和免疫组织化学分析表明,PRL-R mRNA和蛋白仅在内膜腺上皮(GE)中表达。在腔上皮、基质、子宫肌层或孕体滋养外胚层中未检测到PRL-R mRNA表达。逆转录-聚合酶链反应分析确定,子宫内膜GE表达绵羊PRL-R基因的长、短两种可变剪接形式。狭缝印迹杂交分析表明,子宫肉阜间子宫内膜UTMP mRNA的稳态水平在第20天至第60天之间增加约3倍,在第60天至第80天之间又增加3倍,然后在第120天略有下降。在怀孕母羊中,UTMP mRNA表达局限于海绵层的子宫内膜GE(sGE),在第15天至第17天之间大幅增加,并且在妊娠第17天至第50天期间,上sGE中的表达明显高于下sGE。第50天后,sGE的增生伴随着所有sGE中UTMP mRNA表达的增加。总体而言,结果表明:1)子宫内膜sGE是催乳激素作用的主要靶标;2)UTMP mRNA表达与滋养外胚层的PL产生以及妊娠期间sGE的分化状态相关。有人提出,PRL和PL激活PRL-R信号转导通路在妊娠期间子宫内膜GE重塑和分化功能中起主要作用,以支持孕体的生长和发育。