Mehta D V, Kim Y-S, Dixon D, Jetten A M
Cell Biology Section, Division of Intramural Research, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA.
Placenta. 2002 Apr;23(4):281-7. doi: 10.1053/plac.2001.0779.
Previous studies have provided evidence indicating that the nuclear orphan receptor RTR plays an important role during embryonic development and in spermatogenesis. In this study, we examine the expression of RTR in murine placenta and several human placental choriocarcinoma cell lines. Northern blot analysis showed high expression of RTR mRNA in placental tissue. In contrast to murine testis, which contains 7.4 and 2.3 kb transcripts, placental tissue expressed only the larger transcript. Examination of RTR expression in murine placental tissue by immunohistochemistry demonstrated the presence of RTR protein in the nuclei of giant trophoblasts and spongiotrophoblasts. RTR mRNA was also expressed in rat choriocarcinoma Rcho-1 cells and in the human placental choriocarcinoma cell lines BeWo, JAR, and JEG-3. In trophoblasts, RTR was co-expressed with the estrogen-related receptors ERR alpha and ERR beta. Giant trophoblast differentiation in Rcho-1 cells, characterized by induction of placental lactogen I (PL-I), was accompanied by a steady decrease in the expression of RTR mRNA and down-regulation of ERR beta expression while levels of ERR alpha mRNA did not change significantly. RTR was able to inhibit ERR alpha-mediated transactivation through the consensus RTR-response element (RTRE) likely by competing with ERR alpha for binding to the RTRE. These results suggest the possibility of cross-talk between RTR and ERR alpha receptor signalling pathways in trophoblasts.
先前的研究已提供证据表明,核孤儿受体RTR在胚胎发育和精子发生过程中发挥重要作用。在本研究中,我们检测了RTR在小鼠胎盘和几种人胎盘绒毛膜癌细胞系中的表达。Northern印迹分析显示RTR mRNA在胎盘组织中高表达。与含有7.4 kb和2.3 kb转录本的小鼠睾丸不同,胎盘组织仅表达较大的转录本。通过免疫组织化学检测小鼠胎盘组织中RTR的表达,结果表明在巨大滋养层细胞和海绵滋养层细胞的细胞核中存在RTR蛋白。RTR mRNA也在大鼠绒毛膜癌Rcho-1细胞以及人胎盘绒毛膜癌细胞系BeWo、JAR和JEG-3中表达。在滋养层细胞中,RTR与雌激素相关受体ERRα和ERRβ共表达。以胎盘催乳素I(PL-I)诱导为特征的Rcho-1细胞中巨大滋养层细胞分化,伴随着RTR mRNA表达的稳步下降以及ERRβ表达的下调,而ERRα mRNA水平没有显著变化。RTR可能通过与ERRα竞争结合RTR反应元件(RTRE),从而抑制ERRα介导的通过共有RTRE的反式激活。这些结果提示了滋养层细胞中RTR与ERRα受体信号通路之间存在相互作用的可能性。