Department of Physiology, Southern Illinois University School of Medicine, Carbondale, 62901, IL, USA.
Cell Tissue Res. 2011 Jun;344(3):567-76. doi: 10.1007/s00441-011-1171-0. Epub 2011 May 12.
Tumor necrosis factor receptor subfamily 9 (TNFRSF9) plays a potentially important general role in immune function. Tnfrsf9 gene expression has previously been characterized in late pregnant mouse uterus and placenta. However, little is known about its expression in the uterus during the implantation phase of early pregnancy. We have assessed the levels and localization of Tnfrsf9 expression in the mouse uterus and conceptus during implantation. Relative Tnfrsf9 mRNA levels were significantly higher in implantation than in non-implantation site tissue on days 6.5-8.5 of pregnancy. This increase did not depend on the presence of the conceptus, as mRNA levels were not significantly different between pregnant implantation sites and artificially induced deciduomas. Localization by in situ hybridization revealed a subpopulation of endothelial and uterine natural killer cells expressing Tnfrsf9 in the endometrium during implantation. In the developing conceptus, primary trophoblast giant and ectoplacental cells expressed Tnfrsf9 on days 6.5-8.5, followed by expression in the trophoblast giant cell layers surrounding the conceptus on day 9.5 of pregnancy. Two main splice forms of Tnfrsf9 mRNA exist and encode proteins with distinct biological functions; both mRNA splice forms were present in uterine and conceptus tissues as determined by reverse transcription with the polymerase chain reaction. Thus, both membrane and soluble forms of Tnfrsf9 are expressed in specific cell types of the uterus and conceptus during the progression of implantation in mice and possibly have an important function in this process.
肿瘤坏死因子受体超家族 9(TNFRSF9)在免疫功能中发挥着潜在的重要作用。此前,已经在妊娠晚期小鼠子宫和胎盘组织中对 Tnfrsf9 基因表达进行了研究。然而,在妊娠早期着床阶段,其在子宫中的表达情况知之甚少。我们评估了 Tnfrsf9 在小鼠子宫和胚胎着床过程中的表达水平和定位。在妊娠第 6.5-8.5 天,与非着床部位组织相比,Tnfrsf9 的相对 mRNA 水平在着床部位显著升高。这种增加并不依赖于胚胎的存在,因为在妊娠着床部位和人工诱导的蜕膜瘤之间,mRNA 水平没有显著差异。原位杂交定位显示,在着床期子宫内膜中,内皮细胞和子宫自然杀伤细胞亚群表达 Tnfrsf9。在发育中的胚胎中,初级滋养细胞巨细胞和胎盘外细胞在妊娠第 6.5-8.5 天表达 Tnfrsf9,随后在妊娠第 9.5 天,在胚胎周围的滋养细胞巨细胞层表达。存在两种主要的 Tnfrsf9 mRNA 剪接形式,编码具有不同生物学功能的蛋白质;通过聚合酶链反应的逆转录,在子宫和胚胎组织中都存在这两种 mRNA 剪接形式。因此,在小鼠着床过程中,Tnfrsf9 的膜结合和可溶性形式均在子宫和胚胎的特定细胞类型中表达,并且在该过程中可能具有重要功能。