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Tumor necrosis factor receptor subfamily 9 (Tnfrsf9) gene is expressed in distinct cell populations in mouse uterus and conceptus during implantation period of pregnancy

机译:肿瘤坏死因子受体亚家族9(Tnfrsf9)基因在妊娠着床期的小鼠子宫和子宫中的不同细胞群体中表达

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摘要

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.
机译:肿瘤坏死因子受体亚家族9(TNFRSF9)在免疫功能中起着潜在重要的一般作用。 Tnfrsf9基因表达以前已在晚期妊娠小鼠子宫和胎盘中表征。然而,关于其在早期妊娠的植入阶段在子宫中的表达知之甚少。我们评估了植入过程中小鼠子宫和概念子宫中Tnfrsf9表达的水平和定位。在妊娠的第6.5-8.5天,相对于非植入部位组织,Tnfrsf9 mRNA的相对水平显着更高。这种增加并不取决于概念的存在,因为在怀孕的植入部位和人工诱导的蜕皮瘤之间,mRNA水平没有显着差异。通过原位杂交的定位揭示了在植入期间子宫内膜中表达Tnfrsf9的内皮和子宫自然杀伤细胞亚群。在发育中的概念中,原代滋养层巨细胞和外胎盘细胞在6.5-8.5天表达Tnfrsf9,然后在怀孕的第9.5天在围绕概念的滋养层巨细胞层表达。存在两种主要的Tnfrsf9 mRNA剪接形式,它们编码具有不同生物学功能的蛋白质。通过聚合酶链反应逆转录测定,两种mRNA剪接形式均存在于子宫和概念组织中。因此,在小鼠着床过程中,Tnfrsf9的膜形式和可溶性形式都在子宫和子宫的特定细胞类型中表达,并且可能在此过程中起重要作用。

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