Sonderegger S, Husslein H, Leisser C, Knöfler M
Department of Obstetrics and Gynecology, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria.
Placenta. 2007 Apr;28 Suppl A(Suppl A):S97-102. doi: 10.1016/j.placenta.2006.11.003. Epub 2007 Jan 2.
Canonical Wingless (Wnt) signalling provoked by exogenous and endogenous Wnt ligands was recently shown to play a crucial role in the invasive differentiation of human trophoblasts. To gain insights into the expression pattern of the developmental regulators, we analysed all human Wnt ligands and their frizzled (FZD) receptors in the human placenta and different trophoblast model systems using semi-quantitative PCR. Fourteen out of 19 Wnt ligands and 8 out of 10 FZD receptors were detectable in placental tissues, however, expression patterns varied with gestational age and between different trophoblast subtypes suggesting cell-specific functions. Besides Wnt ligands acting through the canonical pathway, non-canonical ligands such as Wnt-5a, which may also activate alternative Wnt signalling pathways or inhibit canonical Wnt signalling, could be identified. Western blot analyses revealed secretion of Wnt-5a from primary trophoblast cultures and trophoblastic cell lines. To evaluate the potential role of Wnt-5a, SGHPL-5 trophoblast cells were transfected with luciferase reporter plasmids harbouring eight T-cell factor (TCF) DNA-recognition sequences which are exclusively activated through the canonical Wnt signalling pathway. Luciferase assays revealed that Wnt-3a-induced reporter activity was repressed by recombinant Wnt-5a indicating an antagonistic role in trophoblasts. The data suggest that a complex network of Wnt ligands and FZD receptors may regulate developmental processes of the human placenta.
最近研究表明,外源性和内源性Wnt配体引发的经典无翅型(Wnt)信号通路在人滋养层细胞的侵袭性分化中起关键作用。为深入了解发育调节因子的表达模式,我们使用半定量PCR分析了人胎盘和不同滋养层模型系统中所有人类Wnt配体及其卷曲蛋白(FZD)受体。在胎盘组织中可检测到19种Wnt配体中的14种以及10种FZD受体中的8种,然而,表达模式随胎龄以及不同滋养层亚型而变化,提示其具有细胞特异性功能。除了通过经典途径起作用的Wnt配体,还可鉴定出非经典配体,如Wnt-5a,其可能还会激活其他Wnt信号通路或抑制经典Wnt信号通路。蛋白质免疫印迹分析显示,原代滋养层细胞培养物和滋养层细胞系可分泌Wnt-5a。为评估Wnt-5a的潜在作用,用含有八个T细胞因子(TCF)DNA识别序列的荧光素酶报告质粒转染SGHPL-5滋养层细胞,这些序列仅通过经典Wnt信号通路被激活。荧光素酶检测显示,重组Wnt-5a可抑制Wnt-3a诱导的报告基因活性,表明其在滋养层细胞中起拮抗作用。数据表明,Wnt配体和FZD受体的复杂网络可能调节人胎盘的发育过程。