首页> 外文期刊>Molecular and Cellular Endocrinology >Chui, A.a b , Kalionis, B.a b , Abumaree, M.c , Cocquebert, M.d e f , Fournier, T.d e f , Evain-Brion, D.d e f , Brennecke, S.P.a b , Murthi, P.a b Downstream targets of the homeobox gene DLX3 are differentially expressed in the placentae of pregnancies affected by human idiopathic fetal growth restriction
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Chui, A.a b , Kalionis, B.a b , Abumaree, M.c , Cocquebert, M.d e f , Fournier, T.d e f , Evain-Brion, D.d e f , Brennecke, S.P.a b , Murthi, P.a b Downstream targets of the homeobox gene DLX3 are differentially expressed in the placentae of pregnancies affected by human idiopathic fetal growth restriction

机译:Chui,Aa b,Kalionis,Ba b,Abumaree,Mc,Cocquebert,Md ef,Fournier,Td ef,Evain-Brion,Dd ef,Brennecke,SPa b,Murthi,Pa b同源盒基因DLX3的下游靶标差异表达在人类特发性胎儿生长受限的影响下怀孕的胎盘中

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摘要

Human idiopathic fetal growth restriction (FGR) is associated with placental insufficiency. Previously, we reported that the expression of homeobox gene Distal-less 3 (DLX3) is increased in idiopathic FGR placentae and is a regulator of villous trophoblast differentiation. Here, we identify the downstream targets of DLX3 in trophoblast-derived cell lines. We modelled the high levels of DLX3 in FGR using an over-expression plasmid construct and complemented this using short-interference RNA (siRNA) for inactivation in cultured cells. Using a real-time PCR-based gene profiling, candidate target genes of DLX3 over-expression and inactivation were identified as regulators of trophoblast differentiation; GATA2 and PPARγ. The expression of GATA2 and PPARγ were further assessed in placental tissues and showed increased mRNA and protein levels in FGR-affected tissues compared with gestation-matched controls. We conclude that DLX3 orchestrates the expression of multiple regulators of trophoblast differentiation and that expression of these regulatory genes is abnormal in FGR.
机译:人类特发性胎儿生长受限(FGR)与胎盘功能不全相关。以前,我们报道特发性FGR胎盘中同源盒基因Distal-less 3(DLX3)的表达增加,并且是绒毛滋养细胞分化的调节因子。在这里,我们确定了滋养层细胞来源的细胞系中DLX3的下游目标。我们使用过表达质粒构建体对FGR中高水平的DLX3进行建模,并使用短干扰RNA(siRNA)对其进行补充,以在培养的细胞中失活。使用基于实时PCR的基因谱分析,DLX3过表达和失活的候选目标基因被鉴定为滋养细胞分化的调控因子。 GATA2和PPARγ。进一步评估了胎盘组织中GATA2和PPARγ的表达,并显示与妊娠匹配的对照组相比,受FGR影响的组织中的mRNA和蛋白质水平升高。我们得出的结论是,DLX3协调了滋养层细胞分化的多个调控因子的表达,而这些调控基因的表达在FGR中是异常的。

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