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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,腹部,MC,CocQuebert,MD EF,Fournier,Td EF,Evain-Brion,DD EF,Brennecke,Spa B,Murthi,PA B差异表达 在受人特发敏病胎儿生长限制影响的怀孕的胎盘中

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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:人发育性胎儿生长限制(FGR)与胎盘不足有关。以前,我们报道,在特发性FBR胎盘中,Homeobox基因远端3(DLX3)的表达增加,是绒毛滋养细胞分化的调节剂。在此,我们鉴定滋养细胞衍生细胞系中DLX3的下游靶标。我们使用过表达质粒构建体建模了FGR中的高水平DLX3,并使用短干扰RNA(siRNA)在培养的细胞中灭活。使用基于PCR的基因分析,将DLX3过表达和失活的候选靶基因鉴定为滋养细胞分化的调节剂; gata2和pparγ。在胎盘组织中进一步评估了GATA2和PPARγ的表达,与妊娠匹配的对照相比,FGR影响组织中的mRNA和蛋白质水平增加。我们得出结论,DLX3策划了多种调节剂分化的表达,并且这种调节基因的表达在FGR中异常。

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  • 作者单位

    Department of Perinatal Medicine Pregnancy Research Centre Royal Women's Hospital Parkville VIC;

    Department of Perinatal Medicine Pregnancy Research Centre Royal Women's Hospital Parkville VIC;

    College of Medicine King Saud Bin Abdulaziz University for Health Sciences King Abdullah;

    INSERM U767 Faculté des Sciences Pharmaceutiques et Biologiques Paris F-75006 France;

    INSERM U767 Faculté des Sciences Pharmaceutiques et Biologiques Paris F-75006 France;

    INSERM U767 Faculté des Sciences Pharmaceutiques et Biologiques Paris F-75006 France;

    Department of Perinatal Medicine Pregnancy Research Centre Royal Women's Hospital Parkville VIC;

    Department of Perinatal Medicine Pregnancy Research Centre Royal Women's Hospital Parkville VIC;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 内分泌腺疾病及代谢病;
  • 关键词

    Fetal growth; Homeobox genes; Human placenta; Trophoblast;

    机译:胎儿生长;Homeobox基因;人胎盘;滋养板;

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