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首页> 外文期刊>Placenta >JunB/Cyclin-D1 imbalance in placental mesenchymal stromal cells derived from preeclamptic pregnancies with fetal-placental compromise
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JunB/Cyclin-D1 imbalance in placental mesenchymal stromal cells derived from preeclamptic pregnancies with fetal-placental compromise

机译:子痫前期妊娠合并胎盘损伤的胎盘间质基质细胞中的JunB / Cyclin-D1不平衡

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Introduction In the present study, we characterized the expression of Activating Protein 1 (AP-1) factors, key cell cycle regulators, in primary placental mesenchymal stromal cells (PDMSCs) derived from normal and preeclamptic (PE) pregnancies with fetal-placental compromise. Methods PDMSCs were isolated from control (n = 20) and preeclamptic (n = 24) placentae. AP-1 expression was determined by semi-quantitative RT-PCR (sqRT-PCR), Real Time PCR and Western Blot assay. PDMSCs were plated and JunB siRNA was performed. JunB and Cyclin-D1 expression were assessed by Real Time and Western Blot analyses. Results JunB expression was significantly increased while Cyclin-D1 expression was significantly down-regulated in PE relative to control PDMSCs. JunB siRNA was accompanied by JunB down-regulation and increased Cyclin-D1 in normal PDMSCs. Conclusions We described, for the first time, AP-1 expression in PDMSCs derived from physiological and PE placentae. Importantly, we demonstrated that JunB over-expression in PE-PDMSCs affects Cyclin-D1 regulation. Our data suggest a possible contribution of these pathological placental cells to the altered cell cycle regulation typical of preeclamptic placentae.
机译:引言在本研究中,我们表征了活化蛋白1(AP-1)因子,关键细胞周期调节因子在源自胎盘正常和先兆子痫(PE)妊娠且胎盘受损的胎盘间质基质细胞(PDMSC)中的表达。方法从对照组(n = 20)和先兆子痫(n = 24)胎盘中分离PDMSC。通过半定量RT-PCR(sqRT-PCR),实时PCR和Western Blot检测确定AP-1的表达。将PDMSC铺板并进行JunB siRNA。通过实时和Western Blot分析评估JunB和Cyclin-D1表达。结果与对照PDMSC相比,PE中JunB表达显着增加,而Cyclin-D1表达显着下调。在正常PDMSC中,JunB siRNA伴随JunB下调和Cyclin-D1增加。结论我们首次描述了在生理和PE胎盘来源的PDMSC中AP-1的表达。重要的是,我们证明了PE-PDMSC中的JunB过表达会影响Cyclin-D1的调控。我们的数据表明这些病理性胎盘细胞可能对子痫前胎盘典型的改变的细胞周期调控有贡献。

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