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首页> 外文期刊>Journal of Perinatal Medicine >Peroxisome proliferator-activated receptor-gamma (PPARγ) is down regulated in trophoblast cells of gestational diabetes mellitus (GDM) and in trophoblast tumour cells BeWo in vitro after stimulation with PPARγ agonists.
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Peroxisome proliferator-activated receptor-gamma (PPARγ) is down regulated in trophoblast cells of gestational diabetes mellitus (GDM) and in trophoblast tumour cells BeWo in vitro after stimulation with PPARγ agonists.

机译:过氧化物酶体增殖物激活受体-γ(PPARγ)在体外受妊娠糖尿病(GDM)的滋养层细胞和受PPARγ激动剂刺激后在滋养层肿瘤细胞中被下调。

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摘要

Peroxisome proliferator-activated receptor-gamma (PPARγ) plays an important role in insulin metabolism, trophoblast differentiation and anti-inflammatory circuits. The aim of this study was to investigate the expression of PPARγ in the placenta of patients with gestational diabetes mellitus (GDM) and the regulation of PPARγ by its agonists in trophoblast tumour cells BeWo in vitro.PPARγ expression in a total of 80 placentas (40 GDM/40 controls) was analysed by immunohistochemistry using the semi-quantitative immunoreactive score. Furthermore, a quantitative reverse transcription-polymerase chain reaction (PCR) was performed to determine the PPARγ mRNA-expression in both groups. We used a fused and a non-fused BeWo cell culture model for the stimulation with arachidonic acid and 15-Deoxy-Δ12,14-prostaglandin J2 (15d-PGJ2). Afterwards PPARγ mRNA-expression was analysed by quantitative real-time PCR (RT-PCR) (TaqMan).Using immunohistochemistry we identified a decreased expression of PPARγ in the syncytiotrophoblast and the extravillous trophoblast of GDM placentas compared to normal controls. Furthermore, PPARγ mRNA-expression was reduced in GDM placentas. Stimulation of BeWo cells with arachidonic acid and 15d-PGJ2 caused a downregulation of PPARγ expression.As PPARγ is down regulated by arachidonic acid and 15d-PGJ2, the reduced PPARγ expression in GDM placentas may be due to an altered concentration of fatty acid derivates.
机译:过氧化物酶体增殖物激活受体-γ(PPARγ)在胰岛素代谢,滋养细胞分化和抗炎回路中起重要作用。这项研究的目的是研究妊娠糖尿病(GDM)患者胎盘中PPARγ的表达以及其激动剂在体外滋养层肿瘤细胞中对PPARγ的调节.PPARγ在总共80个胎盘中表达(40使用半定量免疫反应评分,通过免疫组织化学分析了GDM / 40对照)。此外,进行定量逆转录-聚合酶链反应(PCR)以确定两组中的PPARγmRNA表达。我们使用一种融合的和非融合的BeWo细胞培养模型分别用花生四烯酸和15-脱氧-Δ12,14-前列腺素J2(15d-PGJ2)进行刺激。然后通过定量实时PCR(RT-PCR)(TaqMan)分析PPARγmRNA的表达。使用免疫组织化学,我们确定与正常对照相比,GDM胎盘的滋养层滋养层和绒毛层滋养层中PPARγ的表达降低。此外,GDM胎盘中PPARγmRNA的表达降低。花生四烯酸和15d-PGJ2刺激BeWo细胞导致PPARγ表达下调。由于花生四烯酸和15d-PGJ2下调了PPARγ,因此GDM胎盘中PPARγ表达降低可能是由于脂肪酸衍生物浓度的改变。

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