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The role of p38α mitogen-activated protein kinase gene in the HELLP syndrome

机译:p38α丝裂原活化蛋白激酶基因在HELLP综合征中的作用

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Mitogen-activated protein kinase (MAPK) p38α was shown to be implicated in the organogenesis of the placenta, and such placental alteration is crucial for the development of hemolysis, elevated liver enzymes, and low platelets (HELLP) syndrome. We aimed to analyze for the first time human placental expression of MAPK p38α in pregnancies complicated by HELLP. The placental expression of MAPK p38α was investigated by semiquantitative polymerase chain reaction using cDNA extracted from placental tissue of 15 pregnancies with HELLP syndrome and 15 gestational age-matched controls. Seven patients with HELLP also had intrauterine fetal growth restriction (IUGR). In placenta from pregnancy complicated by HELLP, the expression of MAPK p38α is significantly decreased compared to the group with normal pregnancy (p?
机译:丝裂原激活的蛋白激酶(MAPK)p38α被证明与胎盘的器官发生有关,这种胎盘的改变对于溶血,肝酶升高和低血小板(HELLP)综合征的发生至关重要。我们旨在首次分析妊娠合并HELLP的人胎盘中MAPKp38α的表达。通过半定量聚合酶链反应,使用从15例HELLP综合征孕妇和15个胎龄匹配对照胎盘组织中提取的cDNA,研究了MAPKp38α的胎盘表达。七名HELLP患者也有宫内胎儿生长受限(IUGR)。与正常妊娠组相比,妊娠并发HELLP引起的胎盘中MAPKp38α的表达显着降低(p <0.001),而IULP亚群的HELLP和HELLP之间无差异。我们的研究首次表明MAPKp38α在人胎盘中表达。具有胎盘功能障碍和高血压并发症的孕妇的特征在于MAPKp38α的表达显着降低。我们的观察结果表明,p38 MAPK信号传导可能在胎盘血管生成和功能中至关重要。

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