首页> 外文期刊>The Tohoku Journal of Experimental Medicine >Expression of nuclear factor-kappa B and placental apoptosis in pregnancies complicated with intrauterine growth restriction and preeclampsia: an immunohistochemical study.
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Expression of nuclear factor-kappa B and placental apoptosis in pregnancies complicated with intrauterine growth restriction and preeclampsia: an immunohistochemical study.

机译:妊娠并发宫内生长受限和先兆子痫的核因子-κB和胎盘细胞凋亡的表达:一项免疫组织化学研究。

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摘要

Preeclampsia affects 7-10% of all pregnancies, and is a major cause of maternal and fetal morbidity and mortality. Although enhanced apoptosis is well known in placentas with preeclampsia, the role of transcription factor nuclear factor-kappa B (NF-kappa B) in the process is still being debated. In this work, we investigate the relationship between NF-kappa B expression and trophoblastic cell apoptosis in pregnancies complicated with preeclampsia or intrauterine growth restriction (IUGR) by immunohistochemical analysis of NF-kappa B and three apoptosis related markers: bcl-2, caspase-3, and M30 CytoDeath antibody that identifies early apoptotic changes in the cytoskeleton related to action of caspase. The study was conducted on placental samples from 19 preeclamptic, 5 IUGR-complicated and 10 normal pregnant women. The three conclusions from the statistical analysis of the data are obtained; (i) Significantly higher expression of NF-kappa B in IUGR-complicated (p = 0.003) and preeclamptic placentas (p = 0.004) than the control placentas, (ii) significantly higher M30 index and caspase 3 expression in IUGR and preeclampsia placentas (p = 0.003), and (iii) decreased expression of bcl-2 in IUGR and preeclampsia placentas (p = 0.001). Based on these observations, we suggest that increased trophoblastic apoptosis is at least partially induced by NF-kappa B and reduced bcl-2 expression.
机译:子痫前症影响所有怀孕的7-10%,是母婴发病率和死亡率的主要原因。尽管子痫前期胎盘中增强的细胞凋亡是众所周知的,但是转录因子核因子-κB(NF-κB)在该过程中的作用仍在争论中。在这项工作中,我们通过对NF-κB的免疫组织化学分析和三种凋亡相关标记:bcl-2,caspase- 3和M30 CytoDeath抗体,可识别与caspase作用有关的细胞骨架中的早期凋亡变化。该研究是从19名先兆子痫,5名IUGR并发症和10名正常孕妇的胎盘样本中进行的。从数据的统计分析中得出三个结论。 (i)IUGR并发症(p = 0.003)和先兆子痫胎盘(p = 0.004)中的NF-κB表达明显高于对照胎盘(ii)IUGR和先兆子痫胎盘中M30指数和caspase 3的表达显着更高p = 0.003),以及(iii)IUGR和先兆子痫胎盘中bcl-2的表达降低(p = 0.001)。基于这些观察,我们建议增加的滋养细胞凋亡至少部分是由NF-κB和降低的bcl-2表达诱导的。

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