缺氧-再氧化:人胎盘细胞凋亡改变的有效诱导剂和子痫前期可能的病因

T. Hung, Jeremy N. Skepper, D. Charnock-Jones, G. Burton
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引用次数: 410

摘要

子痫前期是人类妊娠的一种严重疾病,其特征是母体内皮细胞的普遍活化。胎盘的氧化应激被认为是一个关键的中间步骤,促使凋亡片段被驱逐到母体循环中,但原因尚不清楚。我们假设间歇性胎盘灌注,继发于滋养细胞侵袭子宫内膜动脉不足,导致缺血-再灌注型损伤。因此,我们测试了体外缺氧-再氧化(H/R)是否刺激人胎盘组织的凋亡,并与对照组保持低氧或常氧相比。H/R后,线粒体细胞色素c的释放显著增加,并与合胞滋养细胞和胎儿内皮细胞中活性caspase 3的强烈免疫标记有关。同时,细胞滋养层细胞核对裂解的聚腺苷核糖(adp)聚合酶(PARP)的标记增多,Western blot检测到裂解的PARP片段细胞质浓度升高。合胞滋养层细胞核染色质凝聚增加,TUNEL阳性比例显著增加。这些变化伴随着乳酸脱氢酶释放到培养基中的增加。预先给予自由基清除剂去铁胺,减少细胞色素c的释放和tunel阳性指数,表明羟基自由基的产生介导了这些过程。相比之下,低氧单独引起tunel阳性指数的增加较小,并且大多数合胞滋养细胞细胞核表现出核溶解,而常氧对照则保持常染色。我们得出结论,H/R刺激合胞滋养细胞内的凋亡变化,而缺氧主要诱导坏死。因此,胎盘灌注的质量可能是子痫前期病理生理中比绝对数量更重要的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypoxia-Reoxygenation: A Potent Inducer of Apoptotic Changes in the Human Placenta and Possible Etiological Factor in Preeclampsia
Preeclampsia is a severe disorder of human pregnancy characterized by generalized activation of maternal endothelial cells. Oxidative stress of the placenta is considered a key intermediary step, precipitating deportation of apoptotic fragments into the maternal circulation, but the cause remains unknown. We hypothesize that intermittent placental perfusion, secondary to deficient trophoblast invasion of the endometrial arteries, leads to an ischemia-reperfusion–type insult. We therefore tested whether hypoxia-reoxygenation (H/R) in vitro stimulates apoptosis in human placental tissues compared with controls kept hypoxic or normoxic throughout. After H/R, release of cytochrome c from mitochondria was significantly increased and was associated with intense immunolabeling for active caspase 3 in the syncytiotrophoblast and fetal endothelial cells. There was also increased labeling of syncytiotrophoblastic nuclei for cleaved poly (ADP-ribose) polymerase (PARP), and higher cytosolic concentrations of cleaved PARP fragment were detected by Western blot. Syncytiotrophoblastic nuclei displayed increased chromatin condensation, and a significantly greater percentage was TUNEL positive. These changes were accompanied by increased lactate dehydrogenase release into the medium. Preadministration of the free radical scavenger, desferrioxamine, reduced cytochrome c release and the TUNEL-positive index, suggesting generation of hydroxyl radicals mediates these processes. By contrast, hypoxia alone caused a smaller increase in the TUNEL-positive index, and the majority of syncytiotrophoblastic nuclei displayed karyolysis, whereas normoxic controls remained euchromatic. We conclude that H/R stimulates apoptotic changes within the syncytiotrophoblast, whereas hypoxia principally induces necrosis. The quality of placental perfusion may therefore be a more important factor in the pathophysiology of preeclampsia than the absolute quantity.
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