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首页> 外文期刊>Clinical Science >Human placenta-derived stromal cells decrease inflammation, placental injury and blood pressure in hypertensive pregnant mice
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Human placenta-derived stromal cells decrease inflammation, placental injury and blood pressure in hypertensive pregnant mice

机译:人胎盘来源的基质细胞减少高血压妊娠小鼠的炎症,胎盘损伤和血压

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摘要

Pre-eclampsia, the development of hypertension and proteinuria or end-organ damage during pregnancy, is a leading cause of both maternal and fetal morbidity and mortality, and there are no effective clinical treatments for pre-eclampsia aside from delivery. The development of pre-eclampsia is characterized by maladaptation of the maternal immune system, excessive inflammation and endothelial dysfunction. We have reported that detection of extracellular RNA by the Toll-like receptors (TLRs) 3 and 7 is a key initiating signal that contributes to the development of pre-eclampsia. PLacental eXpanded (PLX-PAD) cells are human placenta-derived, mesenchymal-like, adherent stromal cells that have anti-inflammatory, proangiogenic, cytoprotective and regenerative properties, secondary to paracrine secretion of various molecules in response to environmental stimulation. We hypothesized that PLX-PAD cells would reduce the associated inflammation and tissue damage and lower blood pressure in mice with pre-eclampsia induced by TLR3 or TLR7 activation. Injection of PLX-PAD cells on gestational day 14 significantly decreased systolic blood pressure by day 17 in TLR3-induced and TLR7-induced hypertensive mice (TLR3 144-111 mmHg; TLR7 145-106 mmHg; both P<0.05), and also normalized their elevated urinary protein: creatinine ratios (TLR3 5.68-3.72; TLR7 5.57-3.84; both P<0.05). On gestational day 17, aortic endothelium-dependent relaxation responses improved significantly in TLR3-induced and TLR7-induced hypertensive mice that received PLX-PAD cells on gestational day 14 (TLR3 35-65 %; TLR7 37-63 %; both P<0.05). In addition, markers of systemic inflammation and placental injury, increased markedly in both groups of TLR-induced hypertensive mice, were reduced by PLX-PAD cells. Importantly, PLX-PAD cell therapy had no effects on these measures in pregnant control mice or on the fetuses. These data demonstrate that PLX-PAD cell therapy can safely reverse pre-eclampsia-like features during pregnancy and have a potential therapeutic role in pre-eclampsia treatment.
机译:子痫前期是妊娠期间高血压和蛋白尿或终末器官损害的发展,是母婴发病率和死亡率的主要原因,除分娩外,尚无有效的临床治疗子痫前期的方法。子痫前期的发展特征在于母体免疫系统的适应不良,过度炎症和内皮功能障碍。我们已经报道了由Toll样受体(TLRs)3和7检测细胞外RNA是促成先兆子痫的关键起始信号。 PLacental eXpanded(PLX-PAD)细胞是人类胎盘来源的间充质样贴壁基质细胞,具有抗炎,促血管生成,细胞保护和再生特性,可随环境刺激而分泌各种分子。我们假设PLX-PAD细胞将减少由TLR3或TLR7激活引起的先兆子痫小鼠的相关炎症和组织损伤,并降低血压。在妊娠第14天注射PLX-PAD细胞后,到第17天,TLR3诱导和TLR7诱导的高血压小鼠(TLR3 144-111 mmHg; TLR7 145-106 mmHg;均P <0.05)可使收缩压显着降低,并且也已标准化尿蛋白:肌酐比例升高(TLR3 5.68-3.72; TLR7 5.57-3.84;两者均P <0.05)。在妊娠第17天,在妊娠第14天接受PLX-PAD细胞的TLR3诱导和TLR7诱导的高血压小鼠中,主动脉内皮依赖性舒张反应显着改善(TLR3 35-65%; TLR7 37-63%;两者均P <0.05 )。此外,PLX-PAD细胞减少了全身炎症和胎盘损伤的标志物,在两组TLR诱导的高血压小鼠中均显着增加。重要的是,在孕妇对照小鼠或胎儿中,PLX-PAD细胞疗法对这些措施没有影响。这些数据表明,PLX-PAD细胞疗法可以安全地逆转妊娠期子痫前期样特征,并在子痫前期治疗中具有潜在的治疗作用。

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