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Placenta-derived extracellular vesicles induce preeclampsia in mouse models

机译:胎盘衍生的细胞外囊囊泡在小鼠模型中诱导预先普利克斯

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Preeclampsia is a pregnancy-induced condition that impairs the mother's health and results in pregnancy termination or premature delivery. Elevated levels of placenta-derived extracellular vesides (pcEV) in the circulation have been consistently associated with preeclampsia, but whether these vesicles induce preeclampsia or are the product of preeclampsia is not known. Guided by a small cohort study of preeclamptic patients, we examined the impact of pcEV on the pathogenesis of preeclampsia in mouse models. We detected pcEV in pregnant C56BL/6J mice with a peak level of 3.8 +/- 0.9x10(7)/mL at 17-18 days postcoitum. However, these pregnant mice developed hypertension and proteinuria only after being infused with vesicles purified from injured placenta. These extracellular vesicles released from injured placenta disrupted endothelial integrity and induced vasoconstriction. Enhancing the dearance of extracellular vesides prevented the development of the extracellular vesicle-induced preeclampsia in mice. Our results demonstrate a causal role of pcEV in preeclampsia and identify microveside dearance as a new therapeutic strategy for the treatment of this pregnancy-associated complication.
机译:预口普拉姆斯是一种妊娠诱导的条件,损害母亲的健康,并导致怀孕终止或过早递送。循环中的胎盘衍生细胞外符号(PCEV)升高一直与先兆子痫有关,但这些囊泡是否诱导预先升板或是预先坦克西亚的产物。由一小群队患者的小队列研究指导,我们检查了PCEV对小鼠模型预坦克西亚发病机制的影响。在17-18天的Postcoitum,我们检测到怀孕C56BL / 6J小鼠中的PCEV,峰值水平为3.8 +/- 0.9x10(7)/ mL。然而,这些怀孕的小鼠才能在注入受伤胎盘纯化的囊泡后产生高血压和蛋白尿。这些细胞外囊泡从受伤的胎盘中释放出内皮完整性并诱导血管收缩。增强细胞外血晶的耐益,防止了小鼠细胞外囊泡诱导的预胰抗的发育。我们的结果表明,PCEV在预坦克西氏症中的因果作用,并鉴定微缺酰均衡作为治疗这种妊娠相关并发症的新治疗策略。

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