Pregnancy-specific beta-1-glycoprotein 1-enriched exosomes are involved in the regulation of vascular endothelial cell function during pregnancy

微泡 怀孕 脐静脉 外体 胎盘 内皮 内科学 内分泌学 内皮干细胞 滋养层 免疫学 医学 生物 胎儿 生物化学 体外 小RNA 遗传学 基因
作者
Linyan Jia,Xiaojie Huang,Hao Peng,Yuanhui Jia,Ruonan Zhang,Yingying Wei,Mengtian Wei,Ruixue Wang,Han Li,Qizhi He,Kai Wang
出处
期刊:Placenta [Elsevier BV]
卷期号:139: 138-147 被引量:6
标识
DOI:10.1016/j.placenta.2023.06.014
摘要

Pregnancy is a dynamic time period associated with significant physiological changes in the cardiovascular system. It is well known that during pregnancy, the placenta secretes a variety of molecular signals, including exosomes, into the maternal circulation to adapt to increased blood volume and maintain blood pressure at normotensive levels.In the present study, we compared the effects of exosomes derived from the peripheral blood serum of nonpregnant women (NP-Exo) and pregnant women with uncomplicated pregnancy (P-Exo) on endothelial cell function. We also analyzed the proteomic profiles of these two groups of exosomes and the molecular mechanisms underlying the effect of exosome cargoes on vascular endothelial cell function.We found that P-Exo were positively involved in regulating the function of human umbilical vein endothelial cell (HUVEC) and promoting the release of nitric oxide (NO). Furthermore, we revealed that trophoblast-derived pregnancy-specific beta-1-glycoprotein 1 (PSG1)-enriched exosomes treatment induced the promotion of HUVEC proliferation and migration as well as the release of NO. In addition, we found that P-Exo maintained blood pressure at normal levels in mice.These results suggested that PSG1-enriched exosomes derived from maternal peripheral blood regulate the function of vascular endothelial cells and play an important role in maintaining maternal blood pressure during pregnancy.
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