Department of Gynecology and Obstetrics, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China (mainland).
Department of Gynecology and Obstetrics, Provincial Clinical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian, China (mainland).
Med Sci Monit. 2019 Apr 19;25:2868-2878. doi: 10.12659/MSM.915449.
BACKGROUND Atrial natriuretic peptide (ANP) is a cardiac hormone that regulates blood pressure and the salt-water balance in the blood. It acts through natriuretic peptide receptors (NPR), and the major biologically active ANP receptor is natriuretic peptide receptor-A (NPR-A). Aberrant forms of ANP and its receptors have been reported in patients with preeclampsia. However, whether aberrant forms of ANP or NPR-A are present in preeclamptic placenta, and what their role is in preeclampsia pathogenesis, has not yet been elucidated clearly. The aim of this study was to assess the expression of ANP and NPR-A in the placenta and decidua and its role in preeclampsia development. MATERIAL AND METHODS The expression of ANP and NPR-A in the first-trimester villous and decidua, full-term placenta, and preeclamptic placenta was determined using immunohistochemistry and Western blot analysis. The HTR8/SVneo cell line was used to investigate the role of NPR-A in proliferation, apoptosis, and invasion using Cell Counting Kit-8 analysis, flow cytometry analysis, and a Transwell invasion assay, respectively. RESULTS ANP and NPR-A were localized in the syncytiotrophoblasts, cytotrophoblasts, and trophoblast columns of human first-trimester villous trophoblast cells of decidua, and in the glandular epithelium and extravillous trophoblast cells of decidua. ANP-positive and NPR-A-positive cells in the decidual stroma were clustered around and infiltrated into the vascular wall of the spiral artery undergoing remodeling. NPR-A expression was significantly reduced in preeclamptic placentas, and NPR-A knockdown significantly impaired the invasion ability of HTR8/SVneo cells, although it had no effect on cell proliferation and apoptosis. CONCLUSIONS ANP and NPR-A are involved in human placental development. Decreased levels of NPR-A may contribute to the development of preeclampsia.
心钠肽(ANP)是一种心脏激素,可调节血压和血液中的盐水平衡。它通过利钠肽受体(NPR)发挥作用,主要的生物活性 ANP 受体是利钠肽受体-A(NPR-A)。子痫前期患者中已报道存在异常形式的 ANP 和其受体。然而,异常形式的 ANP 或 NPR-A 是否存在于子痫前期胎盘,以及它们在子痫前期发病机制中的作用尚未阐明。本研究旨在评估 ANP 和 NPR-A 在胎盘和蜕膜中的表达及其在子痫前期发病中的作用。
采用免疫组织化学和 Western blot 分析检测第一孕期绒毛和蜕膜、足月胎盘和子痫前期胎盘的 ANP 和 NPR-A 表达。使用 HTR8/SVneo 细胞系分别通过细胞计数试剂盒-8 分析、流式细胞术分析和 Transwell 侵袭试验研究 NPR-A 在增殖、凋亡和侵袭中的作用。
ANP 和 NPR-A 定位于人第一孕期绒毛滋养层细胞的合体滋养层细胞、细胞滋养层细胞和滋养层柱,以及蜕膜的腺体上皮细胞和绒毛外滋养层细胞。蜕膜基质中 ANP 阳性和 NPR-A 阳性细胞聚集并浸润到正在重塑的螺旋动脉的血管壁周围。子痫前期胎盘 NPR-A 表达显著降低,NPR-A 敲低显著损害 HTR8/SVneo 细胞的侵袭能力,尽管它对细胞增殖和凋亡没有影响。
ANP 和 NPR-A 参与了人类胎盘的发育。NPR-A 水平的降低可能导致子痫前期的发生。