Lumbers Eugenie R, Wang Yu, Delforce Sarah J, Corbisier de Meaultsart Celine, Logan Philip C, Mitchell Murray D, Pringle Kirsty G
School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, Australia and Mothers and Babies Research Centre, Hunter Medical Research Institute, Level 3 East, 1 Kookaburra Circuit, New Lambton Heights, NSW, 2305, Australia.
The Liggins Institute, University of Auckland, Auckland, New Zealand.
Reprod Biol Endocrinol. 2015 Nov 25;13:129. doi: 10.1186/s12958-015-0127-8.
In pregnancy, the decidualised endometrium expresses high levels of prorenin and other genes of the renin-angiotensin system (RAS) pathway. In this study we aimed to determined if the RAS was present in endometrial stromal cells and if decidualisation upregulated the expression of prorenin, the prorenin receptor ((P)RR) and associated RAS pathways. Immortalised human endometrial stromal cells (HESCs) can be stimulated to decidualise by combined treatment with medroxyprogesterone acetate (MPA), 17β-estradiol (E2) and cAMP (MPA-mix) or with 5-aza-2'-deoxycytidine (AZA), a global demethylating agent.
HESCs were incubated for 10 days with one of the following treatments: vehicle, MPA-mix, a combination of medroxyprogesterone acetate (MPA) and estradiol-17β alone, or AZA. Messenger RNA abundance and protein levels of prorenin (REN), the (P)RR (ATP6AP2), angiotensinogen (AGT), angiotensin converting enzyme (ACE), angiotensin II type 1 receptor (AGTR1), vascular endothelial growth factor (VEGF), and plasminogen activator inhibitor-1 (PAI-1) were measured by real-time PCR and ELISA's, respectively. Promyelocytic zinc finger (PLZF) and phospho-inositol-3 kinase (PIK3R1) mRNA abundances were also measured.
HESCs expressed the prorenin receptor (ATP6AP2), REN, AGT, ACE and low levels of AGTR1. MPA-mix and AZA stimulated expression of REN. Prorenin protein secretion was increased in MPA-mix treated HESCs. E2 + MPA had no effect on any RAS genes. MPA-mix treatment was associated with increased VEGF (VEGFA) and PAI-1 (SERPINE1) mRNA and VEGF protein.
An endometrial prorenin receptor/renin angiotensin system is activated by decidualisation. Since (P)RR is abundant, the increase in prorenin secretion could have stimulated VEGF A and SERPINE1 expression via Ang II, as both ACE and AGTR1 are present, or by Ang II independent pathways. Activation of the RAS in human endometrium with decidualisation, through stimulation of VEGF expression and secretion, could be critical in establishing an adequate blood supply to the developing maternal placental vascular bed.
在妊娠期间,蜕膜化的子宫内膜表达高水平的肾素原和肾素 - 血管紧张素系统(RAS)途径的其他基因。在本研究中,我们旨在确定RAS是否存在于子宫内膜基质细胞中,以及蜕膜化是否上调肾素原、肾素原受体((P)RR)和相关RAS途径的表达。永生化的人子宫内膜基质细胞(HESC)可以通过醋酸甲羟孕酮(MPA)、17β - 雌二醇(E2)和cAMP(MPA混合物)联合处理或用5 - 氮杂 - 2'-脱氧胞苷(AZA,一种全局去甲基化剂)刺激而发生蜕膜化。
将HESC用以下处理之一孵育10天:溶剂、MPA混合物、醋酸甲羟孕酮(MPA)和单独的雌二醇 - 17β的组合或AZA。分别通过实时PCR和ELISA测量肾素原(REN)、(P)RR(ATP6AP2)、血管紧张素原(AGT)、血管紧张素转换酶(ACE)、血管紧张素II 1型受体(AGTR1)、血管内皮生长因子(VEGF)和纤溶酶原激活物抑制剂 - 1(PAI - 1)的信使RNA丰度和蛋白质水平。还测量了早幼粒细胞锌指(PLZF)和磷酸化肌醇 - 3激酶(PIK3R1)的信使RNA丰度。
HESC表达肾素原受体(ATP6AP2)、REN、AGT、ACE和低水平的AGTR1。MPA混合物和AZA刺激REN的表达。在MPA混合物处理的HESC中肾素原蛋白分泌增加。E2 + MPA对任何RAS基因均无影响。MPA混合物处理与VEGF(VEGFA)和PAI - 1(SERPINE1)信使RNA及VEGF蛋白增加有关。
蜕膜化激活子宫内膜肾素原受体/肾素血管紧张素系统。由于(P)RR丰富,肾素原分泌增加可能通过Ang II刺激VEGF A和SERPINE1表达,因为ACE和AGTR1均存在,或者通过Ang II非依赖途径。蜕膜化通过刺激VEGF表达和分泌激活人子宫内膜中的RAS,这对于为发育中的母体胎盘血管床建立充足的血液供应可能至关重要。