Laboratory of Reproductive Biology, Center for Biomedical Research and Innovation (CIIB), Universidad de los Andes, Santiago 7620001, Chile.
Faculty of Medicine, Universidad de los Andes, Santiago 7620001, Chile.
Int J Mol Sci. 2022 Aug 13;23(16):9071. doi: 10.3390/ijms23169071.
Endometrial stromal cells play an important role in reproductive success, especially in implantation and placentation. Although Mesenchymal stem cells (MSCs) have been studied to assess decidualization disorders in preeclampsia (PE), their role during trophoblast invasion remains unclear. This study aims to determine: (i) whether MSCs isolated from menstrual fluid (MenSCs) from nulliparous, multiparous, and women with a previous history of preeclampsia exhibited different patterns of proliferation and migration and (ii) whether reproductive history (i.e., prior pregnancy or prior history of PE) was able to produce changes in MenSCs, thus altering trophoblast invasion capacity. MenSCs were collected from nulliparous and multiparous women without a history of PE and from non-pregnant women with a history of PE. Proliferation and migration assays were performed on MenSCs with sulforhodamine B and transwell assays, respectively. Trophoblast invasion was analyzed by culturing HTR-8/SVneo trophospheres on a matrigel overlying MenSCs for 72 h at 5% O, simulating a 3D implantation model. A previous history of pregnancy or PE did not impact the proliferative capacity or migratory behavior of MenSCs. Following exposure to physiological endometrial conditions, MenSCs demonstrated upregulated expression of and mRNA, decidualization and window of implantation markers, respectively. The mRNA expression of , , and was upregulated upon trophosphere formation. Relative to co-culture with multiparous MenSCs, co-culture with PE-MenSCs was associated with reduced trophoblast invasion. The findings of this study suggest a potential role for communication between maternal MenSCs and invading trophoblast cells during the implantation process that could be implicated in the etiology of PE.
子宫内膜基质细胞在生殖成功中起着重要作用,特别是在着床和胎盘形成中。虽然间充质干细胞(MSCs)已被研究用于评估子痫前期(PE)中的蜕膜化障碍,但它们在滋养细胞浸润中的作用尚不清楚。本研究旨在确定:(i)从初产妇、经产妇和有 PE 病史的妇女的月经血中分离的间充质干细胞(MenSCs)是否表现出不同的增殖和迁移模式;(ii)生殖史(即既往妊娠或既往 PE 病史)是否能够改变 MenSCs,从而改变滋养细胞浸润能力。MenSCs 从无 PE 病史的初产妇和经产妇以及有 PE 病史的非妊娠妇女中收集。用磺酰罗丹明 B 进行增殖实验,用 Transwell 进行迁移实验。通过在覆盖 MenSCs 的 Matrigel 上培养 HTR-8/SVneo 滋养球 72 小时,在 5%O 下模拟 3D 着床模型,分析滋养细胞的侵袭能力。既往妊娠或 PE 病史不影响 MenSCs 的增殖能力或迁移行为。在暴露于生理子宫内膜条件下,MenSCs 分别表现出上调的 和 mRNA 表达,即蜕膜化和着床窗口标志物。当形成滋养球时, 、 和 的 mRNA 表达上调。与与经产妇 MenSCs 共培养相比,与 PE-MenSCs 共培养与减少的滋养细胞侵袭有关。本研究的结果表明,母体 MenSCs 和入侵的滋养细胞之间的通讯在着床过程中可能起着重要作用,这可能与 PE 的病因有关。