Department of Biological Sciences, Mount Holyoke College, South Hadley, Massachusetts, USA.
J Anat. 2024 Jun;244(6):1054-1066. doi: 10.1111/joa.14019. Epub 2024 Jan 30.
The mammalian placenta's interface with the parent is a richly vascularized tissue whose development relies upon communication between many different cell types within the uterine microenvironment. The uterine blood vessels of the interface are reshaped during pregnancy into wide-bore, flaccid vessels that convey parental blood to the exchange region of the placenta. Invasive trophoblast as well as parental uterine macrophages and Natural Killer cells are involved in the stepwise remodeling of these vessels and their respective contributions to this crucial process are still being delineated. However, the earliest steps in arteriole remodeling are understudied as they are difficult to study in humans, and other species lack the deep trophoblast invasion that is so prominent a feature of placentation in humans. Here, we further characterize the rat, with deep hemochorial placentation akin to humans, as a model system in which to tease apart the earliest, relatively understudied events in spiral arteriole remodeling. We show that the rat uterine-placental interface increases in size and vascularity rapidly, before trophoblast invasion. The remodeling stages in the arterioles of the rat uterine-placental interface follow a sequence of anatomical changes similar to those in humans, and there are changes to the arterioles' muscular tunica media prior to the marked influx of immune cells. The rat is a tractable model in which to better understand the cell/cell interactions occurring in vivo in an intact tissue microenvironment over time.
哺乳动物胎盘与母体的界面是一个富含血管的组织,其发育依赖于子宫微环境中许多不同细胞类型之间的通讯。妊娠期间,界面的子宫血管重塑为宽口径、松弛的血管,将母体血液输送到胎盘的交换区域。侵袭性滋养层以及母体子宫巨噬细胞和自然杀伤细胞参与这些血管的逐步重塑,它们各自对这一关键过程的贡献仍在阐明之中。然而,由于在人类中难以研究,因此对小动脉重塑的最早步骤研究不足,而且其他物种缺乏人类胎盘形成中如此突出的深滋养层侵袭特征。在这里,我们进一步将具有与人相似的深绒毛膜胎盘的大鼠作为模型系统进行研究,以剖析螺旋小动脉重塑中最早、相对研究较少的事件。我们发现,在滋养层侵袭之前,大鼠的子宫胎盘界面迅速增大并增加血管密度。大鼠子宫胎盘界面中小动脉的重塑阶段遵循与人类相似的解剖学变化序列,并且在大量免疫细胞涌入之前,动脉的中膜肌层发生变化。大鼠是一种易于处理的模型,可以更好地理解在完整的组织微环境中随时间发生的细胞/细胞相互作用。