Kusuma G D, Manuelpillai U, Abumaree M H, Pertile M D, Brennecke S P, Kalionis B
University of Melbourne, Department of Obstetrics and Gynaecology, Royal Women's Hospital, Parkville, Victoria 3052, Australia; Pregnancy Research Centre, Department of Perinatal Medicine, Royal Women's Hospital, Parkville, Victoria 3052, Australia.
Pregnancy Research Centre, Department of Perinatal Medicine, Royal Women's Hospital, Parkville, Victoria 3052, Australia; Centre for Genetic Diseases, Monash Institute of Medical Research, Monash University, Clayton, Victoria 3168, Australia; Prince Henry's Institute of Medical Research, Monash University, Clayton, Victoria 3168, Australia.
Placenta. 2015 Mar;36(3):312-21. doi: 10.1016/j.placenta.2014.12.014. Epub 2014 Dec 24.
Maternal decidua basalis tissue attached to the placenta following delivery is a source of decidual mesenchymal stem cells (DMSCs). The in vitro characteristics of DMSCs have been partly defined but their in vivo function(s) are poorly understood. The anatomic location, or niche, provides clues regarding potential in vivo function(s) of DMSCs, but the niche has not been described.
Cells were isolated from the decidua basalis and flow cytometric analyses showed the expected phenotypic profile for MSC cell surface markers. In vitro, the cells differentiated into adipocytes, osteocytes, and chondrocytes. DMSCs were then stained with antibodies by immunofluorescence detection.
Immunocytochemistry revealed that DMSCs were positive for FZD-9, STRO-1, 3G5, and α-SMA as expected and lacked expression of vWF and Ck7. Fluorescence in situ hybridization analysis showed the cultured cells were of maternal origin. Immunofluorescence was carried out on placental bed biopsies using the FZD-9, STRO-1, 3G5, and α-SMA antibodies. DMSCs were located in the vascular niche in decidua basalis. Immunofluorescence with antibodies to FZD-9, Ck7 and vWF revealed DMSCs in the vascular niche surrounding intact non-transformed spiral arterioles but DMSCs were absent in fully transformed spiral arterioles.
Spiral arteriole remodelling is a critical feature of human pregnancy. The DMSC niche was investigated in fully transformed and non-transformed spiral arterioles. DMSCs have not been previously implicated in spiral arteriole remodelling. The absence of DMSCs around fully transformed spiral arterioles suggests they are a target for replacement or destruction by invading placental extravillous trophoblast cells, which carry out spiral arteriole remodelling.
分娩后附着于胎盘的母体基蜕膜组织是蜕膜间充质干细胞(DMSC)的来源。DMSC的体外特性已部分明确,但其体内功能尚不清楚。解剖位置或微环境可为DMSC的潜在体内功能提供线索,但该微环境尚未被描述。
从基蜕膜中分离细胞,流式细胞术分析显示其具有间充质干细胞(MSC)细胞表面标志物的预期表型特征。在体外,这些细胞可分化为脂肪细胞、骨细胞和软骨细胞。然后通过免疫荧光检测用抗体对DMSC进行染色。
免疫细胞化学显示,DMSC如预期的那样对FZD - 9、STRO - 1、3G5和α - SMA呈阳性,且不表达vWF和Ck7。荧光原位杂交分析表明培养的细胞来源于母体。使用FZD - 9、STRO - 1、3G5和α - SMA抗体对胎盘床活检组织进行免疫荧光检测。DMSC位于基蜕膜的血管微环境中。用FZD - 9、Ck7和vWF抗体进行免疫荧光检测发现,完整未转化的螺旋小动脉周围的血管微环境中有DMSC,但在完全转化的螺旋小动脉中没有DMSC。
螺旋小动脉重塑是人类妊娠的一个关键特征。在完全转化和未转化的螺旋小动脉中研究了DMSC微环境。此前DMSC未被认为与螺旋小动脉重塑有关。完全转化的螺旋小动脉周围没有DMSC,这表明它们是进行螺旋小动脉重塑的侵入性胎盘绒毛外滋养层细胞替代或破坏的目标。