Blankenship T N, Enders A C
Department of Cell Biology and Human Anatomy, School of Medicine, University of California, Davis 95616-8643, USA.
Anat Rec. 1997 Mar;247(3):413-9. doi: 10.1002/(SICI)1097-0185(199703)247:3<413::AID-AR13>3.0.CO;2-S.
Placental development in higher primates is characterized by the invasion of uterine blood vessels by trophoblast cells. These cells proceed to migrate within uterine spiral arteries, opposite to the direction of normal blood flow. Observations indicate adhesion of intra-arterial trophoblast to endothelium as well as to adjacent trophoblast cells.
Macaque placenta and endometrial tissues were collected from day 15 of pregnancy (implantation begins on day 9) to term. Standard indirect immunoperoxidase methods were used to identify platelet-endothelial cell adhesion molecule-1 (PECAM), cytokeratins, and factor VIII-related antigen.
In early specimens arterioles were often nearly occluded by cytokeratin-labeled trophoblast cells. Adjacent sections revealed the presence of PECAM on these trophoblast cells and on the endothelium. After day 30 the invaded arteries usually contained a re-formed lumen, and trophoblast cells were increasingly evident in the modified walls of arteries, where PECAM labeling was often reduced on cells distant from the lumen. Endothelium of both invaded and uninvaded uterine vessels retained PECAM reactivity throughout gestation. Trophoblast cells of the cell columns, cytotrophoblastic shell, and mid- to late-gestation chorionic plate were also reactive for PECAM. Villous cytotrophoblast cells did not express PECAM, but a dense border of PECAM was consistently present on the apical surfaces of syncytial trophoblast.
Because PECAM functions as a counter-ligand for PECAM via homophilic binding, we conclude that this molecule is directly involved in adhesion of trophoblast cells to arterial endothelium in addition to maintaining cohesion between some subpopulations of cytotrophoblast cells.
高等灵长类动物的胎盘发育以滋养层细胞侵入子宫血管为特征。这些细胞在子宫螺旋动脉内迁移,与正常血流方向相反。观察结果表明动脉内滋养层细胞与内皮以及相邻滋养层细胞之间存在黏附。
从妊娠第15天(第9天开始着床)至足月收集猕猴胎盘和子宫内膜组织。采用标准间接免疫过氧化物酶方法鉴定血小板内皮细胞黏附分子-1(PECAM)、细胞角蛋白和因子VIII相关抗原。
在早期标本中,小动脉常被细胞角蛋白标记的滋养层细胞几乎完全阻塞。相邻切片显示这些滋养层细胞和内皮上存在PECAM。30天后,被侵入的动脉通常含有重新形成的管腔,并且在动脉的改良壁中滋养层细胞越来越明显,在远离管腔的细胞上PECAM标记常常减少。在整个妊娠期,被侵入和未被侵入的子宫血管内皮均保持PECAM反应性。细胞柱、细胞滋养层壳以及妊娠中期至晚期绒毛膜板的滋养层细胞对PECAM也有反应。绒毛细胞滋养层细胞不表达PECAM,但在合体滋养层的顶端表面始终存在一层致密的PECAM边界。
由于PECAM通过同源性结合作为PECAM的反配体发挥作用,我们得出结论,该分子除了维持某些细胞滋养层细胞亚群之间的黏附外,还直接参与滋养层细胞与动脉内皮的黏附。