Goldman-Wohl D, Greenfield C, Haimov-Kochman R, Ariel I, Anteby E Y, Hochner-Celnikier D, Farhat M, Yagel S
Department of Obstetrics and Gynecology, Hadassah University Hospital - Mt. Scopus, PO Box 24035, Jerusalem, Israel 91240.
Placenta. 2004 Aug;25(7):623-30. doi: 10.1016/j.placenta.2004.01.016.
Eph receptors and their ephrin ligands play a fundamental role in embryogenesis. Their functions include cell targeting and angiogenesis. In placental development, trophoblasts migrate and invade maternal tissue and spiral arteries, where they play a role in both anchoring the placenta to the uterus and increasing blood flow to the developing fetus (interstitial and endovascular invasions). We investigated the cellular distribution and expression patterns of representative Eph and ephrin RNA and protein in an effort to identify the molecules involved in trophoblast migration during normal placental development and placental pathologies. We found ephrin-A1 expressed exclusively in the invasive extravillous trophoblast (EVT) cell lineage. We therefore proceeded to investigate ephrin-A1 in placental pathologies with defects in EVT invasion. In preeclampsia, where trophoblast invasion is shallow, we observed ephrin-A1 expression similar to normal placenta. Furthermore, in initial experiments on the deeply invading trophoblasts of placenta accreta, which lacks decidua, ephrin-A1 is found to be expressed highly in extravillous trophoblasts that have invaded the myometrium. In addition, we found the prototype ephrin-A1 receptor, EphA2, localized in several placental cell types. EphB4 and ephrin-B2 molecules, which have specific expression patterns during artery and vein development, respectively, were also expressed in the placenta. The cell specific distribution of ephrin-A1 suggests that it may play a role in targeting and migration of trophoblasts, and in the vascular remodeling induced by the invading extravillous trophoblasts. Failure of ephrin-A1 expression is unlikely to be the primary cause in defective migration of trophoblasts observed in preeclampsia. Specific roles for other Eph and ephrin proteins remain to be investigated.
Eph受体及其Ephrin配体在胚胎发育过程中发挥着重要作用。它们的功能包括细胞靶向和血管生成。在胎盘发育过程中,滋养层细胞迁移并侵入母体组织和螺旋动脉,在将胎盘锚定到子宫以及增加流向发育中胎儿的血流量(间质和血管内侵入)方面发挥作用。我们研究了代表性Eph和Ephrin RNA及蛋白质的细胞分布和表达模式,以确定在正常胎盘发育和胎盘病理过程中参与滋养层细胞迁移的分子。我们发现Ephrin-A1仅在侵袭性绒毛外滋养层(EVT)细胞谱系中表达。因此,我们继续研究在EVT侵袭存在缺陷的胎盘病理情况下的Ephrin-A1。在先兆子痫中,滋养层侵袭较浅,我们观察到Ephrin-A1的表达与正常胎盘相似。此外,在对缺乏蜕膜的胎盘植入的深度侵袭性滋养层细胞进行的初步实验中,发现Ephrin-A1在侵入子宫肌层的绒毛外滋养层细胞中高度表达。此外,我们发现原型Ephrin-A1受体EphA2定位于几种胎盘细胞类型中。分别在动脉和静脉发育过程中具有特定表达模式的EphB4和Ephrin-B2分子也在胎盘中表达。Ephrin-A1的细胞特异性分布表明它可能在滋养层细胞的靶向和迁移以及由侵入性绒毛外滋养层细胞诱导的血管重塑中发挥作用。Ephrin-A1表达缺失不太可能是先兆子痫中观察到的滋养层细胞迁移缺陷的主要原因。其他Eph和Ephrin蛋白的具体作用仍有待研究。