Gratton R J, Asano H, Han V K M
Department of Obstetrics and Gynecology, CIHR Group in Fetal and Neonatal Health and Development, The Child Health Research Institute, The Lawson Health Research Institute, The University of Western Ontario, London, Canada.
Placenta. 2002 Apr;23(4):303-10. doi: 10.1053/plac.2001.0780.
Insulin-like growth factors and their binding proteins regulate cellular proliferation, differentiation and function, and play an important role in placental development. IGF-II and IGFBP-1 are abundantly expressed by cells at the maternal-fetal interface and mediate cell-to-cell communication between trophoblasts and decidua. Placentae of pre-eclamptic pregnancies show villous cytotrophoblast proliferation, increased syncytial sprout formation and impaired trophoblast invasion. We hypothesized that the expression of IGF-II and IGFBP-1 by cells at the maternal-fetal interface is altered in pre-eclampsia. We determined the regional abundance and cellular localization of IGF-II mRNA and IGFBP-1 mRNA and protein in placentae from normotensive control and pre-eclamptic pregnancies. IGF-II mRNA was expressed in both the chorionic villi and basal plate decidua regions. Increased IGF-II mRNA abundance was observed in the intermediate trophoblasts of peri-infarct regions. IGFBP-1 expression was present only in the decidua of the basal plate and membranes, and this expression was decreased significantly in pre-eclamptic placentae. The increased IGF-II expression in the intermediate trophoblast surrounding placental infarcts suggests a role for IGF-II in placental repair or remodelling. Decreased IGFBP-1 mRNA expression in the basal plate decidua suggests that the increased concentrations of IGFBP-1 the circulation of pre-eclamptic women is not of decidual origin. The altered IGF-II and IGFBP-1 expression at the fetomaternal interface may be important in the pathophysiology of pre-eclampsia.
胰岛素样生长因子及其结合蛋白调节细胞增殖、分化和功能,并在胎盘发育中发挥重要作用。IGF-II和IGFBP-1在母胎界面的细胞中大量表达,介导滋养层细胞与蜕膜之间的细胞间通讯。子痫前期妊娠的胎盘表现出绒毛细胞滋养层增殖、合体滋养层芽形成增加以及滋养层侵袭受损。我们推测子痫前期母胎界面细胞中IGF-II和IGFBP-1的表达发生了改变。我们测定了正常血压对照组和子痫前期妊娠胎盘组织中IGF-II mRNA和IGFBP-1 mRNA及蛋白的区域丰度和细胞定位。IGF-II mRNA在绒毛膜绒毛和基底板蜕膜区域均有表达。在梗死周围区域的中间滋养层中观察到IGF-II mRNA丰度增加。IGFBP-1仅在基底板和胎膜的蜕膜中表达,且在子痫前期胎盘中该表达显著降低。胎盘梗死周围中间滋养层中IGF-II表达增加提示IGF-II在胎盘修复或重塑中起作用。基底板蜕膜中IGFBP-1 mRNA表达降低表明子痫前期妇女循环中IGFBP-1浓度升高并非来源于蜕膜。母胎界面处IGF-II和IGFBP-1表达的改变可能在子痫前期的病理生理学中具有重要意义。