Caniggia I, Winter J L
Program in Development and Fetal Health, Samuel Lunenfeld Research Institute, Mt Sinai Hospital, Toronto, Ontario, Canada.
Placenta. 2002 Apr;23 Suppl A:S47-57. doi: 10.1053/plac.2002.0815.
During early pregnancy, trophoblast differentiation occurs in an environment of relative low oxygen tension which is essential for normal embryonic and placental development. At around 10-12 weeks' gestation, when the intervillous space opens to maternal blood, there is an increase in Po(2). This increase correlates with the time of maximal trophoblast invasion into the maternal decidua, which allows extravillous trophoblast cells to access and remodel the maternal spiral arteries. Hypoxia Inducible Factor 1(HIF-1) is a transcription factor which activates gene transcription in response to varying oxygen concentration of cells. HIF-1 is a heterodimer composed of the inducible HIF-1alpha and the constitutively expressed HIF-1beta/ARNT subunits. Using villous explants, we have demonstrated that the oxygen-regulated events of early trophoblast differentiation are in part mediated by TGFbeta(3), an inhibitor of trophoblast differentiation, via HIF-1alpha. Pre-eclampsia is a disease of pregnancy that is characterized by shallow trophoblast invasion. Recently, we have reported that TGFbeta(3) is over-expressed in pre-eclamptic pregnancy and that its down-regulation restores invasive capability to trophoblast cells. Because TGFbeta(3) is downstream of HIF-1alpha, in the present study we investigated the expression of HIF-1alpha in pre-eclamptic placentae and age-matched controls using in situ hybridization and histochemical analyses. We found that HIF-1alpha mRNA and protein expression are abnormally elevated in pre-eclamptic placental tissue when compared to normal placental tissue. We conclude that pre-eclampsia may result from a developmental failure of oxygen to increase or of trophoblast cells to respond and/or sense an increase in oxygen. This will prevent the normal TGFbeta3 down-regulation and will lead to poor trophoblast invasion predisposing the pregnancy to pre-eclampsia.
在妊娠早期,滋养层细胞分化发生在相对低氧张力的环境中,这对正常胚胎和胎盘发育至关重要。在妊娠约10 - 12周时,当绒毛间隙向母体血液开放时,氧分压(Po₂)会升高。这种升高与滋养层细胞向母体蜕膜最大程度浸润的时间相关,这使得绒毛外滋养层细胞能够接触并重塑母体螺旋动脉。缺氧诱导因子1(HIF - 1)是一种转录因子,可根据细胞内不同的氧浓度激活基因转录。HIF - 1是一种异二聚体,由可诱导的HIF - 1α和组成型表达的HIF - 1β/ARNT亚基组成。利用绒毛外植体,我们已经证明早期滋养层细胞分化的氧调节事件部分是由转化生长因子β3(TGFβ3)介导的,TGFβ3是一种滋养层细胞分化抑制剂,通过HIF - 1α起作用。子痫前期是一种妊娠期疾病,其特征是滋养层细胞浸润浅。最近,我们报道TGFβ3在子痫前期妊娠中过度表达,并且其下调可恢复滋养层细胞的浸润能力。因为TGFβ3在HIF - 1α的下游,所以在本研究中,我们使用原位杂交和组织化学分析研究了子痫前期胎盘组织和年龄匹配对照组中HIF - 1α的表达。我们发现,与正常胎盘组织相比,子痫前期胎盘组织中HIF - 1α mRNA和蛋白表达异常升高。我们得出结论,子痫前期可能是由于氧增加的发育失败,或者是滋养层细胞对氧增加的反应和/或感知失败所致。这将阻止正常的TGFβ3下调,并导致滋养层细胞浸润不良,使妊娠易患子痫前期。