Department of Molecular Pathology and Innovative Therapies, Marche Polytechnic University, Via Tronto, 10/a - I-60126 Ancona, Italy.
Placenta. 2010 Oct;31(10):919-27. doi: 10.1016/j.placenta.2010.08.001. Epub 2010 Aug 30.
Preeclampsia (PE) is a serious disorder of human pregnancy, it is often associated with fetal growth restriction (FGR) which is a failure of the fetus to reach its own growth potential. Activator protein-1 (AP-1) is a family of transcription factors inducible in response to a variety of extracellular stimuli and functions. AP-1 plays a complex role in the regulation of different fundamental cellular processes, including cell proliferation, survival, death and transformation. We investigate the expression pattern of AP-1 transcription factors in normal placentas during gestation and in placentas from PE without and with FGR using semiquantitative RT-PCR and immunohistochemistry techniques. The most interesting data concern the alterations of protein expression patterns of c-fos, Jun D and c-jun in normal gestation as well as in PE and PE-FGR pathologies. In addition, alterations but not significant changes are detected in mRNA expressions for these transcription factors. We strongly suggest that c-fos is implicated in regulating invasiveness mechanism of extravillous trophoblast in normal gestation as well as in PE placentas. In addition, we suggest that the opposite modulation of Jun D and c-jun in PE and PE-FGR supports the recent hypothesis that PE and PE-FGR could be considered two pathologies with different origin (maternal and placental) each of which has a different molecular pattern of expression.
子痫前期 (PE) 是一种严重的妊娠疾病,常伴有胎儿生长受限 (FGR),即胎儿未能达到其自身生长潜力。激活蛋白-1 (AP-1) 是一种转录因子家族,可响应多种细胞外刺激而诱导产生,并发挥作用。AP-1 在调节不同基本细胞过程中发挥着复杂的作用,包括细胞增殖、存活、死亡和转化。我们使用半定量 RT-PCR 和免疫组织化学技术研究了正常妊娠期间和无 FGR 及有 FGR 的 PE 胎盘 AP-1 转录因子的表达模式。最有趣的数据涉及 c-fos、Jun D 和 c-jun 蛋白表达模式在正常妊娠以及 PE 和 PE-FGR 病理中的改变。此外,这些转录因子的 mRNA 表达也发生了改变,但并不显著。我们强烈认为,c-fos 参与调节正常妊娠和 PE 胎盘中绒毛外滋养细胞的侵袭机制。此外,我们认为 Jun D 和 c-jun 在 PE 和 PE-FGR 中的相反调节支持了最近的假说,即 PE 和 PE-FGR 可以被认为是两种具有不同起源(母体和胎盘)的疾病,每种疾病都有不同的分子表达模式。