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激活蛋白-1 转录因子家族在人胎盘的表达与子痫前期及其合并胎儿生长受限的关系。

Activating protein-1 family of transcription factors in the human placenta complicated by preeclampsia with and without fetal growth restriction.

机构信息

Department of Molecular Pathology and Innovative Therapies, Marche Polytechnic University, Via Tronto, 10/a - I-60126 Ancona, Italy.

出版信息

Placenta. 2010 Oct;31(10):919-27. doi: 10.1016/j.placenta.2010.08.001. Epub 2010 Aug 30.

Abstract

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.

摘要

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。

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