Regulation of trophoblast differentiation during embryo implantation and placentation: Implications in pregnancy complications

Sudha Saryu Malhotra, Priyanka Banerjee, Satish Kumar Gupta
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引用次数: 6

Abstract

A significant proportion of pregnancy related complications like preterm birth, preeclampsia, intra-uterine growth restriction (IUGR) and spontaneous abortion may be due to defects at various stages of embryo implantation process, in particular, placentation. One of these defects is impaired syncytialization. This may also be responsible for low success rate of embryo implantation during Assisted Reproductive Technology (ART). As it is an early differentiation event of the trophectoderm, unveiling its elementary molecular network might help in understanding the cause behind such complications and even ameliorate the success rate of pregnancies. Therefore, the current review highlights the available information with respect to effector molecules such as syncytins, syndecan-1, CD98, connexin-43, proteases and protease convertase in trophoblast syncytialization. Promotion of syncytialization by EGF, hCG, IGFs, LIF etc. and its inhibition by TGF-β1 and TNF-α is also discussed. The signaling pathways, such as PKA-CREB, MAPK, STAT, Wnt/β-catenin etc. through which various factors modulate the process of syncytialization have also been presented. Post-transcriptional regulation via microRNAs has also been discussed. The information provided in this review will help in our understanding of the molecular mechanisms associated with syncytialization and their implications in pregnancy related complications.

胚胎着床和胎盘过程中滋养细胞分化的调控:对妊娠并发症的影响
妊娠相关并发症,如早产、先兆子痫、宫内生长受限(IUGR)和自然流产,很大一部分可能是由于胚胎着床过程中各个阶段的缺陷,特别是胎盘植入。其中一个缺陷是合胞受损。这也可能是辅助生殖技术(ART)中胚胎着床成功率低的原因。由于这是滋养外胚层的早期分化事件,揭示其基本分子网络可能有助于了解这些并发症背后的原因,甚至可以提高怀孕成功率。因此,本综述重点介绍了有关滋养细胞合胞素、syndecan-1、CD98、connexin-43、蛋白酶和蛋白酶转化酶等效应分子在滋养细胞合胞过程中的作用。还讨论了EGF、hCG、igf、LIF等对合胞的促进作用以及TGF-β1和TNF-α对合胞的抑制作用。各种因子通过PKA-CREB、MAPK、STAT、Wnt/β-catenin等信号通路调节合胞过程。通过microrna的转录后调控也进行了讨论。本综述提供的信息将有助于我们了解与合胞相关的分子机制及其在妊娠相关并发症中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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