Ang1 immunoexpression vs vascular profile in chorio-villous germinative status in early term compromised pregnancies

Valeriu David, V. Fulga, V. Petrovici, Ecaterina Carpenco, L. Saptefrati
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Abstract

Background: A normal maternal-fetal system is essential for the functioning of the placenta during placentation and the establishment of the maternalembryofetal vascular circulation. The angiopoietin/TIE pathway is involved in vascular morphogenesis through regulation, survival and maturation of endothelial cells concomitant with vascular remodeling. Deregulation of pro-angiogenic factor secretion and expression is associated with disruption of vascular morphogenesis, reduction of vascular bed and installation of primary placental insufficiency. The aim: Evaluation of Ang 1 immunoexpression in early term compromised pregnancies in the context of chorio-villary circulatory dysfunction in primary placental insufficiency. Material and methods: Abortion product from 61 patients (stagnant pregnancies – 39 cases, early miscarriage – 8 cases, control group – 14 cases of pregnancies solved on social indications/ desire) were immunohistochemically evaluated with the marker for anti-Ang1 and anti-CD31. Results: The villous syncytiotrophoblast was the most immunoreactive area. Most of cases of the pregnancies terminated on social indications/ desire were anti-Ang1 negative. The levels of anti-Ang1 immunoexpression were statistically significantly different in case of syncytiotrophoblast of early miscarriages and abortions terminated on social indications/ desire. The highest chorio-villous vascular density was noticed in the abortions on social indications/ desire and early misscariages group. Conclusions: The placental period is characterized by a weak angiogenic Ang1 differentiated cellular environment in the chorio-villous germinal site in the group of short term compromised pregnancies. The selectively immunoexpressed cellular profile statistically significantly correlates with placental vascular index and chorio-villous vascular density in stagnant pregnancies.
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早产儿绒毛膜胚芽状态中的 Ang1 免疫表达与血管概况
背景:正常的母胎系统对于胎盘在胎儿期的功能和母胎血管循环的建立至关重要。血管生成素/TIE通路通过调节、存活和成熟内皮细胞,与血管重塑同时参与血管形态发生。促血管生成因子分泌和表达的失调与血管形态发生的破坏、血管床的减少和原发性胎盘功能不全有关。目的:在原发性胎盘功能不全绒毛-毛细血管循环功能障碍的背景下,评估早产妊娠中 Ang 1 的免疫表达。材料和方法使用抗 Ang1 和抗 CD31 标记对 61 例患者(停滞妊娠 39 例,早期流产 8 例,对照组--14 例因社会适应症/愿望而解决的妊娠)的流产产物进行免疫组化评估。结果显示绒毛合体滋养细胞是免疫反应最强的区域。大多数因社会指征/愿望而终止妊娠的病例抗 Ang1 阴性。早期流产和社会指征/意愿终止妊娠的合胞滋养细胞的抗Ang1免疫表达水平在统计学上有显著差异。社会指征/意愿流产组和早期流产组的绒毛血管密度最高。结论在短期受损妊娠组中,胎盘期的特点是绒毛生殖部位的血管生成Ang1分化细胞环境较弱。选择性免疫表达的细胞特征与停滞妊娠的胎盘血管指数和绒毛血管密度有显著的统计学相关性。
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