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子痫前期与正常胎盘组织中 Foxp3 和 CD68 的分布:一项组织形态学评估。

The Distribution of Foxp3 and CD68 in Preeclamptic and Healthy Placentas: A Histomorphological Evaluation.

机构信息

Department of Histology and Embryology, School of Medicine, Bahcesehir University, Istanbul, Turkey.

Department of Histology and Embryology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

出版信息

J Histochem Cytochem. 2023 Apr;71(4):211-225. doi: 10.1369/00221554231170662. Epub 2023 Apr 18.

DOI:10.1369/00221554231170662
PMID:37070940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10149892/
Abstract

Preeclampsia is a complication of pregnancy that affects 3-5% of pregnancies and is one of the major causes of maternal/neonatal mortality and morbidities worldwide. We aimed to investigate the distribution of Foxp3+ regulatory T-cells and CD68+ Hofbauer cells in the placenta of preeclamptic and healthy pregnant women with a special focus on correlating these findings with placental histology. Decidua and chorionic villi of the placenta obtained from healthy and preeclamptic pregnancies were evaluated in full-thickness sections. Sections were stained with hematoxylin and eosin and Masson's trichrome and immunostained for Foxp3 and CD68 for histological analyses. The total histomorphological score for placentas was found to be higher in preeclamptic placentas than that in the controls. The CD68 immunoreactivity was higher in the chorionic villi of preeclamptic placentas than that in the controls. The immunoreactivity of Foxp3 was found widely distributed within the decidua in both the groups and did not differ significantly. Interestingly, Foxp3 immunoreactivity in the chorionic villi was found mainly in the villous core and, to a lesser extent, in the syncytiotrophoblasts. We found no significant relation between Foxp3 expressions and morphological changes observed in preeclamptic placentas. Although extensive research is being carried out regarding the pathophysiology of preeclampsia, the findings are still controversial.

摘要

子痫前期是一种妊娠并发症,影响 3-5%的妊娠,是全球孕产妇/新生儿死亡和发病的主要原因之一。我们旨在研究子痫前期和健康孕妇胎盘组织中 Foxp3+调节性 T 细胞和 CD68+Hofbauer 细胞的分布,并特别关注这些发现与胎盘组织学的相关性。对来自健康和子痫前期妊娠的胎盘蜕膜和绒毛进行全层切片评估。用苏木精和伊红、Masson 三色和 Foxp3 和 CD68 免疫染色进行组织学分析。与对照组相比,子痫前期胎盘的总组织形态学评分更高。子痫前期胎盘的绒毛 CD68 免疫反应性高于对照组。Foxp3 的免疫反应性在两组蜕膜中广泛分布,无显著差异。有趣的是,绒毛中的 Foxp3 免疫反应性主要位于绒毛核心,其次是合体滋养层。我们没有发现 Foxp3 表达与子痫前期胎盘观察到的形态变化之间有显著关系。尽管针对子痫前期的病理生理学进行了广泛的研究,但结果仍然存在争议。

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本文引用的文献

1
CHARACTERISTICS OF CD68+ AND CD163+ EXPRESSION IN PLACENTA OF WOMEN WITH PREECLAMPSIA AND OBESITY.子痫前期合并肥胖孕妇胎盘 CD68+ 和 CD163+ 表达的特征。
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Contribution of macrophages to fetomaternal immunological tolerance.巨噬细胞在胎母免疫耐受中的作用。
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Role of the Macrophage Migration Inhibitory Factor in the Pathophysiology of Pre-Eclampsia.巨噬细胞移动抑制因子在子痫前期发病机制中的作用。
Int J Mol Sci. 2021 Feb 12;22(4):1823. doi: 10.3390/ijms22041823.
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Placental macrophages: Origin, heterogeneity, function and role in pregnancy-associated infections.胎盘巨噬细胞:起源、异质性、功能及其在妊娠相关感染中的作用。
Placenta. 2021 Jan 1;103:94-103. doi: 10.1016/j.placenta.2020.10.017. Epub 2020 Oct 17.
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Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia.早发型和晚发型子痫前期关键固有免疫细胞的机制
Front Immunol. 2020 Aug 18;11:1864. doi: 10.3389/fimmu.2020.01864. eCollection 2020.
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Altered Levels of Decidual Immune Cell Subsets in Fetal Growth Restriction, Stillbirth, and Placental Pathology.胎儿生长受限、死胎和胎盘病理学中蜕膜免疫细胞亚群水平的改变。
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Abnormal placental CD8 T-cell infiltration is a feature of fetal growth restriction and pre-eclampsia.异常的胎盘 CD8+T 细胞浸润是胎儿生长受限和子痫前期的一个特征。
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8
Maternal Obesity and the Uterine Immune Cell Landscape: The Shaping Role of Inflammation.母体肥胖与子宫免疫细胞景观:炎症的塑造作用。
Int J Mol Sci. 2020 May 27;21(11):3776. doi: 10.3390/ijms21113776.
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Immune tolerance at the maternal-placental interface in healthy pregnancy and pre-eclampsia.健康妊娠和子痫前期中母胎界面的免疫耐受
J Obstet Gynaecol Res. 2020 Jul;46(7):1067-1076. doi: 10.1111/jog.14309. Epub 2020 May 19.
10
The role of two common gene promoter polymorphisms in preeclampsia in a Turkish population: a case-control study.两种常见基因启动子多态性在土耳其人群子痫前期中的作用:一项病例对照研究。
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