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子痫前期胎盘的补体激活与调节

Complement activation and regulation in preeclamptic placenta.

作者信息

Lokki Anna Inkeri, Heikkinen-Eloranta Jenni, Jarva Hanna, Saisto Terhi, Lokki Marja-Liisa, Laivuori Hannele, Meri Seppo

机构信息

Department of Medical Genetics, Haartman Institute, University of Helsinki , Helsinki , Finland ; Department of Bacteriology and Immunology, Haartman Institute, University of Helsinki , Helsinki , Finland ; Immunobiology Research Program, Research Programs Unit, University of Helsinki , Helsinki , Finland.

Department of Medical Genetics, Haartman Institute, University of Helsinki , Helsinki , Finland ; Department of Obstetrics and Gynaecology, Helsinki University Central Hospital , Helsinki , Finland.

出版信息

Front Immunol. 2014 Jul 9;5:312. doi: 10.3389/fimmu.2014.00312. eCollection 2014.

Abstract

Preeclampsia (PE) is a common disorder of pregnancy originating in the placenta. We examined whether excessive activation or poor regulation of the complement system at the maternal-fetal interface could contribute to the development of PE. Location and occurrence of complement components and regulators in placentae were analyzed. Cryostat sections of placentae were processed from 7 early-onset PE (diagnosis <34 weeks of gestation), 5 late-onset PE, 10 control pregnancies, and immunostained for 6 complement activators and 6 inhibitors. Fluorescence was quantified and compared between PE and control placentae. Gene copy numbers of complement components C4A and C4B were assessed by a quantitative PCR method. Maternal C4 deficiencies (≥1 missing or non-functional C4) were most common in the early-onset PE group (71%), and more frequent in late-onset PE compared to healthy controls (60 vs. 38%). Complement C1q deposition differed significantly between control and patient groups: controls and early-onset PE patients had more C1q than late-onset PE patients (mean p = 0.01 and p = 0.005, respectively). C3 activation was analyzed by staining for C3b/iC3b and C3d. C3d was mostly specific to the basal syncytium and C3b/iC3b diffuse in other structures, but there were no clear differences between the study groups. Activated C4 and membrane-bound regulators CD55, CD46, and CD59 were observed abundantly in the syncytiotrophoblast. Syncytial knots, structures enriched in PE, stained specifically for the classical pathway inhibitor C4bp, whereas the key regulator alternative pathway, factor H (FH) showed a wider distribution in the placenta. Differences in C1q deposition between late- and early-onset PE groups may be indicative of the different etiology of PE symptoms in these patients. Irregular distribution of the complement regulators C4bp and FH in the PE placenta and a higher frequency of C4A deficiencies suggest a disturbed balance between complement activation and regulation in PE.

摘要

子痫前期(PE)是一种起源于胎盘的常见妊娠疾病。我们研究了母胎界面处补体系统的过度激活或调节不良是否会导致PE的发生。分析了胎盘组织中补体成分和调节因子的定位及出现情况。对7例早发型PE(诊断孕周<34周)、5例晚发型PE及10例对照妊娠的胎盘进行冷冻切片处理,并对6种补体激活剂和6种抑制剂进行免疫染色。对荧光进行定量分析,并在PE组和对照胎盘之间进行比较。采用定量PCR方法评估补体成分C4A和C4B的基因拷贝数。母源性C4缺陷(≥1个缺失或无功能的C4)在早发型PE组最为常见(71%),与健康对照相比,在晚发型PE中更常见(60%对38%)。补体C1q沉积在对照组和患者组之间存在显著差异:对照组和早发型PE患者的C1q比晚发型PE患者更多(平均p值分别为0.01和0.005)。通过对C3b/iC3b和C3d进行染色分析C3激活情况。C3d主要特异性定位于基底合体滋养层,C3b/iC3b在其他结构中呈弥漫性分布,但研究组之间无明显差异。在合体滋养层中大量观察到活化的C4以及膜结合调节因子CD55、CD46和CD59。合体结节是PE中富集的结构,对经典途径抑制剂C4bp进行特异性染色,而替代途径的关键调节因子因子H(FH)在胎盘中分布更广泛。早发型和晚发型PE组之间C1q沉积的差异可能表明这些患者PE症状的病因不同。PE胎盘中补体调节因子C4bp和FH的分布不规则以及C4A缺陷的高频率表明PE中补体激活与调节之间的平衡受到干扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9e/4088925/006bcc97ba99/fimmu-05-00312-g001.jpg

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