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伴有或不伴有子痫前期的胎儿生长受限妊娠中胎盘的凋亡及胎盘和母体胎盘床中黏附分子的表达

Placental apoptosis and adhesion molecules expression in the placenta and the maternal placental bed of pregnancies complicated by fetal growth restriction with and without pre-eclampsia.

作者信息

Madazli R, Benian A, Ilvan S, Calay Z

机构信息

Department of Obstetrics, Gynecology and Pathology, Cerrahpasa Medical Faculty, University of Istanbul, Istanbul, Turkey.

出版信息

J Obstet Gynaecol. 2006 Jan;26(1):5-10. doi: 10.1080/01443610500363840.

Abstract

The aim of the study was to examine the expression of adhesion molecules VCAM-1 and ICAM-3 in placental tissue samples and placental bed (maternal decidual tissue) biopsies of pregnancies complicated by pre-eclampsia (PE) and fetal growth restriction (FGR), and to determine whether PE and FGR are associated with an increase in placental apoptosis. We studied placentas and placental bed samples of 49 third trimester pregnancies complicated by FGR (26 with associated PE, 23 without PE) and 25 normotensive healthy pregnant women. Placental apoptosis was assessed by the TUNEL method. Immunohistochemistry was used to assess expression of the VCAM-1 and ICAM-3. There was no significant difference in the staining intensity of VCAM-1 in placentas (p=0.472) and placental bed biopsies (p=0.754) of women delivering appropriate for gestational age and growth restricted fetuses (with and without associated PE). The amount of lymphocytes staining positively with ICAM-3 was significantly higher in both placental and placental bed biopsies of women delivering growth restricted fetuses compared with control pregnancies (p<0.001). Fetal growth restricted pregnancies with associated PE showed higher staining of ICAM-3 in placental compared with placental bed samples (p=0.049). In fetal growth restricted placentas, apoptotic nuclei were more abundant compared with control placentas (p<0.001). Increased expression of ICAM-3 on lymphocyte surface of both maternal and fetal side, suggests lymphocyte overactivation in PE and FGR. Increased placental apoptosis may play an important role in the pathogenesis or sequelae of PE.

摘要

本研究的目的是检测子痫前期(PE)和胎儿生长受限(FGR)合并妊娠的胎盘组织样本和胎盘床(母体蜕膜组织)活检中黏附分子血管细胞黏附分子-1(VCAM-1)和细胞间黏附分子-3(ICAM-3)的表达,并确定PE和FGR是否与胎盘细胞凋亡增加有关。我们研究了49例孕晚期合并FGR的妊娠(26例合并PE,23例不合并PE)以及25例血压正常的健康孕妇的胎盘和胎盘床样本。采用TUNEL法评估胎盘细胞凋亡。免疫组织化学法用于评估VCAM-1和ICAM-3的表达。在分娩适于胎龄儿和生长受限胎儿的妇女(合并或不合并PE)的胎盘(p=0.472)和胎盘床活检组织(p=0.754)中,VCAM-1的染色强度无显著差异。与对照妊娠相比,分娩生长受限胎儿的妇女的胎盘和胎盘床活检组织中,ICAM-3阳性染色的淋巴细胞数量显著更高(p<0.001)。合并PE的胎儿生长受限妊娠中,胎盘ICAM-3染色高于胎盘床样本(p=0.049)。与对照胎盘相比,胎儿生长受限的胎盘凋亡核更多(p<0.001)。母胎双方淋巴细胞表面ICAM-3表达增加,提示PE和FGR中淋巴细胞过度激活。胎盘细胞凋亡增加可能在PE的发病机制或后遗症中起重要作用。

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