首页> 外文期刊>Journal of obstetrics and gynaecology: the journal of the Institute of Obstetrics and Gynaecology >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.
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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.

机译:妊娠与无先兆子痫并发胎儿生长受限的胎盘和孕妇胎盘中胎盘凋亡和粘附分子的表达。

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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.
机译:该研究的目的是检查粘附分子VCAM-1和ICAM-3在妊娠合并子痫前期(PE)和胎儿生长受限(FGR)的胎盘组织样品和胎盘床活检组织中的表达。 ,并确定PE和FGR是否与胎盘凋亡增加有关。我们研究了49例妊娠中期合并FGR的胎盘和胎盘床样品(26例伴有PE,23例无PE)和25例血压正常的健康孕妇。通过TUNEL法评估胎盘凋亡。免疫组织化学用于评估VCAM-1和ICAM-3的表达。在分娩时适合胎龄和生长受限的胎儿(有或没有相关PE)的妇女,胎盘(p = 0.472)和胎盘床活检(p = 0.754)中VCAM-1的染色强度没有显着差异。与对照组孕妇相比,在接受生长受限的胎儿的妇女的胎盘和胎盘活检中,ICAM-3阳性染色的淋巴细胞数量明显更高(p <0.001)。与胎盘床样本相比,胎儿生长受限的妊娠与相关的PE显示胎盘中的ICAM-3染色更高(p = 0.049)。在胎儿生长受限的胎盘中,凋亡细胞核比对照胎盘更丰富(p <0.001)。母体和胎儿侧淋巴细胞表面ICAM-3的表达增加,表明PE和FGR中的淋巴细胞过度活化。胎盘凋亡增加可能在PE的发病机制或后遗症中起重要作用。

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