Bandeira Carla Letícia, Urban Borbely Alexandre, Pulcineli Vieira Francisco Rossana, Schultz Regina, Zugaib Marcelo, Bevilacqua Estela
Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, Avenida Professor Lineu Prestes, No. 1524, Cidade Universitária, 05508-900 São Paulo, SP, Brazil.
Department of Obstetrics, Clinics Hospital, School of Medicine, University of São Paulo, Avenida Dr. Enéas de Carvalho Aguiar, No. 255, Cerqueira César, 05403-000 São Paulo, SP, Brazil.
Biomed Res Int. 2014;2014:892856. doi: 10.1155/2014/892856. Epub 2014 Aug 6.
CRIPTO-(CR)1 is a protein associated with tumorigenesis and metastasis. Here we demonstrate that CR-1 expression in normal and creta placentas is associated with various degrees of uterine invasion. Cytokeratin (CK) and CR-1 protein expression was visualized by immunohistochemical staining of formalin-fixed, paraffin-embedded placental specimens (control placentas, n = 9; accreta, n = 6; increta, n = 10; percreta, n = 15). The pattern of extravillous trophoblast (EVT) cell morphology was distinctive in creta placentas: densely-compacted cell columns and large star-shaped cells with a typically migratory phenotype, not common among third trimester control placentas. Quantification revealed higher CR-1 immunoreactivities in accreta (P = 0.001), increta (P = 0.0002), and percreta placentas (P = 0.001) than in controls. In contrast to controls, there was a significant positive relationship between CR-1 and CK reactivity in all creta placentas (accreta, P = 0.02; increta, P = 0.0001, and percreta, P = 0.025). This study demonstrated CR-1 expression in the placental bed, its increased expression in creta placentas, and EVT cells as the main CR-1-producing cell type. Morphological examination revealed an immature and invasive trophoblast profile in creta placentas, suggesting impairment of the trophoblast differentiation pathway. These findings provide important new insights into the pathophysiology of abnormal creta placentation and its gestational consequences.
CRIPTO-(CR)1是一种与肿瘤发生和转移相关的蛋白质。在此我们证明,CR-1在正常胎盘和植入性胎盘(creta placentas)中的表达与不同程度的子宫侵袭有关。通过对福尔马林固定、石蜡包埋的胎盘标本(对照胎盘,n = 9;植入性胎盘,n = 6;穿透性植入性胎盘,n = 10;穿透性胎盘,n = 15)进行免疫组织化学染色,观察细胞角蛋白(CK)和CR-1蛋白的表达。植入性胎盘的绒毛外滋养层(EVT)细胞形态模式具有独特性:细胞柱紧密堆积,有大的星形细胞,具有典型的迁移表型,这在孕晚期对照胎盘中并不常见。定量分析显示,植入性胎盘(P = 0.001)、穿透性植入性胎盘(P = 0.0002)和穿透性胎盘(P = 0.001)中的CR-1免疫反应性高于对照组。与对照组不同,在所有植入性胎盘中,CR-1与CK反应性之间存在显著正相关(植入性胎盘,P = 0.02;穿透性植入性胎盘,P = 0.0001;穿透性胎盘,P = 0.025)。本研究证明了CR-1在胎盘床中的表达,其在植入性胎盘中表达增加,以及EVT细胞是主要的CR-1产生细胞类型。形态学检查显示植入性胎盘的滋养层不成熟且具有侵袭性,提示滋养层分化途径受损。这些发现为异常植入性胎盘形成的病理生理学及其妊娠后果提供了重要的新见解。