Xiao J, Garcia-Lloret M, Winkler-Lowen B, Miller R, Simpson K, Guilbert L J
Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Canada.
Am J Pathol. 1997 May;150(5):1845-60.
Accumulation of maternal monocytes in the villous/intervillous space (villitis) is associated with increased risk of perinatal morbidity and mortality and may initiate in utero transmission of cell-associated infectious agents such cytomegalovirus and HIV-1. We have developed an in vitro model of trophoblast syncytialization and have investigated the adhesive interactions between this tissue and peripheral blood monocytes. We show that monocytes strongly adhere to cultured syncytiotrophoblasts (STs) and that treatment with the inflammatory cytokines interferon-gamma, tumor necrosis factor-alpha, and interleukin-1 alpha greatly increase the number bound. Pretreatment of STs with these cytokines upregulated apical expression of intercellular cell adhesion molecule (ICAM)-1 but not E-or L-selection, ICAM-2 or -3, or various integrins. ICAM-1 expression was cytokine concentration dependent, significantly increased within 6 hours of treatment, peaked after 24 hours, and remained undiminished for 48 hours after cytokine removal from the cultures. Adhesion of monocytes to STs was inhibited > 80% by antibody to ICAM-1 or its cognate ligand LFA-1. ICAM-1 was detected immunohistochemically only in rare foci on intact term placental villi. These results suggest that villous trophoblast expression of ICAM-1 occurs only during an immune inflammatory reaction and that aberrant expression of this molecule may be an important pathological feature in those immunoinflammatory disorders of the placenta characterized by an excessive accumulation of leukocytes in the intervillous/villous space such as spontaneous abortion, perinatal hematogenous infections, and villitis of unknown etiology.
母源性单核细胞在绒毛间隙/绒毛间空间(绒毛炎)的积聚与围产期发病率和死亡率增加相关,并且可能引发细胞相关感染因子如巨细胞病毒和HIV-1的宫内传播。我们建立了一种滋养层细胞融合的体外模型,并研究了该组织与外周血单核细胞之间的黏附相互作用。我们发现单核细胞强烈黏附于培养的合体滋养层细胞(STs),并且用炎性细胞因子干扰素-γ、肿瘤坏死因子-α和白细胞介素-1α处理可大大增加黏附的细胞数量。用这些细胞因子预处理STs可上调细胞间黏附分子(ICAM)-1的顶端表达,但不影响E-或L-选择素、ICAM-2或-3或各种整合素的表达。ICAM-1的表达呈细胞因子浓度依赖性,在处理后6小时内显著增加,24小时后达到峰值,并且在从培养物中去除细胞因子后48小时内仍未减弱。单核细胞与STs的黏附被抗ICAM-1抗体或其同源配体LFA-1抑制>80%。免疫组织化学检测发现ICAM-1仅在足月胎盘绒毛的罕见病灶中存在。这些结果表明,ICAM-1在绒毛滋养层的表达仅发生在免疫炎症反应期间,并且该分子的异常表达可能是胎盘免疫炎症性疾病的一个重要病理特征,这些疾病的特点是在绒毛间隙/绒毛间空间白细胞过度积聚,如自然流产、围产期血源性感染和病因不明的绒毛炎。