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感染淋病奈瑟菌的原代人尿道上皮细胞培养物的超微结构分析。

Ultrastructural analysis of primary human urethral epithelial cell cultures infected with Neisseria gonorrhoeae.

作者信息

Harvey H A, Ketterer M R, Preston A, Lubaroff D, Williams R, Apicella M A

机构信息

Department of Microbiology, University of Iowa, Iowa City 52242, USA.

出版信息

Infect Immun. 1997 Jun;65(6):2420-7. doi: 10.1128/iai.65.6.2420-2427.1997.

Abstract

In men with gonococcal urethritis, the urethral epithelial cell is a site of infection. To study the pathogenesis of gonorrhea in this cell type, we have developed a method to culture primary human urethral epithelial cells obtained at the time of urologic surgery. Fluorescent analysis demonstrated that 100% of the cells stained for keratin. Microscopic analyses indicated that these epithelial cells arrayed in a pattern similar to that seen in urethral epithelium. Using immunoelectron and confocal microscopy, we compared the infection process seen in primary cells with events occurring during natural infection of the same cell type in men with gonococcal urethritis. Immunoelectron microscopy studies of cells infected with Neisseria gonorrhoeae 1291 Opa+ P+ showed adherence of organisms to the epithelial cell membrane, pedestal formation with evidence of intimate association between the gonococcal and the epithelial cell membranes, and intracellular gonococci present in vacuoles. Confocal studies of primary urethral epithelial cells showed actin polymerization upon infection. Polyclonal antibodies to the asialoglycoprotein receptor (ASGP-R) demonstrated the presence of this receptor on infected cells in the primary urethral cell culture. In situ hybridization using a fluorescent-labeled probe specific to the ASGP-R mRNA demonstrated this message in uninfected and infected cells. These features were identical to those seen in urethral epithelial cells in exudates from males with gonorrhea. Infection of primary urethral cells in culture mimics events seen in natural infection and will allow detailed molecular analysis of gonococcal pathogenesis in a human epithelial cell which is commonly infected.

摘要

在患有淋菌性尿道炎的男性中,尿道上皮细胞是感染部位。为了研究这种细胞类型中淋病的发病机制,我们开发了一种方法来培养在泌尿外科手术时获取的原代人尿道上皮细胞。荧光分析表明,100%的细胞角蛋白染色呈阳性。显微镜分析表明,这些上皮细胞排列方式与尿道上皮中所见相似。利用免疫电子显微镜和共聚焦显微镜,我们将原代细胞中的感染过程与患有淋菌性尿道炎男性中相同细胞类型自然感染期间发生的事件进行了比较。对感染淋病奈瑟菌1291 Opa+ P+的细胞进行免疫电子显微镜研究显示,细菌黏附于上皮细胞膜,形成基座,表明淋球菌与上皮细胞膜之间存在紧密联系,并且在液泡中存在细胞内淋球菌。对原代尿道上皮细胞的共聚焦研究显示,感染后肌动蛋白发生聚合。针对去唾液酸糖蛋白受体(ASGP-R)的多克隆抗体证明该受体存在于原代尿道细胞培养物中的感染细胞上。使用对ASGP-R mRNA特异的荧光标记探针进行原位杂交,在未感染和感染细胞中均显示出该信息。这些特征与患有淋病男性渗出物中尿道上皮细胞所见相同。培养中原代尿道细胞的感染模拟了自然感染中所见事件,并将允许对常见感染的人类上皮细胞中淋球菌发病机制进行详细的分子分析。

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