Uitto V J, Pan Y M, Leung W K, Larjava H, Ellen R P, Finlay B B, McBride B C
Department of Oral Biology, University of British Columbia, Vancouver, Canada.
Infect Immun. 1995 Sep;63(9):3401-10. doi: 10.1128/iai.63.9.3401-3410.1995.
The effects of Treponema denticola and its outer membrane-bound chymotrypsin-like proteinase on periodontal ligament epithelial cell cultures at different stages of maturity were studied. In sparse cultures with migrating epithelial cells, large intracellular vacuoles were formed rapidly following exposure to live T. denticola. Treponemes showing structural damage were seen occasionally inside membrane-bound vesicles. Intensive membrane blebbing occurred in infected cells and continued for up to 48 h before the cell died. Blebbing could also be induced by a purified chymotrypsin-like proteinase of T. denticola. Cortical actin and alpha-actinin of the bacterium-treated cells showed disorganization, and pericellular fibronectin was degraded by both whole T. denticola and the isolated proteinase. Epithelial cells with well-formed lateral cell contacts appeared to be more resistant to the effects of T. denticola than migrating isolated cells. In multilayer epithelial cultures, adhesion of T. denticola and membrane blebbing were observed infrequently. There was no evidence of invasion of T. denticola into epithelial multilayers. However, immunogold electron microscopy showed rapid transport of T. denticola chymotrypsin-like proteinase into newly formed large intracellular vacuoles within the epithelial layers. These vacuoles were lined by membranes studded with ribosomes. T. denticola-treated epithelial multilayers had loose cell contacts, collapsed intercellular spaces, and increased permeability. Through its capacity to cause these unique cytopathic effects, the chymotrypsin-like proteinase of T. denticola has the potential to contribute to the initiation of periodontal disease.
研究了齿垢密螺旋体及其外膜结合的类胰凝乳蛋白酶对不同成熟阶段牙周膜上皮细胞培养物的影响。在含有迁移上皮细胞的稀疏培养物中,暴露于活的齿垢密螺旋体后,细胞内迅速形成大的液泡。偶尔可见结构受损的螺旋体位于膜结合囊泡内。受感染的细胞出现强烈的膜泡形成,并在细胞死亡前持续长达48小时。齿垢密螺旋体纯化的类胰凝乳蛋白酶也可诱导膜泡形成。经细菌处理的细胞的皮质肌动蛋白和α-辅肌动蛋白显示出紊乱,全齿垢密螺旋体和分离出的蛋白酶均可降解细胞周围的纤连蛋白。具有良好形成的侧向细胞接触的上皮细胞似乎比迁移的分离细胞对齿垢密螺旋体的作用更具抗性。在多层上皮培养物中,很少观察到齿垢密螺旋体的黏附和膜泡形成。没有证据表明齿垢密螺旋体侵入上皮多层结构。然而,免疫金电子显微镜显示齿垢密螺旋体类胰凝乳蛋白酶迅速转运到上皮层内新形成的大细胞内液泡中。这些液泡内衬有布满核糖体的膜。经齿垢密螺旋体处理的上皮多层结构细胞接触松散,细胞间空间塌陷,通透性增加。齿垢密螺旋体的类胰凝乳蛋白酶通过其引起这些独特细胞病变效应的能力,有可能促进牙周疾病的发生。