In vitro modeling of host-parasite interactions: the 'subgingival' biofilm challenge of primary human epithelial cells

被引:89
作者
Guggenheim, Bernhard [1 ]
Gmuer, Rudolf [1 ]
Galicia, Johnah C. [2 ]
Stathopoulou, Panagiota G. [2 ]
Benakanakere, Manjunatha R. [2 ]
Meier, Andre [1 ]
Thurnheer, Thomas [1 ]
Kinane, Denis F. [2 ,3 ]
机构
[1] Univ Zurich, Inst Oral Biol, Sect Oral Microbiol & Gen Immunol, CH-8032 Zurich, Switzerland
[2] Univ Louisville, Sch Dent, Oral Hlth & Syst Dis Res Grp, Louisville, KY 40222 USA
[3] Univ Penn, Sch Dent Med, Dept Pathol & Periodontol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
GINGIVAL CREVICULAR FLUID; PORPHYROMONAS-GINGIVALIS; BACTERIAL BIOFILMS; MONOCLONAL-ANTIBODIES; SITU HYBRIDIZATION; INTERLEUKIN-8; COMMUNITIES; INTERMEDIUS; RESISTANCE; PROTEIN;
D O I
10.1186/1471-2180-9-280
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Microbial biofilms are known to cause an increasing number of chronic inflammatory and infectious conditions. A classical example is chronic periodontal disease, a condition initiated by the subgingival dental plaque biofilm on gingival epithelial tissues. We describe here a new model that permits the examination of interactions between the bacterial biofilm and host cells in general. We use primary human gingival epithelial cells (HGEC) and an in vitro grown biofilm, comprising nine frequently studied and representative subgingival plaque bacteria. Results: We describe the growth of a mature 'subgingival' in vitro biofilm, its composition during development, its ability to adapt to aerobic conditions and how we expose in vitro a HGEC monolayer to this biofilm. Challenging the host derived HGEC with the biofilm invoked apoptosis in the epithelial cells, triggered release of pro-inflammatory cytokines and in parallel induced rapid degradation of the cytokines by biofilm-generated enzymes. Conclusion: We developed an experimental in vitro model to study processes taking place in the gingival crevice during the initiation of inflammation. The new model takes into account that the microbial challenge derives from a biofilm community and not from planktonically cultured bacterial strains. It will facilitate easily the introduction of additional host cells such as neutrophils for future biofilm: host cell challenge studies. Our methodology may generate particular interest, as it should be widely applicable to other biofilm-related chronic inflammatory diseases.
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页数:12
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