INTERLEUKIN-8 IS A MAJOR NEUTROPHIL CHEMOTACTIC FACTOR DERIVED FROM CULTURED HUMAN GINGIVAL FIBROBLASTS STIMULATED WITH INTERLEUKIN-1-BETA OR TUMOR-NECROSIS-FACTOR-ALPHA

Inflammatory mediators produced by cells in the gingiva have been implicated in the initiation and progression of periodontal disease, a common infectious disease. In this study, we examined the biological activity of neutrophil chemotactic factors and the kinetics of expression of interleukin-8 (IL-8) mRNA derived from normal gingival fibroblasts in response to inflammatory, mediators in an in vitro model. Gingival fibroblasts stimulated by either recombinant human interleukin-1beta or recombinant human tumor necrosis factor alpha produced neutrophil chemotactic factors after 4 h, whereas expression of cell-derived IL-8 mRNA was detected within 1 h after stimulation. Furthermore, in a neutralization assay, rabbit anti-recombinant human IL-8 antiserum inhibited neutrophil chemotactic activity to basal levels. These results provide evidence that gingival fibroblasts synthesize potent chemotactic factors such as IL-8 in the presence of the inflammatory mediators interleukin-1beta and tumor necrosis factor alpha. The activity of these factors may contribute to neutrophil-mediated processes in the pathogenesis of periodontal disease.