INTERLEUKIN-1, INTERLEUKIN-6 AND TRANSFORMING GROWTH-FACTOR-BETA PRODUCTION BY HUMAN GINGIVAL MONONUCLEAR-CELLS FOLLOWING STIMULATION WITH PORPHYROMONAS-GINGIVALIS AND FUSOBACTERIUM-NUCLEATUM
E. Gemmell et Gj. Seymour, INTERLEUKIN-1, INTERLEUKIN-6 AND TRANSFORMING GROWTH-FACTOR-BETA PRODUCTION BY HUMAN GINGIVAL MONONUCLEAR-CELLS FOLLOWING STIMULATION WITH PORPHYROMONAS-GINGIVALIS AND FUSOBACTERIUM-NUCLEATUM, Journal of Periodontal Research, 28(2), 1993, pp. 122-129
Gingival mononuclear cell production of interleukin 1 (IL-1), interleu
kin 6 (IL-6) and transforming growth factor-beta (TGF-beta) after stim
ulation with the putative periodontopathic bacteria, Porphyromonas gin
givalis and Fusobacterium nucleatum was investigated. Using an ELISA m
ethod, gingival mononuclear cells extracted from 18 adult periodontiti
s subjects were found to be producing IL-1. However, IL-1 activity cou
ld only be detected in 5 out of these 18 cases when tested using a thy
mocyte proliferation bio-assay, suggesting the presence of IL-1 inhibi
tors. Depletion of monocytes from peripheral blood cultures resulted i
n a significant decrease in IL-1 activity following P gingivalis stimu
lation while there was no effect in the level of IL-1 activity followi
ng stimulation with F. nucleatum. This suggests that P gingivalis and
F nucleatum stimulate different cell types to produce IL-1. Like IL-1,
IL-6 production by gingival mononuclear cells was significantly great
er than that produced by the control peripheral blood mononuclear cell
s. Following P gingivalis and F nucleatum stimulation, higher levels o
f IL-6 could be detected; however, both organisms stimulated similar l
evels. Intracytoplasmic immunofluorescence staining demonstrated a low
er percent TGF-beta+ cells in bacterial stimulated peripheral blood mo
nonuclear cell cultures compared with cells in medium alone. In the gi
ngival mononuclear cell cultures, the percentage TGF-beta+ cells peake
d at day 1 in F nucleatum-stimulated, whereas in P gingivalis-stimulat
ed cultures the peak TGF-beta+ cells occurred at day 3, again suggesti
ng stimulation of different cell subsets. These results illustrate tha
t different periodontopathic bacteria may stimulate different cell typ
es to produce cytokines which may have synergistic or antagonistic eff
ects.