TABLE 2.
Downregulation of the DNA-binding activity of the p65 subunit of NF-κB in FimA tolerance in THP-1 cellsa
Cell stimulation (primary/secondary) | NF-κB subunit activation (OD450)
|
|
---|---|---|
p50 | p65 | |
Medium/medium (baseline control) | 0.187 ± 0.068 | 0.052 ± 0.019 |
Medium/native fimbriae | 2.124 ± 0.548 | 1.378 ± 0.279 |
Native fimbriae/medium | 1.779 ± 0.354 | 0.176 ± 0.035* |
Native fimbriae/native fimbriae | 2.007 ± 0.432 | 0.389 ± 0.072* |
Medium/rFimA | 1.693 ± 0.267 | 1.401 ± 0.321 |
rFimA/Medium | 1.382 ± 0.298 | 0.209 ± 0.039* |
rFimA/rFimA | 1.538 ± 0.403 | 0.432 ± 0.090* |
THP-1 cells were pretreated for 20 h with medium only or with 1 μg of native fimbriae or rFimA per ml. Subsequently, the cells were washed, rested for 2 h, and restimulated for 1 h as indicated with the stimuli at the same concentration as in pretreatment. NF-κB activation in cellular extracts was analyzed with an NF-κB p50/p65 ELISA-based kit. OD450, optical density at 450 nm. The results are shown are means ± standard deviations (n = 3). Asterisks indicate statistically significant (P < 0.05) inhibition of the DNA-binding activity of NF-κB subunits in tolerant cells with or without restimulation.