Table 3.

IL-17 markedly augments production of proangiogenic factors of fibroblast

Angiogenic factorsFibroblastFibroblast + IL-173-150Fibroblast + IL-17 + mAb
VEGF 2.82 ± 0.18 4.69 ± 0.33 2.77 ± 0.23 
KC 1.3 ± 0.05 26.5 ± 2.15 1.41 ± 0.12 
MIP-2 36.0 ± 1.3 52.0 ± 2.2 37.7 ± 1.5 
PGE1 0.8 ± 0.35 4.8 ± 0.65 0.87 ± 0.33 
PGE2 39.5 ± 2.45 81.1 ± 7.35 38.7 ± 2.86 
NO 8.1 ± 0.95 13.3 ± 1.0 8.21 ± 1.1 
Angiogenic factorsFibroblastFibroblast + IL-173-150Fibroblast + IL-17 + mAb
VEGF 2.82 ± 0.18 4.69 ± 0.33 2.77 ± 0.23 
KC 1.3 ± 0.05 26.5 ± 2.15 1.41 ± 0.12 
MIP-2 36.0 ± 1.3 52.0 ± 2.2 37.7 ± 1.5 
PGE1 0.8 ± 0.35 4.8 ± 0.65 0.87 ± 0.33 
PGE2 39.5 ± 2.45 81.1 ± 7.35 38.7 ± 2.86 
NO 8.1 ± 0.95 13.3 ± 1.0 8.21 ± 1.1 

Cells (1 × 105/mL) were cultured for 48 hours with or without 50 ng/mL IL-17 or 50 ng/mL IL-17 plus 20 μg/mL neutralizing antimouse IL-17 mAb. Cell-free supernatants were collected and assayed for the concentrations of VEGF, KC, MIP-2, PGE1, PGE2, and NO (ng/mL for VEGF, KC, PGE1, and PGE2; pg/mL for MIP-2; μM for NO). Data were expressed as mean ± SD (n = 3 per data point).

F3-150

P < .05.

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