Nasal polyps is a chronic inflammatory disease of the upper airway characte
rized by structural;abnormalities including stromal fibrosis. Fibroblasts a
re a rich soul cr of cytokines and inflammatory mediators and are thought t
o play an important role in the development of fibrosis. In addition. there
is considerable evidence for the participation of eosinophils in the patho
physiology of nasal polyps. Although increased numbers of eosinophils are p
resent in nasal polyps, the mechanisms responsible for their selective accu
mulation are not completely clear. Eotaxin is a chemokine that promotes the
selective recruitment of eosinophils. Thus, it may be an important molecul
e for the recruitment of eosinophils in nasal polyps. The purpose of this s
tudy was to investigate whether nasal polyp fibroblasts synthesize eotaxin
after stimulation with lipopolysaccharide. IL-1 beta or TNF-alpha. Using pr
imary nasal polyp tissue-derived fibroblast lines, we demonstrated that LPS
. IL-1 beta and TNF-alpha induced the gent expression and protein productio
n of cotaxin in nasal polyp fibroblasts. This responsiveness to LPS. IL-1 b
eta and TNF-alpha was time- and dose-dependent. These findings support the
hypothesis that fibroblasts could play an important role in the recruitment
of eosinophils in nasal polyps through the production of eotaxin.