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Title: Combined stimulation of nasal polyp fibroblasts with poly IC, interleukin 4, and tumor necrosis factor alpha potently induces production of thymus- and activation-regulated chemokine. Author: Nonaka M, Ogihara N, Fukumoto A, Sakanushi A, Pawankar R, Yagi T. Journal: Arch Otolaryngol Head Neck Surg; 2008 Jun; 134(6):630-5. PubMed ID: 18559731. Abstract: OBJECTIVE: To examine the effects of cytokines and poly IC on the expression of thymus- and activation-regulated chemokine (TARC), a potent chemoattractant for helper T-cell type 2 (T(H)2) cells, in nasal polyp fibroblasts. DESIGN: Quantitative reverse transcription-polymerase chain reaction (RT-PCR) analysis. SETTING: Academic research. PARTICIPANTS: Primary fibroblast lines were established from human nasal polyp biopsy tissue specimens (n = 5) removed at polypectomy. MAIN OUTCOME MEASURES: The expression of TARC messenger RNA (mRNA) was evaluated by real-time RT-PCR. The amount of TARC in the supernatants was measured by enzyme-linked immunosorbent assay. RESULTS: Combined stimulation with interleukin 4 (IL-4) and tumor necrosis factor alpha (TNF-alpha) or with poly IC and IL-4 induced TARC production. Combined exposure of cells to poly IC, IL-4, and TNF-alpha resulted in substantial amounts of TARC release into the culture medium. Quantitative RT-PCR analysis revealed that simultaneous stimulation with those 3 compounds induced a tremendous increase in the amount of TARC mRNA in the nasal polyp fibroblasts. CONCLUSION: Nasal polyp fibroblasts contribute to T(H)2 cell infiltration and RNA virus-induced exacerbation of T(H)2-type airway inflammatory conditions such as allergic chronic sinusitis.[Abstract] [Full Text] [Related] [New Search]