Abstract
Background: Many cystic fibrosis (CF) patients display airway hyperresponsiveness and have symptoms of asthma such as cough, wheezing and reversible airway obstruction. Chronic airway bacterial colonization, associated with neutrophilic inflammation and high levels of interleukin-8 (IL-8) is also a common occurrence in these patients. The aim of this work was to determine the responsiveness of airway smooth muscle to IL-8 in CF patients compared to non-CF individuals.Methods: Experiments were conducted on cultured ASM cells harvested from subjects with and without CF (control subjects). Cells from the 2ndto 5thpassage were studied. Expression of the IL-8 receptors CXCR1 and CXCR2 was assessed by flow cytometry. The cell response to IL-8 was determined by measuring intracellular calcium concentration ([Ca2+]i), cell contraction, migration and proliferation.Results: The IL-8 receptors CXCR1 and CXCR2 were expressed in both non-CF and CF ASM cells to a comparable extent. IL-8 (100 nM) induced a peak Ca2+release that was higher in control than in CF cells: 228 ± 7 versus 198 ± 10 nM (p < 0.05). IL-8 induced contraction was greater in CF cells compared to control. Furthermore, IL-8 exposure resulted in greater phosphorylation of myosin light chain (MLC20) in CF than in control cells. In addition, MLC20expression was also increased in CF cells. Exposure to IL-8 induced migration and proliferation of both groups of ASM cells but was not different between CF and non-CF cells.Conclusion: ASM cells of CF patients are more contractile to IL-8 than non-CF ASM cells. This enhanced contractility may be due to an increase in the amount of contractile protein MLC20. Higher expression of MLC20by CF cells could contribute to airway hyperresponsiveness to IL-8 in CF patients. © 2008 Govindaraju et al; licensee BioMed Central Ltd.
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CITATION STYLE
Govindaraju, V., Michoud, M. C., Ferraro, P., Arkinson, J., Safka, K., Valderrama-Carvajal, H., & Martin, J. G. (2008). The effects of interleukin-8 on airway smooth muscle contraction in cystic fibrosis. Respiratory Research, 9. https://doi.org/10.1186/1465-9921-9-76
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