BACKGROUND: Glutaredoxins (GRX)-1 is glutathione-dependent oxidoreductase. However, the role of these enzymes remains unknown in airway inflammatory diseases. Therefore, we aimed to establish the expression pattern of GRX-1 in the nasal polyps (NPs) and to assess the regulatory mechanisms associated with GRX-1 expression in interleukin (IL)-1 beta-treated airway epithelial cells. METHODS: The expression of GRX-1 in NPs and normal nasal mucosa were analyzed by reverse-transcription polymerase chain reaction and immunohistochemical staining. IL-1 beta-induced reactive oxygen species (ROS) formation and GRX-1 expression in the airway epithelial cells was determined by flow cytometry and immunoassay. RESULTS: The expression level of GRX-1 in NPs was significantly higher than in the normal nasal mucosa (p < 0.05). GRX-1 was highly expressed in the surface epithelial cells and the submucosal glandular cells in the NPs. IL-1 beta increased the intracellular ROS formation and GRX-1 expression in airway epithelial cells. The inhibition of IL-1 beta-induced ROS production by N-acetyl-cystein, an ROS scavenger, reduced GRX-1 expression. Diphenyleneiodonium and apocynin, NADPH oxidase inhibitors, did not abolish IL-1 beta-induced ROS formation and GRX-1 expression, whereas budesonide attenuated it. CONCLUSION: High GRX-1 expression in NPs might be a primary defense against chronic inflammatory oxidative stress in nasal mucosa. IL-1 beta-induced up-regulation of GRX-1 in airway epithelial cells is probably mediated by ROS. Glucocorticoids can regulate IL-1 beta-induced ROS formation and GRX-1 expression.
BACKGROUND: Glutaredoxins (GRX)-1 is glutathione-dependent oxidoreductase. However, the role of these enzymes remains unknown in airway inflammatory diseases. Therefore, we aimed to establish the expression pattern of GRX-1 in the nasal polyps (NPs) and to assess the regulatory mechanisms associated with GRX-1 expression in interleukin (IL)-1 beta-treated airway epithelial cells. METHODS: The expression of GRX-1 in NPs and normal nasal mucosa were analyzed by reverse-transcription polymerase chain reaction and immunohistochemical staining. IL-1 beta-induced reactive oxygen species (ROS) formation and GRX-1 expression in the airway epithelial cells was determined by flow cytometry and immunoassay. RESULTS: The expression level of GRX-1 in NPs was significantly higher than in the normal nasal mucosa (p < 0.05). GRX-1 was highly expressed in the surface epithelial cells and the submucosal glandular cells in the NPs. IL-1 beta increased the intracellular ROS formation and GRX-1 expression in airway epithelial cells. The inhibition of IL-1 beta-induced ROS production by N-acetyl-cystein, an ROS scavenger, reduced GRX-1 expression. Diphenyleneiodonium and apocynin, NADPH oxidase inhibitors, did not abolish IL-1 beta-induced ROS formation and GRX-1 expression, whereas budesonide attenuated it. CONCLUSION: High GRX-1 expression in NPs might be a primary defense against chronic inflammatory oxidative stress in nasal mucosa. IL-1 beta-induced up-regulation of GRX-1 in airway epithelial cells is probably mediated by ROS. Glucocorticoids can regulate IL-1 beta-induced ROS formation and GRX-1 expression.
Authors: Philip N Sanders; Olha M Koval; Omar A Jaffer; Anand M Prasad; Thomas R Businga; Jason A Scott; Patrick J Hayden; Elizabeth D Luczak; David D Dickey; Chantal Allamargot; Alicia K Olivier; David K Meyerholz; Alfred J Robison; Danny G Winder; Timothy S Blackwell; Ryszard Dworski; David Sammut; Brett A Wagner; Garry R Buettner; Robert M Pope; Francis J Miller; Megan E Dibbern; Hans Michael Haitchi; Peter J Mohler; Peter H Howarth; Joseph Zabner; Joel N Kline; Isabella M Grumbach; Mark E Anderson Journal: Sci Transl Med Date: 2013-07-24 Impact factor: 17.956