Glucocorticoid receptor expression in human bronchial epithelial cells: effects of smoking and COPD
Author(s) -
M. M. Verheggen,
P. W. C. Adriaansen-Soeting,
Cor Berrevoets,
Peter Th. W. van Hal,
A.O. Brinkmann,
H. C. Hoogsteden,
Marjan A. Versnel
Publication year - 1998
Publication title -
mediators of inflammation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.37
H-Index - 97
eISSN - 1466-1861
pISSN - 0962-9351
DOI - 10.1080/09629359890965
Subject(s) - copd , glucocorticoid receptor , dissociation constant , glucocorticoid , receptor , inflammation , epithelium , medicine , endocrinology , respiratory epithelium , immunology , cell culture , lung , chemistry , biology , pathology , genetics
Previously, we found that inflammatory mediators modulated the number and binding affinity of glucocorticoid receptors (GR) in human bronchial epithelial cell lines. In this study we investigated whether smoking and chronic obstructive pulmonary disease (COPD), both characterized by airway inflammation with increased levels of inflammatory mediators, affect GR characteristics in cultured human bronchial epithelial cells (HBEC). A statistically significant difference was found between the dissociation constant (Kd) values in HBEC from smoking (Kd = 0.98+/-0.08 nM; n = 6) and nonsmoking controls (Kd = 0.76+/-0.10 nM, P = 0.03; n = 5), but no significant difference was found between the mean number of binding sites. Our results are the first indication that cultured HBEC from smokers possess GR with a lower binding affinity. This may result from the inflammation found in the airways from smokers. Furthermore, these results provide further evidence that the bronchial epithelium may be an actual target for inhaled glucocorticoid therapy.
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