Glucocorticoid receptor expression in human bronchial epithelial cells: effects of smoking and COPD

被引:9
|
作者
Verheggen, MM
Adriaansen-Soeting, PWC
Berrevoets, CA
van Hal, PTW
Brinkmann, AO
Hoogsteden, HC
Versnel, MA
机构
[1] Erasmus Univ, Dept Immunol, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus Univ, Dept Pulm Med, NL-3000 DR Rotterdam, Netherlands
[3] Erasmus Univ, Dept Endocrinol & Reprod, NL-3000 DR Rotterdam, Netherlands
[4] Univ Hosp Rotterdam Dijkzigt, Dept Immunol, NL-3000 DR Rotterdam, Netherlands
[5] Univ Hosp Rotterdam Dijkzigt, Dept Pulm Med, NL-3000 DR Rotterdam, Netherlands
[6] Univ Hosp Rotterdam Dijkzigt, Dept Endocrinol & Reprod, NL-3000 DR Rotterdam, Netherlands
关键词
glucocorticoid receptors; human bronchial epithelial cells; chronic obstructive pulmonary disease; smoking;
D O I
10.1080/09629359890965
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 (K-d) values in HBEC from smoking (K-d = 0.98 +/- 0.08 nM; n = 6) and nonsmoking controls (K-d = 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.
引用
收藏
页码:275 / 281
页数:7
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