Open AccessDecreased expression of human aquaporin‐5 correlated with mucus overproduction in airways of chronic obstructive pulmonary disease 1
Author(s) -
WANG Ke,
FENG Yulin,
WEN Fuqiang,
CHEN Xuerong,
OU Xuemei,
XU Dan,
YANG Jie,
DENG Zhiping
Publication year - 2007
Publication title -
acta pharmacologica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.514
H-Index - 90
eISSN - 1745-7254
pISSN - 1671-4083
DOI - 10.1111/j.1745-7254.2007.00608.x
Subject(s) - copd , mucus , medicine , submucosal glands , mucin , periodic acid–schiff stain , vital capacity , pathology , gastroenterology , pulmonary function testing , lung , chronic bronchitis , immunohistochemistry , endocrinology , biology , lung function , diffusing capacity , ecology
Aim: To investigate the relationship between aquaporin‐5 (AQP 5 ) expression and mucus overproduction in the airways of Chinese patients with chronic obstructive pulmonary disease (COPD) and the correlation with pulmonary function change. Methods: Bronchial tissues were obtained from fiberoptic bronchoscopy and bronchial biopsy in West China Hospital from April to July 2004. Twenty‐five patients were diagnosed as COPD patients, and another 20 were diagnosed as the control patients. The expressions of AQP 5 , mucin 5 AC (MUC5AC), and mucin in bronchial tissues were detected by semiquantitative RT‐PCR, in situ hybridization, and immunohistochemical and alcian blue‐periodic acid‐Schiff (AB‐PAS) staining, respectively. Results: Compared with the control group, an attenuated expression of AQP 5 was detected throughout the bronchial tissues from patients with COPD ( P < 0.01), but no difference existed in the lung tissues ( P > 0.05). Simultaneously, increased staining of MUC5 AC and mucus in submucosal glands were noted ( P < 0.01, respectively). Smoking attenuated the expressions of AQP 5 and increased the staining of MUC5AC and mucus in submucosal glands in the COPD groups ( P < 0.01), while there were no significant differences observed in the control group ( P > 0.05). The decreased expression of AQP 5 mRNA was correlated with forced expiratory volume in 1 s (FEV 1 )/forced vital capacity (FVC) ( r = 0.60, P < 0.01), FEV 1 % predicted value ( r = 0.60, P < 0.01), maximal expiratory flow in 50% vital capacity ( V 50 )% predicted value ( r = 0.55, P < 0.01), and maximal expiratory flow in 25% vital capacity ( V 25 ) % predicted value ( r = 0.45, P < 0.01). The decreased expression was negatively correlated with MUC5 AC mRNA of the epithelium airways ( r =−0.45, P < 0.01) and the AB‐PAS‐stained area of submucosal glands ( r =−0.61, P < 0.01). The upregulation of MUC5AC mRNA correlated with the positively AB‐PAS‐stained area of submucosal glands and correlated negatively with FEV 1 /FVC ( r =−0.53; P < 0.01), FEV 1 % predicted value ( r =−0.53; P < 0.01), V 50 % predicted value ( r =−0.48; P < 0.01), and V 25 % predicted value ( r =−0.43; P < 0.01). Conclusion: The attenuated gene expression of AQP 5 existed in the airways of Chinese COPD patients, which was complicated by mucus hypersecretion. The decreased expression of AQP 5 mRNA may be related to the severity of airflow obstruction.