Cigarette smoke exposure induces CFTR internalization and insolubility, leading to airway surface liquid dehydration

被引:211
作者
Clunes, Lucy A. [1 ]
Davies, Catrin M. [1 ]
Coakley, Raymond D. [1 ]
Aleksandrov, Andrei A. [1 ]
Henderson, Ashley G. [1 ]
Zeman, Kirby L. [1 ]
Worthington, Erin N. [1 ]
Gentzsch, Martina [1 ]
Kreda, Silvia M. [1 ]
Cholon, Deborah [1 ]
Bennett, William D. [1 ]
Riordan, John R. [1 ]
Boucher, Richard C. [1 ]
Tarran, Robert [1 ]
机构
[1] Univ N Carolina, Cyst Fibrosis Pulm Res & Treatment Ctr, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
aggresome; chronic bronchitis; ion channel; lung disease; TRANSMEMBRANE CONDUCTANCE REGULATOR; CYSTIC-FIBROSIS; ENDOCYTIC TRAFFICKING; AGGRESOME FORMATION; MUCUS CLEARANCE; IN-VITRO; PROTEASOME; INFLAMMATION; DEGRADATION; VIVO;
D O I
10.1096/fj.11-192377
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cigarette smoke (CS) exposure induces mucus obstruction and the development of chronic bronchitis (CB). While many of these responses are determined genetically, little is known about the effects CS can exert on pulmonary epithelia at the protein level. We, therefore, tested the hypothesis that CS exerts direct effects on the CFTR protein, which could impair airway hydration, leading to the mucus stasis characteristic of both cystic fibrosis and CB. In vivo and in vitro studies demonstrated that CS rapidly decreased CFTR activity, leading to airway surface liquid (ASL) volume depletion (i.e., dehydration). Further studies revealed that CS induced internalization of CFTR. Surprisingly, CS-internalized CFTR did not colocalize with lysosomal proteins. Instead, the bulk of CFTR shifted to a detergent-resistant fraction within the cell and colocalized with the intermediate filament vimentin, suggesting that CS induced CFTR movement into an aggresome-like, perinuclear compartment. To test whether airway dehydration could be reversed, we used hypertonic saline (HS) as an osmolyte to rehydrate ASL. HS restored ASL height in CS-exposed, dehydrated airway cultures. Similarly, inhaled HS restored mucus transport and increased clearance in patients with CB. Thus, we propose that CS exposure rapidly impairs CFTR function by internalizing CFTR, leading to ASL dehydration, which promotes mucus stasis and a failure of mucus clearance, leaving smokers at risk for developing CB. Furthermore, our data suggest that strategies to rehydrate airway surfaces may provide a novel form of therapy for patients with CB.-Clunes, L. A., Davies, C. M., Coakley, R. D., Aleksandrov, A. A., Henderson, A. G., Zeman, K. L., Worthington, E. N., Gentzsch, M., Kreda, S. M., Cholon, D., Bennett, W. D., Riordan, J. R., Boucher, R. C., Tarran, R. Cigarette smoke exposure induces CFTR internalization and insolubility, leading to airway surface liquid dehydration. FASEB J. 26, 533-545 (2012). www.fasebj.org
引用
收藏
页码:533 / 545
页数:13
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