A Periciliary Brush Promotes the Lung Health by Separating the Mucus Layer from Airway Epithelia

被引:623
作者
Button, Brian [2 ]
Cai, Li-Heng [1 ]
Ehre, Camille [2 ]
Kesimer, Mehmet [2 ,3 ]
Hill, David B. [2 ]
Sheehan, John K. [3 ]
Boucher, Richard C. [2 ]
Rubinstein, Michael [1 ,4 ]
机构
[1] Univ N Carolina, Curriculum Appl Sci & Engn, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Cyst Fibrosis Res & Treatment Ctr, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
CYSTIC-FIBROSIS; SURFACE LIQUID; PSEUDOMONAS-AERUGINOSA; MUCOCILIARY CLEARANCE; RESPIRATORY-TRACT; IN-VIVO; MUCIN; TRANSPORT; DISEASE; IDENTIFICATION;
D O I
10.1126/science.1223012
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mucus clearance is the primary defense mechanism that protects airways from inhaled infectious and toxic agents. In the current gel-on-liquid mucus clearance model, a mucus gel is propelled on top of a "watery" periciliary layer surrounding the cilia. However, this model fails to explain the formation of a distinct mucus layer in health or why mucus clearance fails in disease. We propose a gel-on-brush model in which the periciliary layer is occupied by membrane-spanning mucins and mucopolysaccharides densely tethered to the airway surface. This brush prevents mucus penetration into the periciliary space and causes mucus to form a distinct layer. The relative osmotic moduli of the mucus and periciliary brush layers explain both the stability of mucus clearance in health and its failure in airway disease.
引用
收藏
页码:937 / 941
页数:5
相关论文
共 44 条
[1]  
Arfken G. B., 2000, Mathematical Methods for Physicists
[2]   IMMUNOHISTOPATHOLOGIC LOCALIZATION OF PSEUDOMONAS-AERUGINOSA IN LUNGS FROM PATIENTS WITH CYSTIC-FIBROSIS - IMPLICATIONS FOR THE PATHOGENESIS OF PROGRESSIVE LUNG DETERIORATION [J].
BALTIMORE, RS ;
CHRISTIE, CDC ;
SMITH, GJW .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 140 (06) :1650-1661
[3]   New concepts of the pathogenesis of cystic fibrosis lung disease [J].
Boucher, RC .
EUROPEAN RESPIRATORY JOURNAL, 2004, 23 (01) :146-158
[4]   Airway surface dehydration in cystic fibrosis: Pathogenesis and therapy [J].
Boucher, Richard C. .
ANNUAL REVIEW OF MEDICINE, 2007, 58 :157-170
[5]   Cigarette smoke exposure induces CFTR internalization and insolubility, leading to airway surface liquid dehydration [J].
Clunes, Lucy A. ;
Davies, Catrin M. ;
Coakley, Raymond D. ;
Aleksandrov, Andrei A. ;
Henderson, Ashley G. ;
Zeman, Kirby L. ;
Worthington, Erin N. ;
Gentzsch, Martina ;
Kreda, Silvia M. ;
Cholon, Deborah ;
Bennett, William D. ;
Riordan, John R. ;
Boucher, Richard C. ;
Tarran, Robert .
FASEB JOURNAL, 2012, 26 (02) :533-545
[6]   MEDICAL PROGRESS Airway Mucus Function and Dysfunction [J].
Fahy, John V. ;
Dickey, Burton F. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (23) :2233-2247
[7]   Cystic fibrosis and the relationship between mucin and chloride secretion by cultures of human airway gland mucous cells [J].
Finkbeiner, Walter E. ;
Zlock, Lorna T. ;
Morikawa, Masatoshi ;
Lao, Anna Y. ;
Dasari, Vijay ;
Widdicombe, Jonathan H. .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2011, 301 (04) :L402-L414
[8]  
Hattrup CL, 2008, ANNU REV PHYSIOL, V70, P431, DOI 10.1146/annurev.physiol.70.113006.100659
[9]  
Hilding A C, 1967, Minn Med, V50, P915
[10]   The nature of small-airway obstruction in chronic obstructive pulmonary disease [J].
Hogg, JC ;
Chu, F ;
Utokaparch, S ;
Woods, R ;
Elliott, WM ;
Buzatu, L ;
Cherniack, RM ;
Rogers, RM ;
Sciurba, FC ;
Coxson, HO ;
Paré, PD .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (26) :2645-2653