Airway mucus - From production to secretion

被引:217
作者
Williams, OW
Sharafkhaneh, A
Kim, V
Dickey, BF
Evans, CM
机构
[1] MD Anderson Canc Ctr, Dept Pulm Med, Inst Biosci & Technol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Michael E Debakey Houston VA Med Ctr, Dept Pediat Med, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Michael E Debakey Houston VA Med Ctr, Dept Med, Houston, TX 77030 USA
[4] Temple Univ Hosp & Med Sch, Temple Lung Ctr, Div Pulm & Crit Care Med, Philadelphia, PA 19140 USA
关键词
epithelium; lung; metaplasia; mucin; secretion;
D O I
10.1165/rcmb.2005-0436SF
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
Mucus hypersecretion is a phenotype associated with multiple obstructive lung diseases. However, in spite of its nefarious reputation under pathologic conditions, there are significant benefits to having low levels of mucus present in the airways at baseline, such as the ability to trap and eliminate inhaled particles and to prevent desiccation of airway surfaces. Mucins are high-molecular-weight glycoproteins that are the chief components that render viscoelastic and gel-forming properties to mucus. Recent advances in animal models and in vitro systems have provided a wealth of information regarding the identification of the mucin genes that are expressed in the lungs, the signal transduction pathways that regulate the expression of these mucins, and the secretory pathways that mediate their release into the airways. In addition, the clinical and pathologic literature has corroborated many of the basic laboratory findings. As a result, mucin overproduction and hypersecretion are moving away from being markers of disease and toward being testable as functional components of lung disease processes.
引用
收藏
页码:527 / 536
页数:10
相关论文
共 123 条
[1]   Muc-5/5ac mucin messenger RNA and protein expression is a marker of goblet cell metaplasia in murine airways [J].
Alimam, MZ ;
Piazza, FM ;
Selby, DM ;
Letwin, N ;
Huang, L ;
Rose, MC .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 22 (03) :253-260
[2]   Drosophila Unc-13 is essential for synaptic transmission [J].
Aravamudan, B ;
Fergestad, T ;
Davis, WS ;
Rodesch, CK ;
Broadie, K .
NATURE NEUROSCIENCE, 1999, 2 (11) :965-971
[3]   Munc13-1 is essential for fusion competence of glutamatergic synoptic vesicles [J].
Augustin, I ;
Rosenmund, C ;
Südhof, TC ;
Brose, N .
NATURE, 1999, 400 (6743) :457-461
[4]   Expression of MUC1, MUC2, MUC5AC, and MUC6 in atypical adenomatous hyperplasia, bronchioloalveolar carcinoma, adenocarcinoma with mixed subtypes, and mucinous bronchioloalveolar carcinoma of the lung [J].
Awaya, H ;
Takeshima, Y ;
Yamasaki, M ;
Inai, K .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2004, 121 (05) :644-653
[5]   The melanosome as a model to study organelle motility in mammals [J].
Barral, DC ;
Seabra, MC .
PIGMENT CELL RESEARCH, 2004, 17 (02) :111-118
[6]   Respiratory viral infections in patients with chronic, obstructive pulmonary disease [J].
Beckham, JD ;
Cadena, A ;
Lin, JJ ;
Piedra, PA ;
Glezen, WP ;
Greenberg, SB ;
Atmar, RL .
JOURNAL OF INFECTION, 2005, 50 (04) :322-330
[7]   LUNG IN CYSTIC-FIBROSIS - QUANTITATIVE STUDY INCLUDING PREVALENCE OF PATHOLOGIC FINDINGS AMONG DIFFERENT AGE-GROUPS [J].
BEDROSSIAN, CWM ;
GREENBERG, SD ;
SINGER, DB ;
HANSEN, JJ ;
ROSENBERG, HS .
HUMAN PATHOLOGY, 1976, 7 (02) :195-204
[8]   Mucin gene expression during differentiation of human airway epithelia in vitro -: MUC4 and MUC5B are strongly induced [J].
Bernacki, SH ;
Nelson, AL ;
Abdullah, L ;
Sheehan, JK ;
Harris, A ;
Davis, CW ;
Randell, SH .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 20 (04) :595-604
[9]   Number and proliferation of Clara cells in normal human airway epithelium [J].
Boers, JE ;
Ambergen, AW ;
Thunnissen, FBJM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (05) :1585-1591
[10]   New concepts of the pathogenesis of cystic fibrosis lung disease [J].
Boucher, RC .
EUROPEAN RESPIRATORY JOURNAL, 2004, 23 (01) :146-158