Regulated mucin secretion from airway epithelial cells

KB Adler, MJ Tuvim, BF Dickey - Frontiers in endocrinology, 2013 - frontiersin.org
Secretory epithelial cells of the proximal airways synthesize and secrete gel-forming
polymeric mucins. The secreted mucins adsorb water to form mucus that is propelled by …

Mucociliary clearance–a critical upper airway host defense mechanism and methods of assessment

MB Antunes, NA Cohen - Current opinion in allergy and clinical …, 2007 - journals.lww.com
Advancements in techniques for analysis of mucociliary clearance have improved our
understanding of the interaction between the respiratory epithelium and the airway surface …

Secretion properties, clearance, and therapy in airway disease

BK Rubin - Translational respiratory medicine, 2014 - Springer
Chronic airway diseases like cystic fibrosis, chronic bronchitis, asthma, diffuse
panbronchiolitis, and bronchiectasis are all associated with chronic inflammation. The …

Coordinated release of nucleotides and mucin from human airway epithelial Calu‐3 cells

SM Kreda, SF Okada, CA Van Heusden… - The Journal of …, 2007 - Wiley Online Library
The efficiency of the mucociliary clearance (MCC) process that removes noxious materials
from airway surfaces depends on the balance between mucin secretion, airway surface …

Chronic effects of mechanical force on airways

DJ Tschumperlin, JM Drazen - Annu. Rev. Physiol., 2006 - annualreviews.org
▪ Abstract Airways are embedded in the mechanically dynamic environment of the lung. In
utero, this mechanical environment is defined largely by fluid secretion into the developing …

TMEM16A Protein: A New Identity for Ca2+-Dependent Cl Channels

L Ferrera, A Caputo, LJV Galietta - Physiology, 2010 - journals.physiology.org
Ca+-dependent Cl− channels (CaCCs) play a variety of physiological roles in different
organs and tissues, including transepithelial Cl− secretion, smooth muscle contraction …

Cystic fibrosis: the mechanisms of pathogenesis of an inherited lung disorder

MT Clunes, RC Boucher - Drug Discovery Today: Disease Mechanisms, 2007 - Elsevier
Cystic fibrosis patients exhibit lung disease consistent with a failure of innate airway defense
mechanisms. The link between abnormal ion transport and disease initiation and …

Deletion of the ubiquitin ligase Nedd4L in lung epithelia causes cystic fibrosis-like disease

T Kimura, H Kawabe, C Jiang… - Proceedings of the …, 2011 - National Acad Sciences
Cystic fibrosis is caused by impaired ion transport due to mutated cystic fibrosis
transmembrane conductance regulator, accompanied by elevated activity of the amiloride …

P2X3-receptor antagonists as potential antitussives: summary of current clinical trials in chronic cough

PV Dicpinigaitis, LP McGarvey, BJ Canning - Lung, 2020 - Springer
Cough is among the most common complaints for which patients worldwide seek medical
attention. In a majority of patients with chronic cough (defined as cough of greater than 8 …

Airway hydration and COPD

A Ghosh, RC Boucher, R Tarran - Cellular and Molecular Life Sciences, 2015 - Springer
Chronic obstructive pulmonary disease (COPD) is one of the prevalent causes of worldwide
mortality and encompasses two major clinical phenotypes, ie, chronic bronchitis (CB) and …