Regulation of airway surface liquid volume by human airway epithelia
- PMID: 12548395
- DOI: 10.1007/s00424-002-0955-1
Regulation of airway surface liquid volume by human airway epithelia
Abstract
Mucus clearance on airway surfaces is a primary form of pulmonary defense. The efficiency of mucus clearance in large part depends on the volume of the airway surface liquid components, including both the periciliary liquid (PCL) layer and the mucus layer. Studies with in vitro model systems suggest that the mucus layer acts as a passive reservoir to redistribute water to and from, as needed, the PCL layer. In contrast, the overall volume of airway surface liquid is determined by active transepithelial salt transport. Data from in vitro systems suggest that airway epithelia have the capacity to both absorb and secrete liquid in response to the volume requirements on the apical surface. At present, the nature of the signals that transmit information about airway surface liquid volume to epithelia and their sensors are unknown. However, progress in elucidation of this system is important, because it appears that these systems are deranged in the genetic disease cystic fibrosis, which is characterized by airway surface liquid volume depletion, mucus stasis, and chronic infection. Thus, insights into these systems may offer novel therapeutic opportunities to correct this physiologic dysfunction of airway epithelia.
Similar articles
-
Regulation of airway surface liquid volume and mucus transport by active ion transport.Proc Am Thorac Soc. 2004;1(1):42-6. doi: 10.1513/pats.2306014. Proc Am Thorac Soc. 2004. PMID: 16113411 Review.
-
Altered NaCl concentration of airway surface liquid in cystic fibrosis.Pflugers Arch. 2001;443 Suppl 1:S8-10. doi: 10.1007/s004240100636. Epub 2001 Jun 28. Pflugers Arch. 2001. PMID: 11845295
-
Adenosine receptors, cystic fibrosis, and airway hydration.Handb Exp Pharmacol. 2009;(193):363-81. doi: 10.1007/978-3-540-89615-9_12. Handb Exp Pharmacol. 2009. PMID: 19639288 Review.
-
Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia.Int J Mol Sci. 2020 Feb 21;21(4):1488. doi: 10.3390/ijms21041488. Int J Mol Sci. 2020. PMID: 32098269 Free PMC article.
-
Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.Nat Med. 2004 May;10(5):487-93. doi: 10.1038/nm1028. Epub 2004 Apr 11. Nat Med. 2004. PMID: 15077107
Cited by
-
Physiological impact of abnormal lipoxin A₄ production on cystic fibrosis airway epithelium and therapeutic potential.Biomed Res Int. 2015;2015:781087. doi: 10.1155/2015/781087. Epub 2015 Mar 19. Biomed Res Int. 2015. PMID: 25866809 Free PMC article. Review.
-
Lipoxin A4 stimulates calcium-activated chloride currents and increases airway surface liquid height in normal and cystic fibrosis airway epithelia.PLoS One. 2012;7(5):e37746. doi: 10.1371/journal.pone.0037746. Epub 2012 May 25. PLoS One. 2012. PMID: 22662206 Free PMC article.
-
Vitamin C controls the cystic fibrosis transmembrane conductance regulator chloride channel.Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3691-6. doi: 10.1073/pnas.0308393100. Epub 2004 Mar 1. Proc Natl Acad Sci U S A. 2004. PMID: 14993613 Free PMC article.
-
Serially passaged, conditionally reprogrammed nasal epithelial cells as a model to study epithelial functions and SARS-CoV-2 infection.Am J Physiol Cell Physiol. 2022 Apr 1;322(4):C591-C604. doi: 10.1152/ajpcell.00363.2021. Epub 2022 Feb 23. Am J Physiol Cell Physiol. 2022. PMID: 35196166 Free PMC article.
-
Linking increased airway hydration, ciliary beating, and mucociliary clearance through ENaC inhibition.Am J Physiol Lung Cell Mol Physiol. 2015 Jan 1;308(1):L22-32. doi: 10.1152/ajplung.00163.2014. Epub 2014 Oct 31. Am J Physiol Lung Cell Mol Physiol. 2015. PMID: 25361567 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical