Cited by 335Cystic Fibrosis Research AdvancesIon Transport and Channel RegulationRespiratory and Cough-Related Research

Effective mucus clearance is essential for respiratory health

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Randell, Scott H., Boucher, Richard C.·2006·American Journal of Respiratory Cell and Molecular Biology

Abstract

Studies of the pathogenesis of cystic fibrosis (CF) and primary ciliary dyskinesia (PCD), as well as novel genetic mouse models, vividly illustrate that effective "mucus clearance" is a critical innate airway defense mechanism.Modern physics, physical chemistry, biochemistry, and cell and systems biology are revealing the structure of the mucus clearance apparatus and elucidating key parameters underlying its efficient function.New paradigms are evolving to describe the interaction of the near-cell surface environment with overlying mucus, the dominant role of adequate hydration for effective mucus clearance, the role of nucleotide and nucleoside signaling to regulate airway surface hydration, the physiochemical basis of mucus adhesion, and the pathophysiologic consequences of impaired mucus clearance.The recent success of hypertonic saline to restore surface hydration and improve mucus clearance in CF suggests that novel therapeutic strategies will be similarly efficacious in other airway diseases, including chronic obstructive pulmonary disease (COPD).

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Crossref · 10.1165/rcmb.2006-0082sf

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  • Low humidity in the respiratory tract leads to impaired mucociliary function and increases the risk of both upper and lower respiratory tract infections.

    “Low humidity in the respiratory tract leads to impaired mucociliary function and increases the risk of both upper and lower respiratory tract infections [6].”

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  1. [63]Hirsh AJ, Picher M, Boucher RC. Adenosine metabolism and transport by human airway epithelium [abstract]. Pediatr Pulmonol Suppl 2001;22:241. [Google Scholar]

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Authors
Randell, S. H., & Boucher, R. C.
Affiliations
University of North Carolina at Chapel Hill (US)
Venue
American Journal of Respiratory Cell and Molecular Biology
Published
2006-07-01
Volume
35
Issue
1
Pages
20-28
ISSN
  • 1044-1549 (ISSN-L)
  • 1535-4989
OpenAlex
W2104048715
Cited by
335
References
67
Citations by year
2026: 9 · 2025: 11 · 2024: 17 · 2023: 25 · 2022: 11 · 2021: 21 · 2020: 13 · 2019: 23 · 2018: 16 · 2017: 14 · 2016: 17 · 2015: 11 · 2014: 30 · 2013: 24 · 2012: 24
FWCI
2.26
Type
journal article
Language
en
Open access
Locations
  • American Journal of Respiratory Cell and Molecular Biology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institutes of Health
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Respiratory and Cough-Related Research
Keywords
mucus clearance, cystic fibrosis, primary ciliary dyskinesia, mucus adhesion, nucleotide signaling, hypertonic saline, airway defense, chronic obstructive pulmonary disease
MeSH terms
Animals, Body Water, Humans, Inflammation, Mucociliary Clearance, Respiratory System, Immunity, Mucosal

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