» Articles » PMID: 35356083

Regional Differences in Mucociliary Clearance in the Upper and Lower Airways

Overview
Journal Front Physiol
Date 2022 Mar 31
PMID 35356083
Authors
Affiliations
Soon will be listed here.
Abstract

As the nasal cavity is the portal of entry for inspired air in mammals, this region is exposed to the highest concentration of inhaled particulate matter and pathogens, which must be removed to keep the lower airways sterile. Thus, one might expect vigorous removal of these substances via mucociliary clearance (MCC) in this region. We have investigated the rate of MCC in the murine nasal cavity compared to the more distal airways (trachea). The rate of MCC in the nasal cavity (posterior nasopharynx, PNP) was ∼3-4× greater than on the tracheal wall. This appeared to be due to a more abundant population of ciliated cells in the nasal cavity (∼80%) compared to the more sparsely ciliated trachea (∼40%). Interestingly, the tracheal ventral wall exhibited a significantly lower rate of MCC than the tracheal posterior membrane. The trachealis muscle underlying the ciliated epithelium on the posterior membrane appeared to control the surface architecture and likely in part the rate of MCC in this tracheal region. In one of our mouse models ( KO) exhibiting a 3-fold increase in MUC5B protein in lavage fluid, MCC particle transport on the tracheal walls was severely compromised, yet normal MCC occurred on the tracheal posterior membrane. While a blanket of mucus covered the surface of both the PNP and trachea, this mucus appeared to be transported as a blanket by MCC only in the PNP. In contrast, particles appeared to be transported as discrete patches or streams of mucus in the trachea. In addition, particle transport in the PNP was fairly linear, in contrast transport of particles in the trachea often followed a more non-linear route. The thick, viscoelastic mucus blanket that covered the PNP, which exhibited ∼10-fold greater mass of mucus than did the blanket covering the surface of the trachea, could be transported over large areas completely devoid of cells (made by a breach in the epithelial layer). In contrast, particles could not be transported over even a small epithelial breach in the trachea. The thick mucus blanket in the PNP likely aids in particle transport over the non-ciliated olfactory cells in the nasal cavity and likely contributes to humidification and more efficient particle trapping in this upper airway region.

Citing Articles

Structure and function relationships of mucociliary clearance in human and rat airways.

Roth D, Sahin A, Ling F, Tepho N, Senger C, Quiroz E Nat Commun. 2025; 16(1):2446.

PMID: 40069153 PMC: 11897160. DOI: 10.1038/s41467-025-57667-z.


Developing human upper, lower, and deep lung airway models: Combining different scaffolds and developing complex co-cultures.

Murkar R, Wiese-Rischke C, Weigel T, Kopp S, Walles H J Tissue Eng. 2025; 16:20417314241299076.

PMID: 39885949 PMC: 11780661. DOI: 10.1177/20417314241299076.


Development of an inhalable contrast agent targeting the respiratory tract mucus layer for pulmonary ultrasonic imaging.

Tsuruta J, Sears P, Rebuli M, Weitz A, Durham P, Clapp P Sci Rep. 2024; 14(1):29840.

PMID: 39617759 PMC: 11609298. DOI: 10.1038/s41598-024-80933-x.


CFTR dysfunction leads to defective bacterial eradication on cystic fibrosis airways.

Wu M, Chen J Front Physiol. 2024; 15:1385661.

PMID: 38699141 PMC: 11063615. DOI: 10.3389/fphys.2024.1385661.


Structure and Function Relationships of Mucociliary Clearance in Human and Rat Airways.

Roth D, Sahin A, Ling F, Tepho N, Senger C, Quiroz E bioRxiv. 2024; .

PMID: 38187619 PMC: 10769450. DOI: 10.1101/2023.12.24.572054.


References
1.
Mall M, Mayer-Hamblett N, Rowe S . Cystic Fibrosis: Emergence of Highly Effective Targeted Therapeutics and Potential Clinical Implications. Am J Respir Crit Care Med. 2019; 201(10):1193-1208. PMC: 7233349. DOI: 10.1164/rccm.201910-1943SO. View

2.
Fahy J, Dickey B . Airway mucus function and dysfunction. N Engl J Med. 2010; 363(23):2233-47. PMC: 4048736. DOI: 10.1056/NEJMra0910061. View

3.
Evans C, Williams O, Tuvim M, Nigam R, Mixides G, Blackburn M . Mucin is produced by clara cells in the proximal airways of antigen-challenged mice. Am J Respir Cell Mol Biol. 2004; 31(4):382-94. PMC: 10862391. DOI: 10.1165/rcmb.2004-0060OC. View

4.
Chen G, Volmer A, Wilkinson K, Deng Y, Jones L, Yu D . Role of Spdef in the Regulation of Muc5b Expression in the Airways of Naive and Mucoobstructed Mice. Am J Respir Cell Mol Biol. 2018; 59(3):383-396. PMC: 6189647. DOI: 10.1165/rcmb.2017-0127OC. View

5.
COBURN R . Squeegee of fluid in the compressed canine trachea. Respir Physiol. 1972; 16(1):33-40. DOI: 10.1016/0034-5687(72)90086-2. View