Related Experiment Video
Updated: Jul 12, 2026

Rapid Viscoelastic Characterization of Airway Mucus Using a Benchtop Rheometer
Published on: April 21, 2022
Particle size determines mucociliary transport mechanisms in normal and cystic fibrosis airways
Michael Scott1,2, Kaleb C Bierstedt1,2, Weijie Du3,2
1Roy J. Carver Department of Biomedical Engineering, College of Engineering, University of Iowa, USA.
Abstract:
A wide spectrum of microparticles is inhaled with each breath, deposited on airway surfaces, entrapped in the mucus, and removed by mucociliary transport (MCT). However, the influence of particle size on MCT remains largely unknown. Here, we investigated the MCT of microparticles with a trachea-on-a-chip method that integrates a micro-machined device with a trachea explant from newborn pigs. This method preserves airway structures for mucus secretion and cilia beating (e.g., airway surface epithelia and submucosal glands), maintains physiological air-liquid-interface on the airway surface, and allows tracks motion of microparticles with high resolution. Using this method, we found that, in normal airways, 6 μm polystyrene particles clear rapidly, whereas 102 μm particles clear slower and require mucus strands for motion. In cystic fibrosis (CF) airways, MCT of microparticles reduces, but particle size-dependence persists. Methacholine increases particle motion in normal airways, but not in CF airways. These findings suggest two distinct MCT processes, in which large particles rely on mucus strands for clearance, small particles can be cleared independent of mucus strands, and CF disrupts both.
Insights
Particle size significantly impacts airway clearance via mucociliary transport (MCT). Larger particles require mucus, while smaller ones do not, and cystic fibrosis (CF) impairs this process.
Area of Science:
- Pulmonary Science
- Biomedical Engineering
- Respiratory Physiology
Background:
- Microparticles are inhaled daily and cleared by mucociliary transport (MCT).
- The effect of particle size on MCT is not well understood.
- Understanding particle clearance is crucial for respiratory health and disease.
Purpose of the Study:
- To investigate the influence of microparticle size on MCT.
- To compare MCT in normal versus cystic fibrosis (CF) airways.
- To examine the effect of methacholine on particle clearance.
Main Methods:
- Development of a novel trachea-on-a-chip model using pig trachea explants.
- Preservation of airway structures, mucus secretion, and cilia beating.
- High-resolution tracking of microparticle motion in controlled environments.
Main Results:
- In normal airways, 6 µm particles cleared faster than 102 µm particles, which required mucus strands.
- MCT was reduced in CF airways, but particle size-dependence remained.
- Methacholine enhanced particle motion in normal airways but not in CF airways.
Conclusions:
- Two distinct MCT mechanisms exist: mucus-dependent for large particles and mucus-independent for small particles.
- Cystic fibrosis disrupts both MCT pathways.
- Particle size and airway condition are critical factors in respiratory clearance.
Related Concept Videos
Cystic Fibrosis: Management
Sinus disease and chronic sinusitis...
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Chronic Obstructive Pulmonary Disease III: Chronic Bronchitis Features
Drugs Used in Upper Respiratory Disorders: Overview
Antihistamines (e.g., Benadryl) block histamines from binding. Histamines are chemicals released during an allergic reaction in the body. As a...
Chronic Obstructive Pulmonary Disease-II: Pathophysiology
Chronic Inflammation
The Bronchial Tree
The trachea, commonly known as the windpipe, is a tube that connects the larynx (voice box) to the bronchi. At a point called the carina, it bifurcates into two primary bronchi. The right primary bronchus is wider, shorter, and more vertical than the left primary...

