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pmid: 23276626
To date, there is only a fragmentary understanding of the fundamental mechanisms of airway mucociliary transport. Application of the latest measurement techniques can aid in deciphering the complex interplay between ciliary beat and airway surface liquid (ASL) transport. In the present study, direct, quasi-simultaneous measurements of the cilia-induced fluid and bead transport were performed to gain a better insight into both transport mechanisms. In this study cilia-induced periciliary liquid (PCL) transport is measured by means of micro Particle Image Velocimetry (μPIV) with neutrally buoyant tracers. Particle Tracking Velocimetry (PTV) with heavier polystyrene-ferrite beads is performed to simulate particle transport. Contrary to recent literature, in which the presence of mucus was deemed necessary to maintain periciliary liquid (PCL) transport, effective particle and fluid transport was measured in our experiments in the absence of mucus. In response to muscarine or ATP stimulation, maximum fluid transport rates of 250 μm/s at 15 μm distance to the tracheal epithelia were measured while bead transport rates over the epithelia surfaces reached 200 μm/s. We estimated that the mean bead transport is dominated by viscous drag compared to inertial fluid forces. Furthermore, mean bead transport velocities appear to be two orders of magnitude larger compared to bead sedimentation velocities. Therefore, beads are expected to closely follow the mean PCL flow in non-ciliated epithelium regions. Based on our results, we have shown that PCL transport can be directly driven by the cilia beat and that the PCL motion may be capable of driving bead transport by fluid drag.
380, Rehabilitation, Biophysics, Biomedical Engineering, ?PIV, Biological Transport, Active, Respiratory Mucosa, ASL transport, Muscarinic Agonists, μPIV, Trachea, Mice, Mucus, Adenosine Triphosphate, Muscarine, Mouse trachea, Animals, Orthopedics and Sports Medicine, Cilia, PCL transport
380, Rehabilitation, Biophysics, Biomedical Engineering, ?PIV, Biological Transport, Active, Respiratory Mucosa, ASL transport, Muscarinic Agonists, μPIV, Trachea, Mice, Mucus, Adenosine Triphosphate, Muscarine, Mouse trachea, Animals, Orthopedics and Sports Medicine, Cilia, PCL transport
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