Physiology and pathophysiology of human airway mucus

DB Hill, B Button, M Rubinstein… - Physiological …, 2022 - journals.physiology.org
The mucus clearance system is the dominant mechanical host defense system of the human
lung. Mucus is cleared from the lung by cilia and airflow, including both two-phase gas-liquid …

Biofilm aggregates and the host airway-microbial interface

L Hall-Stoodley, KS McCoy - Frontiers in Cellular and Infection …, 2022 - frontiersin.org
Biofilms are multicellular microbial aggregates that can be associated with host mucosal
epithelia in the airway, gut, and genitourinary tract. The host environment plays a critical role …

Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties via hydration

CB Morrison, KM Shaffer, KC Araba… - European …, 2022 - Eur Respiratory Soc
Question Cystic fibrosis (CF) is characterised by the accumulation of viscous adherent
mucus in the lungs. While several hypotheses invoke a direct relationship with cystic fibrosis …

The effect of CFTR modulators on airway infection in cystic fibrosis

C Harvey, S Weldon, S Elborn, DG Downey… - International Journal of …, 2022 - mdpi.com
The advent of Cystic fibrosis transmembrane receptor (CFTR) modulators in 2012 was a
critical event in the history of cystic fibrosis (CF) treatment. Unlike traditional therapies that …

Models using native tracheobronchial mucus in the context of pulmonary drug delivery research: composition, structure and barrier properties

BC Huck, X Murgia, S Frisch, M Hittinger… - Advanced Drug Delivery …, 2022 - Elsevier
Mucus covers all wet epithelia and acts as a protective barrier. In the airways of the lungs,
the viscoelastic mucus meshwork entraps and clears inhaled materials and efficiently …

Mucins and CFTR: their close relationship

K Okuda, KM Shaffer, C Ehre - International journal of molecular sciences, 2022 - mdpi.com
Mucociliary clearance is a critical defense mechanism for the lungs governed by regionally
coordinated epithelial cellular activities, including mucin secretion, cilia beating, and …

Mucus concentration–dependent biophysical abnormalities unify submucosal gland and superficial airway dysfunction in cystic fibrosis

T Kato, G Radicioni, MJ Papanikolas, GV Stoychev… - Science …, 2022 - science.org
Cystic fibrosis (CF) is characterized by abnormal transepithelial ion transport. However, a
description of CF lung disease pathophysiology unifying superficial epithelial and …

[HTML][HTML] Airway surface hyperviscosity and defective mucociliary transport by IL-17/TNF-α are corrected by β-adrenergic stimulus

D Guidone, M Buccirossi, P Scudieri, M Genovese… - JCI insight, 2022 - ncbi.nlm.nih.gov
The fluid covering the surface of airway epithelia represents a first barrier against
pathogens. The chemical and physical properties of the airway surface fluid are controlled …

Mucus and mucus flake composition and abundance reflect inflammatory and infection status in cystic fibrosis

MR Markovetz, IC Garbarine, CB Morrison… - Journal of Cystic …, 2022 - Elsevier
Background Mucus hyperconcentration in cystic fibrosis (CF) lung disease is marked by
increases in both mucin and DNA concentration. Additionally, it has been shown that half of …

[HTML][HTML] IL-13–programmed airway tuft cells produce PGE2, which promotes CFTR-dependent mucociliary function

ME Kotas, CM Moore, JG Gurrola, SD Pletcher… - JCI insight, 2022 - ncbi.nlm.nih.gov
Abstract Chronic type 2 (T2) inflammatory diseases of the respiratory tract are characterized
by mucus overproduction and disordered mucociliary function, which are largely attributed to …