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 …

Modeling mucus physiology and pathophysiology in human organs-on-chips

Z Izadifar, A Sontheimer-Phelps, BA Lubamba… - Advanced Drug Delivery …, 2022 - Elsevier
The surfaces of human internal organs are lined by a mucus layer that ensures symbiotic
relationships with commensal microbiome while protecting against potentially injurious …

Mucus-targeting therapies of defective mucus clearance for cystic fibrosis: a short review

MF Figueira, CMP Ribeiro, B Button - Current opinion in pharmacology, 2022 - Elsevier
In the lungs, defective CFTR associated with cystic fibrosis (CF) represents the nidus for
abnormal mucus clearance in the airways and consequently a progressive lung disease …

Pseudomonas aeruginosa in the Cystic Fibrosis Lung

J King, R Murphy, JC Davies - Pseudomonas aeruginosa: Biology …, 2022 - Springer
Cystic fibrosis is a common genetically inherited, multisystem disorder caused by loss of
function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein, an …

[PDF][PDF] Toward an optimized strategy of using various airway mucus clearance techniques to treat critically ill COVID-19 patients

M Luo, K Ni, Y Sun, J Guo, K Wen, L Deng - Biocell, 2022 - academia.edu
Toward an optimized strategy of using various airway mucus clearance techniques to treat
critically ill COVID-19 patients Page 1 Toward an optimized strategy of using various airway …

[HTML][HTML] Drug repurposing for cystic fibrosis: Identification of drugs that induce CFTR-independent fluid secretion in nasal organoids

LW Rodenburg, L Delpiano, V Railean… - International Journal of …, 2022 - mdpi.com
Individuals with cystic fibrosis (CF) suffer from severe respiratory disease due to a genetic
defect in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which …

[PDF][PDF] Mimicking the host and its microenvironment in vitro for studying

A Crabbé, MA Ledesma, CA Nickerson - academia.edu
Why is a healthy person protected from Pseudomonas aeruginosa infections, while
individuals with cystic fibrosis or damaged epithelium are particularly susceptible to this …

Proteomics of Pseudomonas aeruginosa cystic fibrosis isolates to understand host adaptation

KS Kamath - 2022 - figshare.mq.edu.au
Pseudomonas aeruginosa is an opportunistic bacterial pathogen commonly associated with
cystic fibrosis (CF) lung infection. Numerous studies have investigated the mechanism of …