M Bäck, WS Powell, SE Dahlén… - British journal of …, 2014 - Wiley Online Library
The endogenous ligands for the LT, lipoxin (LX) and oxoeicosanoid receptors are bioactive products produced by the action of the lipoxygenase family of enzymes. The LT receptors …
M Weitnauer, V Mijošek, AH Dalpke - Mucosal immunology, 2016 - Elsevier
The lung is ventilated by thousand liters of air per day. Inevitably, the respiratory system comes into contact with airborne microbial compounds, most of them harmless …
J Simonin, E Bille, G Crambert, S Noel, E Dreano… - Scientific reports, 2019 - nature.com
Cystic fibrosis (CF) is caused by defective Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein. Morbidity is mainly due to early airway infection. We hypothesized …
M Briottet, K Sy, C London, A Aissat… - Proceedings of the …, 2024 - National Acad Sciences
In cystic fibrosis (CF), impaired mucociliary clearance leads to chronic infection and inflammation. However, cilia beating features in a CF altered environment, consisting of …
Airborne pathogens and environmental stimuli evoke immune responses in the lung. It is critical to health that these responses be controlled to prevent tissue damage and the …
RI Jaén, S Sánchez-García… - Frontiers in …, 2021 - frontiersin.org
Inflammation is an a physiological response instead an essential response of the organism to injury and its adequate resolution is essential to restore homeostasis. However, defective …
FC Ringholz, PJ Buchanan, DT Clarke… - European …, 2014 - Eur Respiratory Soc
Airway disease in cystic fibrosis (CF) is characterised by impaired mucociliary clearance, persistent bacterial infection and neutrophilic inflammation. Lipoxin A4 (LXA4) initiates the …
R Bhowmick, H Gappa-Fahlenkamp - Lung, 2016 - Springer
The pulmonary epithelium is divided into upper, lower, and alveolar (or small) airway epithelia and acts as the mechanical and immunological barrier between the external …
K Kunzelmann, A Mehta - The FEBS journal, 2013 - Wiley Online Library
Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR). The resulting disease is pleiotropic consistent with the idea that CFTR acts as a …