Physiology and pathophysiology of human airway mucus
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 …
lung. Mucus is cleared from the lung by cilia and airflow, including both two-phase gas-liquid …
[HTML][HTML] Respiratory epithelial cells orchestrate pulmonary innate immunity
JA Whitsett, T Alenghat - Nature immunology, 2015 - nature.com
The epithelial surfaces of the lungs are in direct contact with the environment and are
subjected to dynamic physical forces as airway tubes and alveoli are stretched and …
subjected to dynamic physical forces as airway tubes and alveoli are stretched and …
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules
The humoral arm of innate immunity includes diverse molecules with antibody-like functions,
some of which serve as disease severity biomarkers in coronavirus disease 2019 (COVID …
some of which serve as disease severity biomarkers in coronavirus disease 2019 (COVID …
Structure and function of TMEM16 proteins (anoctamins)
N Pedemonte, LJV Galietta - Physiological reviews, 2014 - journals.physiology.org
TMEM16 proteins, also known as anoctamins, are involved in a variety of functions that
include ion transport, phospholipid scrambling, and regulation of other membrane proteins …
include ion transport, phospholipid scrambling, and regulation of other membrane proteins …
Cystic fibrosis: emergence of highly effective targeted therapeutics and potential clinical implications
MA Mall, N Mayer-Hamblett… - American journal of …, 2020 - atsjournals.org
Cystic fibrosis (CF) remains the most common life-shortening hereditary disease in white
populations, with high morbidity and mortality related to chronic airway mucus obstruction …
populations, with high morbidity and mortality related to chronic airway mucus obstruction …
Mucus, mucins, and cystic fibrosis
Cystic fibrosis (CF) is both the most common and most lethal genetic disease in the
Caucasian population. CF is caused by mutations in the cystic fibrosis transmembrane …
Caucasian population. CF is caused by mutations in the cystic fibrosis transmembrane …
[HTML][HTML] The groovy TMEM16 family: molecular mechanisms of lipid scrambling and ion conduction
V Kalienkova, VC Mosina, C Paulino - Journal of Molecular Biology, 2021 - Elsevier
The TMEM16 family of membrane proteins displays a remarkable functional dichotomy–
while some family members function as Ca 2+-activated anion channels, the majority of …
while some family members function as Ca 2+-activated anion channels, the majority of …
Cellular functions of TMEM16/anoctamin
U Oh, J Jung - Pflügers Archiv-European Journal of Physiology, 2016 - Springer
Abstract Ca 2+-activated Cl− channels (CaCCs) are a class of Cl− channels activated by
intracellular Ca 2+ that are known to mediate numerous physiological functions. In 2008, the …
intracellular Ca 2+ that are known to mediate numerous physiological functions. In 2008, the …
TMEM16A potentiation: a novel therapeutic approach for the treatment of cystic fibrosis
HL Danahay, S Lilley, R Fox, H Charlton… - American journal of …, 2020 - atsjournals.org
Rationale: Enhancing non–CFTR (cystic fibrosis transmembrane conductance regulator)-
mediated anion secretion is an attractive therapeutic approach for the treatment of cystic …
mediated anion secretion is an attractive therapeutic approach for the treatment of cystic …
Drug repurposing: the anthelmintics niclosamide and nitazoxanide are potent TMEM16A antagonists that fully bronchodilate airways
K Miner, K Labitzke, B Liu, P Wang… - Frontiers in …, 2019 - frontiersin.org
There is an unmet need in severe asthma where approximately 40% of patients exhibit poor
β-agonist responsiveness, suffer daily symptoms and show frequent exacerbations …
β-agonist responsiveness, suffer daily symptoms and show frequent exacerbations …