[HTML][HTML] Inflammation as a regulator of the airway surface liquid pH in cystic fibrosis

T Rehman, MJ Welsh - Cells, 2023 - mdpi.com
The airway surface liquid (ASL) is a thin sheet of fluid that covers the luminal aspect of the
airway epithelium. The ASL is a site of several first-line host defenses, and its composition is …

[HTML][HTML] Human conjunctiva organoids to study ocular surface homeostasis and disease

M Bannier-Hélaouët, J Korving, Z Ma, H Begthel… - Cell Stem Cell, 2024 - cell.com
The conjunctival epithelium covering the eye contains two main cell types: mucus-producing
goblet cells and water-secreting keratinocytes, which present mucins on their apical surface …

The mechanisms of chromogranin B-regulated Cl homeostasis

QX Jiang, G Yadav - Biochemical Society Transactions, 2022 - portlandpress.com
Chloride is the most abundant inorganic anions in almost all cells and in human circulation
systems. Its homeostasis is therefore important for systems physiology and normal cellular …

CFTR dysfunction leads to defective bacterial eradication on cystic fibrosis airways

M Wu, JH Chen - Frontiers in Physiology, 2024 - frontiersin.org
Dysfunction of the cystic fibrosis transmembrane conductance regulator (CFTR) anion
channel by genetic mutations causes the inherited disease cystic fibrosis (CF). CF lung …

VSI: The Anoctamins: Structure and Function

R Schreiber, J Ousingsawat, K Kunzelmann - Cell Calcium, 2024 - Elsevier
When activated by increase in intracellular Ca 2+, anoctamins (TMEM16 proteins) operate
as phospholipid scramblases and as ion channels. Anoctamin 1 (ANO1) is the Ca 2+ …

[PDF][PDF] Epithelial Anoctamins

R Schreiber, J Ousingsawat, K Kunzelmann - Cell Calcium, 2024 - epub.uni-regensburg.de
When activated by increase in intracellular Ca2+, anoctamins (TMEM16 proteins) operate as
phospholipid scramblases and as ion channels. Anoctamin 1 (ANO1) is the Ca2+-activated …

Airway succinate chemosensing induces CFTR-dependent anion secretion and mucus clearance which is impaired in cystic fibrosis.

T Apablaza, M Barros-Poblete, L Delpiano… - bioRxiv, 2024 - biorxiv.org
The respiratory tract possesses a highly regulated innate defense system which includes
efficient cilia-mediated mucus transport or mucociliary clearance (MCC). This essential …

The Physiology of Epithelial ION and Fluid Transport: Beyond CFTR Modulators

L Delpiano, MA Gray - Hodson and Geddes' Cystic Fibrosis, 2023 - taylorfrancis.com
Ion and fluid transport are critical for the functioning of epithelial tissues affected in cystic
fibrosis (CF), such as those lining the airways, pancreatic and biliary ducts, intestines and …

Identification of Key Genes and Underlying Mechanisms in Cystic Fibrosis and its Associated Complications Based on Bioinformatics Analysis of Next Generation …

B Vastrad, C Vastrad - bioRxiv, 2022 - biorxiv.org
Cystic fibrosis (CF) is one of the inherited autosomal recessive disorders with very
complicated pathogenesis. Identifying the molecular signatures and specific biomarkers of …

Alternate channel therapy for cystic fibrosis lung disease

L Delpiano - 2023 - theses.ncl.ac.uk
Cystic Fibrosis (CF) is the most common, severe, autosomal recessive disease in the
Caucasian population, and is caused by mutations in the cystic fibrosis transmembrane …