[HTML][HTML] Functional interplay between CFTR and pendrin: physiological and pathophysiological relevance

G Tamma, S Dossena - Frontiers in Bioscience-Landmark, 2022 - imrpress.com
The transport of chloride and bicarbonate across epithelia controls the pH and volume of the
intracellular and luminal fluids, as well as the systemic pH and vascular volume. The anion …

Pendrin mediates bicarbonate secretion and enhances cystic fibrosis transmembrane conductance regulator function in airway surface epithelia

D Kim, J Huang, A Billet, A Abu-Arish… - American journal of …, 2019 - atsjournals.org
Bicarbonate facilitates mucin unpacking and bacterial killing; however, its transport
mechanisms in the airways are not well understood. cAMP stimulates anion efflux through …

Novel role for pendrin in orchestrating bicarbonate secretion in cystic fibrosis transmembrane conductance regulator (CFTR)-expressing airway serous cells

JP Garnett, E Hickman, R Burrows, P Hegyi… - Journal of Biological …, 2011 - ASBMB
In most HCO 3−-secreting epithelial tissues, SLC26 Cl−/HCO 3− transporters work in concert
with the cystic fibrosis transmembrane conductance regulator (CFTR) to regulate the …

Pendrin mediates bicarbonate secretion and enhances CFTR function in airway surface epithelia

D Kim, J Huang, A Billet, A Abu-Arish… - American Journal of …, 2019 - hal.science
Bicarbonate facilitates mucin unpacking and bacterial killing; however, its transport
mechanisms in the airways are not well understood. cAMP stimulates anion efflux through …

Pendrin: physiology, molecular biology and clinical importance

R Grimaldi, P Capuano, N Miranda… - Giornale italiano di …, 2007 - europepmc.org
Pendrin, first identified in 1997, belongs to a superfamily of anion transporters localized in
the thyroid gland, inner ear and kidney. Immunohistochemical studies have shown that …

[HTML][HTML] Pendrin stimulates a chloride absorption pathway to increase CFTR‐mediated chloride secretion from Cystic Fibrosis airway epithelia

J Bajko, M Duguid, S Altmann, GD Hurlbut… - FASEB …, 2020 - ncbi.nlm.nih.gov
Cystic Fibrosis (CF), an inherited multi‐system disease, is caused by mutations in the Cystic
Fibrosis Transmembrane Conductance Regulator (CFTR) that disrupt its ability to secrete …

[HTML][HTML] Inhibitors of pendrin anion exchange identified in a small molecule screen increase airway surface liquid volume in cystic fibrosis

PM Haggie, PW Phuan, JA Tan, L Zlock… - The FASEB …, 2016 - ncbi.nlm.nih.gov
Abstract Pendrin (SLC26A4) is a Cl−/anion exchanger expressed in the epithelium of
inflamed airways where it is thought to facilitate Cl− absorption and HCO 3− secretion …

Pendrin function in airway epithelia

C Nofziger, S Dossena, S Suzuki, K Izuhara… - Cellular Physiology and …, 2011 - karger.com
The expression and function of the anion exchanger pendrin (SLC26A4) was thought to be
limited mainly to the inner ear, kidney and thyroid. Recent data indicates that pendrin is also …

Effect of known inhibitors of ion transport on pendrin (SLC26A4) activity in a human kidney cell line

E Bernardinelli, R Costa, C Nofziger… - Cellular physiology and …, 2016 - karger.com
Abstract Background/Aims: Pendrin is a Cl-/I-/HCO3-exchanger playing a fundamental role
in controlling blood pressure and airway function, therefore representing an attractive target …

[HTML][HTML] A FRET-based approach for quantitative evaluation of forskolin-induced pendrin trafficking at the plasma membrane in bronchial NCI H292 cells

G Tamma, M Ranieri, S Dossena, A Di Mise… - Cellular physiology and …, 2013 - karger.com
Background: Human pendrin (SLC26A4, PDS) is an integral membrane protein acting as an
electroneutral anion exchanger. Loss of function mutations in pendrin protein cause …