Adenosine receptors, cystic fibrosis, and airway hydration

G Com, JP Clancy - Adenosine Receptors in Health and Disease, 2009 - Springer
Adenosine (Ado) regulates diverse cellular functions in the lung through its local production,
release, metabolism, and subsequent stimulation of G-protein-coupled P1 purinergic …

Relationships between cystic fibrosis transmembrane conductance regulator, extracellular nucleotides and cystic fibrosis

B Marcet, JM Boeynaems - Pharmacology & therapeutics, 2006 - Elsevier
Cystic fibrosis (CF) is one of the most common lethal autosomal recessive genetic diseases
in the Caucasian population, with a frequency of about 1 in 3000 livebirths. CF is due to a …

[HTML][HTML] Attenuated amiloride-sensitive current and augmented calcium-activated chloride current in marsh rice rat (Oryzomys palustris) airways

SP Kuan, YSJ Liao, KM Davis, JG Messer, J Zubcevic… - Iscience, 2019 - cell.com
Prolonged heat and sea salt aerosols pose a challenge for the mammalian airway, placing
the protective airway surface liquid (ASL) at risk for desiccation. Thus, mammals inhabiting …

KCa3. 1 differentially regulates trachea and bronchi epithelial gene expression in a chronic-asthma mouse model

AR Philp, F Miranda, A Gianotti… - Physiological …, 2022 - journals.physiology.org
Ion channels are potentially exploitable as pharmacological targets to treat asthma. This
study evaluated the role of KCa3. 1 channels, encoded by Kcnn4, in regulating the gene …

Haemolysin produced by Vibrio mimicus activates two Cl secretory pathways in cultured intestinal‐like Caco‐2 cells

A Takahashi, S Miyoshi, N Takata… - Cellular …, 2007 - Wiley Online Library
Haemolysin (VMH) is a virulent factor produced by Vibrio mimicus, a human pathogen that
causes diarrhoea. As intestinal epithelial cells are the primary targets of haemolysin, we …

Gene therapy for cystic fibrosis airway disease-is clinical success imminent?

DS Anson, GJ Smith, DW Parsons - Current gene therapy, 2006 - ingentaconnect.com
Cystic fibrosis (CF) was one of the first inherited disorders for which gene therapy was
seriously considered as a realistic option for treatment, and as such, it has long provided a …

Targeted therapy for cystic fibrosis: cystic fibrosis transmembrane conductance regulator mutation-specific pharmacologic strategies

RC Rubenstein - Molecular Diagnosis & Therapy, 2006 - Springer
Cystic fibrosis (CF) results from the absence or dysfunction of a single protein, the CF
transmembrane conductance regulator (CFTR). CFTR plays a critical role in the regulation of …

CFTR regulation of aquaporin-mediated water transport

DF Carrageta, RL Bernardino, MG Alves… - Vitamins and …, 2020 - Elsevier
The cystic fibrosis transmembrane conductance regulator (CFTR) is an anion channel
responsible for the direct transport of bicarbonate and chloride. CFTR-dependent ionic …

Infections in chronic lung diseases

GI Parameswaran, TF Murphy - Infectious disease clinics of North America, 2007 - Elsevier
Chronic lung diseases are prevalent worldwide and cause significant mortality and suffering.
This article discusses infections that occur in three chronic lung diseases: chronic …

Apical localization of ITPK1 enhances its ability to be a modifier gene product in a murine tracheal cell model of cystic fibrosis

L Yang, J Reece, SE Gabriel… - Journal of cell …, 2006 - journals.biologists.com
A new aspect of research into the pathogenesis of cystic fibrosis (CF) is a genetics-based
search formodifier genes' that may affect the severity of CF lung disease. Using an …