The adenosine A2B receptor is involved in anion secretion in human pancreatic duct Capan-1 epithelial cells

Autor: Ivana Novak, Hiroko Matsuda, Akihiro Inagaki, Mikio Hayashi
Jazyk: angličtina
Předmět:
Male
0301 basic medicine
Adenosine
Physiology
Clinical Biochemistry
Aminopyridines
Cystic Fibrosis Transmembrane Conductance Regulator
Membrane Potentials
chemistry.chemical_compound
0302 clinical medicine
CFTR
Receptor
Adenosine receptor
Purinergic signalling
Cell biology
Female
Ion Channels
Receptors and Transporters

medicine.drug
Anions
medicine.medical_specialty
Guinea Pigs
Biology
Receptor
Adenosine A2B

Cell Line
03 medical and health sciences
Adenosine A1 receptor
Chlorides
Internal medicine
Physiology (medical)
Phenethylamines
medicine
Animals
Humans
Duct
Rats
Wistar

Uridine
Pancreas
Transepithelial potential difference
CGS-21680
Pancreatic Ducts
Cl− channel
Epithelial Cells
Rats
Cl channel
030104 developmental biology
Endocrinology
chemistry
030217 neurology & neurosurgery
Adenosine A2B receptor
Zdroj: Hayashi, M, Inagaki, A, Novak, I & Matsuda, H 2016, ' The adenosine A 2B receptor is involved in anion secretion in human pancreatic duct Capan-1 epithelial cells ', Pfluegers Archiv, vol. 468, no. 7, pp. 1171-1181 . https://doi.org/10.1007/s00424-016-1806-9
Europe PubMed Central
Pflugers Archiv
ISSN: 0031-6768
DOI: 10.1007/s00424-016-1806-9
Popis: Adenosine modulates a wide variety of biological processes via adenosine receptors. In the exocrine pancreas, adenosine regulates transepithelial anion secretion in duct cells and is considered to play a role in acini-to-duct signaling. To identify the functional adenosine receptors and Cl− channels important for anion secretion, we herein performed experiments on Capan-1, a human pancreatic duct cell line, using open-circuit Ussing chamber and gramicidin-perforated patch-clamp techniques. The luminal addition of adenosine increased the negative transepithelial potential difference (Vte) in Capan-1 monolayers with a half-maximal effective concentration value of approximately 10 μM, which corresponded to the value obtained on whole-cell Cl− currents in Capan-1 single cells. The effects of adenosine on Vte, an equivalent short-circuit current (Isc), and whole-cell Cl− currents were inhibited by CFTRinh-172, a cystic fibrosis transmembrane conductance regulator (CFTR) Cl− channel inhibitor. The adenosine A2B receptor agonist, BAY 60-6583, increased Isc and whole-cell Cl− currents through CFTR Cl− channels, whereas the A2A receptor agonist, CGS 21680, had negligible effects. The A2B receptor antagonist, PSB 603, inhibited the response of Isc to adenosine. Immunohistochemical analysis showed that the A2A and A2B receptors colocalized with Ezrin in the luminal membranes of Capan-1 monolayers and in rat pancreatic ducts. Adenosine elicited the whole-cell Cl− currents in guinea pig duct cells. These results demonstrate that luminal adenosine regulates anion secretion by activating CFTR Cl− channels via adenosine A2B receptors on the luminal membranes of Capan-1 cells. The present study endorses that purinergic signaling is important in the regulation of pancreatic secretion.
Databáze: OpenAIRE