» Articles » PMID: 25074489

Potassium Channels in Pancreatic Duct Epithelial Cells: Their Role, Function and Pathophysiological Relevance

Overview
Journal Pflugers Arch
Specialty Physiology
Date 2014 Jul 31
PMID 25074489
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Pancreatic ductal epithelial cells play a fundamental role in HCO3 (-) secretion, a process which is essential for maintaining the integrity of the pancreas. Although several studies have implicated impaired HCO3 (-) and fluid secretion as a triggering factor in the development of pancreatitis, the mechanism and regulation of HCO3 (-) secretion is still not completely understood. To date, most studies on the ion transporters that orchestrate ductal HCO3 (-) secretion have focussed on the role of Cl(-)/HCO3 (-) exchangers and Cl(-) channels, whereas much less is known about the role of K(+) channels. However, there is growing evidence that many types of K(+) channels are present in ductal cells where they have an essential role in establishing and maintaining the electrochemical driving force for anion secretion. For this reason, strategies that increase K(+) channel function may help to restore impaired HCO3 (-) and fluid secretion, such as in pancreatitis, and therefore provide novel directions for future pancreatic therapy. In this review, our aims are to summarize the types of K(+) channels found in pancreatic ductal cells and to discuss their individual roles in ductal HCO3 (-) secretion. We will also describe how K(+) channels are involved in pathophysiological conditions and discuss how they could act as new molecular targets for the development of therapeutic approaches to treat pancreatic diseases.

Citing Articles

Single-cell analysis of nasal epithelial cell development in domestic pigs.

Wang W, Liu R, Zhong Q, Cao Y, Qi J, Li Y Vet Res. 2024; 55(1):140.

PMID: 39478588 PMC: 11523856. DOI: 10.1186/s13567-024-01403-w.


Synergistic effects of agonists and two-pore-domain potassium channels on secretory responses of human pancreatic duct cells Capan-1.

Sorensen C, Trauzold A, Christensen N, Tawfik D, Szczepanowski M, Novak I Pflugers Arch. 2022; 475(3):361-379.

PMID: 36534232 PMC: 9908661. DOI: 10.1007/s00424-022-02782-9.


BK Channel in the Physiology and in the Cancer of Pancreatic Duct: Impact and Reliability of BK Openers.

Zuccolini P, Gavazzo P, Pusch M Front Pharmacol. 2022; 13:906608.

PMID: 35685628 PMC: 9171006. DOI: 10.3389/fphar.2022.906608.


Ion Channel Signature in Healthy Pancreas and Pancreatic Ductal Adenocarcinoma.

Schnipper J, Dhennin-Duthille I, Ahidouch A, Ouadid-Ahidouch H Front Pharmacol. 2020; 11:568993.

PMID: 33178018 PMC: 7596276. DOI: 10.3389/fphar.2020.568993.


Mouse pancreatic ductal organoid culture as a relevant model to study exocrine pancreatic ion secretion.

Molnar R, Madacsy T, Varga A, Nemeth M, Katona X, Gorog M Lab Invest. 2019; 100(1):84-97.

PMID: 31409889 DOI: 10.1038/s41374-019-0300-3.


References
1.
Joiner W, Basavappa S, Vidyasagar S, Nehrke K, Krishnan S, Binder H . Active K+ secretion through multiple KCa-type channels and regulation by IKCa channels in rat proximal colon. Am J Physiol Gastrointest Liver Physiol. 2003; 285(1):G185-96. DOI: 10.1152/ajpgi.00337.2002. View

2.
Liu Y, Holmgren M, Jurman M, Yellen G . Gated access to the pore of a voltage-dependent K+ channel. Neuron. 1997; 19(1):175-84. DOI: 10.1016/s0896-6273(00)80357-8. View

3.
Shuck M, Piser T, Bock J, Slightom J, Lee K, Bienkowski M . Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3). J Biol Chem. 1997; 272(1):586-93. DOI: 10.1074/jbc.272.1.586. View

4.
Ketchum K, Joiner W, Sellers A, Kaczmarek L, Goldstein S . A new family of outwardly rectifying potassium channel proteins with two pore domains in tandem. Nature. 1995; 376(6542):690-5. DOI: 10.1038/376690a0. View

5.
Kiehn J, Lacerda A, Wible B, Brown A . Molecular physiology and pharmacology of HERG. Single-channel currents and block by dofetilide. Circulation. 1996; 94(10):2572-9. DOI: 10.1161/01.cir.94.10.2572. View