Molecular characterisation of pancreatic zymogen granule ion channel and regulator proteins involved in exocytosis.
10.3346/jkms.2000.15.S.S51
- Author:
Frank THEVENOD
1
;
Matthias BRAUN
;
Eleni ROUSSA
;
Catherine M FULLER
Author Information
1. Department of Physiology, Universitat des Saarlandes, Homburg/Saar, Germany. frank.thevenod@man.ac.uk
- Publication Type:Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S. ; Review
- Keywords:
Secretion;
Acinar Cells;
Anion Channels;
mdr1 P-Glycoprotein;
Sulfonylurea Receptor
- MeSH:
Animal;
Chloride Channels/metabolism*;
Chloride Channels/genetics;
Exocytosis/physiology*;
Gene Expression/physiology;
P-Glycoprotein/metabolism;
P-Glycoprotein/genetics;
Pancreas/secretion*;
Pancreas/cytology;
Potassium Channels/metabolism*;
Potassium Channels/genetics;
Secretory Vesicles/secretion;
Secretory Vesicles/metabolism*;
Support, U.S. Gov't, P.H.S.
- From:Journal of Korean Medical Science
2000;15(Suppl):S51-S52
- CountryRepublic of Korea
- Language:English
-
Abstract:
In pancreatic acinar cells Ca(2+)-dependent secretagogues promote the fusion of zymogen granules (ZG) with the apical plasma membrane (PM) and exocytosis of digestive enzymes. In addition to exocytotic fusion complexes between SNARE proteins in the ZG membrane (ZGM) and the apical PM, enzyme secretion elicited by Ca(2+)-dependent secretagogues requires cytosolic Cl and K+ and is inhibited by blockers of Cl- and K+-channels. We have identified a Cl-conductance activated by ATP, and a K+-conductance (with properties similar to ATP-sensitive K+-channels), regulated by the granule matrix protein Zg-16p in the ZGM. Both conductances are inversely regulated by a 65-kD mdr1 gene product. We have also identified a novel Ca(2+)-activated anion conductance in ZGM, the Ca(2+)-sensitivity of which increases 50-fold when Cl is replaced by 1. This conductance is blocked by micromolar H2-DIDS or DTT, reminiscent of a family of epithelial Ca(2+)-activated Cl -channels (CaCC). Expression of a CaCC in exocrine pancreas has been confirmed by RT-PCR analysis, and by immunoblotting and immunogold labeling of ZG membranes. These data suggest that ion channels in the ZGM are essential elements in pancreatic exocytosis.
