Histochemistry and Cell Biology

, Volume 115, Issue 2, pp 131–145

Guanylin in the human pancreas: a novel luminocrine regulatory pathway of electrolyte secretion via cGMP and CFTR in the ductal system

Authors

  • Hasan Kulaksiz
    • Department of Molecular Cell Biology, Institute of Anatomy and Cell Biology, Philipps University, Robert-Koch-Strasse 6, 35033 Marburg, Germany
  • Andreas Schmid
    • Department of Physiology II, University of Saarland, Homburg/Saar, Germany
  • Matthias Hönscheid
    • Department of Physiology II, University of Saarland, Homburg/Saar, Germany
  • Rolf Eissele
    • Department of Gastroenterology and Endocrinology, Philipps University, Marburg, Germany
  • Jürgen Klempnauer
    • Clinics for Visceral and Transplantation Surgery, Hannover Medical School, Hannover, Germany
  • Yalcin Cetin
    • Department of Molecular Cell Biology, Institute of Anatomy and Cell Biology, Philipps University, Robert-Koch-Strasse 6, 35033 Marburg, Germany
Original Paper

DOI: 10.1007/s004180000244

Cite this article as:
Kulaksiz, H., Schmid, A., Hönscheid, M. et al. Histochem Cell Biol (2001) 115: 131. doi:10.1007/s004180000244

Abstract.

Cystic fibrosis transmembrane conductance regulator (CFTR) is a channel and regulator protein that is crucially involved in transepithelial ion transport. In the exocrine pancreas, the CFTR-mediated secretion of an electrolyte-rich fluid is a major but as yet incompletely understood function. We show here that the peptide guanylin is a specific activator of CFTR function in the human pancreas implicating regulation of pancreatic electrolyte secretion. Guanylin and its affiliated signaling and effector proteins including guanylate cyclase C, cGMP-dependent protein kinase II, CFTR, and the epithelial \(Cl^-/HCO_3^-\) exchanger, anion exchanger 2, are highly expressed in the human pancreas. Guanylin is localized specifically to the typical centroacinar cells and proximal duct cells which, based on its additional presence in the pancreatic juice, is obviously released luminally into the pancreatic ducts. The guanylin receptor and the respective functional downstream proteins are all confined to the apical membrane of the duct cells implicating an as yet unknown route of luminal regulatory pathway of electrolyte secretion in the ductal system. Functional studies in two different human pancreatic duct cell lines expressing the CFTR Cl channel that is functionally intact in CAPAN-1 cells but defective (ΔF508) in CFPAC-1 cells clearly identify guanylin as a specific regulator of pancreatic CFTR channel function. Whole-cell patch-clamp recordings in CAPAN-1 cells revealed that forskolin induces an increase of Cl conductance mediated by cAMP. In contrast, guanylin increased Cl conductance in the same cells via cGMP but not cAMP; the respective membrane current was largely blockable by the sulfonylurea glibenclamide. In CFPAC-1 cells, however, neither guanylin nor forskolin produced a current activation. Based on the present findings we conclude that guanylin is an intrinsic pancreatic regulator of Cl current activation in pancreatic duct cells via cGMP and CFTR. Remarkably, in the pancreas guanylin may exert its function through an intriguing luminocrine mode via the pancreatic juice.

Pancreas Regulatory peptides Guanylate cyclase Protein kinase Anion exchanger

Copyright information

© Springer-Verlag 2001