Differentiation Potential of Pancreatic Fibroblastoid Cells/Stellate Cells: Effects of Peroxisome Proliferator-Activated Receptor Gamma Ligands

Author:

Kruse M.-L.1,Hopf-Jensen S.12,Timke C.13,Agricola B.4,Sparmann G.15,Schmid A.67,Sipos B.89,Arlt A.1,Schäfer H.1

Affiliation:

1. Laboratory for Molecular Gastroenterology and Hepatology, Department for General Internal Medicine, University Hospital Schleswig-Holstein, Campus Kiel, Arnold-Heller-Str. 3 (Building 6), 24105 Kiel, Germany

2. Klinik fuer Diagnostische und Interventionelle Radiologie/Neuroradiologie, Diakonissenanstalt zu Flensburg, Knuthstr. 1, 24939 Flensburg, Germany

3. Department of Pediatrics, University Hospital Schleswig-Holstein, Campus Kiel, Arnold-Heller-Str. 3 (Building 9), 24105 Kiel, Germany

4. Institute for Clinical Cytobiology and Cytopathology, University of Marburg, Robert-Koch-Str. 6, 35037 Marburg, Germany

5. Division of Gastroenterology, Department of Internal Medicine, University of Rostock, Ernst-Heydemann-Straße 6, 18057 Rostock, Germany

6. Department for General and Thoracic Surgery, University Hospital Schleswig-Holstein, Campus Kiel, Arnold-Heller-Str. 3 (Building 18), 24105 Kiel, Germany

7. DRK Krankenhaus Moelln-Ratzeburg, Röpersberg 2, 23909 Ratzeburg, Germany

8. Institute for Pathology, University Hospital Schleswig-Holstein, Campus Kiel, Arnold-Heller-Str. 3 (Building 14), 24105 Kiel, Germany

9. Department of General Pathology, University of Tuebingen, Liebermeisterstraße 8, 72076 Tuebingen, Germany

Abstract

Pancreatic stellate cells have been investigated mostly for their activation process, supposed to support the development of pancreatic disease. Few studies have been presented on reversal of the activation process in vitro. Thiazolidinediones (TZDs) have been used as antidiabetics and have now been reported to exert antifibrotic activity. We tested effects of natural and synthetic ligands of peroxisome proliferator-activated receptor gamma (PPARγ) on human pancreatic fibroblastoid cells (hPFCs) in search for specificity of action. Ciglitazone, as a prototype of TZDs, was shown to have reversible growth inhibitory effects on human pancreatic fibroblastoid cells/stellate cells. Cells treated with ciglitazone for three days showed enhanced lipid content and induction of proteins involved in lipid metabolism. Collagen synthesis was reduced in hPFC. Interaction of PPARγwith DNA binding sites upon ligand binding was shown by gel shift analysis. These findings point toward a potential for adipocyte differentiation in human pancreatic fibroblastoid cells.

Funder

Christian-Albrechts-Universität zu Kiel

Publisher

Hindawi Limited

Subject

Cell Biology

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