Peroxisome proliferator ‐ activated receptor γ overexpression inhibits pro‐fibrogenic activities of immortalised rat pancreatic stellate cells

• Published in: Journal of cellular and molecular medicine 2005-07, Vol.9 (3), p.670-682
• Main Authors: Jaster, Robert, Lichte, Philipp, Fitzner, Brit, Brock, Peter, Glass, Änne, Karopka, Thomas, Gierl, Lothar, Koczan, Dirk, Thiesen, Hans‐Jürgen, Sparmann, Gisela, Emmrich, Jörg, Liebe, Stefan
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Cell activation; Cell death; Cell Line; Cell proliferation; Cellular signal transduction; Collagen; DNA microarrays; Extracellular matrix; Fibrinolytic Agents - pharmacology; Fibrosis; Gene expression; Genes; Hepatocytes; Ligands; Lipid metabolism; Overexpression; Pancreas - cytology; Pancreas - drug effects; Pancreatic cancer; pancreatic stellate cells; Pancreatitis; Peroxisome proliferator-activated receptors; peroxisome proliferator‐activated receptor γ; Phenotypes; PPAR gamma - genetics; Rats; Signal transduction; Stellate cells; Tetracycline; Tetracyclines; Thiazolidinediones
• ISSN: 1582-1838; 1582-4934
• DOI: 10.1111/j.1582-4934.2005.tb00497.x

Pancreatic stellate cells (PSCs) play a key role in the development of pancreatic fibrosis, a constant feature of chronic pancreatitis and pancreatic cancer. In response to pro‐fibrogenic mediators, PSCs undergo an activation process that involves proliferation, enhanced production of extracellular matrix proteins and a phenotypic transition towards myofibroblasts. Ligands of the peroxisome proliferator‐activated receptor gamma (PPARγ), such as thiazolidinediones, are potent inhibitors of stellate cell activation and fibrogenesis in pancreas and liver. The effects of PPARγ ligands, however, however, are at least in part mediated through PPARγ‐independent pathways. Here, we have chosen a different approach to study regulatory functions of PPARγ in PSCs. Using immortalised rat PSCs, we have established a model of tetracycline (tet)‐regulated PPARγ over‐expression. Induction of PPARγ expression strongly inhibited proliferation and enhanced the rate of apoptotic cell death. Furthermore, PPARγ‐overexpressing cells synthesised less collagen than controls. To monitor effects of PPARγ on PSC gene expression, we employed Affymetrix microarray technology. Using stringent selection criteria, we identified 21 up‐ and 19 down‐regualated genes in PPARγ‐overexpressing cells. Most of the corresponding gene products are either involved in lipid metabolism, play a role in signal transduction, or are secreted molecules that regulate cell growth and differentition. In conclusion, our data suggest an active role of PPARγ in the induction of a quiescent PSC phenotype. PPARγ‐regulated genes in PSCs may serve as novel targets for the development of antifibrotic therapies.