PPARγ2 expression in growth plate chondrocytes is regulated by p38 and GSK‐3

• Published in: Journal of cellular and molecular medicine Vol. 14; no. 1‐2; pp. 242 - 256
• Main Authors: Stanton, Lee‐Anne, Li, Jennifer Ruizhe, Beier, Frank
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.01.2010; John Wiley & Sons, Inc
• Subjects: Adipocytes; Apoptosis; Arteriosclerosis; Body fat; Bone cancer; Bones; chondrocyte; Chondrocytes; Chondrogenesis; Collagen (type X); Fatty acids; Gene expression; Growth plate; GSK‐3; Hedgehog protein; Lipid metabolism; Lipids; Metabolism; Morphogenesis; p38; Penicillin; Peptides; Peroxisome proliferator-activated receptors; PPARγ; Protein turnover; Proteins; Signal transduction; Troglitazone; Canada; United States > US
• ISSN: 1582-1838; 1582-4934
• DOI: 10.1111/j.1582-4934.2008.00396.x

Although peroxisome proliferator activated receptor (PPAR)γ remains a critical regulator of preadipocyte differentiation, new roles have been discovered in inflammation, bone morphogenesis, endothelial function, cancer, longevity and atherosclerosis. Despite the demonstration of PPARγ expression in chondrocytes, its role and the pathways affecting its expression and activity in chondrocytes remain largely unknown. We investigated the effects of PPARγ activation on chondrocyte differentiation and its participation in chondrocyte lipid metabolism. PPARγ2 expression is highly regulated during chondrocyte differentiation in vivo and in vitro PPARγ activation with troglitazone resulted in increased Indian hedgehog expression and reduced collagen X expression, confirming previously described roles in the inhibition of differentiation. However, the major effect of PPARγ2 in chondrocytes appears to be on lipid metabolism. During differentiation chondrocytes increase expression of the lipid‐associated metabolizing protein, Lpl, which is accompanied by increased gene expression of PPARγ. PPARγ expression is suppressed by p38 activity, but requires GSK‐3 activity. Furthermore, Lpl expression is regulated by p38 and GSK‐3 signalling. This is the first study demonstrating a relationship between PPARγ2 expression and chondrocyte lipid metabolism and its regulation by p38 and GSK‐3 signalling.