期刊
BRITISH JOURNAL OF DERMATOLOGY
卷 160, 期 4, 页码 762-770出版社
WILEY
DOI: 10.1111/j.1365-2133.2008.08989.x
关键词
collagen; keloid; peroxisome proliferator-activated receptor-gamma; transforming growth factor-beta 1; wound healing
类别
资金
- National Nature Science Foundation of China [30772260, 30672189]
Background Peroxisome proliferator-activated receptor (PPAR)-gamma agonists are increasingly used in patients with diabetes and some studies have suggested a beneficial effect on organ fibrosis. However their effects on dermal fibrosis in keloids are unknown. Objective To investigate the effect of the PPAR-c agonist troglitazone on transforming growth factor (TGF)-beta 1-induced collagen type I expression in keloid fibroblasts. Methods Keloid fibroblasts were cultured and exposed to different concentrations of troglitazone in the presence of TGF-beta 1. The mRNA expression of PPAR-c was determined by semiquantitative reverse transcriptase -polymerase chain reaction. The protein of PPAR-gamma, Smad2, Smad3, phoshpo-Smad2/3 and collagen type I was determined by Western blotting and collagen synthesis was evaluated by measuring H-3-proline incorporation. The effect of troglitazone on cell viability was evaluated by the colorimetric conversion of 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide. Results PPAR-gamma was expressed at a moderate level in keloid fibroblasts. Troglitazone depressed TGF-beta 1-stimulated collagen type I expression and collagen synthesis in keloid fibroblasts in a concentration-dependent manner. Moreover, troglitazone inhibited expression and phosphorylation of TGF-beta 1-induced Smad2 / 3. Cell viability was unaffected. These inhibitory effects of troglitazone were reversed by the PPAR-gamma-specific antagonist GW9662. Conclusions Our data suggest that PPAR-gamma is present in keloid fibroblasts and PPAR-gamma activation inhibits TGF-beta 1-induced collagen type I expression at least in part by decreasing collagen synthesis. PPAR-gamma may be a promising therapeutic target for keloids.
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